Mary Norton, MD

Title(s)Professor, Ob/Gyn, Reproductive Sciences
SchoolSchool of Medicine
Address490 Illinois Street, #102S
San Francisco CA 94158
Phone415-353-7865
ORCID ORCID Icon0000-0002-5967-1701 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of California, San FranciscoPost-Doc Fellow/Scholar1991 Medicine (Obstetrics & Gynecology)
    University of California, San FranciscoResidency

    Collapse Overview 
    Collapse Overview
    Mary E. Norton is a perinatologist and clinical geneticist at UCSF Medical Center's Prenatal Diagnostic Center. She primarily cares for pregnant women who have a fetus with a birth defect or genetic disorder or are at risk for such a condition. Norton performs obstetrical ultrasounds, counsels women in whom ultrasound detects a problem with the fetus and performs such prenatal tests as amniocentesis and chorionic villus sampling. She also interprets complex genetic tests, especially when abnormalities are found. Her areas of interest in research include applying new genetic tests to prenatal diagnosis and fetal disease, as well as patient decision-making around genetic testing and obstetrical ultrasound. She is also the chair of the obstetrics, gynecology and reproductive sciences at UCSF.

    Norton earned her undergraduate degree at the University of Washington in 1982. She completed her internship and residency in Obstetrics and Gynecology at Tuft University in Boston in 1990. She completed a fellowship in Maternal Fetal Medicine and Clinical Genetics at UCSF in 1993. After several years at Brigham and Women's Hospital and Harvard Medical School, she returned to San Francisco where she joined UCSF Medical Center in 1998. She is a professor of obstetrics, gynecology and reproductive sciences at UCSF.

    Collapse Research 
    Collapse Research Activities and Funding
    Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
    NIH U01HG009599Aug 4, 2017 - May 31, 2022
    Role: Co-Principal Investigator
    Maternal Fetal Units Network: Stanford University and Santa Clara Valley
    NIH U10HD068268Apr 7, 2011 - Mar 30, 2016
    Role: Co-Principal Investigator
    Women's Reproductive Health Research
    NIH K12HD001262Sep 30, 1998 - Jun 30, 2025
    Role: Principal Investigator

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    Collapse Clinical Trials

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Trends in Reporting of Nuchal Translucency Measurements After the Clinical Introduction of Cell-Free DNA Screening. Obstet Gynecol. 2024 Apr 11. Wen T, Thornburg LL, Norton ME, Platt LD, Dugoff L, Hesson A, Spitz JL, Toland G, Bromley B, Nuchal Translucency Quality Review Program of the Perinatal Quality Foundation. PMID: 38603781.
      View in: PubMed   Mentions:
    2. The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model. Am J Obstet Gynecol. 2024 Mar 01. Khalil A, Bellesia G, Norton ME, Jacobsson B, Haeri S, Egbert M, Malone FD, Wapner RJ, Roman A, Faro R, Madankumar R, Strong N, Silver RM, Vohra N, Hyett J, Macpherson C, Prigmore B, Ahmed E, Demko Z, Ortiz JB, Souter V, Dar P. PMID: 38432413.
      View in: PubMed   Mentions:    Fields:    
    3. Achievement of Target Gain Larger than Unity in an Inertial Fusion Experiment. Phys Rev Lett. 2024 Feb 09; 132(6):065102. Abu-Shawareb H, Acree R, Adams P, Adams J, Addis B, Aden R, Adrian P, Afeyan BB, Aggleton M, Aghaian L, Aguirre A, Aikens D, Akre J, Albert F, Albrecht M, Albright BJ, Albritton J, Alcala J, Alday C, Alessi DA, Alexander N, Alfonso J, Alfonso N, Alger E, Ali SJ, Ali ZA, Allen A, Alley WE, Amala P, Amendt PA, Amick P, Ammula S, Amorin C, Ampleford DJ, Anderson RW, Anklam T, Antipa N, Appelbe B, Aracne-Ruddle C, Araya E, Archuleta TN, Arend M, Arnold P, Arnold T, Arsenlis A, Asay J, Atherton LJ, Atkinson D, Atkinson R, Auerbach JM, Austin B, Auyang L, Awwal AAS, Aybar N, Ayers J, Ayers S, Ayers T, Azevedo S, Bachmann B, Back CA, Bae J, Bailey DS, Bailey J, Baisden T, Baker KL, Baldis H, Barber D, Barberis M, Barker D, Barnes A, Barnes CW, Barrios MA, Barty C, Bass I, Batha SH, Baxamusa SH, Bazan G, Beagle JK, Beale R, Beck BR, Beck JB, Bedzyk M, Beeler RG, Beeler RG, Behrendt W, Belk L, Bell P, Belyaev M, Benage JF, Bennett G, Benedetti LR, Benedict LX, Berger RL, Bernat T, Bernstein LA, Berry B, Bertolini L, Besenbruch G, Betcher J, Bettenhausen R, Betti R, Bezzerides B, Bhandarkar SD, Bickel R, Biener J, Biesiada T, Bigelow K, Bigelow-Granillo J, Bigman V, Bionta RM, Birge NW, Bitter M, Black AC, Bleile R, Bleuel DL, Bliss E, Bliss E, Blue B, Boehly T, Boehm K, Boley CD, Bonanno R, Bond EJ, Bond T, Bonino MJ, Borden M, Bourgade JL, Bousquet J, Bowers J, Bowers M, Boyd R, Boyle D, Bozek A, Bradley DK, Bradley KS, Bradley PA, Bradley L, Brannon L, Brantley PS, Braun D, Braun T, Brienza-Larsen K, Briggs R, Briggs TM, Britten J, Brooks ED, Browning D, Bruhn MW, Brunner TA, Bruns H, Brunton G, Bryant B, Buczek T, Bude J, Buitano L, Burkhart S, Burmark J, Burnham A, Burr R, Busby LE, Butlin B, Cabeltis R, Cable M, Cabot WH, Cagadas B, Caggiano J, Cahayag R, Caldwell SE, Calkins S, Callahan DA, Calleja-Aguirre J, Camara L, Camp D, Campbell EM, Campbell JH, Carey B, Carey R, Carlisle K, Carlson L, Carman L, Carmichael J, Carpenter A, Carr C, Carrera JA, Casavant D, Casey A, Casey DT, Castillo A, Castillo E, Castor JI, Castro C, Caughey W, Cavitt R, Celeste J, Celliers PM, Cerjan C, Chandler G, Chang B, Chang C, Chang J, Chang L, Chapman R, Chapman TD, Chase L, Chen H, Chen H, Chen K, Chen LY, Cheng B, Chittenden J, Choate C, Chou J, Chrien RE, Chrisp M, Christensen K, Christensen M, Christiansen NS, Christopherson AR, Chung M, Church JA, Clark A, Clark DS, Clark K, Clark R, Claus L, Cline B, Cline JA, Cobble JA, Cochrane K, Cohen B, Cohen S, Collette MR, Collins GW, Collins LA, Collins TJB, Conder A, Conrad B, Conyers M, Cook AW, Cook D, Cook R, Cooley JC, Cooper G, Cope T, Copeland SR, Coppari F, Cortez J, Cox J, Crandall DH, Crane J, Craxton RS, Cray M, Crilly A, Crippen JW, Cross D, Cuneo M, Cuotts G, Czajka CE, Czechowicz D, Daly T, Danforth P, Danly C, Darbee R, Darlington B, Datte P, Dauffy L, Davalos G, Davidovits S, Davis P, Davis J, Dawson S, Day RD, Day TH, Dayton M, Deck C, Decker C, Deeney C, DeFriend KA, Deis G, Delamater ND, Delettrez JA, Demaret R, Demos S, Dempsey SM, Desjardin R, Desjardins T, Desjarlais MP, Dewald EL, DeYoreo J, Diaz S, Dimonte G, Dittrich TR, Divol L, Dixit SN, Dixon J, Do A, Dodd ES, Dolan D, Donovan A, Donovan M, Döppner T, Dorrer C, Dorsano N, Douglas MR, Dow D, Downie J, Downing E, Dozieres M, Draggoo V, Drake D, Drake RP, Drake T, Dreifuerst G, Drury O, DuBois DF, DuBois PF, Dunham G, Durocher M, Dylla-Spears R, Dymoke-Bradshaw AKL, Dzenitis B, Ebbers C, Eckart M, Eddinger S, Eder D, Edgell D, Edwards MJ, Efthimion P, Eggert JH, Ehrlich B, Ehrmann P, Elhadj S, Ellerbee C, Elliott NS, Ellison CL, Elsner F, Emerich M, Engelhorn K, England T, English E, Epperson P, Epstein R, Erbert G, Erickson MA, Erskine DJ, Erlandson A, Espinosa RJ, Estes C, Estabrook KG, Evans S, Fabyan A, Fair J, Fallejo R, Farmer N, et al. PMID: 38394591.
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    4. Genetic ancestry and diagnostic yield of exome sequencing in a diverse population. NPJ Genom Med. 2024 Jan 03; 9(1):1. Mavura Y, Sahin-Hodoglugil N, Hodoglugil U, Kvale M, Martin PM, Van Ziffle J, Devine WP, Ackerman SL, Koenig BA, Kwok PY, Norton ME, Slavotinek A, Risch N. PMID: 38172272; PMCID: PMC10764913.
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    5. Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study. Prenat Diagn. 2023 12; 43(13):1574-1580. Martin K, Norton ME, MacPherson C, Demko Z, Egbert M, Haeri S, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Silver R, Vohra N, Hyett J, Kao C, Hakonarson H, Jacobson B, Dar P. PMID: 38066724.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis. Prenat Diagn. 2024 Apr; 44(4):422-431. Blayney GV, Laffan E, Jacob PA, Baptiste CD, Gabriel H, Sparks TN, Yaron Y, Norton ME, Diderich K, Wang Y, Chong K, Chitayat D, Saini N, Aggarwal S, Pauta M, Borrell A, Gilmore K, Chandler NJ, Allen S, Vora N, Noor A, Monaghan C, Kilby MD, Wapner RJ, Chitty LS, Mone F. PMID: 38054560.
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    7. Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 Oct 23; 8(1):34. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37872195; PMCID: PMC10593851.
      View in: PubMed   Mentions:
    8. Corrigendum to 'Prenatal Exome and Genome Sequencing for Fetal Structural Abnormalities': [American Journal of Obstetrics and Gynecology 228 (2023) 140-149]. Am J Obstet Gynecol. 2023 Dec; 229(6):709. Vora NL, Norton ME. PMID: 37816656.
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    9. Perinatal Outcomes Associated With Management of Stage 1 Hypertension. Obstet Gynecol. 2023 Dec 01; 142(6):1395-1404. Bailey EJ, Tita ATN, Leach J, Boggess K, Dugoff L, Sibai B, Lawrence K, Hughes BL, Bell J, Aagaard K, Edwards RK, Gibson K, Haas DM, Plante L, Metz TD, Casey BM, Esplin S, Longo S, Hoffman M, Saade GR, Foroutan J, Tuuli MG, Owens MY, Simhan HN, Frey HA, Rosen T, Palatnik A, Baker S, August P, Reddy UM, Kinzler W, Su EJ, Krishna I, Nguyen N, Norton ME, Skupski D, El-Sayed YY, Ogunyemi D, Galis ZS, Harper L, Ambalavanan N, Oparil S, Kuo HC, Szychowski JM, Hoppe K. PMID: 37769314; PMCID: PMC10840706.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US. Prenat Diagn. 2023 10; 43(11):1394-1405. Sahin-Hodoglugil NN, Lianoglou BR, Ackerman S, Sparks TN, Norton ME. PMID: 37752660; PMCID: PMC10846391.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age. Am J Obstet Gynecol. 2024 Mar; 230(3):368.e1-368.e12. Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kazmierczak A, Vermeesch JR, Devriendt K, Busa T, Sigaudy S, Vigneswaran T, Simpson JM, Dungan J, Gotteiner N, Gloning KP, Digilio MC, Unolt M, Putotto C, Marino B, Repetto G, Fadic M, Garcia-Minaur S, Achón Buil A, Thomas MA, Fruitman D, Beecroft T, Hui PW, Oskarsdottir S, Bradshaw R, Criebaum A, Norton ME, Lee T, Geiger M, Dunnington L, Isaac J, Wilkins-Haug L, Hunter L, Izzi C, Toscano M, Ghi T, McGlynn J, Romana Grati F, Emanuel BS, Gaiser K, Gaynor JW, Goldmuntz E, McGinn DE, Schindewolf E, Tran O, Zackai EH, Yan Q, Bassett AS, Wapner R, McDonald-McGinn DM. PMID: 37717890.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    12. The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction. Prenat Diagn. 2024 02; 44(2):196-204. Brar BK, Blakemore K, Hertenstein C, Miller JL, Miller KA, Shamseldin H, Maddirevula S, Hays T, Lianoglou B, Dukhovny S, Baker LA, Sparks TN, Wapner R, Alkuraya FS, Norton ME, Jelin AC, Fetal Sequencing Consortium. PMID: 37594370.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    13. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. Am J Hum Genet. 2023 09 07; 110(9):1454-1469. Lowther C, Valkanas E, Giordano JL, Wang HZ, Currall BB, O'Keefe K, Pierce-Hoffman E, Kurtas NE, Whelan CW, Hao SP, Weisburd B, Jalili V, Fu J, Wong I, Collins RL, Zhao X, Austin-Tse CA, Evangelista E, Lemire G, Aggarwal VS, Lucente D, Gauthier LD, Tolonen C, Sahakian N, Stevens C, An JY, Dong S, Norton ME, MacKenzie TC, Devlin B, Gilmore K, Powell BC, Brandt A, Vetrini F, DiVito M, Sanders SJ, MacArthur DG, Hodge JC, O'Donnell-Luria A, Rehm HL, Vora NL, Levy B, Brand H, Wapner RJ, Talkowski ME. PMID: 37595579; PMCID: PMC10502737.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    14. Parent-Reported Clinical Utility of Pediatric Genomic Sequencing. Pediatrics. 2023 08 01; 152(2). Smith HS, Ferket BS, Gelb BD, Hindorff L, Ferar KD, Norton ME, Sahin-Hodoglugil N, Slavotinek A, Lich KH, Berg JS, Russell HV. PMID: 37470118; PMCID: PMC10812387.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    15. Spectrum of Fetal Intraparenchymal Hemorrhage in COL4A1/A2-Related Disorders. Pediatr Neurol. 2023 10; 147:63-67. George E, Vassar R, Mogga A, Li Y, Norton ME, Gano D, Glenn OA. PMID: 37562171.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    16. Cell-free DNA Screening for Aneuploidy. Clin Obstet Gynecol. 2023 09 01; 66(3):557-567. Norton ME. PMID: 37650668.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    17. Society for Maternal-Fetal Medicine response to Cuneo et al. Am J Obstet Gynecol. 2023 Oct; 229(4):364-365. Society for Maternal-Fetal Medicine (SMFM), Osmundson SS, Grobman W, Silver R, Craigo S, Porter F, Norton ME, Louis J, Kuller JA, SMFM Publications Committee. Electronic address: pubs@smfm.org. PMID: 37453909.
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    18. Breastfeeding initiation and duration among people with mild chronic hypertension: a secondary analysis of the Chronic Hypertension and Pregnancy trial. Am J Obstet Gynecol MFM. 2023 09; 5(9):101086. Goulding AN, Antoniewicz L, Leach JM, Boggess K, Dugoff L, Sibai B, Lawrence K, Hughes BL, Bell J, Edwards RK, Gibson K, Haas DM, Plante L, Metz TD, Casey B, Esplin S, Longo S, Hoffman M, Saade GR, Hoppe KK, Foroutan J, Tuuli M, Owens MY, Simhan HN, Frey H, Rosen T, Palatnik A, Baker S, Reddy UM, Kinzler W, Su E, Krishna I, Nguyen N, Norton ME, Skupski D, El-Sayed YY, Ogunyemi D, Harper LM, Ambalavanan N, Oparil S, Szychowski JM, Tita AT, Chronic Hypertension and Pregnancy Trial Consortium. PMID: 37437694; PMCID: PMC10528420.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 May 26; 8(1):10. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37236975; PMCID: PMC10220040.
      View in: PubMed   Mentions: 6  
    20. Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry. medRxiv. 2023 May 24. Mavura Y, Sahin-Hodoglugil N, Hodoglugil U, Kvale M, Martin PM, Van Ziffle J, Devine WP, Ackerman SL, Koenig BA, Kwok PY, Norton ME, Slavotinek A, Risch N. PMID: 37293051; PMCID: PMC10246153.
      View in: PubMed   Mentions:
    21. Performance of prenatal cfDNA screening for sex chromosomes. Genet Med. 2023 08; 25(8):100879. Martin K, Dar P, MacPherson C, Egbert M, Demko Z, Parmar S, Hashimoto K, Haeri S, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Silver RM, Vohra N, Hyett J, Rabinowitz M, Kao C, Hakonarson H, Jacobsson B, Norton ME. PMID: 37154148.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    22. Nonreportable cell free DNA results in high-risk vs low-risk patients. Am J Obstet Gynecol. 2023 Oct; 229(4):475-476. Norton ME, MacPherson C, Dar P. PMID: 37120052.
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    23. Noninvasive prenatal screening and maternal malignancy: role of imaging. Abdom Radiol (NY). 2023 05; 48(5):1590-1598. Jha P, Lenaerts L, Vermeesch J, Norton M, Amant F, Glanc P, Poder L. PMID: 37095202.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    24. Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening results. Am J Obstet Gynecol. 2023 09; 229(3):300.e1-300.e9. Norton ME, MacPherson C, Demko Z, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Haeri S, Silver R, Vohra N, Hyett J, Martin K, Rabinowitz M, Jacobsson B, Dar P. PMID: 36965866.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    25. The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry. Blood Adv. 2023 01 24; 7(2):269-279. Schwab ME, Lianoglou BR, Gano D, Gonzalez Velez J, Allen IE, Arvon R, Baschat A, Bianchi DW, Bitanga M, Bourguignon A, Brown RN, Chen B, Chien M, Davis-Nelson S, de Laat MWM, Ekwattanakit S, Gollin Y, Hirata G, Jelin A, Jolley J, Meyer P, Miller J, Norton ME, Ogasawara KK, Panchalee T, Schindewolf E, Shaw SW, Stumbaugh T, Thompson AA, Towner D, Tsai PS, Viprakasit V, Volanakis E, Zhang L, Vichinsky E, MacKenzie TC. PMID: 36306387; PMCID: PMC9860434.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenat Diagn. 2023 02; 43(2):133-143. Shear MA, Swanson K, Garg R, Jelin AC, Boscardin J, Norton ME, Sparks TN. PMID: 36588186; PMCID: PMC10268789.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    27. Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes (Basel). 2023 01 06; 14(1). Schneider H, Hadj-Rabia S, Faschingbauer F, Bodemer C, Grange DK, Norton ME, Cavalli R, Tadini G, Stepan H, Clarke A, Guillén-Navarro E, Maier-Wohlfart S, Bouroubi A, Porte F. PMID: 36672894; PMCID: PMC9858920.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCTClinical Trials
    28. Understanding Preterm Birth in Pregnancies Complicated by Nonimmune Hydrops Fetalis. Am J Perinatol. 2023 07; 40(9):917-922. Swanson K, Norton ME, Downum SL, Gonzalez-Velez JM, Sparks TN. PMID: 36603834; PMCID: PMC10330491.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    29. Evaluating Expanded Noninvasive Prenatal Screening. Obstet Gynecol. 2022 Dec 01; 140(6):1078-1079. Dar P, Norton M. PMID: 36441933.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    30. Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenat Diagn. 2022 12; 42(13):1686-1693. Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC, Fetal Sequencing Consortium. PMID: 36403095; PMCID: PMC9805891.
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    31. ISPD 2022 debate-When offering a first trimester ultrasound at 11 + 0 to 13 + 6 weeks, a detailed review of fetal anatomy should be included. Prenat Diagn. 2023 04; 43(4):421-427. Hui L, Johnson JA, Norton ME. PMID: 36289589.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. Circulating Cell-free DNA and Screening for Trisomies. N Engl J Med. 2022 10 06; 387(14):1322-1324. Norton ME. PMID: 36170494.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    33. Curriculum and Competency Assessment Program for Training Maternal-Fetal Medicine Fellows in the Performance of the Detailed Obstetric Ultrasound Examination. J Ultrasound Med. 2022 12; 41(12):2925-2932. Stone J, Abu-Rustum RS, Bromley B, Fuchs KM, Anton T, Cooper T, Minton KK, Dashe J, Lee W, Platt LD, Porche LM, Norton ME, Benacerraf BR, Abuhamad AZ. PMID: 36073175.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    34. Curriculum and competency assessment program for training maternal-fetal medicine fellows in the performance of the detailed obstetric ultrasound examination: A consensus report. Am J Obstet Gynecol. 2023 02; 228(2):B2-B9. Stone J, Abu-Rustum RS, Bromley B, Fuchs KM, Anton T, Cooper T, Minton KK, Dashe J, Lee W, Platt LD, Porche LM, Norton ME, Benacerraf BR, Abuhamad AZ. PMID: 36087741.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    35. Society for Maternal-Fetal Medicine Consult Series #64: Systemic lupus erythematosus in pregnancy. Am J Obstet Gynecol. 2023 03; 228(3):B41-B60. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Silver R, Craigo S, Porter F, Osmundson SS, Kuller JA, Norton ME. PMID: 36084704.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    36. Prenatal exome and genome sequencing for fetal structural abnormalities. Am J Obstet Gynecol. 2023 02; 228(2):140-149. Vora NL, Norton ME. PMID: 36027950; PMCID: PMC9877148.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    37. Universal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing for Obstetric Inpatient Units Across the United States. Clin Infect Dis. 2022 08 24; 75(1):e322-e328. Gilner J, Kansal N, Biggio JR, Delaney S, Grotegut CA, Hardy E, Hirshberg A, Kachikis A, LaCourse SM, Martin J, Metz TD, Miller ES, Norton ME, Sinkey R, Sobhani NC, Son SL, Srinivas S, Tita A, Werner EF, Hughes BL. PMID: 34791093; PMCID: PMC8689996.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    38. Cost-Effectiveness of Exome Sequencing versus Targeted Gene Panels for Prenatal Diagnosis of Fetal Effusions and Non-Immune Hydrops Fetalis. Am J Obstet Gynecol MFM. 2022 11; 4(6):100724. Avram CM, Caughey AB, Norton ME, Sparks TN. PMID: 35995366; PMCID: PMC9938838.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    39. Lawson Criterion for Ignition Exceeded in an Inertial Fusion Experiment. Phys Rev Lett. 2022 Aug 12; 129(7):075001. Abu-Shawareb H, Acree R, Adams P, Adams J, Addis B, Aden R, Adrian P, Afeyan BB, Aggleton M, Aghaian L, Aguirre A, Aikens D, Akre J, Albert F, Albrecht M, Albright BJ, Albritton J, Alcala J, Alday C, Alessi DA, Alexander N, Alfonso J, Alfonso N, Alger E, Ali SJ, Ali ZA, Alley WE, Amala P, Amendt PA, Amick P, Ammula S, Amorin C, Ampleford DJ, Anderson RW, Anklam T, Antipa N, Appelbe B, Aracne-Ruddle C, Araya E, Arend M, Arnold P, Arnold T, Asay J, Atherton LJ, Atkinson D, Atkinson R, Auerbach JM, Austin B, Auyang L, Awwal AS, Ayers J, Ayers S, Ayers T, Azevedo S, Bachmann B, Back CA, Bae J, Bailey DS, Bailey J, Baisden T, Baker KL, Baldis H, Barber D, Barberis M, Barker D, Barnes A, Barnes CW, Barrios MA, Barty C, Bass I, Batha SH, Baxamusa SH, Bazan G, Beagle JK, Beale R, Beck BR, Beck JB, Bedzyk M, Beeler RG, Beeler RG, Behrendt W, Belk L, Bell P, Belyaev M, Benage JF, Bennett G, Benedetti LR, Benedict LX, Berger R, Bernat T, Bernstein LA, Berry B, Bertolini L, Besenbruch G, Betcher J, Bettenhausen R, Betti R, Bezzerides B, Bhandarkar SD, Bickel R, Biener J, Biesiada T, Bigelow K, Bigelow-Granillo J, Bigman V, Bionta RM, Birge NW, Bitter M, Black AC, Bleile R, Bleuel DL, Bliss E, Bliss E, Blue B, Boehly T, Boehm K, Boley CD, Bonanno R, Bond EJ, Bond T, Bonino MJ, Borden M, Bourgade JL, Bousquet J, Bowers J, Bowers M, Boyd R, Bozek A, Bradley DK, Bradley KS, Bradley PA, Bradley L, Brannon L, Brantley PS, Braun D, Braun T, Brienza-Larsen K, Briggs TM, Britten J, Brooks ED, Browning D, Bruhn MW, Brunner TA, Bruns H, Brunton G, Bryant B, Buczek T, Bude J, Buitano L, Burkhart S, Burmark J, Burnham A, Burr R, Busby LE, Butlin B, Cabeltis R, Cable M, Cabot WH, Cagadas B, Caggiano J, Cahayag R, Caldwell SE, Calkins S, Callahan DA, Calleja-Aguirre J, Camara L, Camp D, Campbell EM, Campbell JH, Carey B, Carey R, Carlisle K, Carlson L, Carman L, Carmichael J, Carpenter A, Carr C, Carrera JA, Casavant D, Casey A, Casey DT, Castillo A, Castillo E, Castor JI, Castro C, Caughey W, Cavitt R, Celeste J, Celliers PM, Cerjan C, Chandler G, Chang B, Chang C, Chang J, Chang L, Chapman R, Chapman T, Chase L, Chen H, Chen H, Chen K, Chen LY, Cheng B, Chittenden J, Choate C, Chou J, Chrien RE, Chrisp M, Christensen K, Christensen M, Christopherson AR, Chung M, Church JA, Clark A, Clark DS, Clark K, Clark R, Claus L, Cline B, Cline JA, Cobble JA, Cochrane K, Cohen B, Cohen S, Collette MR, Collins G, Collins LA, Collins TJB, Conder A, Conrad B, Conyers M, Cook AW, Cook D, Cook R, Cooley JC, Cooper G, Cope T, Copeland SR, Coppari F, Cortez J, Cox J, Crandall DH, Crane J, Craxton RS, Cray M, Crilly A, Crippen JW, Cross D, Cuneo M, Cuotts G, Czajka CE, Czechowicz D, Daly T, Danforth P, Darbee R, Darlington B, Datte P, Dauffy L, Davalos G, Davidovits S, Davis P, Davis J, Dawson S, Day RD, Day TH, Dayton M, Deck C, Decker C, Deeney C, DeFriend KA, Deis G, Delamater ND, Delettrez JA, Demaret R, Demos S, Dempsey SM, Desjardin R, Desjardins T, Desjarlais MP, Dewald EL, DeYoreo J, Diaz S, Dimonte G, Dittrich TR, Divol L, Dixit SN, Dixon J, Dodd ES, Dolan D, Donovan A, Donovan M, Döppner T, Dorrer C, Dorsano N, Douglas MR, Dow D, Downie J, Downing E, Dozieres M, Draggoo V, Drake D, Drake RP, Drake T, Dreifuerst G, DuBois DF, DuBois PF, Dunham G, Dylla-Spears R, Dymoke-Bradshaw AKL, Dzenitis B, Ebbers C, Eckart M, Eddinger S, Eder D, Edgell D, Edwards MJ, Efthimion P, Eggert JH, Ehrlich B, Ehrmann P, Elhadj S, Ellerbee C, Elliott NS, Ellison CL, Elsner F, Emerich M, Engelhorn K, England T, English E, Epperson P, Epstein R, Erbert G, Erickson MA, Erskine DJ, Erlandson A, Espinosa RJ, Estes C, Estabrook KG, Evans S, Fabyan A, Fair J, Fallejo R, Farmer N, Farmer WA, Farrell M, Fatherley VE, Fedorov M, Feigenbaum E, Feit M, Ferguson W, Fernandez JC, Fernandez-Panella A, Fess S, Field JE, Filip CV, Fincke JR, Finn T, Finnegan SM, et al. PMID: 36018710.
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    40. The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing. Prenat Diagn. 2022 09; 42(10):1288-1294. Swanson K, Norton ME, Lianoglou BR, Jelin AC, Hodoglugil U, Van Ziffle J, Devine P, Sparks TN. PMID: 35723972; PMCID: PMC9531346.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    41. Incidental Detection of Maternal Malignancy by Fetal Cell-Free DNA Screening. Obstet Gynecol. 2022 07 01; 140(1):121-131. Rink BD, Stevens BK, Norton ME. PMID: 35849469.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    42. "Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research. Front Genet. 2022; 13:882703. Brown JEH, Zamora AN, Outram S, Sparks TN, Lianoglou BR, Norstad M, Sahin Hodoglugil NN, Norton ME, Ackerman SL. PMID: 35669190; PMCID: PMC9164104.
      View in: PubMed   Mentions: 2  
    43. Care Levels for Fetal Therapy Centers. Obstet Gynecol. 2022 06 01; 139(6):1027-1042. Baschat AA, Blackwell SB, Chatterjee D, Cummings JJ, Emery SP, Hirose S, Hollier LM, Johnson A, Kilpatrick SJ, Luks FI, Menard MK, McCullough LB, Moldenhauer JS, Moon-Grady AJ, Mychaliska GB, Narvey M, Norton ME, Rollins MD, Skarsgard ED, Tsao K, Warner BB, Wilpers A, Ryan G. PMID: 35675600; PMCID: PMC9202072.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    44. Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach. Genet Med. 2022 06; 24(6):1206-1216. Rego S, Hoban H, Outram S, Zamora AN, Chen F, Sahin-Hodoglugil N, Anguiano B, Norstad M, Yip T, Lianoglou B, Sparks TN, Norton ME, Koenig BA, Slavotinek AM, Ackerman SL. PMID: 35396980; PMCID: PMC9536515.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    45. Treatment for Mild Chronic Hypertension during Pregnancy. N Engl J Med. 2022 05 12; 386(19):1781-1792. Tita AT, Szychowski JM, Boggess K, Dugoff L, Sibai B, Lawrence K, Hughes BL, Bell J, Aagaard K, Edwards RK, Gibson K, Haas DM, Plante L, Metz T, Casey B, Esplin S, Longo S, Hoffman M, Saade GR, Hoppe KK, Foroutan J, Tuuli M, Owens MY, Simhan HN, Frey H, Rosen T, Palatnik A, Baker S, August P, Reddy UM, Kinzler W, Su E, Krishna I, Nguyen N, Norton ME, Skupski D, El-Sayed YY, Ogunyemi D, Galis ZS, Harper L, Ambalavanan N, Geller NL, Oparil S, Cutter GR, Andrews WW, Chronic Hypertension and Pregnancy (CHAP) Trial Consortium. PMID: 35363951; PMCID: PMC9575330.
      View in: PubMed   Mentions: 71     Fields:    Translation:Humans
    46. Perinatal outcomes and 2017 ACC/AHA blood pressure categories. Pregnancy Hypertens. 2022 Jun; 28:134-138. Tesfalul MA, Sperling JD, Blat C, Parikh NI, Gonzalez-Velez JM, Zlatnik MG, Norton ME. PMID: 35381471.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    47. Primary cell-free DNA screening or contingent screening for the common trisomies: a response. Am J Obstet Gynecol. 2022 07; 227(1):127-128. Dar P, Norton ME. PMID: 35218698.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    48. Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis. Prenat Diagn. 2022 05; 42(5):611-616. Swanson K, Loeliger KB, Chetty SP, Sparks TN, Norton ME. PMID: 35106791; PMCID: PMC9116240.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    49. Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study. Am J Obstet Gynecol. 2022 07; 227(1):124-125. Dar P, Norton ME. PMID: 35120885.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    50. Cell-free DNA screening for trisomies 21, 18, and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmation. Am J Obstet Gynecol. 2022 08; 227(2):259.e1-259.e14. Dar P, Jacobsson B, MacPherson C, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Edwards L, Haeri S, Silver R, Vohra N, Hyett J, Clunie G, Demko Z, Martin K, Rabinowitz M, Flood K, Carlsson Y, Doulaveris G, Malone C, Hallingstrom M, Klugman S, Clifton R, Kao C, Hakonarson H, Norton ME. PMID: 35085538.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    51. Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome. Am J Obstet Gynecol. 2022 07; 227(1):79.e1-79.e11. Dar P, Jacobsson B, Clifton R, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Edwards L, Strong N, Haeri S, Silver R, Vohra N, Hyett J, Demko Z, Martin K, Rabinowitz M, Flood K, Carlsson Y, Doulaveris G, Daly S, Hallingström M, MacPherson C, Kao C, Hakonarson H, Norton ME. PMID: 35033576.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    52. Consensus statement for the perinatal management of patients with α thalassemia major. Blood Adv. 2021 12 28; 5(24):5636-5639. MacKenzie TC, Amid A, Angastiniotis M, Butler C, Gilbert S, Gonzalez J, Keller RL, Kharbanda S, Kirby-Allen M, Koenig BA, Kyono W, Lal A, Lianoglou BR, Norton ME, Ogasawara KK, Panchalee T, Rosner M, Schwab M, Thompson A, Waye JS, Vichinsky E. PMID: 34749399; PMCID: PMC8714716.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    53. Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A. Eur J Med Genet. 2022 Feb; 65(2):104407. Slavotinek A, Lefebvre M, Brehin AC, Thauvin C, Patrier S, Sparks TN, Norton M, Yu J, Huang E. PMID: 34942405; PMCID: PMC9162882.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    54. An Introduction: Prenatal Screening, Diagnosis, and Treatment of Single Gene Disorders. Clin Obstet Gynecol. 2021 12 01; 64(4):852-860. Wapner RJ, Norton ME. PMID: 34618720.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    55. Foreword: Gene Therapy in Obstetrics. Clin Obstet Gynecol. 2021 12 01; 64(4):850-851. Wapner RJ, Norton ME. PMID: 34608016.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    56. In Utero Gene Therapy for Primary Immunodeficiencies. Clin Obstet Gynecol. 2021 12 01; 64(4):886-897. Mardy AH, Norton ME. PMID: 34482336.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    57. The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research. Genet Med. 2022 02; 24(2):410-418. Norstad M, Outram S, Brown JEH, Zamora AN, Koenig BA, Risch N, Norton ME, Slavotinek A, Ackerman SL. PMID: 34906477.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    58. Bystander cardiopulmonary resuscitation for paediatric out-of-hospital cardiac arrest in England: An observational registry cohort study. Resuscitation. 2022 01; 170:17-25. Albargi H, Mallett S, Berhane S, Booth S, Hawkes C, Perkins GD, Norton M, Foster T, Scholefield B. PMID: 34748765.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    59. Society for Maternal-Fetal Medicine Consult Series #59: The use of analgesia and anesthesia for maternal-fetal procedures. Contraception. 2022 02; 106:10-15. Medicine SFM, Planning SOF, Norton ME, Cassidy A, Ralston SJ, Chatterjee D, Farmer D, Beasley AD, Dragoman M. PMID: 34740602.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    60. United States' experience in nuchal translucency measurement: variation according to provider characteristics in over five million ultrasound examinations. Ultrasound Obstet Gynecol. 2021 Nov; 58(5):732-737. Thornburg LL, Bromley B, Dugoff L, Platt LD, Fuchs KM, Norton ME, McIntosh J, Toland GJ, Cuckle H, Nuchal Translucency Quality Review Program of the Perinatal Quality Foundation. PMID: 33634915.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    61. Response to "Further genetic testing in prenatal cases of nonimmune hydrops fetalis with a normal array: a targeted panel or exome?" Am J Obstet Gynecol. 2022 02; 226(2):277. Norton ME, Sparks TN. PMID: 34606761; PMCID: PMC8810662.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    62. Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis. Ultrasound Obstet Gynecol. 2021 Oct; 58(4):509-518. Mone F, Eberhardt RY, Hurles ME, Mcmullan DJ, Maher ER, Lord J, Chitty LS, Dempsey E, Homfray T, Giordano JL, Wapner RJ, Sun L, Sparks TN, Norton ME, Kilby MD. PMID: 33847422; PMCID: PMC8487902.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    63. Urinoma. Am J Obstet Gynecol. 2021 11; 225(5):B34-B35. Society for Maternal-Fetal Medicine (SMFM), Connolly K, Norton ME. PMID: 34507797.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    64. Society for Maternal-Fetal Medicine Consult Series #59: The use of analgesia and anesthesia for maternal-fetal procedures. Am J Obstet Gynecol. 2021 12; 225(6):B2-B8. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Society of Family Planning (SFP), Norton ME, Cassidy A, Ralston SJ, Chatterjee D, Farmer D, Beasley AD, Dragoman M. PMID: 34461076.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    65. Diagnostic testing after positive results on cell free DNA screening: CVS or Amnio? Prenat Diagn. 2021 Sep; 41(10):1249-1254. Mardy AH, Norton ME. PMID: 34386984.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    66. Influenza Complicating Delivery Hospitalization and Its Association With Severe Maternal Morbidity in the United States, 2000-2018. Obstet Gynecol. 2021 08 01; 138(2):218-227. Wen T, Arditi B, Riley LE, Sobhani NC, Norton M, D'Alton M, Friedman AM, Venkatesh KK. PMID: 34237767.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    67. SMFM Fetal Anomalies Consult Series #4: Genitourinary anomalies. Am J Obstet Gynecol. 2021 11; 225(5):B2-B35. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Norton ME, Cheng Y, Chetty S, Chyu JK, Connolly K, Ghaffari N, Hopkins LM, Jelin A, Mardy A, Osmundson SS, Sparks TN, Sperling J, Swanson K, Zuckerwise LC, Kuller JA. PMID: 34507800; PMCID: PMC8763622.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    68. Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis. Am J Obstet Gynecol. 2022 01; 226(1):128.e1-128.e11. Norton ME, Ziffle JV, Lianoglou BR, Hodoglugil U, Devine WP, Sparks TN. PMID: 34331894; PMCID: PMC8748274.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    69. Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants. Am J Surg. 2022 Jan; 223(1):182-186. Schwab ME, Dong S, Lianoglou BR, Aguilar Lucero AF, Schwartz GB, Norton ME, MacKenzie TC, Sanders SJ. PMID: 34315577.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    70. Twin chorionicity and zygosity both vary with maternal age. Prenat Diagn. 2021 08; 41(9):1074-1079. Yeaton-Massey A, Sparks TN, Norton ME, Jelliffe-Pawlowski L, Currier RJ. PMID: 35280337; PMCID: PMC8916645.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    71. Risk of pregnancy loss before 20 weeks' gestation in study participants with COVID-19. Am J Obstet Gynecol. 2021 10; 225(4):456-457. Jacoby VL, Murtha A, Afshar Y, Gaw SL, Asiodu I, Tolosa J, Norton ME, Boscardin WJ, Flaherman V. PMID: 34175267; PMCID: PMC8225313.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    72. Preference for secondary findings in prenatal and pediatric exome sequencing. Prenat Diagn. 2022 05; 42(6):753-761. Swanson K, Sparks TN, Lianoglou BR, Chen F, Downum S, Patel S, Rego S, Yip T, Van Ziffle J, Koenig BA, Slavotinek AM, Norton ME. PMID: 34057224; PMCID: PMC8630094.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    73. Evaluation of Hypoglycemia in Neonates of Women at Risk for Late Preterm Delivery: An Antenatal Late Preterm Steroids Trial Cohort Study. Am J Perinatol. 2023 04; 40(5):532-538. Gyamfi-Bannerman C, Jablonski KA, Blackwell SC, Tita ATN, Reddy UM, Jain L, Saade GR, Rouse DJ, Clark EAS, Thorp JM, Chien EK, Peaceman AM, Gibbs RS, Swamy GK, Norton ME, Casey BM, Caritis SN, Tolosa JE, Sorokin Y, VanDorsten JP, Eunice Kennedy Shriver National Institute of Child Health Human Development Maternal-Fetal Medicine . PMID: 34044454; PMCID: PMC8626537.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    74. Response to Letter. Obstet Gynecol. 2021 05 01; 137(5):960. Silver J, Norton ME. PMID: 33878054.
      View in: PubMed   Mentions:    Fields:    
    75. Society for Maternal-Fetal Medicine Special Statement: Maternal-fetal medicine subspecialist survey on abortion training and service provision. Am J Obstet Gynecol. 2021 07; 225(1):B2-B11. Society for Maternal-Fetal Medicine. Electronic address: RHProject@smfm.org, Lappen JR, Vricella LK, Andrews V, Christensen E, Heuser CC, Horvath S, Johnson CT, Louis JM, Luchowski AT, Norton ME, Sagaser KG, Srinivas SK, Werner E, Zahedi-Spung L, Blackwell S. PMID: 33845031.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    76. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. J Pers Med. 2021 Mar 13; 11(3). Suckiel SA, O'Daniel JM, Donohue KE, Gallagher KM, Gilmore MJ, Hendon LG, Joseph G, Lianoglou BR, Mathews JM, Norton ME, Odgis JA, Poss AF, Rego S, Scollon S, Yip T, Amendola LM. PMID: 33805616; PMCID: PMC7998798.
      View in: PubMed   Mentions: 4  
    77. Expanded Carrier Screening and the Complexity of Implementation. Obstet Gynecol. 2021 02 01; 137(2):345-350. Silver J, Norton ME. PMID: 33416279.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    78. Society for Maternal-Fetal Medicine Special Statement: Grading of Recommendations Assessment, Development, and Evaluation (GRADE) update. Am J Obstet Gynecol. 2021 04; 224(4):B24-B28. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Norton ME, Kuller JA, Metz TD. PMID: 33347844.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    79. Society for Maternal-Fetal Medicine Consult Series #55: Counseling women at increased risk of maternal morbidity and mortality. Am J Obstet Gynecol. 2021 04; 224(4):B16-B23. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Kaimal A, Norton ME. PMID: 33309561.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    80. Blake's Pouch Cyst. Am J Obstet Gynecol. 2020 12; 223(6):B47-B50. Society for Maternal-Fetal Medicine (SMFM), Post A, Norton ME, Monteagudo A. PMID: 33757627.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    81. Fetal Ventriculomegaly. Am J Obstet Gynecol. 2020 12; 223(6):B30-B33. Society for Maternal-Fetal Medicine (SMFM), Norton ME, Fox NS, Monteagudo A, Kuller JA, Craigo S. PMID: 33168210.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    82. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. N Engl J Med. 2020 10 29; 383(18):1746-1756. Sparks TN, Lianoglou BR, Adami RR, Pluym ID, Holliman K, Duffy J, Downum SL, Patel S, Faubel A, Boe NM, Field NT, Murphy A, Laurent LC, Jolley J, Uy C, Slavotinek AM, Devine P, Hodoglugil U, Van Ziffle J, Sanders SJ, MacKenzie TC, Norton ME, University of California Fetal–Maternal Consortium, University of California, San Francisco Center for Maternal–Fetal Precision Medicine. PMID: 33027564; PMCID: PMC7650529.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    83. Gross morphologic appearance of chorionic villi and the risk of chromosomal abnormalities. Reprod Sci. 2021 02; 28(2):570-574. Sobhani NC, Cassidy AG, Qi Z, Yu J, Chetty S, Norton ME. PMID: 32989629.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    84. COVID-19 Testing, Personal Protective Equipment, and Staffing Strategies Vary at Obstetrics Centers across the Country. Am J Perinatol. 2020 12; 37(14):1482-1484. Johnson JD, Melvin E, Srinivas SK, Louis JM, Hughes B, Han CS, Norton ME, Werner EF. PMID: 32979850; PMCID: PMC7724575.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCellsPHPublic Health
    85. SMFM Fetal Anomalies Consult Series #3: Intracranial Anomalies. Am J Obstet Gynecol. 2020 12; 223(6):B2-B50. Society for Maternal-Fetal Medicine (SMFM), Monteagudo A, Kuller JA, Craigo S, Fox NS, Norton ME, Post A, Rotmensch S, Ward A, Yeaton-Massey A. PMID: 33168215.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    86. Variants of uncertain significance in prenatal microarrays: a retrospective cohort study. BJOG. 2021 01; 128(2):431-438. Mardy AH, Wiita AP, Wayman BV, Drexler K, Sparks TN, Norton ME. PMID: 32702189; PMCID: PMC7856034.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    87. Community Obstetrical Units Less Likely than Academic Units to Have Universal COVID-19 Testing. Am J Perinatol. 2020 08; 37(10):1074-1076. Werner EF, Louis JM, Hughes B, Han CS, Norton ME, Srinivas SK. PMID: 32428963; PMCID: PMC7416201.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    88. Environmental and Socioeconomic Factors Influence the Live-Born Incidence of Congenital Heart Disease: A Population-Based Study in California. J Am Heart Assoc. 2020 04 21; 9(8):e015255. Peyvandi S, Baer RJ, Chambers CD, Norton ME, Rajagopal S, Ryckman KK, Moon-Grady A, Jelliffe-Pawlowski LL, Steurer MA. PMID: 32306820; PMCID: PMC7428546.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansPHPublic Health
    89. Reproductive services for women at high risk for maternal mortality: a report of the workshop of the Society for Maternal-Fetal Medicine, the American College of Obstetricians and Gynecologists, the Fellowship in Family Planning, and the Society of Family Planning. Am J Obstet Gynecol. 2020 04; 222(4):B2-B18. Blackwell S, Louis JM, Norton ME, Lappen JR, Pettker CM, Kaimal A, Landy U, Edelman A, Teal S, Landis R. PMID: 32252942.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    90. Etiology and management of early pregnancy renal anhydramnios: Is there a place for serial amnioinfusions? Prenat Diagn. 2020 04; 40(5):528-537. Jelin AC, Sagaser KG, Forster KR, Ibekwe T, Norton ME, Jelin EB. PMID: 32003482; PMCID: PMC7780162.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    91. Maternal genetic disorders and fetal development. Prenat Diagn. 2020 08; 40(9):1056-1065. Mardy AH, Chetty SP, Norton ME. PMID: 32010984.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    92. Utility of chromosomal microarray for diagnosis in cases of nonimmune hydrops fetalis. Prenat Diagn. 2020 03; 40(4):492-496. Mardy AH, Rangwala N, Hernandez-Cruz Y, Gosnell KA, Gonzalez JM, Norton ME, Sparks TN. PMID: 31981373; PMCID: PMC7153803.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    93. The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell-free DNA screening. Prenat Diagn. 2020 01; 40(2):185-190. Berger VK, Norton ME, Sparks TN, Flessel M, Baer RJ, Currier RJ. PMID: 31652356; PMCID: PMC7002253.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    94. Impaired Fetal Environment and Gestational Age: What Is Driving Mortality in Neonates With Critical Congenital Heart Disease? J Am Heart Assoc. 2019 11 19; 8(22):e013194. Steurer MA, Peyvandi S, Baer RJ, Oltman SP, Chambers CD, Norton ME, Ryckman KK, Moon-Grady AJ, Keller RL, Shiboski SC, Jelliffe-Pawlowski LL. PMID: 31726960; PMCID: PMC6915289.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    95. Laboratory screening and diagnosis of open neural tube defects, 2019 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2020 03; 22(3):462-474. Palomaki GE, Bupp C, Gregg AR, Norton ME, Oglesbee D, Best RG, ACMG Biochemical Genetics Subcommittee of the Laboratory Quality Assurance Committee. PMID: 31700163.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    96. Assessing the multidisciplinary team approaches to placenta accreta spectrum across five institutions within the University of California fetal Consortium (UCfC). J Matern Fetal Neonatal Med. 2021 Sep; 34(18):2971-2976. Fratto VM, Conturie CL, Ballas J, Pettit KE, Stephenson ML, Truong YN, Henry D, Afshar Y, Murphy A, Kim L, Field N, Wing DA, Norton ME, Ramos GA, University of California fetal Consortium. PMID: 31645153.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    97. Association Between Features of Spontaneous Late Preterm Labor and Late Preterm Birth. Am J Perinatol. 2020 03; 37(4):357-364. Glover AV, Battarbee AN, Gyamfi-Bannerman C, Boggess KA, Sandoval G, Blackwell SC, Tita ATN, Reddy UM, Jain L, Saade GR, Rouse DJ, Iams JD, Clark EAS, Chien EK, Peaceman AM, Gibbs RS, Swamy GK, Norton ME, Casey BM, Caritis SN, Tolosa JE, Sorokin Y, Manuck TA, Eunice Kennedy Shriver National Institute of Child Health Human Development Maternal-Fetal Medicine . PMID: 31529452; PMCID: PMC7058482.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    98. Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS). Genet Med. 2020 02; 22(2):283-291. Trosman JR, Weldon CB, Slavotinek A, Norton ME, Douglas MP, Phillips KA. PMID: 31501586; PMCID: PMC7004856.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    99. The Society for Maternal-Fetal Medicine (SMFM) Fetal Anomalies Consult Series. Am J Obstet Gynecol. 2019 11; 221(5):B2-B24. Society for Maternal-Fetal Medicine, Stone JE, Kuller JA, Norton ME, Abuhamad A. PMID: 31679590.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    100. Pregnancy loss after amniocentesis in monochorionic and dichorionic twin pregnancies: Results from a large population-based dataset. Prenat Diagn. 2019 09; 39(10):896-900. Sperling JD, Zlatnik MG, Norton ME, Currier RJ. PMID: 31218716.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    101. A system-based approach to the genetic etiologies of non-immune hydrops fetalis. Prenat Diagn. 2019 08; 39(9):732-750. Mardy AH, Chetty SP, Norton ME, Sparks TN. PMID: 31087399; PMCID: PMC6699893.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    102. Cost-effectiveness of Antenatal Corticosteroid Therapy vs No Therapy in Women at Risk of Late Preterm Delivery: A Secondary Analysis of a Randomized Clinical Trial. JAMA Pediatr. 2019 05 01; 173(5):462-468. Gyamfi-Bannerman C, Zupancic JAF, Sandoval G, Grobman WA, Blackwell SC, Tita ATN, Reddy UM, Jain L, Saade GR, Rouse DJ, Iams JD, Clark EAS, Thorp JM, Chien EK, Peaceman AM, Gibbs RS, Swamy GK, Norton ME, Casey BM, Caritis SN, Tolosa JE, Sorokin Y, VanDorsten JP, Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal-Fetal Medic. PMID: 30855640; PMCID: PMC6503503.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    103. Effect of Trial of Labor before Cesarean and Risk of Subsequent Placenta Accreta Spectrum Disorders. Am J Perinatol. 2020 05; 37(6):633-637. O'Malley KN, Norton ME, Osmundson SS. PMID: 30991440.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    104. Previous Adverse Outcome of Term Pregnancy and Risk of Preterm Birth in Subsequent Pregnancy. Matern Child Health J. 2019 Apr; 23(4):443-450. Baer RJ, Berghella V, Muglia LJ, Norton ME, Rand L, Ryckman KK, Jelliffe-Pawlowski LL, McLemore MR. PMID: 30539421.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    105. How does Fetal Autopsy after Pregnancy Loss or Termination for Anomalies and other Complications Change Recurrence Risk? AJP Rep. 2019 Jan; 9(1):e30-e35. Cassidy A, Herrick C, Norton ME, Ursell PC, Vargas J, Kerns JL. PMID: 30783547; PMCID: PMC6379179.
      View in: PubMed   Mentions: 2  
    106. Association of Gestational Diabetes Mellitus With Neonatal Respiratory Morbidity. Obstet Gynecol. 2019 02; 133(2):349-353. Werner EF, Romano ME, Rouse DJ, Sandoval G, Gyamfi-Bannerman C, Blackwell SC, Tita ATN, Reddy UM, Jain L, Saade GR, Iams JD, Clark EAS, Thorp JM, Chien EK, Peaceman AM, Swamy GK, Norton ME, Casey BM, Caritis SN, Tolosa JE, Sorokin Y, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Maternal-Fet. PMID: 30633135; PMCID: PMC6357223.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    107. Gender Differences in Academic Rank and NIH Funding among Academic Maternal-Fetal Medicine Physicians in the United States. Am J Perinatol. 2019 04; 36(5):443-448. Sperling JD, Shulman R, Blat C, Miller EE, Kokroko J, Zlatnik MG, Gonzalez-Velez J, Norton ME, Gossett DR. PMID: 30414602.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    108. Nonimmune hydrops fetalis: identifying the underlying genetic etiology. Genet Med. 2019 06; 21(6):1339-1344. Sparks TN, Thao K, Lianoglou BR, Boe NM, Bruce KG, Datkhaeva I, Field NT, Fratto VM, Jolley J, Laurent LC, Mardy AH, Murphy AM, Ngan E, Rangwala N, Rottkamp CAM, Wilson L, Wu E, Uy CC, Valdez Lopez P, Norton ME, University of California Fetal–Maternal Consortium (UCfC). PMID: 30410095; PMCID: PMC6509016.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    109. Socioeconomic Mediators of Racial and Ethnic Disparities in Congenital Heart Disease Outcomes: A Population-Based Study in California. J Am Heart Assoc. 2018 10 16; 7(20):e010342. Peyvandi S, Baer RJ, Moon-Grady AJ, Oltman SP, Chambers CD, Norton ME, Rajagopal S, Ryckman KK, Jelliffe-Pawlowski LL, Steurer MA. PMID: 30371284; PMCID: PMC6474947.
      View in: PubMed   Mentions: 52     Fields:    Translation:Humans
    110. Fetal Congenital Pulmonary Airway Malformation: The Role of an Objective Measurement of Cardiomediastinal Shift. Am J Perinatol. 2019 02; 36(3):225-232. Shulman R, Sparks TN, Gosnell K, Blat C, Norton ME, Lee H, Gonzalez-Velez J, Goldstein RB. PMID: 30199894; PMCID: PMC6372337.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    111. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. Am J Hum Genet. 2018 09 06; 103(3):319-327. Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hassmiller-Lich K, Joseph G, Kenny EE, Koenig BA, Knight S, Kwok PY, Lewis KL, McGuire AL, Norton ME, Ou J, Parsons DW, Powell BC, Risch N, Robinson M, Rini C, Scollon S, Slavotinek AM, Veenstra DL, Wasserstein MP, Wilfond BS, Hindorff LA, CSER consortium, Plon SE, Jarvik GP. PMID: 30193136; PMCID: PMC6128306.
      View in: PubMed   Mentions: 80     Fields:    Translation:Humans
    112. Effect of Fetal Growth on 1-Year Mortality in Neonates With Critical Congenital Heart Disease. J Am Heart Assoc. 2018 09 04; 7(17):e009693. Steurer MA, Baer RJ, Burke E, Peyvandi S, Oltman S, Chambers CD, Norton ME, Rand L, Rajagopal S, Ryckman KK, Feuer SK, Liang L, Paynter RA, McCarthy M, Moon-Grady AJ, Keller RL, Jelliffe-Pawlowski LL. PMID: 30371167; PMCID: PMC6201429.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    113. What are the goals of prenatal genetic testing? Semin Perinatol. 2018 08; 42(5):270-274. Dukhovny S, Norton ME. PMID: 30195989.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    114. Optimizing use of existing prenatal genetic tests: Screening and diagnostic testing for aneuploidy. Semin Perinatol. 2018 08; 42(5):296-302. Stoll K, Norton ME. PMID: 30209012.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    115. Preface. Semin Perinatol. 2018 08; 42(5):269. Norton ME, Wapner RJ. PMID: 30195988.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    116. Hypertensive Disorders of Pregnancy and Preterm Birth Rates among Black Women. Am J Perinatol. 2019 01; 36(2):148-154. Premkumar A, Baer RJ, Jelliffe-Pawlowski LL, Norton ME. PMID: 29980155.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    117. Correction: Prediction of preterm birth with and without preeclampsia using mid-pregnancy immune and growth-related molecular factors and maternal characteristics. J Perinatol. 2018 07; 38(7):946. Jelliffe-Pawlowski LL, Rand L, Bedell B, Baer RJ, Oltman SP, Norton ME, Shaw GM, Stevenson DK, Murray JC, Ryckman KK. PMID: 29941898; PMCID: PMC6151530.
      View in: PubMed   Mentions: 1     Fields:    
    118. Prediction of preterm birth with and without preeclampsia using mid-pregnancy immune and growth-related molecular factors and maternal characteristics. J Perinatol. 2018 08; 38(8):963-972. Jelliffe-Pawlowski LL, Rand L, Bedell B, Baer RJ, Oltman SP, Norton ME, Shaw GM, Stevenson DK, Murray JC, Ryckman KK. PMID: 29795450; PMCID: PMC6089890.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    119. Classification of Preterm Birth With Placental Correlates. Pediatr Dev Pathol. 2018 Nov-Dec; 21(6):548-560. Chisholm KM, Norton ME, Penn AA, Heerema-McKenney A. PMID: 29759046.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    120. Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrate. Haemophilia. 2018 Nov; 24(6):941-949. Liesner R, Akanezi C, Norton M, Payne J. PMID: 29707881.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCTClinical Trials
    121. Mild fetal ventriculomegaly: diagnosis, evaluation, and management. Am J Obstet Gynecol. 2018 07; 219(1):B2-B9. Society for Maternal-Fetal Medicine (SMFM);. Electronic address: pubs@smfm.org, Fox NS, Monteagudo A, Kuller JA, Craigo S, Norton ME. PMID: 29705191.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    122. Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in women and girls with hereditary factor X deficiency. J Thromb Haemost. 2018 05; 16(5):849-857. Kulkarni R, James AH, Norton M, Shapiro A. PMID: 29460388.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCTClinical Trials
    123. Investigating human placentation and pregnancy using first trimester chorionic villi. Placenta. 2018 05; 65:65-75. Hannibal RL, Cardoso-Moreira M, Chetty SP, Lau J, Qi Z, Gonzalez-Maldonado E, Cherry AM, Yu J, Norton ME, Baker JC. PMID: 29908643.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    124. Cell-Free DNA Screening for Aneuploidy and Microdeletion Syndromes. Obstet Gynecol Clin North Am. 2018 Mar; 45(1):13-26. Shaffer BL, Norton ME. PMID: 29428281.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    125. Obstetric Sonography: Why Are We Still Terrifying Pregnant Women? J Ultrasound Med. 2018 Sep; 37(9):2277-2278. Filly RA, Norton ME. PMID: 29480571.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    126. What is the real "price" of more prenatal screening and fewer diagnostic procedures? Costs and trade-offs in the genomic era. Prenat Diagn. 2018 03; 38(4):246-249. Hui L, Norton M. PMID: 29441593.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansPHPublic Health
    127. Jordanian adolescents' health behaviour and school climate. J Res Nurs. 2018 Feb; 23(1):58-73. Nassar O, Shaheen AM, Jarrah SS, Norton ME, Khalaf IA, Mohammad Hamdan K. PMID: 34394408; PMCID: PMC7932250.
      View in: PubMed   Mentions: 2  
    128. Current controversies in prenatal diagnosis 2: Cell-free DNA prenatal screening should be used to identify all chromosome abnormalities. Prenat Diagn. 2018 02; 38(3):160-165. Chitty LS, Hudgins L, Norton ME. PMID: 29417608.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    129. Prenatal Diagnosis of Congenital Diaphragmatic Hernia: Does Laterality Predict Perinatal Outcomes? Am J Perinatol. 2018 08; 35(10):919-924. Sperling JD, Sparks TN, Berger VK, Farrell JA, Gosnell K, Keller RL, Norton ME, Gonzalez JM. PMID: 29304545; PMCID: PMC6033692.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    130. Utility of chromosomal microarray in anomalous fetuses. Prenat Diagn. 2018 01; 38(2):140-147. Parchem JG, Sparks TN, Gosnell K, Norton ME. PMID: 29297200; PMCID: PMC5828907.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    131. Placental Alpha Microglobulin-1 Compared With Fetal Fibronectin to Predict Preterm Delivery in Symptomatic Women. Obstet Gynecol. 2017 12; 130(6):1183-1191. Wing DA, Haeri S, Silber AC, Roth CK, Weiner CP, Echebiri NC, Franco A, Pappas LM, Yeast JD, Brebnor AA, Quirk JG, Murphy AM, Laurent LC, Field NT, Norton ME. PMID: 29112664.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    132. Gestational Age and Outcomes in Critical Congenital Heart Disease. Pediatrics. 2017 Oct; 140(4). Steurer MA, Baer RJ, Keller RL, Oltman S, Chambers CD, Norton ME, Peyvandi S, Rand L, Rajagopal S, Ryckman KK, Moon-Grady AJ, Jelliffe-Pawlowski LL. PMID: 28885171.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    133. Expanded Carrier Screening: A Rational Approach to Screening for Rare Diseases. Obstet Gynecol. 2017 08; 130(2):260-261. Norton ME. PMID: 28697096.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    134. Testing for Noonan syndrome after increased nuchal translucency. Prenat Diagn. 2017 Aug; 37(8):750-753. Ali MM, Chasen ST, Norton ME. PMID: 28569377.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    135. Fetal Treatment 2017: The Evolution of Fetal Therapy Centers - A Joint Opinion from the International Fetal Medicine and Surgical Society (IFMSS) and the North American Fetal Therapy Network (NAFTNet). Fetal Diagn Ther. 2017; 42(4):241-248. Moon-Grady AJ, Baschat A, Cass D, Choolani M, Copel JA, Crombleholme TM, Deprest J, Emery SP, Evans MI, Luks FI, Norton ME, Ryan G, Tsao K, Welch R, Harrison M. PMID: 28531885; PMCID: PMC5739586.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    136. Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis-Insights from a Population-Based Dataset. J Pediatr. 2017 08; 187:182-188.e3. Steurer MA, Peyvandi S, Baer RJ, MacKenzie T, Li BC, Norton ME, Jelliffe-Pawlowski LL, Moon-Grady AJ. PMID: 28533037.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    137. Particle damage sources for fused silica optics and their mitigation on high energy laser systems. Opt Express. 2017 May 15; 25(10):11414-11435. Bude J, Carr CW, Miller PE, Parham T, Whitman P, Monticelli M, Raman R, Cross D, Welday B, Ravizza F, Suratwala T, Davis J, Fischer M, Hawley R, Lee H, Matthews M, Norton M, Nostrand M, VanBlarcom D, Sommer S. PMID: 28788823.
      View in: PubMed   Mentions: 6     Fields:    
    138. Prenatal screening: it is not just about Down syndrome. BJOG. 2017 07; 124(8):1162. Norton ME. PMID: 28301716.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    139. Mosaic trisomy 16: what are the obstetric and long-term childhood outcomes? Genet Med. 2017 10; 19(10):1164-1170. Sparks TN, Thao K, Norton ME. PMID: 28383546; PMCID: PMC6029708.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    140. The association of maternal lymphatic markers and critical congenital heart defects in the fetus-A population based case-control study. Am J Med Genet A. 2017 May; 173(5):1231-1236. Steurer MA, Norton ME, Baer RJ, Shaw GM, Keating S, Moon-Grady AJ, Chambers CD, Jelliffe-Pawlowski LL. PMID: 28323386.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    141. Obstetric care in women with genetic disorders. Best Pract Res Clin Obstet Gynaecol. 2017 Jul; 42:86-99. Chetty S, Norton ME. PMID: 28392223.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    142. The role of ultrasound in women who undergo cell-free DNA screening. Am J Obstet Gynecol. 2017 03; 216(3):B2-B7. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Norton ME, Biggio JR, Kuller JA, Blackwell SC. PMID: 28108156.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    143. Risk of preterm birth among women using drugs during pregnancy with elevated α-fetoprotein. J Perinatol. 2017 03; 37(3):220-225. Baer RJ, Chambers CD, Ryckman KK, Oltman SP, Norton ME, Jelliffe-Pawlowski LL. PMID: 27929528.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    144. Noninvasive prenatal testing to analyze the fetal genome. Proc Natl Acad Sci U S A. 2016 12 13; 113(50):14173-14175. Norton ME. PMID: 27911833; PMCID: PMC5167201.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    145. Observed Rate of Down Syndrome in Twin Pregnancies. Obstet Gynecol. 2016 11; 128(5):1127-1133. Sparks TN, Norton ME, Flessel M, Goldman S, Currier RJ. PMID: 27741202.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    146. Women should decide which conditions matter. Am J Obstet Gynecol. 2016 Nov; 215(5):583-587.e1. Norton ME, Kuppermann M. PMID: 27793311.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    147. What Is New in the Prevention of Preeclampsia?: Best Articles From the Past Year. Obstet Gynecol. 2016 Sep; 128(3):651-652. Norton ME. PMID: 27500324.
      View in: PubMed   Mentions:    Fields:    
    148. Maternal and neonatal outcomes after antenatal corticosteroid administration for PPROM at 32 to 33 6/7 weeks gestational age. J Matern Fetal Neonatal Med. 2017 Jul; 30(14):1676-1680. Sheibani L, Fong A, Henry DE, Norton ME, Truong YN, Anyikam A, Laurent LC, Rao R, Wing DA, University of California Fetal Consortium (UCfC). PMID: 27578238.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    149. The interaction between maternal race/ethnicity and chronic hypertension on preterm birth. Am J Obstet Gynecol. 2016 Dec; 215(6):787.e1-787.e8. Premkumar A, Henry DE, Moghadassi M, Nakagawa S, Norton ME. PMID: 27555318.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    150. The association between nitroglycerin use and adverse outcomes in women undergoing cesarean delivery in the second stage of labor. J Matern Fetal Neonatal Med. 2017 Jun; 30(11):1297-1301. Isquick S, Henry D, Nakagawa S, Moghadassi M, Thiet MP, Norton M, Lucero J. PMID: 27405400.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    151. Recurrence of Preterm Birth and Early Term Birth. Obstet Gynecol. 2016 08; 128(2):364-372. Yang J, Baer RJ, Berghella V, Chambers C, Chung P, Coker T, Currier RJ, Druzin ML, Kuppermann M, Muglia LJ, Norton ME, Rand L, Ryckman K, Shaw GM, Stevenson D, Jelliffe-Pawlowski LL. PMID: 27400000; PMCID: PMC5055875.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    152. The use of chromosomal microarray for prenatal diagnosis. Am J Obstet Gynecol. 2016 10; 215(4):B2-9. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Dugoff L, Norton ME, Kuller JA. PMID: 27427470.
      View in: PubMed   Mentions: 48     Fields:    Translation:Humans
    153. Ensuring Access to Safe, Legal Abortion in an Increasingly Complex Regulatory Environment. Obstet Gynecol. 2016 07; 128(1):171-5. Paul M, Norton ME. PMID: 27275804.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    154. Experience of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency undergoing surgery. Haemophilia. 2016 Sep; 22(5):713-20. Escobar MA, Auerswald G, Austin S, Huang JN, Norton M, Millar CM. PMID: 27217097.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCTClinical Trials
    155. Reply. Am J Obstet Gynecol. 2016 08; 215(2):253-4. Norton ME, Kuppermann M, Jelliffe-Pawlowski LL. PMID: 27094963.
      View in: PubMed   Mentions:    Fields:    
    156. 'Global health' and 'global nursing': proposed definitions from The Global Advisory Panel on the Future of Nursing. J Adv Nurs. 2016 Jul; 72(7):1529-40. Wilson L, Mendes IA, Klopper H, Catrambone C, Al-Maaitah R, Norton ME, Hill M. PMID: 27062286.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    157. Preferences regarding contemporary prenatal genetic tests among women desiring testing: implications for optimal testing strategies. Prenat Diagn. 2016 May; 36(5):469-75. Kuppermann M, Norton ME, Thao K, O'Leary A, Nseyo O, Cortez A, Kaimal AJ. PMID: 26946227.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    158. Genetic Counseling for Patients Considering Screening and Diagnosis for Chromosomal Abnormalities. Clin Lab Med. 2016 Jun; 36(2):227-36. Chard RL, Norton ME. PMID: 27235908.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    159. Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency. Haemophilia. 2016 May; 22(3):419-25. Austin SK, Kavakli K, Norton M, Peyvandi F, Shapiro A, FX Investigators Group. PMID: 27197801.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCTClinical Trials
    160. Pharmacokinetics of a high-purity plasma-derived factor X concentrate in subjects with moderate or severe hereditary factor X deficiency. Haemophilia. 2016 May; 22(3):426-32. Austin SK, Brindley C, Kavakli K, Norton M, Shapiro A, FX Investigators Group. PMID: 26879266.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCTClinical Trials
    161. Antenatal Betamethasone for Women at Risk for Late Preterm Delivery. N Engl J Med. 2016 Apr 07; 374(14):1311-20. Gyamfi-Bannerman C, Thom EA, Blackwell SC, Tita AT, Reddy UM, Saade GR, Rouse DJ, McKenna DS, Clark EA, Thorp JM, Chien EK, Peaceman AM, Gibbs RS, Swamy GK, Norton ME, Casey BM, Caritis SN, Tolosa JE, Sorokin Y, VanDorsten JP, Jain L, NICHD Maternal–Fetal Medicine Units Network. PMID: 26842679; PMCID: PMC4823164.
      View in: PubMed   Mentions: 146     Fields:    Translation:Humans
    162. First trimester pregnancy-associated plasma protein-A and birth weight. Eur J Obstet Gynecol Reprod Biol. 2016 Mar; 198:1-6. Baer RJ, Lyell DJ, Norton ME, Currier RJ, Jelliffe-Pawlowski LL. PMID: 26773241.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    163. Screening for fetal aneuploidy. Semin Perinatol. 2016 Feb; 40(1):35-43. Rink BD, Norton ME. PMID: 26725144.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    164. Cell-free DNA Analysis for Noninvasive Examination of Trisomy. N Engl J Med. 2015 12 24; 373(26):2582. Norton ME, Wapner RJ. PMID: 26699179.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    165. Changing indications for invasive testing in an era of improved screening. Semin Perinatol. 2016 Feb; 40(1):56-66. Norton ME, Rink BD. PMID: 26725145.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    166. Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities. Am J Obstet Gynecol. 2016 Jun; 214(6):727.e1-6. Norton ME, Baer RJ, Wapner RJ, Kuppermann M, Jelliffe-Pawlowski LL, Currier RJ. PMID: 26709085.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    167. Gestational dating by metabolic profile at birth: a California cohort study. Am J Obstet Gynecol. 2016 Apr; 214(4):511.e1-511.e13. Jelliffe-Pawlowski LL, Norton ME, Baer RJ, Santos N, Rutherford GW. PMID: 26688490; PMCID: PMC4822537.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    168. Outcomes of pregnancies with more than one positive prenatal screening result in the first or second trimester. Prenat Diagn. 2015 Dec; 35(12):1223-31. Baer RJ, Currier RJ, Norton ME, Flessel MC, Goldman S, Towner D, Jelliffe-Pawlowski LL. PMID: 26288069.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    169. Detection Rates for Aneuploidy by First-Trimester and Sequential Screening. Obstet Gynecol. 2015 Oct; 126(4):753-759. Baer RJ, Flessel MC, Jelliffe-Pawlowski LL, Goldman S, Hudgins L, Hull AD, Norton ME, Currier RJ. PMID: 26348180.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    170. Prenatal Testing in the Genomic Age: Clinical Outcomes, Quality of Life, and Costs. Obstet Gynecol. 2015 Oct; 126(4):737-746. Kaimal AJ, Norton ME, Kuppermann M. PMID: 26348190.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    171. Early Screening and Treatment of Women with Prediabetes: A Randomized Controlled Trial. Am J Perinatol. 2016 Jan; 33(2):172-9. Osmundson SS, Norton ME, El-Sayed YY, Carter S, Faig JC, Kitzmiller JL. PMID: 26344009.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    172. Should cell-free DNA testing be used to target antenatal rhesus immune globulin administration? J Matern Fetal Neonatal Med. 2016; 29(11):1866-70. Ma KK, Rodriguez MI, Cheng YW, Norton ME, Caughey AB. PMID: 26169705.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    173. What Is New in Prenatal Aneuploidy Screening?: Best Articles From the Past Year. Obstet Gynecol. 2015 Jul; 126(1):211-2. Norton ME. PMID: 26241275.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    174. Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn. 2015 Aug; 35(8):725-34. Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, Gross S, Huang T, Johnson J, Maymon R, Norton M, Odibo A, Schielen P, Spencer K, Wright D, Yaron Y. PMID: 25970088.
      View in: PubMed   Mentions: 84     Fields:    Translation:Humans
    175. Variation in Women's Understanding of Prenatal Testing. Obstet Gynecol. 2015 Jun; 125(6):1306-1312. Bryant AS, Norton ME, Nakagawa S, Bishop JT, Pena S, Gregorich SE, Kuppermann M. PMID: 26000501; PMCID: PMC4509625.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    176. Cell-free DNA analysis for noninvasive examination of trisomy. N Engl J Med. 2015 Apr 23; 372(17):1589-97. Norton ME, Jacobsson B, Swamy GK, Laurent LC, Ranzini AC, Brar H, Tomlinson MW, Pereira L, Spitz JL, Hollemon D, Cuckle H, Musci TJ, Wapner RJ. PMID: 25830321.
      View in: PubMed   Mentions: 231     Fields:    Translation:HumansCTClinical Trials
    177. Society for Maternal-Fetal Medicine (SMFM) Clinical Guideline #8: the fetus at risk for anemia--diagnosis and management. Am J Obstet Gynecol. 2015 Jun; 212(6):697-710. Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org, Mari G, Norton ME, Stone J, Berghella V, Sciscione AC, Tate D, Schenone MH. PMID: 25824811.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    178. Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine. Obstet Gynecol. 2015 Mar; 125(3):653-662. Edwards JG, Feldman G, Goldberg J, Gregg AR, Norton ME, Rose NC, Schneider A, Stoll K, Wapner R, Watson MS. PMID: 25730230.
      View in: PubMed   Mentions: 128     Fields:    Translation:HumansPHPublic Health
    179. Decision-support guide and use of prenatal genetic testing--reply. JAMA. 2015 Jan 13; 313(2):200-1. Kuppermann M, Norton ME. PMID: 25585336.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    180. Society for maternal-fetal medicine (SMFM) clinical guideline #7: nonimmune hydrops fetalis. Am J Obstet Gynecol. 2015 Feb; 212(2):127-39. Society for Maternal-Fetal Medicine (SMFM), Norton ME, Chauhan SP, Dashe JS. PMID: 25557883.
      View in: PubMed   Mentions: 53     Fields:    Translation:Humans
    181. Chromosome abnormalities detected by current prenatal screening and noninvasive prenatal testing. Obstet Gynecol. 2014 Nov; 124(5):979-986. Norton ME, Jelliffe-Pawlowski LL, Currier RJ. PMID: 25437727.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    182. Risk of critical congenital heart defects by nuchal translucency norms. Am J Obstet Gynecol. 2015 Apr; 212(4):518.e1-10. Jelliffe-Pawlowski LL, Norton ME, Shaw GM, Baer RJ, Flessel MC, Goldman S, Currier RJ. PMID: 25448520.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    183. Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial. JAMA. 2014 Sep 24; 312(12):1210-7. Kuppermann M, Pena S, Bishop JT, Nakagawa S, Gregorich SE, Sit A, Vargas J, Caughey AB, Sykes S, Pierce L, Norton ME. PMID: 25247517; PMCID: PMC4445462.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    184. Factors associated with gastroschisis outcomes. Obstet Gynecol. 2014 Sep; 124(3):551-557. Overcash RT, DeUgarte DA, Stephenson ML, Gutkin RM, Norton ME, Parmar S, Porto M, Poulain FR, Schrimmer DB, University of California Fetal Consortium*. PMID: 25162255; PMCID: PMC4147679.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    185. Risk of selected structural abnormalities in infants after increased nuchal translucency measurement. Am J Obstet Gynecol. 2014 Dec; 211(6):675.e1-19. Baer RJ, Norton ME, Shaw GM, Flessel MC, Goldman S, Currier RJ, Jelliffe-Pawlowski LL. PMID: 24949541.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    186. Noninvasive prenatal screening by next-generation sequencing. Annu Rev Genomics Hum Genet. 2014; 15:327-47. Gregg AR, Van den Veyver IB, Gross SJ, Madankumar R, Rink BD, Norton ME. PMID: 24849140.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    187. Evaluation of serial urine viral cultures for the diagnosis of cytomegalovirus infection in neonates and infants. Pediatr Dev Pathol. 2014 May-Jun; 17(3):176-80. Chisholm KM, Aziz N, McDowell M, Guo FP, Srinivas N, Benitz WE, Norton ME, Gutierrez K, Folkins AK, Pinsky BA. PMID: 24617645.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    188. Obstetric, perinatal, and fetal outcomes in pregnancies with false-positive integrated screening results. Obstet Gynecol. 2014 Mar; 123(3):603-609. Baer RJ, Currier RJ, Norton ME, Flessel MC, Goldman S, Towner D, Jelliffe-Pawlowski LL. PMID: 24499760.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    189. Does augmentation or induction of labor with oxytocin increase the risk for autism? Am J Obstet Gynecol. 2014 May; 210(5):495-6. Rosenstein MG, Newman TB, Norton ME. PMID: 24534186; PMCID: PMC4621006.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    190. Noninvasive prenatal testing. Obstet Gynecol Surv. 2014 Feb; 69(2):89-99. Lo JO, Cori D F, Norton ME, Caughey AB. PMID: 25112487.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    191. Women's Attitudes Regarding Prenatal Testing for a Range of Congenital Disorders of Varying Severity. J Clin Med. 2014 Jan 21; 3(1):144-52. Norton ME, Nakagawa S, Kuppermann M. PMID: 26237253; PMCID: PMC4449668.
      View in: PubMed   Mentions: 5  
    192. Response to "On gestational weeks and maths". Prenat Diagn. 2013 Dec; 33(12):1218-9. Benn P, Borrell A, Chiu R, Cuckle H, Dugoff L, Faas B, Gross S, Johnson J, Maymon R, Norton M, Odibo A, Schielen P, Spencer K, Huang T, Wright D, Yaron Y. PMID: 24307534.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    193. Follow-up of sonographically detected soft markers for fetal aneuploidy. Semin Perinatol. 2013 Oct; 37(5):365-9. Norton ME. PMID: 24176161.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    194. Fetal blood sampling. Am J Obstet Gynecol. 2013 Sep; 209(3):170-80. Society for Maternal-Fetal Medicine (SMFM), Berry SM, Stone J, Norton ME, Johnson D, Berghella V. PMID: 23978246.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    195. Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening. Prenat Diagn. 2013 Jun; 33(6):542-6. Chetty S, Garabedian MJ, Norton ME. PMID: 23592525.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    196. Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn. 2013 Jul; 33(7):622-9. Benn P, Borell A, Chiu R, Cuckle H, Dugoff L, Faas B, Gross S, Johnson J, Maymon R, Norton M, Odibo A, Schielen P, Spencer K, Huang T, Wright D, Yaron Y. PMID: 23616385.
      View in: PubMed   Mentions: 56     Fields:    Translation:Humans
    197. Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing. Prenat Diagn. 2013 Jul; 33(7):656-61. Allyse MA, Sayres LC, Havard M, King JS, Greely HT, Hudgins L, Taylor J, Norton ME, Cho MK, Magnus D, Ormond KE. PMID: 23613322; PMCID: PMC4057377.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    198. Noninvasive prenatal testing for fetal aneuploidy: clinical assessment and a plea for restraint. Obstet Gynecol. 2013 Apr; 121(4):847-850. Norton ME, Rose NC, Benn P. PMID: 23635685.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    199. Effects of changes in prenatal aneuploidy screening policies in an integrated health care system. Obstet Gynecol. 2013 Feb; 121(2 Pt 1):265-271. Norton ME, Nakagawa S, Norem C, Gregorich SE, Kuppermann M. PMID: 23344275.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    200. A first look at chorioamnionitis management practice variation among US obstetricians. Infect Dis Obstet Gynecol. 2012; 2012:628362. Greenberg MB, Anderson BL, Schulkin J, Norton ME, Aziz N. PMID: 23319852; PMCID: PMC3540735.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    201. Congenital heart defects in a large, unselected cohort of monochorionic twins. J Perinatol. 2013 Jun; 33(6):457-61. Pettit KE, Merchant M, Machin GA, Tacy TA, Norton ME. PMID: 23223160.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    202. Expanding the gestational age limits for laser treatment for twin-twin transfusion. Am J Obstet Gynecol. 2013 Mar; 208(3):165-6. Kuller JA, Norton ME. PMID: 23201086.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    203. Transdisciplinary translational science and the case of preterm birth. J Perinatol. 2013 Apr; 33(4):251-8. Stevenson DK, Shaw GM, Wise PH, Norton ME, Druzin ML, Valantine HA, McFarland DA, March of Dimes Prematurity Research Center at Stanford University School of Medicine. PMID: 23079774; PMCID: PMC3613736.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    204. Translating cell-free fetal DNA technology: structural lessons from non-invasive RhD blood typing. Trends Biotechnol. 2013 Jan; 31(1):7-9. Goodspeed TA, Allyse M, Sayres LC, Norton ME, Cho MK. PMID: 23040170; PMCID: PMC6309969.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    205. The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy. J Matern Fetal Neonatal Med. 2013 Jan; 26(2):143-5. Brar H, Wang E, Struble C, Musci TJ, Norton ME. PMID: 22913322; PMCID: PMC3545542.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    206. Cell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US context. Hum Reprod. 2012 Nov; 27(11):3123-31. Allyse M, Sayres LC, King JS, Norton ME, Cho MK. PMID: 22863603; PMCID: PMC3472618.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    207. Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. J Med Genet. 2012 Jul; 49(7):473-9. Solomon BD, Bear KA, Wyllie A, Keaton AA, Dubourg C, David V, Mercier S, Odent S, Hehr U, Paulussen A, Clegg NJ, Delgado MR, Bale SJ, Lacbawan F, Ardinger HH, Aylsworth AS, Bhengu NL, Braddock S, Brookhyser K, Burton B, Gaspar H, Grix A, Horovitz D, Kanetzke E, Kayserili H, Lev D, Nikkel SM, Norton M, Roberts R, Saal H, Schaefer GB, Schneider A, Smith EK, Sowry E, Spence MA, Shalev SA, Steiner CE, Thompson EM, Winder TL, Balog JZ, Hadley DW, Zhou N, Pineda-Alvarez DE, Roessler E, Muenke M. PMID: 22791840.
      View in: PubMed   Mentions: 38     Fields:    Translation:Humans
    208. Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. Am J Obstet Gynecol. 2012 Aug; 207(2):137.e1-8. Norton ME, Brar H, Weiss J, Karimi A, Laurent LC, Caughey AB, Rodriguez MH, Williams J, Mitchell ME, Adair CD, Lee H, Jacobsson B, Tomlinson MW, Oepkes D, Hollemon D, Sparks AB, Oliphant A, Song K. PMID: 22742782.
      View in: PubMed   Mentions: 137     Fields:    Translation:HumansCells
    209. Management of pregnancy in women with genetic disorders: Part 2: Inborn errors of metabolism, cystic fibrosis, neurofibromatosis type 1, and Turner syndrome in pregnancy. Obstet Gynecol Surv. 2011 Dec; 66(12):765-76. Chetty SP, Shaffer BL, Norton ME. PMID: 22192461.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    210. Management of pregnancy in women with genetic disorders, Part 1: Disorders of the connective tissue, muscle, vascular, and skeletal systems. Obstet Gynecol Surv. 2011 Nov; 66(11):699-709. Chetty SP, Shaffer BL, Norton ME. PMID: 22186601.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    211. Cell-free fetal DNA testing: a pilot study of obstetric healthcare provider attitudes toward clinical implementation. Prenat Diagn. 2011 Nov; 31(11):1070-6. Sayres LC, Allyse M, Norton ME, Cho MK. PMID: 21793012; PMCID: PMC3200428.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    212. Complete isochromosome 5p in one fetus of a monochorionic twin pair. Prenat Diagn. 2011 Jun; 31(6):605-7. Grams SE, Rand L, Norton ME. PMID: 21425180.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    213. Nuchal translucency measurement in fetuses with spinal muscular atrophy. Prenat Diagn. 2011 Apr; 31(4):327-30. Zadeh N, Hudgins L, Norton ME. PMID: 21287566.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    214. First-trimester screening for chromosomal abnormalities: advantages of an instant results approach. Clin Lab Med. 2010 Sep; 30(3):565-71. Norton ME. PMID: 20638572.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    215. Computerized prenatal genetic testing decision-assisting tool: a randomized controlled trial. Obstet Gynecol. 2009 Jan; 113(1):53-63. Kuppermann M, Norton ME, Gates E, Gregorich SE, Learman LA, Nakagawa S, Feldstein VA, Lewis J, Washington AE, Nease RF. PMID: 19104360.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    216. Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus. AJNR Am J Neuroradiol. 2009 Feb; 30(2):257-63. Tang PH, Bartha AI, Norton ME, Barkovich AJ, Sherr EH, Glenn OA. PMID: 18988682; PMCID: PMC7051410.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    217. Effects of cardiovascular medications on rate of functional decline in Alzheimer disease. Am J Geriatr Psychiatry. 2008 Nov; 16(11):883-92. Rosenberg PB, Mielke MM, Tschanz J, Cook L, Corcoran C, Hayden KM, Norton M, Rabins PV, Green RC, Welsh-Bohmer KA, Breitner JC, Munger R, Lyketsos CG. PMID: 18978249; PMCID: PMC2676234.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    218. Intracranial magnetic resonance imaging findings in the surviving fetus after spontaneous monochorionic cotwin demise. Am J Obstet Gynecol. 2008 Oct; 199(4):398.e1-5. Jelin AC, Norton ME, Bartha AI, Fick AL, Glenn OA. PMID: 18928987.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    219. Google obstetrics: who is educating our patients? Am J Obstet Gynecol. 2008 Jun; 198(6):682.e1-5. Kaimal AJ, Cheng YW, Bryant AS, Norton ME, Shaffer BL, Caughey AB. PMID: 18538152.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    220. Genetic screening and counseling. Curr Opin Obstet Gynecol. 2008 Apr; 20(2):157-63. Norton ME. PMID: 18388816.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    221. Vascular factors predict rate of progression in Alzheimer disease. Neurology. 2007 Nov 06; 69(19):1850-8. Mielke MM, Rosenberg PB, Tschanz J, Cook L, Corcoran C, Hayden KM, Norton M, Rabins PV, Green RC, Welsh-Bohmer KA, Breitner JC, Munger R, Lyketsos CG. PMID: 17984453.
      View in: PubMed   Mentions: 108     Fields:    Translation:Humans
    222. Placenta previa and the risk of preterm delivery. J Matern Fetal Neonatal Med. 2007 Oct; 20(10):719-23. Zlatnik MG, Cheng YW, Norton ME, Thiet MP, Caughey AB. PMID: 17763272.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    223. A prospective, randomized, multicenter trial of amnioreduction vs selective fetoscopic laser photocoagulation for the treatment of severe twin-twin transfusion syndrome. Am J Obstet Gynecol. 2007 Oct; 197(4):396.e1-9. Crombleholme TM, Shera D, Lee H, Johnson M, D'Alton M, Porter F, Chyu J, Silver R, Abuhamad A, Saade G, Shields L, Kauffman D, Stone J, Albanese CT, Bahado-Singh R, Ball RH, Bilaniuk L, Coleman B, Farmer D, Feldstein V, Harrison MR, Hedrick H, Livingston J, Lorenz RP, Miller DA, Norton ME, Polzin WJ, Robinson JN, Rychik J, Sandberg PL, Seri I, Simon E, Simpson LL, Yedigarova L, Wilson RD, Young B. PMID: 17904975; PMCID: PMC2754290.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    224. Does length of labor vary by maternal age? Am J Obstet Gynecol. 2007 Oct; 197(4):428.e1-7. Greenberg MB, Cheng YW, Sullivan M, Norton ME, Hopkins LM, Caughey AB. PMID: 17904990.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    225. First-trimester combined screening: experience with an instant results approach. Am J Obstet Gynecol. 2007 Jun; 196(6):606.e1-5; discussion 606.e5. Norton ME, Hopkins LM, Pena S, Krantz D, Caughey AB. PMID: 17547916; PMCID: PMC2099455.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    226. Evaluation and management of twin-twin transfusion syndrome: still a challenge. Am J Obstet Gynecol. 2007 May; 196(5):419-20. Norton ME. PMID: 17466690.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    227. Chorionic villus sampling compared with amniocentesis and the difference in the rate of pregnancy loss. Obstet Gynecol. 2006 Sep; 108(3 Pt 1):612-6. Caughey AB, Hopkins LM, Norton ME. PMID: 16946222.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    228. Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy. Prenat Diagn. 2006 Aug; 26(8):667-71. Shaffer BL, Caughey AB, Norton ME. PMID: 16724363.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    229. History of miscarriage and increased incidence of fetal aneuploidy in subsequent pregnancy. Obstet Gynecol. 2006 May; 107(5):1098-102. Bianco K, Caughey AB, Shaffer BL, Davis R, Norton ME. PMID: 16648416.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    230. Unequal placental sharing and birth weight discordance in monochorionic diamniotic twins. Am J Obstet Gynecol. 2006 Jul; 195(1):178-83. Fick AL, Feldstein VA, Norton ME, Wassel Fyr C, Caughey AB, Machin GA. PMID: 16643828.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    231. Prenatal diagnosis of familial type I choledochal cyst. Pediatrics. 2006 Mar; 117(3):e596-600. Clifton MS, Goldstein RB, Slavotinek A, Norton ME, Lee H, Farrell J, Nobuhara KK. PMID: 16452322.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    232. Ultrasound screening of fetuses at increased risk for Down syndrome: how many missed diagnoses? Prenat Diagn. 2006 Jan; 26(1):22-7. Caughey AB, Lyell DJ, Washington AE, Filly RA, Norton ME. PMID: 16378329.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    233. Y chromosome heterochromatin variation detected at prenatal diagnosis. Prenat Diagn. 2005 Nov; 25(11):1062-3. Cotter PD, Norton ME. PMID: 16299832.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    234. Prescription of teratogenic medications in United States ambulatory practices. Am J Med. 2005 Nov; 118(11):1240-9. Schwarz EB, Maselli J, Norton M, Gonzales R. PMID: 16271908.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    235. Ethnic variation in the prevalence of echogenic intracardiac foci and the association with Down syndrome. Ultrasound Obstet Gynecol. 2005 Aug; 26(2):158-61. Tran SH, Caughey AB, Norton ME. PMID: 16038014.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    236. Fetal magnetic resonance imaging in the evaluation of fetuses referred for sonographically suspected abnormalities of the corpus callosum. J Ultrasound Med. 2005 Jun; 24(6):791-804. Glenn OA, Goldstein RB, Li KC, Young SJ, Norton ME, Busse RF, Goldberg JD, Barkovich AJ. PMID: 15914683.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    237. Prenatal diagnosis of polymicrogyria by fetal magnetic resonance imaging in monochorionic cotwin death. J Ultrasound Med. 2005 May; 24(5):711-6. Glenn OA, Norton ME, Goldstein RB, Barkovich AJ. PMID: 15840804.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    238. New evidence on birth spacing: promising findings for improving newborn, infant, child, and maternal health. Int J Gynaecol Obstet. 2005 Apr; 89 Suppl 1:S1-6. Norton M. PMID: 15820364.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    239. Prenatal testing guidelines: time for a new approach. Gynecol Obstet Invest. 2005; 60(1):6-10. Kuppermann M, Norton ME. PMID: 15711084.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    240. Prenatal diagnosis of minute supernumerary marker chromosomes. Gynecol Obstet Invest. 2005; 60(1):27-38. Cotter PD, Drexler K, Corley AL, Covert SM, Moland JS, Govberg IJ, Norton ME. PMID: 15689640.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    241. Rapid prenatal diagnosis in translocation carriers by interphase FISH with chromosome-specific subtelomere probes. Am J Med Genet A. 2003 Sep 15; 122A(1):1-5. Cotter PD, Musci TJ, Norton ME. PMID: 12949964.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    242. Ring 21 chromosome and a satellited 1p in the same patient: novel origin for an ectopic NOR. Am J Med Genet A. 2003 Jul 30; 120A(3):365-9. Ki A, Rauen KA, Black LD, Kostiner DR, Sandberg PL, Pinkel D, Albertson DG, Norton ME, Cotter PD. PMID: 12838556.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    243. Risk factors for breast cancer in Jordanian women. J Nurs Scholarsh. 2002; 34(1):19-25. Petro-Nustas W, Norton ME, al-Masarweh I. PMID: 11901963.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    244. The impact of the use of the isolated echogenic intracardiac focus as a screen for Down syndrome in women under the age of 35 years. Am J Obstet Gynecol. 2001 Nov; 185(5):1021-7. Caughey AB, Lyell DJ, Filly RA, Washington AE, Norton ME. PMID: 11717625.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    245. Relationship of twin zygosity and risk of preeclampsia. Am J Obstet Gynecol. 2001 Oct; 185(4):819-21. Maxwell CV, Lieberman E, Norton M, Cohen A, Seely EW, Lee-Parritz A. PMID: 11641658.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    246. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p. Clin Genet. 2001 Apr; 59(4):274-8. McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD. PMID: 11298684.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    247. Predicting the risk of cystic fibrosis with echogenic fetal bowel and one cystic fibrosis mutation. Obstet Gynecol. 1999 Dec; 94(6):1020-3. Bosco AF, Norton ME, Lieberman E. PMID: 10576193.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    248. Preliminary study of the incidence of disomy in sperm fractions after MicroSort flow cytometry. Hum Reprod. 1999 Dec; 14(12):2987-90. Vidal F, Blanco J, Fugger EF, Keyvanfar K, Norton M, Schulman JD, Egozcue J. PMID: 10601083.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    249. Cystic fibrosis and chromosome abnormalities associated with echogenic fetal bowel. Obstet Gynecol. 1999 Jul; 94(1):135-8. Berlin BM, Norton ME, Sugarman EA, Tsipis JE, Allitto BA. PMID: 10389734.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    250. Costello syndrome: phenotype, natural history, differential diagnosis, and possible cause. J Pediatr. 1998 Sep; 133(3):441-8. Johnson JP, Golabi M, Norton ME, Rosenblatt RM, Feldman GM, Yang SP, Hall BD, Fries MH, Carey JC. PMID: 9738731.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    251. Comparison between planar and tomographic radionuclide ventriculography for detecting inferior wall motion abnormalities. Clin Radiol. 1998 Apr; 53(4):264-7. Lee HS, Cross S, Norton M, Walton S. PMID: 9585041.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCTClinical Trials
    252. Efficiency of MicroSort flow cytometry for producing sperm populations enriched in X- or Y-chromosome haplotypes: a blind trial assessed by double and triple colour fluorescent in-situ hybridization. Hum Reprod. 1998 Feb; 13(2):308-12. Vidal F, Fugger EF, Blanco J, Keyvanfar K, Català V, Norton M, Hazelrigg WB, Black SH, Levinson G, Egozcue J, Schulman JD. PMID: 9557828.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCellsCTClinical Trials
    253. Teratogen update: fetal effects of indomethacin administration during pregnancy. Teratology. 1997 Oct; 56(4):282-92. Norton ME. PMID: 9408979.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    254. Behçet's syndrome associated with intrauterine growth restriction: a case report and review of the literature. J Perinatol. 1997 Jul-Aug; 17(4):318-20. Guzelian G, Norton ME. PMID: 9280100.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    255. Cost-effectiveness of strategies used in the evaluation of pregnancies complicated by elevated maternal serum alpha-fetoprotein levels. Obstet Gynecol. 1997 May; 89(5 Pt 1):660-5. Nadel AS, Norton ME, Wilkins-Haug L. PMID: 9166296.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    256. Molecular zygosity studies aid in the management of discordant multiple gestations. J Perinatol. 1997 May-Jun; 17(3):202-7. Norton ME, D'Alton ME, Bianchi DW. PMID: 9210075.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    257. Capital equipment support: a new era in technical service. Biomed Instrum Technol. 1996 Jan-Feb; 30(1):17-24. Lewis J, Kelch D, Cicman JH, Norton M. PMID: 8850591.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    258. Interaction of hypertension and diabetes on renal function in black NIDDM subjects. Kidney Int. 1995 Jun; 47(6):1697-702. Chaiken RL, Palmisano J, Norton ME, Banerji MA, Bard M, Sachimechi I, Behzadi H, Lebovitz HE. PMID: 7643539.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    259. Nonimmune hydrops fetalis. Semin Perinatol. 1994 Aug; 18(4):321-32. Norton ME. PMID: 7985044.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    260. Biochemical and ultrasound screening for chromosomal abnormalities. Semin Perinatol. 1994 Aug; 18(4):256-65. Norton ME. PMID: 7527158.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    261. Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. Am J Hum Genet. 1994 Aug; 55(2):253-65. Eggerding FA, Schonberg SA, Chehab FF, Norton ME, Cox VA, Epstein CJ. PMID: 7913578; PMCID: PMC1918369.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    262. Indomethacin as a tocolytic agent: the controversy continues. J Pediatr. 1994 May; 124(5 Pt 1):734-6. Merrill JD, Clyman RI, Norton ME. PMID: 8176560.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    263. Neonatal complications after the administration of indomethacin for preterm labor. N Engl J Med. 1993 Nov 25; 329(22):1602-7. Norton ME, Merrill J, Cooper BA, Kuller JA, Clyman RI. PMID: 8232428.
      View in: PubMed   Mentions: 62     Fields:    Translation:Humans
    264. Facial features of infants exposed prenatally to cocaine. Teratology. 1993 Nov; 48(5):413-20. Fries MH, Kuller JA, Norton ME, Yankowitz J, Kobori J, Good WV, Ferriero D, Cox V, Donlin SS, Golabi M. PMID: 8303611.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    265. Maternal serum CA 125 for aneuploidy detection in early pregnancy. Prenat Diagn. 1992 Sep; 12(9):779-81. Norton ME, Golbus MS. PMID: 1438070.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    266. Relating patient characteristics at the time of admission to outcomes of hospitalization. J Clin Epidemiol. 1991; 44(10):1063-9. Pompei P, Charlson ME, Ales K, MacKenzie CR, Norton M. PMID: 1940999.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    267. The clinical significance of predictions based on screening second trimester mean arterial pressure: adverse maternal [corrected] and infant outcomes. J Clin Epidemiol. 1990; 43(2):117-24. Ales KL, Norton ME, Druzin ML. PMID: 2331248.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    268. Changes in functional status during pregnancy. Am J Med Sci. 1989 Jun; 297(6):355-60. Ales KL, Norton ME. PMID: 2735341.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    269. Early prediction of antepartum hypertension. Obstet Gynecol. 1989 Jun; 73(6):928-33. Ales KL, Norton ME, Druzin ML. PMID: 2726114.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    270. Trade-offs between hospital charges and patient outcomes. Am J Med Sci. 1988 May; 295(5):418-23. Pompei P, Charlson ME, Sax FL, Ales K, MacKenzie CR, Norton M. PMID: 3132042.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    271. Maternal and neonatal effects of epidural morphine for labor and delivery. Anesth Analg. 1984 Mar; 63(3):319-24. Hughes SC, Rosen MA, Shnider SM, Abboud TK, Stefani SJ, Norton M. PMID: 6703348.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCTClinical Trials
    272. Palliation of airway obstruction from tracheobronchial malignancy: use of the CO2 laser bronchoscope. Otolaryngol Head Neck Surg. 1983 Dec; 91(6):615-9. Shapshay SM, Davis RK, Vaughan CW, Norton M, Strong MS, Simpson GT. PMID: 6198613.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    273. Evaluation of neurotoxicity after subarachnoid injection of large volumes of local anesthetic solutions. Anesth Analg. 1983 Sep; 62(9):802-8. Rosen MA, Baysinger CL, Shnider SM, Dailey PA, Norton M, Curtis JD, Collins M, Davis RL. PMID: 6881568.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
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