Neil Risch, PhD, MS

Title(s)Professor, Epidemiology & Biostatistics
SchoolSchool of Medicine
Address513 Parnassus Ave, HSW, #901F
San Francisco CA 94143
Phone415-476-1127
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    Other Positions
    Title(s)Director, Institute for Human Genetics


    Collapse Overview 

    Collapse Research 
    Collapse Research Activities and Funding
    Pharmacogenomics of Statin Therapy
    NIH P50GM115318Sep 7, 2015 - Aug 31, 2021
    Role: Co-Investigator
    A Resource for Genetic Epidemiology Research in Adult Health and Aging
    NIH RC2AG036607Sep 30, 2009 - Aug 31, 2012
    Role: Principal Investigator
    Pharmacogenetics of Membrane Transporters
    NIH U01GM061390Apr 1, 2000 - Jul 14, 2010
    Role: Co-Investigator
    Linkage Disequilibrium and Human Genetic Studies
    NIH P01GM057672Apr 1, 1998 - Feb 28, 2010
    Role: Co-Investigator
    MOLECULAR GENETICS OF AUTISM
    NIH R01MH052708Jul 1, 1995 - Jun 30, 2001
    Role: Principal Investigator
    STATISTICAL METHODS AND APPLICATIONS IN HUMAN GENETICS
    NIH R01HG000348Sep 30, 1988 - Aug 31, 1998
    Role: Principal Investigator
    STATISTICAL METHODS AND APPLICATIONS IN HUMAN GENETICS
    NIH R01GM039812Sep 30, 1988 - Aug 31, 1993
    Role: Principal Investigator
    TOPICS IN GENETIC EPIDEMIOLOGY
    NIH K04HD000648Jun 1, 1984 - Aug 31, 1987
    Role: Principal Investigator
    Administrative Core - Pharmacogenomics of Statin Therapy (POST)
    NIH/NIGMS P50GM-01
    Role: Co-Investigator

    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. 2023 lifetime achievement award: "If you want to go fast, go alone; if you want to go far, go together". Am J Hum Genet. 2024 Mar 07; 111(3):412-423. Risch N. PMID: 38458162.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. 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.
      View in: PubMed   Mentions:
    3. 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:
    4. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nat Commun. 2023 10 04; 14(1):6172. Budu-Aggrey A, Kilanowski A, Sobczyk MK, 23andMe Research Team, Shringarpure SS, Mitchell R, Reis K, Reigo A, Estonian Biobank Research Team, Mägi R, Nelis M, Tanaka N, Brumpton BM, Thomas LF, Sole-Navais P, Flatley C, Espuela-Ortiz A, Herrera-Luis E, Lominchar JVT, Bork-Jensen J, Marenholz I, Arnau-Soler A, Jeong A, Fawcett KA, Baurecht H, Rodriguez E, Alves AC, Kumar A, Sleiman PM, Chang X, Medina-Gomez C, Hu C, Xu CJ, Qi C, El-Heis S, Titcombe P, Antoun E, Fadista J, Wang CA, Thiering E, Wu B, Kress S, Kothalawala DM, Kadalayil L, Duan J, Zhang H, Hadebe S, Hoffmann T, Jorgenson E, Choquet H, Risch N, Njølstad P, Andreassen OA, Johansson S, Almqvist C, Gong T, Ullemar V, Karlsson R, Magnusson PKE, Szwajda A, Burchard EG, Thyssen JP, Hansen T, Kårhus LL, Dantoft TM, Jeanrenaud ACSN, Ghauri A, Arnold A, Homuth G, Lau S, Nöthen MM, Hübner N, Imboden M, Visconti A, Falchi M, Bataille V, Hysi P, Ballardini N, Boomsma DI, Hottenga JJ, Müller-Nurasyid M, Ahluwalia TS, Stokholm J, Chawes B, Schoos AM, Esplugues A, Bustamante M, Raby B, Arshad S, German C, Esko T, Milani LA, Metspalu A, Terao C, Abuabara K, Løset M, Hveem K, Jacobsson B, Pino-Yanes M, Strachan DP, Grarup N, Linneberg A, Lee YA, Probst-Hensch N, Weidinger S, Jarvelin MR, Melén E, Hakonarson H, Irvine AD, Jarvis D, Nijsten T, Duijts L, Vonk JM, Koppelmann GH, Godfrey KM, Barton SJ, Feenstra B, Pennell CE, Sly PD, Holt PG, Williams LK, Bisgaard H, Bønnelykke K, Curtin J, Simpson A, Murray C, Schikowski T, Bunyavanich S, Weiss ST, Holloway JW, Min JL, Brown SJ, Standl M, Paternoster L. PMID: 37794016; PMCID: PMC10550990.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    5. Low- and High-Density Lipoprotein Cholesterol and Dementia Risk Over 17 Years of Follow-up Among Members of a Large Health Care Plan. Neurology. 2023 Nov 21; 101(21):e2172-e2184. Ferguson EL, Zimmerman SC, Jiang C, Choi M, Swinnerton K, Choudhary V, Meyers TJ, Hoffmann TJ, Gilsanz P, Oni-Orisan A, Whitmer RA, Whitmer RA, Risch N, Krauss RM, Schaefer CA, Glymour MM. PMID: 37793911; PMCID: PMC10663022.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    6. 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  
    7. 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:
    8. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. Nat Commun. 2023 05 15; 14(1):2709. Ollila HM, Sharon E, Lin L, Sinnott-Armstrong N, Ambati A, Yogeshwar SM, Hillary RP, Jolanki O, Faraco J, Einen M, Luo G, Zhang J, Han F, Yan H, Dong XS, Li J, Zhang J, Hong SC, Kim TW, Dauvilliers Y, Barateau L, Lammers GJ, Fronczek R, Mayer G, Santamaria J, Arnulf I, Knudsen-Heier S, Bredahl MKL, Thorsby PM, Plazzi G, Pizza F, Moresco M, Crowe C, Van den Eeden SK, Lecendreux M, Bourgin P, Kanbayashi T, Martínez-Orozco FJ, Peraita-Adrados R, Benetó A, Montplaisir J, Desautels A, Huang YS, FinnGen, Jennum P, Nevsimalova S, Kemlink D, Iranzo A, Overeem S, Wierzbicka A, Geisler P, Sonka K, Honda M, Högl B, Stefani A, Coelho FM, Mantovani V, Feketeova E, Wadelius M, Eriksson N, Smedje H, Hallberg P, Hesla PE, Rye D, Pelin Z, Ferini-Strambi L, Bassetti CL, Mathis J, Khatami R, Aran A, Nampoothiri S, Olsson T, Kockum I, Partinen M, Perola M, Kornum BR, Rueger S, Winkelmann J, Miyagawa T, Toyoda H, Khor SS, Shimada M, Tokunaga K, Rivas M, Pritchard JK, Risch N, Kutalik Z, O'Hara R, Hallmayer J, Ye CJ, Mignot EJ. PMID: 37188663; PMCID: PMC10185546.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    9. A large genome-wide association study of QT interval length utilizing electronic health records. Genetics. 2022 11 30; 222(4). Hoffmann TJ, Lu M, Oni-Orisan A, Lee C, Risch N, Iribarren C. PMID: 36271874; PMCID: PMC9713425.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    10. Polygenic Risk Score and Statin Relative Risk Reduction for Primary Prevention of Myocardial Infarction in a Real-World Population. Clin Pharmacol Ther. 2022 11; 112(5):1070-1078. Oni-Orisan A, Haldar T, Cayabyab MAS, Ranatunga DK, Hoffmann TJ, Iribarren C, Krauss RM, Risch N. PMID: 35862449; PMCID: PMC10112337.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansPHPublic Health
    11. Modest effect of statins on fasting glucose in a longitudinal electronic health record based cohort. Cardiovasc Diabetol. 2022 07 14; 21(1):132. Haldar T, Oni-Orisan A, Hoffmann TJ, Schaefer C, Iribarren C, Krauss RM, Medina MW, Risch N. PMID: 35836181; PMCID: PMC9284686.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    12. Global priorities for large-scale biomarker-based prospective cohorts. Cell Genom. 2022 Jun 08; 2(6):100141. Collins R, Balaconis MK, Brunak S, Chen Z, De Silva M, Gaziano JM, Ginsburg GS, Jha P, Kuri P, Metspalu A, Mulder N, Risch N. PMID: 36778137; PMCID: PMC9903754.
      View in: PubMed   Mentions: 1  
    13. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nat Genet. 2022 05; 54(5):541-547. Palmer DS, Howrigan DP, Chapman SB, Adolfsson R, Bass N, Blackwood D, Boks MPM, Chen CY, Churchhouse C, Corvin AP, Craddock N, Curtis D, Di Florio A, Dickerson F, Freimer NB, Goes FS, Jia X, Jones I, Jones L, Jonsson L, Kahn RS, Landén M, Locke AE, McIntosh AM, McQuillin A, Morris DW, O'Donovan MC, Ophoff RA, Owen MJ, Pedersen NL, Posthuma D, Reif A, Risch N, Schaefer C, Scott L, Singh T, Smoller JW, Solomonson M, Clair DS, Stahl EA, Vreeker A, Walters JTR, Wang W, Watts NA, Yolken R, Zandi PP, Neale BM. PMID: 35410376; PMCID: PMC9117467.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    14. 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
    15. QT Interval Dynamics and Cardiovascular Outcomes: A Cohort Study in an Integrated Health Care Delivery System. J Am Heart Assoc. 2021 10 05; 10(19):e018513. Mantri N, Lu M, Zaroff JG, Risch N, Hoffmann T, Oni-Orisan A, Lee C, Jorgenson E, Iribarren C. PMID: 34581201; PMCID: PMC8649135.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    16. Torsade de pointes: A nested case-control study in an integrated healthcare delivery system. Ann Noninvasive Electrocardiol. 2022 01; 27(1):e12888. Mantri N, Lu M, Zaroff JG, Risch N, Hoffmann T, Oni-Orisan A, Lee C, Iribarren C. PMID: 34547155; PMCID: PMC8739596.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    17. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021 Sep; 26(9):5251. Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ. PMID: 33674754; PMCID: PMC9119210.
      View in: PubMed   Mentions:    Fields:    
    18. Effect of SLCO1B1 T521C on Statin-Related Myotoxicity With Use of Lovastatin and Atorvastatin. Clin Pharmacol Ther. 2021 09; 110(3):733-740. Lu B, Sun L, Seraydarian M, Hoffmann TJ, Medina MW, Risch N, Iribarren C, Krauss RM, Oni-Orisan A. PMID: 34114646; PMCID: PMC8376784.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    19. A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Nat Genet. 2021 07; 53(7):972-981. Veturi Y, Lucas A, Bradford Y, Hui D, Dudek S, Theusch E, Verma A, Miller JE, Kullo I, Hakonarson H, Sleiman P, Schaid D, Stein CM, Edwards DRV, Feng Q, Wei WQ, Medina MW, Krauss RM, Hoffmann TJ, Risch N, Voight BF, Rader DJ, Ritchie MD. PMID: 34140684; PMCID: PMC8555954.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansPHPublic Health
    20. Challenges in providing residual risks in carrier testing. Prenat Diagn. 2021 Aug; 41(9):1049-1056. Nussbaum RL, Slotnick RN, Risch NJ. PMID: 34057205; PMCID: PMC8453722.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    21. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021 09; 26(9):5239-5250. Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ. PMID: 33483695; PMCID: PMC8295400.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    22. Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations. Commun Biol. 2020 12 14; 3(1):765. Jorgenson E, Choquet H, Yin J, Hoffmann TJ, Banda Y, Kvale MN, Risch N, Schaefer C, Asgari MM. PMID: 33318654; PMCID: PMC7736583.
      View in: PubMed   Mentions: 4  Translation:Humans
    23. A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility. Cancer Res. 2021 04 01; 81(7):1695-1703. Emami NC, Cavazos TB, Rashkin SR, Cario CL, Graff RE, Tai CG, Mefford JA, Kachuri L, Wan E, Wong S, Aaronson D, Presti J, Habel LA, Shan J, Ranatunga DK, Chao CR, Ghai NR, Jorgenson E, Sakoda LC, Kvale MN, Kwok PY, Schaefer C, Risch N, Hoffmann TJ, Van Den Eeden SK, Witte JS. PMID: 33293427; PMCID: PMC8137514.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    24. Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. Nat Commun. 2020 10 09; 11(1):5116. Sieh W, Rothstein JH, Klein RJ, Alexeeff SE, Sakoda LC, Jorgenson E, McBride RB, Graff RE, McGuire V, Achacoso N, Acton L, Liang RY, Lipson JA, Rubin DL, Yaffe MJ, Easton DF, Schaefer C, Risch N, Whittemore AS, Habel LA. PMID: 33037222; PMCID: PMC7547012.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    25. The role of exome sequencing in newborn screening for inborn errors of metabolism. Nat Med. 2020 09; 26(9):1392-1397. Adhikari AN, Gallagher RC, Wang Y, Currier RJ, Amatuni G, Bassaganyas L, Chen F, Kundu K, Kvale M, Mooney SD, Nussbaum RL, Randi SS, Sanford J, Shieh JT, Srinivasan R, Sunderam U, Tang H, Vaka D, Zou Y, Koenig BA, Kwok PY, Risch N, Puck JM, Brenner SE. PMID: 32778825; PMCID: PMC8800147.
      View in: PubMed   Mentions: 65     Fields:    Translation:HumansPHPublic Health
    26. Analysis of putative cis-regulatory elements regulating blood pressure variation. Hum Mol Genet. 2020 07 21; 29(11):1922-1932. Nandakumar P, Lee D, Hoffmann TJ, Ehret GB, Arking D, Ranatunga D, Li M, Grove ML, Boerwinkle E, Schaefer C, Kwok PY, Iribarren C, Risch N, Chakravarti A. PMID: 32436959; PMCID: PMC7372556.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    27. Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction. Circ Genom Precis Med. 2020 08; 13(4):e002804. Choquet H, Thai KK, Jiang C, Ranatunga DK, Hoffmann TJ, Go AS, Lindsay AC, Ehm MG, Waterworth DM, Risch N, Schaefer C. PMID: 32605384; PMCID: PMC7446727.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    28. A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness. Commun Biol. 2020 06 11; 3(1):301. Choquet H, Melles RB, Yin J, Hoffmann TJ, Thai KK, Kvale MN, Banda Y, Hardcastle AJ, Tuft SJ, Glymour MM, Schaefer C, Risch N, Nair KS, Hysi PG, Jorgenson E. PMID: 32528159; PMCID: PMC7289804.
      View in: PubMed   Mentions: 13  Translation:Humans
    29. The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. NPJ Genom Med. 2020; 5:1. Oni-Orisan A, Haldar T, Ranatunga DK, Medina MW, Schaefer C, Krauss RM, Iribarren C, Risch N, Hoffmann TJ. PMID: 31969989; PMCID: PMC6965183.
      View in: PubMed   Mentions: 8  
    30. A brief history of human disease genetics. Nature. 2020 01; 577(7789):179-189. Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, Shendure J, Soranzo N, McCarthy MI. PMID: 31915397; PMCID: PMC7405896.
      View in: PubMed   Mentions: 222     Fields:    Translation:HumansAnimals
    31. A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophy. Am J Med Genet A. 2020 03; 182(3):513-520. Mendelsohn BA, Beleford DT, Abu-El-Haija A, Alsaleh NS, Rahbeeni Z, Martin PM, Rego S, Huang A, Capodanno G, Shieh JT, Van Ziffle J, Risch N, Alkuraya FS, Slavotinek AM. PMID: 31880405; PMCID: PMC10335815.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    32. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. JAMA. 2019 11 05; 322(17):1682-1691. Genetics of Glaucoma in People of African Descent (GGLAD) Consortium, Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG, Akafo S, Alhassan MB, Asimadu I, Ayyagari R, Bakayoko S, Nyamsi PB, Bowden DW, Bromley WC, Budenz DL, Carmichael TR, Challa P, Chen YI, Chuka-Okosa CM, Cooke Bailey JN, Costa VP, Cruz DA, DuBiner H, Ervin JF, Feldman RM, Flamme-Wiese M, Gaasterland DE, Garnai SJ, Girkin CA, Guirou N, Guo X, Haines JL, Hammond CJ, Herndon L, Hoffmann TJ, Hulette CM, Hydara A, Igo RP, Jorgenson E, Kabwe J, Kilangalanga NJ, Kizor-Akaraiwe N, Kuchtey RW, Lamari H, Li Z, Liebmann JM, Liu Y, Loos RJF, Melo MB, Moroi SE, Msosa JM, Mullins RF, Nadkarni G, Napo A, Ng MCY, Nunes HF, Obeng-Nyarkoh E, Okeke A, Okeke S, Olaniyi O, Olawoye O, Oliveira MB, Pasquale LR, Perez-Grossmann RA, Pericak-Vance MA, Qin X, Ramsay M, Resnikoff S, Richards JE, Schimiti RB, Sim KS, Sponsel WE, Svidnicki PV, Thiadens AAHJ, Uche NJ, van Duijn CM, de Vasconcellos JPC, Wiggs JL, Zangwill LM, Risch N, Milea D, Ashaye A, Klaver CCW, Weinreb RN, Ashley Koch AE, Fingert JH, Khor CC. PMID: 31688885; PMCID: PMC6865235.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    33. Assessing the clinical impact of CYP2C9 pharmacogenetic variation on phenytoin prescribing practice and patient response in an integrated health system. Pharmacogenet Genomics. 2019 10; 29(8):192-199. Fohner AE, Ranatunga DK, Thai KK, Lawson BL, Risch N, Oni-Orisan A, Jelalian AT, Rettie AE, Liu VX, Schaefer CA. PMID: 31461080; PMCID: PMC6989102.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    34. Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African American subjects in 2 large US cohorts. J Allergy Clin Immunol. 2020 01; 145(1):192-198.e11. Abuabara K, You Y, Margolis DJ, Hoffmann TJ, Risch N, Jorgenson E. PMID: 31369801; PMCID: PMC6949407.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    35. Telomere length and socioeconomic status at neighborhood and individual levels among 80,000 adults in the Genetic Epidemiology Research on Adult Health and Aging cohort. Environ Epidemiol. 2019 Jun; 3(3):e049. Alexeeff SE, Schaefer CA, Kvale MN, Shan J, Blackburn EH, Risch N, Ranatunga DK, Jorgenson E, Hoffmann TJ, Sakoda LC, Quesenberry CP, Van Den Eeden SK. PMID: 33778338; PMCID: PMC7939422.
      View in: PubMed   Mentions: 13  
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    69. Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. JAMA Psychiatry. 2014 Apr; 71(4):375-87. Fears SC, Service SK, Kremeyer B, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Franco J, Lopez MC, Montoya G, Montoya P, Aldana I, Teshiba TM, Abaryan Z, Al-Sharif NB, Ericson M, Jalbrzikowski M, Luykx JJ, Navarro L, Tishler TA, Altshuler L, Bartzokis G, Escobar J, Glahn DC, Ospina-Duque J, Risch N, Ruiz-Linares A, Thompson PM, Cantor RM, Lopez-Jaramillo C, Macaya G, Molina J, Reus VI, Sabatti C, Freimer NB, Bearden CE. PMID: 24522887; PMCID: PMC4045237.
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    73. Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. Am J Hum Genet. 2013 Jun 06; 92(6):904-16. Coram MA, Duan Q, Hoffmann TJ, Thornton T, Knowles JW, Johnson NA, Ochs-Balcom HM, Donlon TA, Martin LW, Eaton CB, Robinson JG, Risch NJ, Zhu X, Kooperberg C, Li Y, Reiner AP, Tang H. PMID: 23726366; PMCID: PMC3675231.
      View in: PubMed   Mentions: 86     Fields:    Translation:HumansCells
    74. Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping. J Hypertens. 2012 Oct; 30(10):1970-6. Shetty PB, Tang H, Tayo BO, Morrison AC, Hanis CL, Rao DC, Young JH, Fox ER, Boerwinkle E, Cooper RS, Risch NJ, Zhu X, Candidate Gene Association Resource (CARe) Consortium. PMID: 22914544; PMCID: PMC3575678.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    75. Estimating kinship in admixed populations. Am J Hum Genet. 2012 Jul 13; 91(1):122-38. Thornton T, Tang H, Hoffmann TJ, Ochs-Balcom HM, Caan BJ, Risch N. PMID: 22748210; PMCID: PMC3397261.
      View in: PubMed   Mentions: 109     Fields:    Translation:Humans
    76. A brief note on the resemblance between relatives in the presence of population stratification. Heredity (Edinb). 2012 May; 108(5):563-8. Sebro R, Risch NJ. PMID: 22234249; PMCID: PMC3330693.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    77. Cystic fibrosis mutations for p.F508del compound heterozygotes predict sweat chloride levels and pancreatic sufficiency. Clin Genet. 2012 Dec; 82(6):546-51. Sebro R, Levy H, Schneck K, Dimmock D, Raby BA, Cannon CL, Broeckel U, Risch NJ. PMID: 22035343; PMCID: PMC4279028.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    78. Differentiating population stratification from genotyping error using family data. Ann Hum Genet. 2012 Jan; 76(1):42-52. Sebro R, Lange C, Laird NM, Rogus JJ, Risch NJ. PMID: 22111716.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    79. Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. Genomics. 2011 Dec; 98(6):422-30. Hoffmann TJ, Zhan Y, Kvale MN, Hesselson SE, Gollub J, Iribarren C, Lu Y, Mei G, Purdy MM, Quesenberry C, Rowell S, Shapero MH, Smethurst D, Somkin CP, Van den Eeden SK, Walter L, Webster T, Whitmer RA, Whitmer RA, Finn A, Schaefer C, Kwok PY, Risch N. PMID: 21903159; PMCID: PMC3502750.
      View in: PubMed   Mentions: 103     Fields:    Translation:Humans
    80. Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry. 2011 Nov; 68(11):1095-102. Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, Risch N. PMID: 21727249; PMCID: PMC4440679.
      View in: PubMed   Mentions: 766     Fields:    Translation:Humans
    81. Charles Joseph Epstein, M.D., 1933–2011, in memoriam. Am J Hum Genet. 2011 Jun 10; 88(6):684-8. Wynshaw-Boris A, Risch N, Motulsky A. PMID: 21805720; PMCID: PMC3113342.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    82. Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics. 2011 Aug; 98(2):79-89. Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, Cao Y, Cawley S, Chung E, Connell S, Eshragh J, Ewing M, Gollub J, Henderson M, Hubbell E, Iribarren C, Kaufman J, Lao RZ, Lu Y, Ludwig D, Mathauda GK, McGuire W, Mei G, Miles S, Purdy MM, Quesenberry C, Ranatunga D, Rowell S, Sadler M, Shapero MH, Shen L, Shenoy TR, Smethurst D, Van den Eeden SK, Walter L, Wan E, Wearley R, Webster T, Wen CC, Weng L, Whitmer RA, Whitmer RA, Williams A, Wong SC, Zau C, Finn A, Schaefer C, Kwok PY, Risch N. PMID: 21565264; PMCID: PMC3146553.
      View in: PubMed   Mentions: 120     Fields:    Translation:Humans
    83. History shaped the geographic distribution of genomic admixture on the island of Puerto Rico. PLoS One. 2011 Jan 31; 6(1):e16513. Via M, Gignoux CR, Roth LA, Fejerman L, Galanter J, Choudhry S, Toro-Labrador G, Viera-Vera J, Oleksyk TK, Beckman K, Ziv E, Risch N, Burchard EG, Martínez-Cruzado JC. PMID: 21304981; PMCID: PMC3031579.
      View in: PubMed   Mentions: 63     Fields:    Translation:Humans
    84. Common variants in P2RY11 are associated with narcolepsy. Nat Genet. 2011 Jan; 43(1):66-71. Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, Winkelmann J, Plazzi G, Nevsimalova S, Hong SC, Honda Y, Honda M, Högl B, Ton TG, Montplaisir J, Bourgin P, Kemlink D, Huang YS, Warby S, Einen M, Eshragh JL, Miyagawa T, Desautels A, Ruppert E, Hesla PE, Poli F, Pizza F, Frauscher B, Jeong JH, Lee SP, Strohl KP, Longstreth WT, Kvale M, Dobrovolna M, Ohayon MM, Nepom GT, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Peppard P, Young T, Jennum P, Steinman L, Tokunaga K, Kwok PY, Risch N, Hallmayer J, Mignot E. PMID: 21170044; PMCID: PMC3019286.
      View in: PubMed   Mentions: 82     Fields:    Translation:Humans
    85. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J Am Coll Cardiol. 2010 Nov 02; 56(19):1552-63. Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, Knowles JW, Thompson JR, Absher D, Iribarren C, Go A, Fortmann SP, Sidney S, Risch N, Tang H, Myers RM, Berger K, Stoll M, Shah SH, Thorgeirsson G, Andersen K, Havulinna AS, Herrera JE, Faraday N, Kim Y, Kral BG, Mathias RA, Ruczinski I, Suktitipat B, Wilson AF, Yanek LR, Becker LC, Linsel-Nitschke P, Lieb W, König IR, Hengstenberg C, Fischer M, Stark K, Reinhard W, Winogradow J, Grassl M, Grosshennig A, Preuss M, Schreiber S, Wichmann HE, Meisinger C, Yee J, Friedlander Y, Do R, Meigs JB, Williams G, Nathan DM, MacRae CA, Qu L, Wilensky RL, Matthai WH, Qasim AN, Hakonarson H, Pichard AD, Kent KM, Satler L, Lindsay JM, Waksman R, Knouff CW, Waterworth DM, Walker MC, Mooser VE, Marrugat J, Lucas G, Subirana I, Sala J, Ramos R, Martinelli N, Olivieri O, Trabetti E, Malerba G, Pignatti PF, Guiducci C, Mirel D, Parkin M, Hirschhorn JN, Asselta R, Duga S, Musunuru K, Daly MJ, Purcell S, Eifert S, Braund PS, Wright BJ, Balmforth AJ, Ball SG, Myocardial Infarction Genetics Consortium, Wellcome Trust Case Control Consortium, Cardiogenics, Ouwehand WH, Deloukas P, Scholz M, Cambien F, Huge A, Scheffold T, Salomaa V, Girelli D, Granger CB, Peltonen L, McKeown PP, Altshuler D, Melander O, Devaney JM, Epstein SE, Rader DJ, Elosua R, Engert JC, Anand SS, Hall AS, Ziegler A, O'Donnell CJ, Spertus JA, Siscovick D, Schwartz SM, Becker D, Thorsteinsdottir U, Stefansson K, Schunkert H, Samani NJ, Quertermous T. PMID: 20933357; PMCID: PMC3084526.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    86. Testing for non-random mating: evidence for ancestry-related assortative mating in the Framingham heart study. Genet Epidemiol. 2010 Nov; 34(7):674-9. Sebro R, Hoffman TJ, Lange C, Rogus JJ, Risch NJ. PMID: 20842694; PMCID: PMC3775670.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    87. Differences in albuminuria between Hispanics and whites: an evaluation by genetic ancestry and country of origin: the multi-ethnic study of atherosclerosis. Circ Cardiovasc Genet. 2010 Jun; 3(3):240-7. Peralta CA, Li Y, Wassel C, Choudhry S, Palmas W, Seldin MF, Risch N, Siscovick D, Arnett D, Psaty B, Shlipak MG. PMID: 20445135; PMCID: PMC2948758.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    88. Human genetic variation recognizes functional elements in noncoding sequence. Genome Res. 2010 Mar; 20(3):311-9. Lomelin D, Jorgenson E, Risch N. PMID: 20032171; PMCID: PMC2840987.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansCells
    89. Characterizing the admixed African ancestry of African Americans. Genome Biol. 2009; 10(12):R141. Zakharia F, Basu A, Absher D, Assimes TL, Go AS, Hlatky MA, Iribarren C, Knowles JW, Li J, Narasimhan B, Sidney S, Southwick A, Myers RM, Quertermous T, Risch N, Tang H. PMID: 20025784; PMCID: PMC2812948.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    90. The Association of African Ancestry and elevated creatinine in the Coronary Artery Risk Development in Young Adults (CARDIA) Study. Am J Nephrol. 2010; 31(3):202-8. Peralta CA, Risch N, Lin F, Shlipak MG, Reiner A, Ziv E, Tang H, Siscovick D, Bibbins-Domingo K. PMID: 20029176; PMCID: PMC3487144.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    91. Ancestry-related assortative mating in Latino populations. Genome Biol. 2009; 10(11):R132. Risch N, Choudhry S, Via M, Basu A, Sebro R, Eng C, Beckman K, Thyne S, Chapela R, Rodriguez-Santana JR, Rodriguez-Cintron W, Avila PC, Ziv E, Gonzalez Burchard E. PMID: 19930545; PMCID: PMC3091325.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    92. Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Neurology. 2009 Oct 20; 73(16):1264-72. Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. PMID: 19841378; PMCID: PMC2764413.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    93. Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. JAMA. 2009 Jun 17; 301(23):2462-71. Risch N, Herrell R, Lehner T, Liang KY, Eaves L, Hoh J, Griem A, Kovacs M, Ott J, Merikangas KR. PMID: 19531786; PMCID: PMC2938776.
      View in: PubMed   Mentions: 599     Fields:    Translation:Humans
    94. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nat Genet. 2009 Jun; 41(6):708-11. Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Hong SS, Honda Y, Honda M, Högl B, Longstreth WT, Montplaisir J, Kemlink D, Einen M, Chen J, Musone SL, Akana M, Miyagawa T, Duan J, Desautels A, Erhardt C, Hesla PE, Poli F, Frauscher B, Jeong JH, Lee SP, Ton TG, Kvale M, Kolesar L, Dobrovolná M, Nepom GT, Salomon D, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Young T, Peppard P, Tokunaga K, Kwok PY, Risch N, Mignot E. PMID: 19412176; PMCID: PMC2803042.
      View in: PubMed   Mentions: 181     Fields:    Translation:HumansAnimalsCells
    95. Admixture mapping of quantitative trait loci for blood lipids in African-Americans. Hum Mol Genet. 2009 Jun 01; 18(11):2091-8. Basu A, Tang H, Lewis CE, North K, Curb JD, Quertermous T, Mosley TH, Boerwinkle E, Zhu X, Risch NJ. PMID: 19304782; PMCID: PMC2722229.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    96. Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q. Obesity (Silver Spring). 2009 Jun; 17(6):1226-31. Basu A, Tang H, Arnett D, Gu CC, Mosley T, Kardia S, Luke A, Tayo B, Cooper R, Zhu X, Risch N. PMID: 19584881; PMCID: PMC2929755.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    97. Genome-wide distribution of ancestry in Mexican Americans. Hum Genet. 2008 Oct; 124(3):207-14. Basu A, Tang H, Zhu X, Gu CC, Hanis C, Boerwinkle E, Risch N. PMID: 18752003; PMCID: PMC3131689.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    98. Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet. 2008 Aug 01; 17(15):2320-8. Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T. PMID: 18443000; PMCID: PMC2733811.
      View in: PubMed   Mentions: 86     Fields:    Translation:HumansCells
    99. Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region. Hum Genet. 2008 Jun; 123(5):455-68. Choudhry S, Taub M, Mei R, Rodriguez-Santana J, Rodriguez-Cintron W, Shriver MD, Ziv E, Risch NJ, Burchard EG. PMID: 18401594; PMCID: PMC2664533.
      View in: PubMed   Mentions: 47     Fields:    Translation:HumansCells
    100. Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD. BMC Med Genet. 2008 Apr 02; 9:23. Knowles JW, Assimes TL, Boerwinkle E, Fortmann SP, Go A, Grove ML, Hlatky M, Iribarren C, Li J, Myers R, Risch N, Sidney S, Southwick A, Volcik KA, Quertermous T. PMID: 18384690; PMCID: PMC2322963.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    101. Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Hum Genet. 2008 May; 123(4):399-408. Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, Iribarren C, Boerwinkle E, Myers R, Risch N, Quertermous T. PMID: 18369664; PMCID: PMC4023692.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    102. Admixture mapping and the role of population structure for localizing disease genes. Adv Genet. 2008; 60:547-69. Zhu X, Tang H, Risch N. PMID: 18358332.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    103. An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus. Proc Natl Acad Sci U S A. 2007 Dec 26; 104(52):20896-901. DeLuca GC, Ramagopalan SV, Herrera BM, Dyment DA, Lincoln MR, Montpetit A, Pugliatti M, Barnardo MC, Risch NJ, Sadovnick AD, Chao M, Sotgiu S, Hudson TJ, Ebers GC. PMID: 18087043; PMCID: PMC2409238.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    104. A genome-wide scan in forty large pedigrees with multiple sclerosis. J Hum Genet. 2007; 52(12):955-962. Willer CJ, Dyment DA, Cherny S, Ramagopalan SV, Herrera BM, Morrison KME, Sadovnick AD, Risch NJ, Ebers GC. PMID: 18000641.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    105. A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease. Atherosclerosis. 2008 May; 198(1):136-44. Assimes TL, Knowles JW, Priest JR, Basu A, Borchert A, Volcik KA, Grove ML, Tabor HK, Southwick A, Tabibiazar R, Sidney S, Boerwinkle E, Go AS, Iribarren C, Hlatky MA, Fortmann SP, Myers RM, Kuhn H, Risch N, Quertermous T. PMID: 17959182; PMCID: PMC2440699.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    106. Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites. Am J Med Genet A. 2007 Sep 15; 143A(18):2098-105. Saunders-Pullman R, Raymond D, Senthil G, Kramer P, Ohmann E, Deligtisch A, Shanker V, Greene P, Tabamo R, Huang N, Tagliati M, Kavanagh P, Soto-Valencia J, Aguiar Pde C, Risch N, Ozelius L, Bressman S. PMID: 17702011.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    107. Minimum incidence of primary cervical dystonia in a multiethnic health care population. Neurology. 2007 Aug 14; 69(7):676-80. Marras C, Van den Eeden SK, Fross RD, Benedict-Albers KS, Klingman J, Leimpeter AD, Nelson LM, Risch N, Karter AJ, Bernstein AL, Tanner CM. PMID: 17698789.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    108. Recent genetic selection in the ancestral admixture of Puerto Ricans. Am J Hum Genet. 2007 Sep; 81(3):626-33. Tang H, Choudhry S, Mei R, Morgan M, Rodriguez-Cintron W, Burchard EG, Risch NJ. PMID: 17701908; PMCID: PMC1950843.
      View in: PubMed   Mentions: 98     Fields:    Translation:HumansCells
    109. Dissecting complex diseases in complex populations: asthma in latino americans. Proc Am Thorac Soc. 2007 Jul; 4(3):226-33. Choudhry S, Seibold MA, Borrell LN, Tang H, Serebrisky D, Chapela R, Rodriguez-Santana JR, Avila PC, Ziv E, Rodriguez-Cintron W, Risch NJ, Burchard EG. PMID: 17607004; PMCID: PMC2647623.
      View in: PubMed   Mentions: 27     Fields:    
    110. A genome scan in a single pedigree with a high prevalence of multiple sclerosis. J Neurol Neurosurg Psychiatry. 2008 Feb; 79(2):158-62. Dyment DA, Cader MZ, Herrera BM, Ramagopalan SV, Orton SM, Chao M, Willer CJ, Sadovnick AD, Risch N, Ebers GC. PMID: 17550985.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    111. Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia. Am J Hum Genet. 2007 Jun; 80(6):1188-93. Risch NJ, Bressman SB, Senthil G, Ozelius LJ. PMID: 17503336; PMCID: PMC1867106.
      View in: PubMed   Mentions: 47     Fields:    Translation:HumansCells
    112. Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene. Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 05; 144B(3):361-4. Heiman GA, Ottman R, Saunders-Pullman RJ, Ozelius LJ, Risch NJ, Bressman SB. PMID: 17066475; PMCID: PMC3694482.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    113. Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study. Am J Hypertens. 2006 Dec; 19(12):1270-7. Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA, SAPPHIRe Study Group. PMID: 17161774.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    114. Ancestry-environment interactions and asthma risk among Puerto Ricans. Am J Respir Crit Care Med. 2006 Nov 15; 174(10):1088-93. Choudhry S, Burchard EG, Borrell LN, Tang H, Gomez I, Naqvi M, Nazario S, Torres A, Casal J, Martinez-Cruzado JC, Ziv E, Avila PC, Rodriguez-Cintron W, Risch NJ. PMID: 16973984; PMCID: PMC2648109.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    115. Twins of mistaken zygosity (TOMZ): evidence for genetic contributions to dietary patterns and physiologic traits. Twin Res Hum Genet. 2006 Aug; 9(4):540-9. Gunderson EP, Tsai AL, Selby JV, Caan B, Mayer-Davis EJ, Risch N. PMID: 16899161.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    116. Global transcriptional response to interferon is a determinant of HCV treatment outcome and is modified by race. Hepatology. 2006 Aug; 44(2):352-9. He XS, Ji X, Hale MB, Cheung R, Ahmed A, Guo Y, Nolan GP, Pfeffer LM, Wright TL, Risch N, Tibshirani R, Greenberg HB. PMID: 16871572.
      View in: PubMed   Mentions: 43     Fields:    Translation:HumansCells
    117. Reconstructing genetic ancestry blocks in admixed individuals. Am J Hum Genet. 2006 Jul; 79(1):1-12. Tang H, Coram M, Wang P, Zhu X, Risch N. PMID: 16773560; PMCID: PMC1474129.
      View in: PubMed   Mentions: 145     Fields:    Translation:Humans
    118. Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans. Hum Genet. 2006 Jul; 119(6):624-33. Tang H, Jorgenson E, Gadde M, Kardia SL, Rao DC, Zhu X, Schork NJ, Hanis CL, Risch N. PMID: 16738946.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    119. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med. 2006 Jan 26; 354(4):424-5. Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB. PMID: 16436782.
      View in: PubMed   Mentions: 245     Fields:    Translation:Humans
    120. Dissecting racial and ethnic differences. N Engl J Med. 2006 Jan 26; 354(4):408-11. Risch N. PMID: 16436773.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    121. Functional genomics of membrane transporters in human populations. Genome Res. 2006 Feb; 16(2):223-30. Urban TJ, Sebro R, Hurowitz EH, Leabman MK, Badagnani I, Lagpacan LL, Risch N, Giacomini KM. PMID: 16354753; PMCID: PMC1361718.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    122. Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16. Neuron. 2005 Dec 08; 48(5):704-5; author reply 705-6. Glatt CE, Carlson E, Taylor TR, Risch N, Reus VI, Schaefer CA. PMID: 16337902.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    123. Population stratification confounds genetic association studies among Latinos. Hum Genet. 2006 Jan; 118(5):652-64. Choudhry S, Coyle NE, Tang H, Salari K, Lind D, Clark SL, Tsai HJ, Naqvi M, Phong A, Ung N, Matallana H, Avila PC, Casal J, Torres A, Nazario S, Castro R, Battle NC, Perez-Stable EJ, Kwok PY, Sheppard D, Shriver MD, Rodriguez-Cintron W, Risch N, Ziv E, Burchard EG, Genetics of Asthma in Latino Americans GALA Study. PMID: 16283388.
      View in: PubMed   Mentions: 116     Fields:    Translation:Humans
    124. Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research. Am J Public Health. 2005 Dec; 95(12):2161-8. González Burchard E, Borrell LN, Choudhry S, Naqvi M, Tsai HJ, Rodriguez-Santana JR, Chapela R, Rogers SD, Mei R, Rodriguez-Cintron W, Arena JF, Kittles R, Perez-Stable EJ, Ziv E, Risch N. PMID: 16257940; PMCID: PMC1449501.
      View in: PubMed   Mentions: 169     Fields:    Translation:Humans
    125. The whole side of it--an interview with Neil Risch by Jane Gitschier. PLoS Genet. 2005 Jul 25; 1(1):e14. Risch N. PMID: 17411332; PMCID: PMC1183530.
      View in: PubMed   Mentions: 1     Fields:    
    126. The whole side of it--an interview with Neil Risch. Interview by Jane Gitschier. PLoS Genet. 2005 Jul; 1(1):3-5. Risch N. PMID: 16103913.
      View in: PubMed   Mentions:    Fields:    
    127. Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics. Genet Epidemiol. 2005 Jul; 29(1):76-86. Salari K, Choudhry S, Tang H, Naqvi M, Lind D, Avila PC, Coyle NE, Ung N, Nazario S, Casal J, Torres-Palacios A, Clark S, Phong A, Gomez I, Matallana H, Pérez-Stable EJ, Shriver MD, Kwok PY, Sheppard D, Rodriguez-Cintron W, Risch NJ, Burchard EG, Ziv E. PMID: 15918156.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    128. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. Hum Mol Genet. 2005 Jul 15; 14(14):2019-26. Dyment DA, Herrera BM, Cader MZ, Willer CJ, Lincoln MR, Sadovnick AD, Risch N, Ebers GC. PMID: 15930013.
      View in: PubMed   Mentions: 73     Fields:    Translation:Humans
    129. Estimation of individual admixture: analytical and study design considerations. Genet Epidemiol. 2005 May; 28(4):289-301. Tang H, Peng J, Wang P, Risch NJ. PMID: 15712363.
      View in: PubMed   Mentions: 344     Fields:    Translation:HumansCells
    130. An autosomal genome-wide scan for loci linked to pre-diabetic phenotypes in nondiabetic Chinese subjects from the Stanford Asia-Pacific Program of Hypertension and Insulin Resistance Family Study. Diabetes. 2005 Apr; 54(4):1200-6. Chiu YF, Chuang LM, Hsiao CF, Hung YJ, Lin MW, Chen YT, Grove J, Jorgenson E, Quertermous T, Risch N, Hsiung CA. PMID: 15793262.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    131. 2004 Curt Stern Award Address. The SNP endgame: a multidisciplinary approach. Am J Hum Genet. 2005 Feb; 76(2):221-6. Risch N. PMID: 15714688; PMCID: PMC1196367.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    132. Admixture mapping for hypertension loci with genome-scan markers. Nat Genet. 2005 Feb; 37(2):177-81. Zhu X, Luke A, Cooper RS, Quertermous T, Hanis C, Mosley T, Gu CC, Tang H, Rao DC, Risch N, Weder A. PMID: 15665825.
      View in: PubMed   Mentions: 142     Fields:    Translation:HumansCells
    133. Haplotype structure and ethnic-specific allele frequencies at the OCTN locus: implications for the genetics of Crohn's disease. Inflamm Bowel Dis. 2005 Jan; 11(1):78-9. Urban TJ, Giacomini KM, Risch N. PMID: 15674120.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    134. Ethnicity and human genetic linkage maps. Am J Hum Genet. 2005 Feb; 76(2):276-90. Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. PMID: 15627237; PMCID: PMC1196373.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    135. Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. Am J Hum Genet. 2005 Feb; 76(2):268-75. Tang H, Quertermous T, Rodriguez B, Kardia SL, Zhu X, Brown A, Pankow JS, Province MA, Hunt SC, Boerwinkle E, Schork NJ, Risch NJ. PMID: 15625622; PMCID: PMC1196372.
      View in: PubMed   Mentions: 192     Fields:    Translation:HumansCells
    136. Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups. Nat Genet. 2004 Nov; 36(11 Suppl):S48-53. Mountain JL, Risch N. PMID: 15508003.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    137. Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population. Am J Med Genet A. 2004 Aug 30; 129A(2):162-4. Ekstein J, Rubin BY, Anderson SL, Weinstein DA, Bach G, Abeliovich D, Webb M, Risch N. PMID: 15316959.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    138. Increased risk for recurrent major depression in DYT1 dystonia mutation carriers. Neurology. 2004 Aug 24; 63(4):631-7. Heiman GA, Ottman R, Saunders-Pullman RJ, Ozelius LJ, Risch NJ, Bressman SB. PMID: 15326234.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    139. TCR beta polymorphisms and multiple sclerosis. Genes Immun. 2004 Aug; 5(5):337-42. Dyment DA, Steckley JL, Morrison K, Willer CJ, Cader MZ, DeLuca GC, Sadovnick AD, Risch N, Ebers GC, Canadian Collaborative Study Group. PMID: 15175643.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    140. Tree-structured supervised learning and the genetics of hypertension. Proc Natl Acad Sci U S A. 2004 Jul 20; 101(29):10529-34. Huang J, Lin A, Narasimhan B, Quertermous T, Hsiung CA, Ho LT, Grove JS, Olivier M, Ranade K, Risch NJ, Olshen RA. PMID: 15249660; PMCID: PMC489971.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    141. Parent-of-origin effect in multiple sclerosis: observations in half-siblings. Lancet. 2004 May 29; 363(9423):1773-4. Ebers GC, Sadovnick AD, Dyment DA, Yee IM, Willer CJ, Risch N. PMID: 15172777.
      View in: PubMed   Mentions: 77     Fields:    Translation:Humans
    142. An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. Hum Mol Genet. 2004 May 15; 13(10):1005-15. Dyment DA, Sadovnick AD, Willer CJ, Armstrong H, Cader ZM, Wiltshire S, Kalman B, Risch N, Ebers GC, Canadian Collaborative Study Group. PMID: 15069025.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    143. Lack of evidence for an association between WNT2 and RELN polymorphisms and autism. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 01; 126B(1):51-7. Li J, Nguyen L, Gleason C, Lotspeich L, Spiker D, Risch N, Myers RM. PMID: 15048648.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    144. Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. Am J Hum Genet. 2004 Apr; 74(4):623-36. Tukel T, Shalata A, Present D, Rachmilewitz D, Mayer L, Grant D, Risch N, Desnick RJ. PMID: 15024686; PMCID: PMC1181940.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    145. Genomic priorities and public health. Science. 2003 Oct 24; 302(5645):599-601. Merikangas KR, Risch N. PMID: 14576422.
      View in: PubMed   Mentions: 64     Fields:    Translation:HumansPHPublic Health
    146. Twin concordance and sibling recurrence rates in multiple sclerosis. Proc Natl Acad Sci U S A. 2003 Oct 28; 100(22):12877-82. Willer CJ, Dyment DA, Risch NJ, Sadovnick AD, Ebers GC, Canadian Collaborative Study Group. PMID: 14569025; PMCID: PMC240712.
      View in: PubMed   Mentions: 138     Fields:    Translation:Humans
    147. Immunology: hepatitis A virus link to atopic disease. Nature. 2003 Oct 09; 425(6958):576. McIntire JJ, Umetsu SE, Macaubas C, Hoyte EG, Cinnioglu C, Cavalli-Sforza LL, Barsh GS, Hallmayer JF, Underhill PA, Risch NJ, Freeman GJ, DeKruyff RH, Umetsu DT. PMID: 14534576.
      View in: PubMed   Mentions: 68     Fields:    Translation:HumansAnimalsCells
    148. Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome. Nat Genet. 2003 Oct; 35(2):185-9. Varon R, Gooding R, Steglich C, Marns L, Tang H, Angelicheva D, Yong KK, Ambrugger P, Reinhold A, Morar B, Baas F, Kwa M, Tournev I, Guerguelcheva V, Kremensky I, Lochmüller H, Müllner-Eidenböck A, Merlini L, Neumann L, Bürger J, Walter M, Swoboda K, Thomas PK, von Moers A, Risch N, Kalaydjieva L. PMID: 14517542.
      View in: PubMed   Mentions: 48     Fields:    Translation:HumansCells
    149. Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. Proc Natl Acad Sci U S A. 2003 May 13; 100(10):5896-901. Leabman MK, Huang CC, DeYoung J, Carlson EJ, Taylor TR, de la Cruz M, Johns SJ, Stryke D, Kawamoto M, Urban TJ, Kroetz DL, Ferrin TE, Clark AG, Risch N, Herskowitz I, Giacomini KM, Pharmacogenetics Of Membrane Transporters Investigators. PMID: 12719533; PMCID: PMC156298.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    150. Will the genomics revolution revolutionize psychiatry? Am J Psychiatry. 2003 Apr; 160(4):625-35. Merikangas KR, Risch N. PMID: 12668348.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    151. The importance of race and ethnic background in biomedical research and clinical practice. N Engl J Med. 2003 Mar 20; 348(12):1170-5. Burchard EG, Ziv E, Coyle N, Gomez SL, Tang H, Karter AJ, Mountain JL, Pérez-Stable EJ, Sheppard D, Risch N. PMID: 12646676.
      View in: PubMed   Mentions: 301     Fields:    Translation:Humans
    152. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet. 2003 Mar; 33 Suppl:228-37. Botstein D, Risch N. PMID: 12610532.
      View in: PubMed   Mentions: 465     Fields:    Translation:Humans
    153. Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection. Am J Hum Genet. 2003 Apr; 72(4):812-22. Risch N, Tang H, Katzenstein H, Ekstein J. PMID: 12612865; PMCID: PMC1180346.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    154. Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science. 2003 Feb 21; 299(5610):1221-5. Kim UK, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D. PMID: 12595690.
      View in: PubMed   Mentions: 283     Fields:    Translation:HumansAnimalsCells
    155. A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. Am J Hypertens. 2003 Feb; 16(2):144-7. Province MA, Kardia SL, Ranade K, Rao DC, Thiel BA, Cooper RS, Risch N, Turner ST, Cox DR, Hunt SC, Weder AB, Boerwinkle E, National Heart, Lung and Blood Institute Family Blood Pressure Program. PMID: 12559682.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    156. A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins. Am J Hypertens. 2003 Feb; 16(2):158-62. Ranade K, Hinds D, Hsiung CA, Chuang LM, Chang MS, Chen YT, Pesich R, Hebert J, Chen YD, Dzau V, Olshen R, Curb D, Botstein D, Cox DR, Risch N. PMID: 12559686.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    157. A model system for identifying genes underlying complex traits. Cold Spring Harb Symp Quant Biol. 2003; 68:365-71. Drayna D, Kim UK, Coon H, Jorgenson E, Risch N, Leppert M. PMID: 15338638.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    158. Diagnostic criteria for dystonia in DYT1 families. Neurology. 2002 Dec 10; 59(11):1780-2. Bressman SB, Raymond D, Wendt K, Saunders-Pullman R, De Leon D, Fahn S, Ozelius L, Risch N. PMID: 12473770.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCTClinical Trials
    159. On the twin risk in autism. Am J Hum Genet. 2002 Oct; 71(4):941-6. Hallmayer J, Glasson EJ, Bower C, Petterson B, Croen L, Grether J, Risch N. PMID: 12297988; PMCID: PMC378547.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    160. A multigenerational family with multiple sclerosis. Brain. 2002 Jul; 125(Pt 7):1474-82. Dyment DA, Cader MZ, Willer CJ, Risch N, Sadovnick AD, Ebers GC. PMID: 12076998.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    161. Categorization of humans in biomedical research: genes, race and disease. Genome Biol. 2002 Jul 01; 3(7):comment2007. Risch N, Burchard E, Ziv E, Tang H. PMID: 12184798; PMCID: PMC139378.
      View in: PubMed   Mentions: 167     Fields:    Translation:Humans
    162. Candidate-gene approaches for studying complex genetic traits: practical considerations. Nat Rev Genet. 2002 05; 3(5):391-7. Tabor HK, Risch NJ, Myers RM. PMID: 11988764.
      View in: PubMed   Mentions: 266     Fields:    Translation:HumansAnimals
    163. Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient. Am J Med Genet. 2002 Mar 08; 114(2):129-36. Spiker D, Lotspeich LJ, Dimiceli S, Myers RM, Risch N. PMID: 11857572.
      View in: PubMed   Mentions: 70     Fields:    Translation:Humans
    164. A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate. Am J Hum Genet. 2002 Apr; 70(4):935-42. Ranade K, Jorgenson E, Sheu WH, Pei D, Hsiung CA, Chiang FT, Chen YD, Pratt R, Olshen RA, Curb D, Cox DR, Botstein D, Risch N. PMID: 11854867; PMCID: PMC379121.
      View in: PubMed   Mentions: 53     Fields:    Translation:Humans
    165. No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study. J Neuroimmunol. 2002 Feb; 123(1-2):193-8. Dyment DA, Steckley JL, Willer CJ, Armstrong H, Sadovnick AD, Risch N, Ebers GC. PMID: 11880164.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    166. Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence. Neurology. 2002 Jan 22; 58(2):242-5. Saunders-Pullman R, Shriberg J, Heiman G, Raymond D, Wendt K, Kramer P, Schilling K, Kurlan R, Klein C, Ozelius LJ, Risch NJ, Bressman SB. PMID: 11805251.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    167. Dropped genetics paper lacked scientific merit. Nature. 2002 Jan 10; 415(6868):115. Risch N, Piazza A, Cavalli-Sforza LL. PMID: 11805804.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    168. The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese origin. Am J Hypertens. 2001 Dec; 14(12):1196-200. Ranade K, Shue WH, Hung YJ, Hsuing CA, Chiang FT, Pesich R, Hebert J, Olivier M, Chen YD, Pratt R, Olshen R, Curb D, Botstein D, Risch N, Cox DR. PMID: 11775126.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    169. Implications of multilocus inheritance for gene-disease association studies. Theor Popul Biol. 2001 Nov; 60(3):215-20. Risch N. PMID: 11855955.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    170. Genetic variation in aldosterone synthase predicts plasma glucose levels. Proc Natl Acad Sci U S A. 2001 Nov 06; 98(23):13219-24. Ranade K, Wu KD, Risch N, Olivier M, Pei D, Hsiao CF, Chuang LM, Ho LT, Jorgenson E, Pesich R, Chen YD, Dzau V, Lin A, Olshen RA, Curb D, Cox DR, Botstein D. PMID: 11687612; PMCID: PMC60851.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    171. Birth order effects on nonverbal IQ scores in autism multiplex families. J Autism Dev Disord. 2001 Oct; 31(5):449-60. Spiker D, Lotspeich LJ, Dimiceli S, Szatmari P, Myers RM, Risch N. PMID: 11794410.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    172. Genetic variation in the human urea transporter-2 is associated with variation in blood pressure. Hum Mol Genet. 2001 Sep 15; 10(19):2157-64. Ranade K, Wu KD, Hwu CM, Ting CT, Pei D, Pesich R, Hebert J, Chen YD, Pratt R, Olshen R, Masaki K, Risch N, Cox DR, Botstein D. PMID: 11590132.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    173. High-throughput genotyping with single nucleotide polymorphisms. Genome Res. 2001 Jul; 11(7):1262-8. Ranade K, Chang MS, Ting CT, Pei D, Hsiao CF, Olivier M, Pesich R, Hebert J, Chen YD, Dzau VJ, Curb D, Olshen R, Risch N, Cox DR, Botstein D. PMID: 11435409; PMCID: PMC311112.
      View in: PubMed   Mentions: 114     Fields:    Translation:Humans
    174. The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol Biomarkers Prev. 2001 Jul; 10(7):733-41. Risch N. PMID: 11440958.
      View in: PubMed   Mentions: 96     Fields:    Translation:Humans
    175. The DYT1 mutation and nonfamilial primary torsion dystonia. Arch Neurol. 2001 Apr; 58(4):681-2. Bressman SB, Fahn S, Ozelius LJ, Kramer PL, Risch NJ. PMID: 11296011.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    176. Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes. Nat Genet. 2001 Apr; 27(4):435-8. Glatt CE, DeYoung JA, Delgado S, Service SK, Giacomini KM, Edwards RH, Risch N, Freimer NB. PMID: 11279528.
      View in: PubMed   Mentions: 51     Fields:    Translation:Humans
    177. Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. Am J Med Genet. 2001 Feb 15; 99(1):70-5. Bach G, Tomczak J, Risch N, Ekstein J. PMID: 11170098.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    178. Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. Am J Hum Genet. 2001 Mar; 68(3):686-99. Mignot E, Lin L, Rogers W, Honda Y, Qiu X, Lin X, Okun M, Hohjoh H, Miki T, Hsu S, Leffell M, Grumet F, Fernandez-Vina M, Honda M, Risch N. PMID: 11179016; PMCID: PMC1274481.
      View in: PubMed   Mentions: 162     Fields:    Translation:Humans
    179. Familial aggregation of absolute pitch. Am J Hum Genet. 2000 Sep; 67(3):755-8. Baharloo S, Service SK, Risch N, Gitschier J, Freimer NB. PMID: 10924408; PMCID: PMC1287535.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    180. Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute. J Hypertens. 2000 Jul; 18(7):867-76. Province MA, Boerwinkle E, Chakravarti A, Cooper R, Fornage M, Leppert M, Risch N, Ranade K. PMID: 10930184.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    181. Searching for genetic determinants in the new millennium. Nature. 2000 Jun 15; 405(6788):847-56. Risch NJ. PMID: 10866211.
      View in: PubMed   Mentions: 405     Fields:    Translation:Humans
    182. Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations. Am J Hypertens. 2000 Jun; 13(6 Pt 1):704-9. Ranade K, Hsuing AC, Wu KD, Chang MS, Chen YT, Hebert J, Chen YI, Olshen R, Curb D, Dzau V, Botstein D, Cox D, Risch N. PMID: 10912757.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    183. Searching for genes in complex diseases: lessons from systemic lupus erythematosus. J Clin Invest. 2000 Jun; 105(11):1503-6. Risch N. PMID: 10841504; PMCID: PMC300868.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    184. The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 2000 May 09; 54(9):1746-52. Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, Brin MF, Fahn S, Breakefield X, Ozelius LJ, Risch NJ. PMID: 10802779.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    185. Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations. Am J Hum Genet. 2000 Jun; 66(6):1821-32. Diaz GA, Gelb BD, Risch N, Nygaard TG, Frisch A, Cohen IJ, Miranda CS, Amaral O, Maire I, Poenaru L, Caillaud C, Weizberg M, Mistry P, Desnick RJ. PMID: 10777718; PMCID: PMC1378046.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    186. Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Canadian Collaborative Study Group. Neurology. 2000 Feb 08; 54(3):729-32. Steckley JL, Dyment DA, Sadovnick AD, Risch N, Hayes C, Ebers GC. PMID: 10680811.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    187. Postnatal experiences and genetic effects on squirrel monkey social affinities and emotional distress. Horm Behav. 1999 Dec; 36(3):266-75. Lyons DM, Martel FL, Levine S, Risch NJ, Schatzberg AF. PMID: 10603290.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimals
    188. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. Am J Med Genet. 1999 Oct 15; 88(5):551-6. Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N. PMID: 10490715.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    189. A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet. 1999 Aug; 65(2):493-507. Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM. PMID: 10417292; PMCID: PMC1377948.
      View in: PubMed   Mentions: 172     Fields:    Translation:HumansCells
    190. Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany. Ann Hum Genet. 1999 Jul; 63(Pt 4):285-91. Klein C, Vieregge P, Hagenah J, Sieberer M, Doyle E, Jacobs H, Gasser T, Breakefield XO, Risch NJ, Ozelius LJ. PMID: 10738540.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    191. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. J Autism Dev Disord. 1999 Jun; 29(3):195-201. Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, Hinds D, Risch N, Myers RM. PMID: 10425582.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    192. Male homosexuality: absence of linkage to microsatellite markers at Xq28. Science. 1999 Apr 23; 284(5414):665-7. Rice G, Anderson C, Risch N, Ebers G. PMID: 10213693.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
    193. The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. II. Individual genotyping. Genome Res. 1999 Mar; 9(3):234-41. Teng J, Risch N. PMID: 10077529.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    194. Sib-pair analysis of the collaborative study on the genetics of alcoholism data set. Genet Epidemiol. 1999; 17 Suppl 1:S187-91. Jorgenson E, Hinds D, Risch N. PMID: 10597434.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    195. Search for a founder mutation in idiopathic focal dystonia from Northern Germany. Am J Hum Genet. 1998 Dec; 63(6):1777-82. Klein C, Ozelius LJ, Hagenah J, Breakefield XO, Risch NJ, Vieregge P. PMID: 9837831; PMCID: PMC1377650.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    196. The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling. Genome Res. 1998 Dec; 8(12):1273-88. Risch N, Teng J. PMID: 9872982.
      View in: PubMed   Mentions: 95     Fields:    Translation:Humans
    197. Canadian collaborative project on genetic susceptibility to MS, phase 2: rationale and method. Canadian Collaborative Study Group. Can J Neurol Sci. 1998 Aug; 25(3):216-21. Sadovnick AD, Risch NJ, Ebers GC. PMID: 9706723.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    198. Co-morbidity and familial aggregation of alcoholism and anxiety disorders. Psychol Med. 1998 Jul; 28(4):773-88. Merikangas KR, Stevens DE, Fenton B, Stolar M, O'Malley S, Woods SW, Risch N. PMID: 9723135.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    199. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet. 1998 Jul; 19(3):292-6. Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. PMID: 9662408.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    200. De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia. Hum Mol Genet. 1998 Jul; 7(7):1133-6. Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ. PMID: 9618171.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    201. Are generalized and localization-related epilepsies genetically distinct? Arch Neurol. 1998 Mar; 55(3):339-44. Ottman R, Lee JH, Hauser WA, Risch N. PMID: 9520007; PMCID: PMC1626267.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    202. Effect of age at onset and parental disease status on sibling risks for MS. Neurology. 1998 Mar; 50(3):719-23. Sadovnick AD, Yee IM, Ebers GC, Risch NJ. PMID: 9521263.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    203. HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups. US Modafinil in Narcolepsy Multicenter Study Group. Tissue Antigens. 1998 Jan; 51(1):96-100. Pelin Z, Guilleminault C, Risch N, Grumet FC, Mignot E. PMID: 9459509.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    204. The role of the DYT1 gene in secondary dystonia. Adv Neurol. 1998; 78:107-15. Bressman SB, de Leon D, Raymond D, Greene PE, Brin MF, Fahn S, Ozelius LJ, Breakefield XO, Kramer PL, Risch NJ. PMID: 9750907.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    205. The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family. Adv Neurol. 1998; 78:93-105. Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Jacoby D, Penney J, Risch NJ, Fahn S, Gusella JF, Breakefield XO. PMID: 9750906.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    206. Clinical-genetic spectrum of primary dystonia. Adv Neurol. 1998; 78:79-91. Bressman SB, de Leon D, Raymond D, Ozelius LJ, Breakefield XO, Nygaard TG, Almasy L, Risch NJ, Kramer PL. PMID: 9750905.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    207. Haemochromatosis, HFE and genetic complexity. Nat Genet. 1997 Dec; 17(4):375-6. Risch N. PMID: 9398831.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    208. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families. Ann Neurol. 1997 Oct; 42(4):670-3. Almasy L, Bressman SB, Raymond D, Kramer PL, Greene PE, Heiman GA, Ford B, Yount J, de Leon D, Chouinard S, Saunders-Pullman R, Brin MF, Kapoor RP, Jones AC, Shen H, Fahn S, Risch NJ, Nygaard TG. PMID: 9382482.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    209. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA. 1997 Oct 22-29; 278(16):1349-56. Farrer LA, Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van Duijn CM. PMID: 9343467.
      View in: PubMed   Mentions: 1680     Fields:    Translation:Humans
    210. Ethnic variation in the clinical expression of idiopathic torsion dystonia. Mov Disord. 1997 Sep; 12(5):715-21. Almasy L, Bressman S, de Leon D, Risch N. PMID: 9380054.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    211. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet. 1997 Sep; 17(1):40-8. Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO. PMID: 9288096.
      View in: PubMed   Mentions: 358     Fields:    Translation:HumansAnimalsCells
    212. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Nat Genet. 1997 Jun; 16(2):202-5. Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP. PMID: 9171836.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansAnimalsCells
    213. Secondary dystonia and the DYTI gene. Neurology. 1997 Jun; 48(6):1571-7. Bressman SB, de Leon D, Raymond D, Greene PE, Brin MF, Fahn S, Ozelius LJ, Breakefield XO, Kramer PL, Risch NJ. PMID: 9191768.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    214. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. Genome Res. 1997 May; 7(5):483-94. Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO. PMID: 9149944.
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    215. Association between migraine and stroke in a large-scale epidemiological study of the United States. Arch Neurol. 1997 Apr; 54(4):362-8. Merikangas KR, Fenton BT, Cheng SH, Stolar MJ, Risch N. PMID: 9109736.
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    216. Genetic analyses of complex behavioral disorders. Proc Natl Acad Sci U S A. 1997 Apr 01; 94(7):2785-6. Uhl GR, Gold LH, Risch N. PMID: 9096294; PMCID: PMC34148.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimals
    217. Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results. Am J Hum Genet. 1997 Mar; 60(3):667-75. Ottman R, Hauser WA, Barker-Cummings C, Lee JH, Risch N. PMID: 9042928; PMCID: PMC1712524.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    218. Evolving methods in genetic epidemiology. II. Genetic linkage from an epidemiologic perspective. Epidemiol Rev. 1997; 19(1):24-32. Risch N. PMID: 9360899.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    219. Autism and the X chromosome. Multipoint sib-pair analysis. Arch Gen Psychiatry. 1996 Nov; 53(11):985-9. Hallmayer J, Hebert JM, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Lin AA, Cavalli-Sforza LL, Risch N, Ciaranello RD. PMID: 8911221.
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    220. Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes. Am J Hum Genet. 1996 Oct; 59(4):951-7. Zhang H, Risch N. PMID: 8808613; PMCID: PMC1914798.
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    221. Exclusion of the DYT1 locus in familial torticollis. Ann Neurol. 1996 Oct; 40(4):681-4. Bressman SB, Warner TT, Almasy L, Uitti RJ, Greene PE, Heiman GA, Raymond D, Ford B, de Leon D, Fahn S, Kramer PL, Risch NJ, Maraganore DM, Nygaard TG, Harding AE. PMID: 8871591.
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    222. The future of genetic studies of complex human diseases. Science. 1996 Sep 13; 273(5281):1516-7. Risch N, Merikangas K. PMID: 8801636.
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    223. Disequilibrium mapping: composite likelihood for pairwise disequilibrium. Genomics. 1996 Aug 15; 36(1):1-16. Devlin B, Risch N, Roeder K. PMID: 8812410.
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    224. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996 Aug; 13(4):399-408. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK. PMID: 8696333.
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    225. A full genome search in multiple sclerosis. Nat Genet. 1996 Aug; 13(4):472-6. Ebers GC, Kukay K, Bulman DE, Sadovnick AD, Rice G, Anderson C, Armstrong H, Cousin K, Bell RB, Hader W, Paty DW, Hashimoto S, Oger J, Duquette P, Warren S, Gray T, O'Connor P, Nath A, Auty A, Metz L, Francis G, Paulseth JE, Murray TJ, Pryse-Phillips W, Nelson R, Freedman M, Brunet D, Bouchard JP, Hinds D, Risch N. PMID: 8696345.
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    226. Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group. Lancet. 1996 Jun 22; 347(9017):1728-30. Sadovnick AD, Ebers GC, Dyment DA, Risch NJ. PMID: 8656905.
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    227. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet. 1996 Jun; 13(2):161-6. Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shepard JM, Williams SR, Risch N, Hinds D, Iwasaki N, Ogata M, Omori Y, Petzold C, Rietzch H, Schröder HE, Schulze J, Cox NJ, Menzel S, Boriraj VV, Chen X, Lim LR, Lindner T, Mereu LE, Wang YQ, Xiang K, Yamagata K, Yang Y, Bell GI. PMID: 8640221.
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    228. The genetic attributable risk of breast and ovarian cancer. Cancer. 1996 Jun 01; 77(11):2318-24. Claus EB, Schildkraut JM, Thompson WD, Risch NJ. PMID: 8635102.
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    229. A manic depressive history. Nat Genet. 1996 Apr; 12(4):351-3. Risch N, Botstein D. PMID: 8630482.
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    230. Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations. Am J Hum Genet. 1996 Apr; 58(4):836-43. Risch NJ, Zhang H. PMID: 8644748; PMCID: PMC1914664.
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    231. Clinical indicators of genetic susceptibility to epilepsy. Epilepsia. 1996 Apr; 37(4):353-61. Ottman R, Lee JH, Risch N, Hauser WA, Susser M. PMID: 8603640.
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    232. Relations of genetic and environmental factors in the etiology of epilepsy. Ann Neurol. 1996 Apr; 39(4):442-9. Ottman R, Annegers JF, Risch N, Hauser WA, Susser M. PMID: 8619522; PMCID: PMC2737460.
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    233. Searching for susceptibility genes in schizophrenia by genetic linkage analysis. Cold Spring Harb Symp Quant Biol. 1996; 61:845-50. Wildenauer DB, Hallmayer J, Schwab SG, Albus M, Eckstein GN, Zill P, Hönig S, Strauss M, Borrmann M, Lichtermann D, Ebstein RP, Lerer B, Risch N, Maier W. PMID: 9246509.
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    234. Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet Epidemiol. 1996; 13(2):117-37. Hauser ER, Boehnke M, Guo SW, Risch N. PMID: 8722742.
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    235. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nat Genet. 1995 Nov; 11(3):325-7. Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N, et al. PMID: 7581458.
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    236. A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics. 1995 Sep 20; 29(2):311-22. Devlin B, Risch N. PMID: 8666377.
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    237. A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group. Nature. 1995 Sep 14; 377(6545):150-1. Ebers GC, Sadovnick AD, Risch NJ. PMID: 7675080.
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    238. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science. 1995 Jun 16; 268(5217):1584-9. Risch N, Zhang H. PMID: 7777857.
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    239. Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nat Genet. 1995 Jun; 10(2):240-2. Rowe RE, Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. PMID: 7663523.
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    240. Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet. 1995 May; 10(1):56-60. Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS, Scheuer ML, et al. PMID: 7647791; PMCID: PMC2823475.
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    241. Birth cohort and familial risk of epilepsy: the effect of diminished recall in studies of lifetime prevalence. Am J Epidemiol. 1995 Feb 01; 141(3):235-41. Ottman R, Lee JH, Hauser WA, Risch N. PMID: 7840097.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    242. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Nat Genet. 1995 Feb; 9(2):152-9. Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S. PMID: 7719342.
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    243. Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. Autoimmunity. 1995; 21(2):127-30. Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. PMID: 8679901.
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    244. Use of sibling risk ratios and components of genetic variance in the characterization of a simulated oligogenic disease. Genet Epidemiol. 1995; 12(6):565-70. Almasy L, Tierney C, Risch N. PMID: 8787974.
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    245. Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation. Ann Neurol. 1994 Nov; 36(5):771-7. Bressman SB, de Leon D, Kramer PL, Ozelius LJ, Brin MF, Greene PE, Fahn S, Breakefield XO, Risch NJ. PMID: 7979224.
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    246. Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease. Nat Genet. 1994 Jun; 7(2):180-4. Corder EH, Saunders AM, Risch NJ, Strittmatter WJ, Schmechel DE, Gaskell PC, Rimmler JB, Locke PA, Conneally PM, Schmader KE, et al. PMID: 7920638.
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    247. Diminished recall and the cohort effect of major depression: a simulation study. Psychol Med. 1994 May; 24(2):375-83. Giuffra LA, Risch N. PMID: 8084933.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    248. Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med. 1994 Apr 14; 330(15):1041-6. Marenberg ME, Risch N, Berkman LF, Floderus B, de Faire U. PMID: 8127331.
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    249. Comorbidity and co-transmission of alcoholism, anxiety and depression. Psychol Med. 1994 Feb; 24(1):69-80. Merikangas KR, Risch NJ, Weissman MM. PMID: 8208896.
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    250. Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. Cancer. 1994 Feb 01; 73(3):643-51. Claus EB, Risch N, Thompson WD. PMID: 8299086.
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    251. Comments on the statistical aspects of the NRC's report on DNA typing. J Forensic Sci. 1994 Jan; 39(1):28-40. Devlin B, Risch N, Roeder K. PMID: 8113709.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    252. Feasibility of half-sibling designs for detecting a genetic component to a disease. Genet Epidemiol. 1994; 11(6):523-38. Tierney C, Merikangas KR, Risch N. PMID: 7713393.
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    253. Male sexual orientation and genetic evidence. Science. 1993 Dec 24; 262(5142):2063-5. Risch N, Squires-Wheeler E, Keats BJ. PMID: 8266107.
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    254. Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nat Genet. 1993 Dec; 5(4):386-91. Nygaard TG, Wilhelmsen KC, Risch NJ, Brown DL, Trugman JM, Gilliam TC, Fahn S, Weeks DE. PMID: 8298648.
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    255. Population genetics of the HRAS1 minisatellite locus. Am J Hum Genet. 1993 Dec; 53(6):1298-305. Devlin B, Krontiris T, Risch N. PMID: 8250046; PMCID: PMC1682480.
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    256. The genetics of infantile hypertrophic pyloric stenosis. A reanalysis. Am J Dis Child. 1993 Nov; 147(11):1203-11. Mitchell LE, Risch N. PMID: 8237916.
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    257. The calculation of breast cancer risk for women with a first degree family history of ovarian cancer. Breast Cancer Res Treat. 1993 Nov; 28(2):115-20. Claus EB, Risch N, Thompson WD. PMID: 8173064.
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    258. Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application to nonobese diabetic (NOD) mouse and human insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet. 1993 Sep; 53(3):702-14. Risch N, Ghosh S, Todd JA. PMID: 8352278; PMCID: PMC1682416.
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    259. An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. N Engl J Med. 1993 Aug 19; 329(8):517-23. Krontiris TG, Devlin B, Karp DD, Robert NJ, Risch N. PMID: 8336750.
      View in: PubMed   Mentions: 57     Fields:    Translation:HumansCells
    260. Physical properties of VNTR data, and their impact on a test of allelic independence. Am J Hum Genet. 1993 Aug; 53(2):324-9. Devlin B, Risch N. PMID: 8328451; PMCID: PMC1682343.
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    261. NRC report on DNA typing. Science. 1993 May 21; 260(5111):1057-9. Devlin B, Risch N, Roeder K. PMID: 8493540.
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    262. Correlates of genetic risk for non-syndromic cleft lip with or without cleft palate. Clin Genet. 1993 May; 43(5):255-60. Mitchell LE, Risch N. PMID: 8375107.
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    263. The A1 allele at the D2 dopamine receptor gene and alcoholism. A reappraisal. JAMA. 1993 Apr 07; 269(13):1673-7. Gelernter J, Goldman D, Risch N. PMID: 8095994.
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    264. Statistical evaluation of DNA fingerprinting: a critique of the NRC's report. Science. 1993 Feb 05; 259(5096):748-9, 837. Devlin B, Risch N, Roeder K. PMID: 8430323.
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    265. Linkage studies of psychiatric disorders. Eur Arch Psychiatry Clin Neurosci. 1993; 243(3-4):143-9. Risch N, Merikangas KR. PMID: 8117757.
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    266. Relationship between breast histopathology and family history of breast cancer. Cancer. 1993 Jan 01; 71(1):147-53. Claus EB, Risch N, Thompson WD, Carter D. PMID: 8380113.
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    267. Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Nat Genet. 1993 Jan; 3(1):49-55. Baron M, Freimer NF, Risch N, Lerer B, Alexander JR, Straub RE, Asokan S, Das K, Peterson A, Amos J, et al. PMID: 8490654.
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    268. Low-density lipoprotein cholesterol responsiveness to diet in normolipidemic subjects. Metabolism. 1993 Jan; 42(1):7-13. Cobb MM, Risch N. PMID: 8446052.
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    269. Risk factors predicting the incidence of second primary breast cancer among women diagnosed with a first primary breast cancer. Am J Epidemiol. 1992 Oct 15; 136(8):925-36. Bernstein JL, Thompson WD, Risch N, Holford TR. PMID: 1456269.
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    270. The genetic epidemiology of second primary breast cancer. Am J Epidemiol. 1992 Oct 15; 136(8):937-48. Bernstein JL, Thompson WD, Risch N, Holford TR. PMID: 1456270.
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    271. Influence of dietary fat, apolipoprotein E phenotype, and sex on plasma lipoprotein levels. Circulation. 1992 Sep; 86(3):849-57. Cobb MM, Teitlebaum H, Risch N, Jekel J, Ostfeld A. PMID: 1516197.
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    272. Corrections to "Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs". Am J Hum Genet. 1992 Sep; 51(3):673-5. Risch N. PMID: 1496996; PMCID: PMC1682718.
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    273. A note on Hardy-Weinberg equilibrium of VNTR data by using the Federal Bureau of Investigation's fixed-bin method. Am J Hum Genet. 1992 Sep; 51(3):549-53. Devlin B, Risch N. PMID: 1496986; PMCID: PMC1682714.
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    274. Ethnic differentiation at VNTR loci, with special reference to forensic applications. Am J Hum Genet. 1992 Sep; 51(3):534-48. Devlin B, Risch N. PMID: 1496985; PMCID: PMC1682699.
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    275. Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. Am J Hum Genet. 1992 Aug; 51(2):323-32. Mitchell LE, Risch N. PMID: 1642234; PMCID: PMC1682664.
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    276. Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. Am J Hum Genet. 1992 Mar; 50(3):619-28. Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF, et al. PMID: 1347197; PMCID: PMC1684274.
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    277. Genetic linkage: interpreting lod scores. Science. 1992 Feb 14; 255(5046):803-4. Risch N. PMID: 1536004.
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    278. On the probability of matching DNA fingerprints. Science. 1992 Feb 07; 255(5045):717-20. Risch NJ, Devlin B. PMID: 1738844.
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    279. Genetic Analysis Workshop 7: summary of the melanoma workshop. Cytogenet Cell Genet. 1992; 59(2-3):148-58. Risch N, Sherman S. PMID: 1737485.
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    280. Model misspecification and multipoint linkage analysis. Hum Hered. 1992; 42(1):77-92. Risch N, Giuffra L. PMID: 1555848.
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    281. Genetic relationship between nevus count or nevus density and cutaneous malignant melanoma. Cytogenet Cell Genet. 1992; 59(2-3):188-90. Claus EB, Giuffra L, Rogers J, Risch N. PMID: 1737496.
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    282. No association between an allele at the D2 dopamine receptor gene (DRD2) and alcoholism. JAMA. 1991 Oct 02; 266(13):1801-7. Gelernter J, O'Malley S, Risch N, Kranzler HR, Krystal J, Merikangas K, Kennedy JL, Kidd KK. PMID: 1832467.
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    283. Estimation of morbid risk and age at onset with missing information. Am J Hum Genet. 1991 Jul; 49(1):76-87. Cupples LA, Risch N, Farrer LA, Myers RH. PMID: 1829582; PMCID: PMC1683228.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    284. A note on multiple testing procedures in linkage analysis. Am J Hum Genet. 1991 Jun; 48(6):1058-64. Risch N. PMID: 2035526; PMCID: PMC1683115.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    285. Developments in gene mapping with linkage methods. Curr Opin Genet Dev. 1991 Jun; 1(1):93-8. Risch N. PMID: 1840884.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    286. Estimation of allele frequencies for VNTR loci. Am J Hum Genet. 1991 Apr; 48(4):662-76. Devlin B, Risch N, Roeder K. PMID: 2014794; PMCID: PMC1682954.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    287. Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet. 1991 Feb; 48(2):232-42. Claus EB, Risch N, Thompson WD. PMID: 1990835; PMCID: PMC1683001.
      View in: PubMed   Mentions: 241     Fields:    Translation:HumansCTClinical Trials
    288. No excess of homozygosity at loci used for DNA fingerprinting. Science. 1990 Sep 21; 249(4975):1416-20. Devlin B, Risch N, Roeder K. PMID: 2205919.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    289. The impact of phenotypic variation on genetic analysis: application to X-linkage in manic-depressive illness. Acta Psychiatr Scand. 1990 Sep; 82(3):196-203. Baron M, Hamburger R, Sandkuyl LA, Risch N, Mandel B, Endicott J, Belmaker RH, Ott J. PMID: 2248044.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    290. Sensitivity of chromosomal mosaicism detection by different tissue culture methods. Prenat Diagn. 1990 Aug; 10(8):519-27. Richkind KE, Risch NJ. PMID: 2267229.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    291. Age at onset as an indicator of familial risk of breast cancer. Am J Epidemiol. 1990 Jun; 131(6):961-72. Claus EB, Risch NJ, Thompson WD. PMID: 2188501.
      View in: PubMed   Mentions: 81     Fields:    Translation:HumansCTClinical Trials
    292. Using age of onset to distinguish between subforms of breast cancer. Ann Hum Genet. 1990 05; 54(2):169-77. Claus EB, Risch NJ, Thompson WD. PMID: 2382970.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    293. Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. Am J Hum Genet. 1990 Mar; 46(3):533-8. Risch NJ, Bressman SB, deLeon D, Brin MF, Burke RE, Greene PE, Shale H, Claus EB, Cupples LA, Fahn S. PMID: 2309703; PMCID: PMC1683634.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    294. Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am J Hum Genet. 1990 Feb; 46(2):229-41. Risch N. PMID: 2301393; PMCID: PMC1684989.
      View in: PubMed   Mentions: 194     Fields:    Translation:Humans
    295. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34. Ann Neurol. 1990 Feb; 27(2):114-20. Kramer PL, de Leon D, Ozelius L, Risch N, Bressman SB, Brin MF, Schuback DE, Burke RE, Kwiatkowski DJ, Shale H, et al. PMID: 2317008.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    296. Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet. 1990 Feb; 46(2):222-8. Risch N. PMID: 2301392; PMCID: PMC1684987.
      View in: PubMed   Mentions: 338     Fields:    Translation:Humans
    297. Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet. 1990 Feb; 46(2):242-53. Risch N. PMID: 2301394; PMCID: PMC1684966.
      View in: PubMed   Mentions: 87     Fields:    Translation:Humans
    298. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genet Epidemiol. 1990; 7(1):3-16; discussion 17-45. Risch N. PMID: 2184091.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    299. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Ann Neurol. 1989 Nov; 26(5):612-20. Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. PMID: 2817837.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    300. Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship. Am J Hum Genet. 1989 Oct; 45(4):521-9. Schildkraut JM, Risch N, Thompson WD. PMID: 2491011; PMCID: PMC1683499.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    301. Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron. 1989 May; 2(5):1427-34. Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D, et al. PMID: 2576373.
      View in: PubMed   Mentions: 42     Fields:    Translation:HumansCells
    302. Genetics of IDDM: evidence for complex inheritance with HLA. Genet Epidemiol. 1989; 6(1):143-8. Risch N. PMID: 2499501.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    303. Linkage detection tests under heterogeneity. Genet Epidemiol. 1989; 6(4):473-80. Risch N. PMID: 2777068.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    304. Description of X-linkage pedigrees. Genet Epidemiol. 1989; 6(1):187-9. Risch N. PMID: 2786483.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    305. Linkage and mode of inheritance in complex traits. Prog Clin Biol Res. 1989; 329:183-8. Risch N, Claus E, Giuffra L. PMID: 2622951.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    306. Genetic analysis of the affective disorders: summary of GAW5. Genet Epidemiol. 1989; 6(1):161-77. Rice J, Risch N. PMID: 2659428.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    307. The Continuous Performance Test, identical pairs version (CPT-IP): I. New findings about sustained attention in normal families. Psychiatry Res. 1988 Nov; 26(2):223-38. Cornblatt BA, Risch NJ, Faris G, Friedman D, Erlenmeyer-Kimling L. PMID: 3237915.
      View in: PubMed   Mentions: 176     Fields:    Translation:Humans
    308. A new statistical test for linkage heterogeneity. Am J Hum Genet. 1988 Feb; 42(2):353-64. Risch N. PMID: 3341384; PMCID: PMC1715251.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    309. Migraine and depression: association and familial transmission. J Psychiatr Res. 1988; 22(2):119-29. Merikangas KR, Risch NJ, Merikangas JR, Weissman MM, Kidd KK. PMID: 3404480.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    310. Inheritance of idiopathic torsion dystonia among Ashkenazi Jews. Adv Neurol. 1988; 50:45-56. Bressman SB, de Leon D, Brin MF, Risch N, Shale H, Burke RE, Greene PE, Fahn S. PMID: 3400502.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    311. Spontaneous mutation and parental age in humans. Am J Hum Genet. 1987 Aug; 41(2):218-48. Risch N, Reich EW, Wishnick MM, McCarthy JG. PMID: 3618593; PMCID: PMC1684215.
      View in: PubMed   Mentions: 72     Fields:    Translation:Humans
    312. Genetic linkage between X-chromosome markers and bipolar affective illness. Nature. 1987 Mar 19-25; 326(6110):289-92. Baron M, Risch N, Hamburger R, Mandel B, Kushner S, Newman M, Drumer D, Belmaker RH. PMID: 3493438.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansCells
    313. Assessing the role of HLA-linked and unlinked determinants of disease. Am J Hum Genet. 1987 Jan; 40(1):1-14. Risch N. PMID: 3468804; PMCID: PMC1684002.
      View in: PubMed   Mentions: 120     Fields:    Translation:Humans
    314. The spectrum concept of schizophrenia: evidence for a genetic-environmental continuum. J Psychiatr Res. 1987; 21(3):257-67. Baron M, Risch N. PMID: 3681761.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    315. The relationship between maternal age and chromosome size in autosomal trisomy. Am J Hum Genet. 1986 Jul; 39(1):68-78. Risch N, Stein Z, Kline J, Warburton D. PMID: 3752082; PMCID: PMC1684020.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    316. Assessing the role of X-linked inheritance in bipolar-related major affective disorder. J Psychiatr Res. 1986; 20(4):275-88. Risch N, Baron M, Mendlewicz J. PMID: 3806423.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    317. Genetic analysis workshop IV: summary of the multiple sclerosis workshop. Genet Epidemiol Suppl. 1986; 1:371-80. Risch N. PMID: 3569867.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    318. Conditional linkage analysis of multiple sclerosis data. Genet Epidemiol Suppl. 1986; 1:387-92. Risch N. PMID: 3569868.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    319. Genetic analysis of plasma amine oxidase activity in schizophrenia. Psychiatry Res. 1985 Jun; 15(2):121-32. Baron M, Risch N, Levitt M, Gruen R. PMID: 3862144.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    320. Genetic analysis of platelet monoamine oxidase activity in families of schizophrenic patients. J Psychiatr Res. 1985; 19(1):9-21. Baron M, Risch N, Levitt M, Gruen R. PMID: 3989738.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    321. Segregation analysis of schizophrenia and related disorders. Am J Hum Genet. 1984 Sep; 36(5):1039-59. Risch N, Baron M. PMID: 6496472; PMCID: PMC1684519.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    322. Segregation analysis incorporating linkage markers. I. Single-locus models with an application to type I diabetes. Am J Hum Genet. 1984 Mar; 36(2):363-86. Risch N. PMID: 6608876; PMCID: PMC1684434.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    323. Genetic Analysis Workshop II: multiple-locus segregation analysis incorporating linkage markers. Genet Epidemiol. 1984; 1(2):207-11. Risch N. PMID: 14971378.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    324. The effects of reduced fertility, method of ascertainment, and a second unlinked locus on affected sib-pair marker allele sharing. Am J Med Genet. 1983 Oct; 16(2):243-59. Risch N. PMID: 6580817.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    325. Estimating morbidity risks in relatives: the effect of reduced fertility. Behav Genet. 1983 Sep; 13(5):441-51. Risch N. PMID: 6667223.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    326. A general model for disease-marker association. Ann Hum Genet. 1983 07; 47(3):245-52. Risch N. PMID: 6577811.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    327. X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data. Ann Hum Genet. 1982 05; 46(2):153-66. Risch N, Baron M. PMID: 6985470.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    328. Age at onset in bipolar-related major affective illness: clinical and genetic implications. J Psychiatr Res. 1982-1983; 17(1):5-18. Baron M, Risch N, Mendlewicz J. PMID: 7183760.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    329. X-linkage in affective and schizoaffective disorders: genetic and diagnostic implications. Neuropsychobiology. 1982; 8(6):304-11. Baron M, Risch N. PMID: 6984491.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    330. X-linkage in bipolar affective illness. Perspectives on genetic heterogeneity, pedigree analysis and the X-chromosome map. J Affect Disord. 1981 Jun; 3(2):141-57. Baron M, Rainer JD, Risch N. PMID: 6454708.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    331. Application of a recombination model in calculating the variance of sib pair genetic identity. Ann Hum Genet. 1979 Oct; 43(2):177-86. Risch N, Lange K. PMID: 525976.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    332. An alternative model of recombination and interference. Ann Hum Genet. 1979 Jul; 43(1):61-70. Risch N, Lange K. PMID: 496395.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
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