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Kyle Walsh, PhD

Title(s)Assistant Professor, Epidemiology & Biostatistics
SchoolSchool of Medicine
AddressLocation Required
Varies CA 00000
Phone415-514-8078
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    Collapse Biography 
    Collapse Education and Training
    The University of California, San FranciscoPostdoctoral2013Program in Cancer Genetics
    Yale UniversityPh.D.2011School of Public Health
    The Ohio State UniversityB.S.2007Department of Anthropology
    The Ohio State UniversityB.S.2007Department of Molecular Genetics
    Collapse Awards and Honors
    The Society for Neuro-Oncology2015Young Investigator Award for Clinical Research
    The Sontag Foundation2015Distinguished Scientist Award
    The Society for Neuro-Oncology2014Award for Excellence in Epidemiology Research
    UCSF Brain Tumor Research Center2013Marvin Barker Award
    The Brain Tumor Epidemiology Consortium2013Junior Investigator Award
    The Brain Tumor Epidemiology Consortium2011Junior Investigator Award
    Yale University School of Public Health2009Master's degree awarded "With Distinction"
    Yale University School of Public Health2007University Fellowship
    American Association for Anthropological Genetics2007Outstanding Student Presentation

    Collapse Research 
    Collapse Research Activities and Funding
    Immune Correlates and Mechanisms of Perinatal Cytomegalovirus Infection and Later Life ALL Development
    NIH/NCI R21CA242439Aug 1, 2019 - Jul 31, 2021
    Role: Principal Investigator
    Genetic Susceptibility to Pediatric Glioma inIndividuals and Diverse populations
    NIH/NCI R01CA194189Sep 9, 2015 - Jan 31, 2021
    Role: Co-Principal Investigator

    Collapse ORNG Applications 
    Collapse Featured Publications
    Collapse Websites

    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.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    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. Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma. Acta Neuropathol Commun. 2020 Oct 28; 8(1):173. Zhang C, Ostrom QT, Semmes EC, Ramaswamy V, Hansen HM, Morimoto L, de Smith AJ, Pekmezci M, Vaksman Z, Hakonarson H, Diskin SJ, Metayer C. PMID: 33115534.
      View in: PubMed   Mentions:    Fields:    
    2. Genetic variation associated with childhood and adult stature and risk of MYCN-amplified neuroblastoma. Cancer Med. 2020 Nov; 9(21):8216-8225. Semmes EC, Shen E, Cohen JL, Zhang C, Wei Q, Hurst JH, Walsh KM. PMID: 32945147.
      View in: PubMed   Mentions:    Fields:    
    3. The Paradoxical Effects of COVID-19 on Cancer Care: Current Context and Potential Lasting Impacts. Clin Cancer Res. 2020 Aug 18. Broom A, Kenny K, Page A, Cort N, Lipp ES, Tan AC, Ashley DM, Walsh KM, Khasraw M. PMID: 32816894.
      View in: PubMed   Mentions:    Fields:    
    4. Cytomegalovirus as an immunomodulator across the lifespan. Curr Opin Virol. 2020 Aug 17; 44:112-120. Semmes EC, Hurst JH, Walsh KM, Permar SR. PMID: 32818717.
      View in: PubMed   Mentions:    Fields:    
    5. Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysis. Neurooncol Adv. 2020 Jan-Dec; 2(1):vdaa089. Muskens IS, Feng Q, Francis SS, Walsh KM, Mckean-Cowdin R, Gauderman WJ, de Smith AJ, Wiemels JL. PMID: 32864610.
      View in: PubMed   Mentions:
    6. Associations of novel variants in PIK3C3, INSR and MAP3K4 of the ATM pathway genes with pancreatic cancer risk. Am J Cancer Res. 2020; 10(7):2128-2144. Zhao LL, Liu HL, Luo S, Walsh KM, Li W, Wei Q. PMID: 32775006.
      View in: PubMed   Mentions:
    7. Germline cancer predisposition variants and pediatric glioma: a population-based study in California. Neuro Oncol. 2020 06 09; 22(6):864-874. Muskens IS, de Smith AJ, Zhang C, Hansen HM, Morimoto L, Metayer C, Ma X, Walsh KM, Wiemels JL. PMID: 31970404.
      View in: PubMed   Mentions: 2     Fields:    
    8. European genetic ancestry associated with risk of childhood ependymoma. Neuro Oncol. 2020 Jun 02. Zhang C, Ostrom QT, Hansen HM, Gonzalez-Maya J, Hu D, Ziv E, Morimoto L, de Smith AJ, Muskens IS, Kline CN, Vaksman Z, Hakonarson H, Diskin SJ, Kruchko C, Barnholtz-Sloan JS, Ramaswamy V, Ali-Osman F, Bondy ML, Taylor MD, Metayer C, Wiemels JL, Walsh KM. PMID: 32607579.
      View in: PubMed   Mentions:    Fields:    
    9. Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic Leukemia. Cancer Epidemiol Biomarkers Prev. 2020 Aug; 29(8):1606-1614. Semmes EC, Vijayakrishnan J, Zhang C, Hurst JH, Houlston RS, Walsh KM. PMID: 32467347.
      View in: PubMed   Mentions:    Fields:    
    10. Genetic variants of the peroxisome proliferator-activated receptor (PPAR) signaling pathway genes and risk of pancreatic cancer. Mol Carcinog. 2020 08; 59(8):930-939. Liu X, Qian D, Liu H, Abbruzzese JL, Luo S, Walsh KM, Wei Q. PMID: 32367578.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. Frequent Mutations of POT1 Distinguish Pulmonary Sarcomatoid Carcinoma From Other Lung Cancer Histologies. Clin Lung Cancer. 2020 Nov; 21(6):e523-e527. Shen E, Xiu J, Bentley R, López GY, Walsh KM. PMID: 32414627.
      View in: PubMed   Mentions:    Fields:    
    12. Telomere Attrition in Childhood Cancer Survivors. Clin Cancer Res. 2020 May 15; 26(10):2281-2283. Walsh KM. PMID: 32198150.
      View in: PubMed   Mentions:    Fields:    
    13. Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemia. Blood Adv. 2020 02 25; 4(4):672-675. Winer P, Muskens IS, Walsh KM, Vora A, Moorman AV, Wiemels JL, Roberts I, Roy A, de Smith AJ. PMID: 32084258.
      View in: PubMed   Mentions:    Fields:    
    14. Temporal Trends in Stroke Incidence Over Time by Sex and Age in the GCNKSS. Stroke. 2020 04; 51(4):1070-1076. Madsen TE, Khoury JC, Leppert M, Alwell K, Moomaw CJ, Sucharew H, Woo D, Ferioli S, Martini S, Adeoye O, Khatri P, Flaherty M, De Los Rios La Rosa F, Mackey J, Mistry E, Demel SL, Coleman E, Jasne A, Slavin SJ, Walsh K, Star M, Broderick JP, Kissela BM, Kleindorfer DO. PMID: 32078459.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    15. POT1 mutation spectrum in tumour types commonly diagnosed among POT1-associated hereditary cancer syndrome families. J Med Genet. 2020 Oct; 57(10):664-670. Shen E, Xiu J, Lopez GY, Bentley R, Jalali A, Heimberger AB, Bainbridge MN, Bondy ML, Walsh KM. PMID: 31937561.
      View in: PubMed   Mentions: 3     Fields:    
    16. Epidemiology of meningiomas. Handb Clin Neurol. 2020; 169:3-15. Walsh KM. PMID: 32553297.
      View in: PubMed   Mentions:    Fields:    
    17. Performance of a nomogram for IDH-wild-type glioblastoma patient survival in an elderly cohort. Neurooncol Adv. 2019 May-Dec; 1(1):vdz036. Shen E, Johnson MO, Lee JW, Lipp ES, Randazzo DM, Desjardins A, McLendon RE, Friedman HS, Ashley DM, Kirkpatrick JP, Peters KB, Walsh KM. PMID: 32642665.
      View in: PubMed   Mentions:
    18. Germline genetic landscape of pediatric central nervous system tumors. Neuro Oncol. 2019 11 04; 21(11):1376-1388. Muskens IS, Zhang C, de Smith AJ, Biegel JA, Walsh KM, Wiemels JL. PMID: 31247102.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    19. Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome. Blood. 2019 10 10; 134(15):1227-1237. Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, Wood BL, Carroll WL, Raetz EA, Feingold E, Devidas M, Barcellos LF, Hansen HM, Morimoto L, Kang AY, Smirnov I, Healy J, Laverdière C, Sinnett D, Taub JW, Birch JM, Thompson P, Spector LG, Pombo-de-Oliveira MS, DeWan AT, Mullighan CG, Hunger SP, Pui CH, Loh ML, Zwick ME, Metayer C, Ma X, Mueller BA, Sherman SL, Wiemels JL, Relling MV, Yang JJ, Lupo PJ, Rabin KR. PMID: 31350265.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    20. Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population. Bone. 2020 01; 130:115070. Zhang C, Hansen HM, Semmes EC, Gonzalez-Maya J, Morimoto L, Wei Q, Eward WC, DeWitt SB, Hurst JH, Metayer C, de Smith AJ, Wiemels JL, Walsh KM. PMID: 31525475.
      View in: PubMed   Mentions: 1     Fields:    
    21. Highlights of the inaugural ten - the launch of Neuro-Oncology Advances. Neurooncol Adv. 2019 May-Dec; 1(1):vdz016. Nassiri F, Aldape K, Alhuwalia M, Brastianos P, Ducray F, Galldiks N, Kim A, Lamszus K, Mitchell D, Nabors LB, Nam DH, Natsume A, Ng HK, Niclou S, Sahm F, Short S, Walsh K, Wick W, Zadeh G. PMID: 32642652.
      View in: PubMed   Mentions:
    22. Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. Leukemia. 2019 11; 33(11):2746-2751. de Smith AJ, Walsh KM, Morimoto LM, Francis SS, Hansen HM, Jeon S, Gonseth S, Chen M, Sun H, Luna-Fineman S, Antillón F, Girón V, Kang AY, Smirnov I, Shao X, Whitehead TP, Barcellos LF, Jolly KW, Healy J, Laverdière C, Sinnett D, Taub JW, Birch JM, Thompson PD, Pombo-de-Oliveira MS, Spector LG, DeWan AT, Mueller BA, Chiang C, Metayer C, Ma X, Wiemels JL. PMID: 31296947.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    23. Diet and risk of glioma: targets for prevention remain elusive. Neuro Oncol. 2019 07 11; 21(7):832-833. Walsh KM, Claus EB. PMID: 31120101.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    24. Potential functional variants in SMC2 and TP53 in the AURORA pathway genes and risk of pancreatic cancer. Carcinogenesis. 2019 06 10; 40(4):521-528. Feng Y, Liu H, Duan B, Liu Z, Abbruzzese J, Walsh KM, Zhang X, Wei Q. PMID: 30794721.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    25. Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children. Genes Chromosomes Cancer. 2019 10; 58(10):723-730. de Smith AJ, Lavoie G, Walsh KM, Aujla S, Evans E, Hansen HM, Smirnov I, Kang AY, Zenker M, Ceremsak JJ, Stieglitz E, Muskens IS, Roberts W, McKean-Cowdin R, Metayer C, Roux PP, Wiemels JL. PMID: 31102422.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    26. Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk. Cancer Sci. 2019 Jun; 110(6):2022-2032. Yang W, Liu H, Duan B, Xu X, Carmody D, Luo S, Walsh KM, Abbruzzese JL, Zhang X, Chen X, Wei Q. PMID: 30972876.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    27. Genetic variants in the liver kinase B1-AMP-activated protein kinase pathway genes and pancreatic cancer risk. Mol Carcinog. 2019 08; 58(8):1338-1348. Xu X, Qian D, Liu H, Cruz D, Luo S, Walsh KM, Abbruzzese JL, Zhang X, Wei Q. PMID: 30997723.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    28. Mendelian randomization provides support for obesity as a risk factor for meningioma. Sci Rep. 2019 01 22; 9(1):309. Takahashi H, Cornish AJ, Sud A, Law PJ, Disney-Hogg L, Calvocoressi L, Lu L, Hansen HM, Smirnov I, Walsh KM, Schramm J, Hoffmann P, Nöthen MM, Jöckel KH, Schildkraut JM, Simon M, Bondy M, Wrensch M, Wiemels JL, Claus EB, Turnbull C, Houlston RS. PMID: 30670737.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    29. Intermediate phenotypes underlying osteosarcoma risk. Oncotarget. 2018 Dec 21; 9(100):37345-37346. Semmes EC, Zhang C, Walsh KM. PMID: 30647834.
      View in: PubMed   Mentions: 1     Fields:    
    30. Genome-wide association analysis identifies a meningioma risk locus at 11p15.5. Neuro Oncol. 2018 10 09; 20(11):1485-1493. Claus EB, Cornish AJ, Broderick P, Schildkraut JM, Dobbins SE, Holroyd A, Calvocoressi L, Lu L, Hansen HM, Smirnov I, Walsh KM, Schramm J, Hoffmann P, Nöthen MM, Jöckel KH, Swerdlow A, Larsen SB, Johansen C, Simon M, Bondy M, Wrensch M, Houlston RS, Wiemels JL. PMID: 29762745.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    31. BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia. Int J Cancer. 2018 12 01; 143(11):2647-2658. de Smith AJ, Walsh KM, Francis SS, Zhang C, Hansen HM, Smirnov I, Morimoto L, Whitehead TP, Kang A, Shao X, Barcellos LF, McKean-Cowdin R, Zhang L, Fu C, Wang R, Yu H, Hoh J, Dewan AT, Metayer C, Ma X, Wiemels JL. PMID: 29923177.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    32. Genetic determinants of childhood and adult height associated with osteosarcoma risk. Cancer. 2018 09 15; 124(18):3742-3752. Zhang C, Morimoto LM, de Smith AJ, Hansen HM, Gonzalez-Maya J, Endicott AA, Smirnov IV, Metayer C, Wei Q, Eward WC, Wiemels JL, Walsh KM. PMID: 30311632.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansPHPublic Health
    33. Disruption of the ß1L Isoform of GABP Reverses Glioblastoma Replicative Immortality in a TERT Promoter Mutation-Dependent Manner. Cancer Cell. 2018 09 10; 34(3):513-528.e8. Mancini A, Xavier-Magalhães A, Woods WS, Nguyen KT, Amen AM, Hayes JL, Fellmann C, Gapinske M, McKinney AM, Hong C, Jones LE, Walsh KM, Bell RJA, Doudna JA, Costa BM, Song JS, Perez-Pinera P, Costello JF. PMID: 30205050.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    34. To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes. Front Genet. 2018; 9:298. Wallace AD, Wendt GA, Barcellos LF, de Smith AJ, Walsh KM, Metayer C, Costello JF, Wiemels JL, Francis SS. PMID: 30154825.
      View in: PubMed   Mentions:
    35. Two HLA Class II Gene Variants Are Independently Associated with Pediatric Osteosarcoma Risk. Cancer Epidemiol Biomarkers Prev. 2018 10; 27(10):1151-1158. Zhang C, Wiemels JL, Hansen HM, Gonzalez-Maya J, Endicott AA, de Smith AJ, Smirnov IV, Witte JS, Morimoto LM, Metayer C, Walsh KM. PMID: 30038050.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    36. Genomic characterization of chronic lymphocytic leukemia (CLL) in radiation-exposed Chornobyl cleanup workers. Environ Health. 2018 05 02; 17(1):43. Ojha J, Dyagil I, Finch SC, Reiss RF, de Smith AJ, Gonseth S, Zhou M, Hansen HM, Sherborne AL, Nakamura J, Bracci PM, Gudzenko N, Hatch M, Babkina N, Little MP, Chumak VV, Walsh KM, Bazyka D, Wiemels JL, Zablotska LB. PMID: 29720177.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansPHPublic Health
    37. Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas. Neuro Oncol. 2018 04 09; 20(5):632-641. Hayes J, Yu Y, Jalbert LE, Mazor T, Jones LE, Wood MD, Walsh KM, Bengtsson H, Hong C, Oberndorfer S, Roetzer T, Smirnov IV, Clarke JL, Aghi MK, Chang SM, Nelson SJ, Woehrer A, Phillips JJ, Solomon DA, Costello JF. PMID: 29077933.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    38. GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Nat Commun. 2018 01 18; 9(1):286. Wiemels JL, Walsh KM, de Smith AJ, Metayer C, Gonseth S, Hansen HM, Francis SS, Ojha J, Smirnov I, Barcellos L, Xiao X, Morimoto L, McKean-Cowdin R, Wang R, Yu H, Hoh J, DeWan AT, Ma X. PMID: 29348612.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    39. A germ-line deletion of APOBEC3B does not contribute to subtype-specific childhood acute lymphoblastic leukemia etiology. Haematologica. 2018 01; 103(1):e29-e31. Wallace AD, Francis SS, Shao X, de Smith AJ, Walsh KM, Mckean-Cowdin R, Ma X, Dahl G, Barcellos LF, Wiemels JL, Metayer C. PMID: 29025908.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    40. Non-additive and epistatic effects of HLA polymorphisms contributing to risk of adult glioma. J Neurooncol. 2017 Nov; 135(2):237-244. Zhang C, de Smith AJ, Smirnov IV, Wiencke JK, Wiemels JL, Witte JS, Walsh KM. PMID: 28721485.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    41. Buccal mucosa micronuclei counts in relation to exposure to low dose-rate radiation from the Chornobyl nuclear accident and other medical and occupational radiation exposures. Environ Health. 2017 06 23; 16(1):70. Bazyka D, Finch SC, Ilienko IM, Lyaskivska O, Dyagil I, Trotsiuk N, Gudzenko N, Chumak VV, Walsh KM, Wiemels J, Little MP, Zablotska LB. PMID: 28645274.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCellsPHPublic Health
    42. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncol. 2017 May 01; 3(5):636-651. Haycock PC, Burgess S, Nounu A, Zheng J, Okoli GN, Bowden J, Wade KH, Timpson NJ, Evans DM, Willeit P, Aviv A, Gaunt TR, Hemani G, Mangino M, Ellis HP, Kurian KM, Pooley KA, Eeles RA, Lee JE, Fang S, Chen WV, Law MH, Bowdler LM, Iles MM, Yang Q, Worrall BB, Markus HS, Hung RJ, Amos CI, Spurdle AB, Thompson DJ, O'Mara TA, Wolpin B, Amundadottir L, Stolzenberg-Solomon R, Trichopoulou A, Onland-Moret NC, Lund E, Duell EJ, Canzian F, Severi G, Overvad K, Gunter MJ, Tumino R, Svenson U, van Rij A, Baas AF, Bown MJ, Samani NJ, van t'Hof FNG, Tromp G, Jones GT, Kuivaniemi H, Elmore JR, Johansson M, Mckay J, Scelo G, Carreras-Torres R, Gaborieau V, Brennan P, Bracci PM, Neale RE, Olson SH, Gallinger S, Li D, Petersen GM, Risch HA, Klein AP, Han J, Abnet CC, Freedman ND, Taylor PR, Maris JM, Aben KK, Kiemeney LA, Vermeulen SH, Wiencke JK, Walsh KM, Wrensch M, Rice T, Turnbull C, Litchfield K, Paternoster L, Standl M, Abecasis GR, SanGiovanni JP, Li Y, Mijatovic V, Sapkota Y, Low SK, Zondervan KT, Montgomery GW, Nyholt DR, van Heel DA, Hunt K, Arking DE, Ashar FN, Sotoodehnia N, Woo D, Rosand J, Comeau ME, Brown WM, Silverman EK, Hokanson JE, Cho MH, Hui J, Ferreira MA, Thompson PJ, Morrison AC, Felix JF, Smith NL, Christiano AM, Petukhova L, Betz RC, Fan X, Zhang X, Zhu C, Langefeld CD, Thompson SD, Wang F, Lin X, Schwartz DA, Fingerlin T, Rotter JI, Cotch MF, Jensen RA, Munz M, Dommisch H, Schaefer AS, Han F, Ollila HM, Hillary RP, Albagha O, Ralston SH, Zeng C, Zheng W, Shu XO, Reis A, Uebe S, Hüffmeier U, Kawamura Y, Otowa T, Sasaki T, Hibberd ML, Davila S, Xie G, Siminovitch K, Bei JX, Zeng YX, Försti A, Chen B, Landi S, Franke A, Fischer A, Ellinghaus D, Flores C, Noth I, Ma SF, Foo JN, Liu J, Kim JW, Cox DG, Delattre O, Mirabeau O, Skibola CF, Tang CS, Garcia-Barcelo M, Chang KP, Su WH, Chang YS, Martin NG, Gordon S, Wade TD, Lee C, Kubo M, Cha PC, Nakamura Y, Levy D, Kimura M, Hwang SJ, Hunt S, Spector T, Soranzo N, Manichaikul AW, Barr RG, Kahali B, Speliotes E, Yerges-Armstrong LM, Cheng CY, Jonas JB, Wong TY, Fogh I, Lin K, Powell JF, Rice K, Relton CL, Martin RM, Davey Smith G. PMID: 28241208.
      View in: PubMed   Mentions: 97     Fields:    Translation:HumansCells
    43. Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT. Acta Neuropathol. 2017 06; 133(6):1001-1016. Pekmezci M, Rice T, Molinaro AM, Walsh KM, Decker PA, Hansen H, Sicotte H, Kollmeyer TM, McCoy LS, Sarkar G, Perry A, Giannini C, Tihan T, Berger MS, Wiemels JL, Bracci PM, Eckel-Passow JE, Lachance DH, Clarke J, Taylor JW, Luks T, Wiencke JK, Jenkins RB, Wrensch MR. PMID: 28255664.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    44. Correlates of Prenatal and Early-Life Tobacco Smoke Exposure and Frequency of Common Gene Deletions in Childhood Acute Lymphoblastic Leukemia. Cancer Res. 2017 04 01; 77(7):1674-1683. de Smith AJ, Kaur M, Gonseth S, Endicott A, Selvin S, Zhang L, Roy R, Shao X, Hansen HM, Kang AY, Walsh KM, Dahl GV, McKean-Cowdin R, Metayer C, Wiemels JL. PMID: 28202519.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCellsPHPublic Health
    45. In utero cytomegalovirus infection and development of childhood acute lymphoblastic leukemia. Blood. 2017 03 23; 129(12):1680-1684. Francis SS, Wallace AD, Wendt GA, Li L, Liu F, Riley LW, Kogan S, Walsh KM, de Smith AJ, Dahl GV, Ma X, Delwart E, Metayer C, Wiemels JL. PMID: 27979823.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansPHPublic Health
    46. Perinatal factors associated with clinical presentation of osteosarcoma in children and adolescents. Pediatr Blood Cancer. 2017 06; 64(6). Endicott AA, Morimoto LM, Kline CN, Wiemels JL, Metayer C, Walsh KM. PMID: 27860191.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCTClinical Trials
    47. Clonal and microclonal mutational heterogeneity in high hyperdiploid acute lymphoblastic leukemia. Oncotarget. 2016 Nov 08; 7(45):72733-72745. de Smith AJ, Ojha J, Francis SS, Sanders E, Endicott AA, Hansen HM, Smirnov I, Termuhlen AM, Walsh KM, Metayer C, Wiemels JL. PMID: 27683039.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    48. Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation Process. Cancer Res. 2016 11 15; 76(22):6680-6689. Ohba S, Mukherjee J, Johannessen TC, Mancini A, Chow TT, Wood M, Jones L, Mazor T, Marshall RE, Viswanath P, Walsh KM, Perry A, Bell RJ, Phillips JJ, Costello JF, Ronen SM, Pieper RO. PMID: 27758882.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimalsCells
    49. Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates. Epigenetics. 2016 09; 11(9):664-673. Gonseth S, de Smith AJ, Roy R, Zhou M, Lee ST, Shao X, Ohja J, Wrensch MR, Walsh KM, Metayer C, Wiemels JL. PMID: 27403598.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    50. Genetic Variation Associated with Longer Telomere Length Increases Risk of Chronic Lymphocytic Leukemia. Cancer Epidemiol Biomarkers Prev. 2016 07; 25(7):1043-9. Ojha J, Codd V, Nelson CP, Samani NJ, Smirnov IV, Madsen NR, Hansen HM, de Smith AJ, Bracci PM, Wiencke JK, Wrensch MR, Wiemels JL, Walsh KM. PMID: 27197291.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    51. Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers. Carcinogenesis. 2016 06; 37(6):576-582. Walsh KM, Whitehead TP, de Smith AJ, Smirnov IV, Park M, Endicott AA, Francis SS, Codd V, Samani NJ, Metayer C, Wiemels JL. PMID: 27207662.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    52. Telomere length connects melanoma and glioma predispositions. Aging (Albany NY). 2016 Mar; 8(3):423-4. Endicott AA, Taylor JW, Walsh KM. PMID: 27029497.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    53. Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. EBioMedicine. 2016 Feb; 4:153-61. David SP, Wang A, Kapphahn K, Hedlin H, Desai M, Henderson M, Yang L, Walsh KM, Schwartz AG, Wiencke JK, Spitz MR, Wenzlaff AS, Wrensch MR, Eaton CB, Furberg H, Mark Brown W, Goldstein BA, Assimes T, Tang H, Kooperberg CL, Quesenberry CP, Tindle H, Patel MI, Amos CI, Bergen AW, Swan GE, Stefanick ML. PMID: 26981579.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    54. Epidemiology. Handb Clin Neurol. 2016; 134:3-18. Walsh KM, Ohgaki H, Wrensch MR. PMID: 26948345.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    55. Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk. Oncotarget. 2015 Dec 15; 6(40):42468-77. Walsh KM, Codd V, Rice T, Nelson CP, Smirnov IV, McCoy LS, Hansen HM, Elhauge E, Ojha J, Francis SS, Madsen NR, Bracci PM, Pico AR, Molinaro AM, Tihan T, Berger MS, Chang SM, Prados MD, Jenkins RB, Wiemels JL, Samani NJ, Wiencke JK, Wrensch MR. PMID: 26646793.
      View in: PubMed   Mentions: 39     Fields:    Translation:HumansCells
    56. Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA. PLoS One. 2015; 10(11):e0143343. de Smith AJ, Walsh KM, Hansen HM, Endicott AA, Wiencke JK, Metayer C, Wiemels JL. PMID: 26575185.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    57. A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution. Cancer Res. 2015 Nov 15; 75(22):4884-94. Walsh KM, de Smith AJ, Hansen HM, Smirnov IV, Gonseth S, Endicott AA, Xiao J, Rice T, Fu CH, McCoy LS, Lachance DH, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR, Ma X, Metayer C, Wiemels JL. PMID: 26527286.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    58. A functional polymorphism in the CEBPE gene promoter influences acute lymphoblastic leukemia risk through interaction with the hematopoietic transcription factor Ikaros. Leukemia. 2016 05; 30(5):1194-7. Wiemels JL, de Smith AJ, Xiao J, Lee ST, Muench MO, Fomin ME, Zhou M, Hansen HM, Termuhlen A, Metayer C, Walsh KM. PMID: 26437776.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    59. Understanding inherited genetic risk of adult glioma - a review. Neurooncol Pract. 2016 Mar; 3(1):10-16. Rice T, Lachance DH, Molinaro AM, Eckel-Passow JE, Walsh KM, Barnholtz-Sloan J, Ostrom QT, Francis SS, Wiemels J, Jenkins RB, Wiencke JK, Wrensch MR. PMID: 26941959.
      View in: PubMed   Mentions:
    60. Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors. N Engl J Med. 2015 Jun 25; 372(26):2499-508. Eckel-Passow JE, Lachance DH, Molinaro AM, Walsh KM, Decker PA, Sicotte H, Pekmezci M, Rice T, Kosel ML, Smirnov IV, Sarkar G, Caron AA, Kollmeyer TM, Praska CE, Chada AR, Halder C, Hansen HM, McCoy LS, Bracci PM, Marshall R, Zheng S, Reis GF, Pico AR, O'Neill BP, Buckner JC, Giannini C, Huse JT, Perry A, Tihan T, Berger MS, Chang SM, Prados MD, Wiemels J, Wiencke JK, Wrensch MR, Jenkins RB. PMID: 26061753.
      View in: PubMed   Mentions: 424     Fields:    Translation:HumansCells
    61. Telomere maintenance and the etiology of adult glioma. Neuro Oncol. 2015 Nov; 17(11):1445-52. Walsh KM, Wiencke JK, Lachance DH, Wiemels JL, Molinaro AM, Eckel-Passow JE, Jenkins RB, Wrensch MR. PMID: 26014050.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    62. Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer. Science. 2015 May 29; 348(6238):1036-9. Bell RJ, Rube HT, Kreig A, Mancini A, Fouse SD, Nagarajan RP, Choi S, Hong C, He D, Pekmezci M, Wiencke JK, Wrensch MR, Chang SM, Walsh KM, Myong S, Song JS, Costello JF. PMID: 25977370.
      View in: PubMed   Mentions: 137     Fields:    Translation:HumansCells
    63. CDKN2A loss is associated with shortened overall survival in lower-grade (World Health Organization Grades II-III) astrocytomas. J Neuropathol Exp Neurol. 2015 May; 74(5):442-52. Reis GF, Pekmezci M, Hansen HM, Rice T, Marshall RE, Molinaro AM, Phillips JJ, Vogel H, Wiencke JK, Wrensch MR, Walsh KM, Perry A. PMID: 25853694.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    64. Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children. Cancer Causes Control. 2015 Apr; 26(4):609-19. Hsu LI, Chokkalingam AP, Briggs FB, Walsh K, Crouse V, Fu C, Metayer C, Wiemels JL, Barcellos LF, Buffler PA. PMID: 25761407.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    65. Survival and low-grade glioma: the emergence of genetic information. Neurosurg Focus. 2015 Jan; 38(1):E6. Claus EB, Walsh KM, Wiencke JK, Molinaro AM, Wiemels JL, Schildkraut JM, Bondy ML, Berger M, Jenkins R, Wrensch M. PMID: 25552286.
      View in: PubMed   Mentions: 58     Fields:    Translation:Humans
    66. Germline mutations in shelterin complex genes are associated with familial glioma. J Natl Cancer Inst. 2015 Jan; 107(1):384. Bainbridge MN, Armstrong GN, Gramatges MM, Bertuch AA, Jhangiani SN, Doddapaneni H, Lewis L, Tombrello J, Tsavachidis S, Liu Y, Jalali A, Plon SE, Lau CC, Parsons DW, Claus EB, Barnholtz-Sloan J, Il'yasova D, Schildkraut J, Ali-Osman F, Sadetzki S, Johansen C, Houlston RS, Jenkins RB, Lachance D, Olson SH, Bernstein JL, Merrell RT, Wrensch MR, Walsh KM, Davis FG, Lai R, Shete S, Aldape K, Amos CI, Thompson PA, Muzny DM, Gibbs RA, Melin BS, Bondy ML. PMID: 25482530.
      View in: PubMed   Mentions: 71     Fields:    Translation:Humans
    67. Familial gliomas: cases in two pairs of brothers. J Neurooncol. 2015 Jan; 121(1):135-40. Osorio JA, Hervey-Jumper SL, Walsh KM, Clarke JL, Butowski NA, Prados MD, Berger MS. PMID: 25208478.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    68. The epidemiology of glioma in adults: a "state of the science" review. Neuro Oncol. 2014 Jul; 16(7):896-913. Ostrom QT, Bauchet L, Davis FG, Deltour I, Fisher JL, Langer CE, Pekmezci M, Schwartzbaum JA, Turner MC, Walsh KM, Wrensch MR, Barnholtz-Sloan JS. PMID: 24842956.
      View in: PubMed   Mentions: 312     Fields:    Translation:Humans
    69. Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat Genet. 2014 Jul; 46(7):731-5. Walsh KM, Codd V, Smirnov IV, Rice T, Decker PA, Hansen HM, Kollmeyer T, Kosel ML, Molinaro AM, McCoy LS, Bracci PM, Cabriga BS, Pekmezci M, Zheng S, Wiemels JL, Pico AR, Tihan T, Berger MS, Chang SM, Prados MD, Lachance DH, O'Neill BP, Sicotte H, Eckel-Passow JE, van der Harst P, Wiencke JK, Samani NJ, Jenkins RB, Wrensch MR. PMID: 24908248.
      View in: PubMed   Mentions: 76     Fields:    Translation:HumansCells
    70. Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia. Am J Hematol. 2014 Jul; 89(7):721-5. Walsh KM, de Smith AJ, Welch TC, Smirnov I, Cunningham MJ, Ma X, Chokkalingam AP, Dahl GV, Roberts W, Barcellos LF, Buffler PA, Metayer C, Wiemels JL. PMID: 24753091.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    71. The role of KIR genes and their cognate HLA class I ligands in childhood acute lymphoblastic leukemia. Blood. 2014 Apr 17; 123(16):2497-503. de Smith AJ, Walsh KM, Ladner MB, Zhang S, Xiao C, Cohen F, Moore TB, Chokkalingam AP, Metayer C, Buffler PA, Trachtenberg EA, Wiemels JL. PMID: 24518758.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    72. GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL. Blood. 2013 Nov 07; 122(19):3385-7. Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Roberts W, Barcellos LF, Wiemels JL, Buffler PA. PMID: 24203929.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    73. Peripheral monocyte count is associated with case fatality after intracerebral hemorrhage. J Stroke Cerebrovasc Dis. 2014 Feb; 23(2):e107-11. Adeoye O, Walsh K, Woo JG, Haverbusch M, Moomaw CJ, Broderick JP, Kissela BM, Kleindorfer D, Flaherty ML, Woo D. PMID: 24119622.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    74. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype. Blood. 2013 Jun 06; 121(23):4808-9. Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Dahl GV, Hsu LI, Barcellos LF, Wiemels JL, Buffler PA. PMID: 23744494.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    75. Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis. Neuro Oncol. 2013 Aug; 15(8):1041-7. Walsh KM, Rice T, Decker PA, Kosel ML, Kollmeyer T, Hansen HM, Zheng S, McCoy LS, Bracci PM, Anderson E, Hsuang G, Wiemels JL, Pico AR, Smirnov I, Molinaro AM, Tihan T, Berger MS, Chang SM, Prados MD, Lachance DH, Sicotte H, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR. PMID: 23733245.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    76. Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children. Leukemia. 2013 Dec; 27(12):2416-9. Walsh KM, Chokkalingam AP, Hsu LI, Metayer C, de Smith AJ, Jacobs DI, Dahl GV, Loh ML, Smirnov IV, Bartley K, Ma X, Wiencke JK, Barcellos LF, Wiemels JL, Buffler PA. PMID: 23615557.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    77. Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology. Neuro Oncol. 2013 May; 15(5):535-41. Rice T, Zheng S, Decker PA, Walsh KM, Bracci P, Xiao Y, McCoy LS, Smirnov I, Patoka JS, Hansen HM, Hsuang G, Wiemels JL, Tihan T, Pico AR, Prados MD, Chang SM, Berger MS, Caron A, Fink S, Kollmeyer T, Rynearson A, Voss J, Kosel ML, Fridley BL, Lachance DH, Eckel-Passow JE, Sicotte H, O'Neill BP, Giannini C, Wiencke JK, Jenkins RB, Wrensch MR. PMID: 23361564.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    78. Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies. Genet Epidemiol. 2013 Feb; 37(2):222-8. Walsh KM, Anderson E, Hansen HM, Decker PA, Kosel ML, Kollmeyer T, Rice T, Zheng S, Xiao Y, Chang JS, McCoy LS, Bracci PM, Wiemels JL, Pico AR, Smirnov I, Lachance DH, Sicotte H, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR. PMID: 23280628.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    79. Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans. Cancer Epidemiol Biomarkers Prev. 2013 Feb; 22(2):251-60. Walsh KM, Gorlov IP, Hansen HM, Wu X, Spitz MR, Zhang H, Lu EY, Wenzlaff AS, Sison JD, Wei C, Lloyd SM, Chen W, Frazier ML, Seldin MF, Bierut LJ, Bracci PM, Wrensch MR, Schwartz AG, Wiencke JK, Amos CI. PMID: 23221128.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    80. Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. Oncotarget. 2012 Nov; 3(11):1428-38. Walsh KM, Amos CI, Wenzlaff AS, Gorlov IP, Sison JD, Wu X, Spitz MR, Hansen HM, Lu EY, Wei C, Zhang H, Chen W, Lloyd SM, Frazier ML, Bracci PM, Seldin MF, Wrensch MR, Schwartz AG, Wiencke JK. PMID: 23232035.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    81. Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach. Front Genet. 2012; 3:203. Jacobs DI, Walsh KM, Wrensch M, Wiencke J, Jenkins R, Houlston RS, Bondy M, Simon M, Sanson M, Gousias K, Schramm J, Labussière M, Di Stefano AL, Wichmann HE, Müller-Nurasyid M, Schreiber S, Franke A, Moebus S, Eisele L, Dewan AT, Dubrow R. PMID: 23091480.
      View in: PubMed   Mentions:
    82. Whole-exome sequencing of a pedigree segregating asthma. BMC Med Genet. 2012 Oct 09; 13:95. DeWan AT, Egan KB, Hellenbrand K, Sorrentino K, Pizzoferrato N, Walsh KM, Bracken MB. PMID: 23046476.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    83. Cigarette smoking associated with lung adenocarcinoma in situ in a large case-control study (SFBALCS). J Thorac Oncol. 2012 Sep; 7(9):1352-60. Bracci PM, Sison J, Hansen H, Walsh KM, Quesenberry CP, Raz DJ, Wrensch M, Wiencke JK. PMID: 22814813.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    84. A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation. Nat Genet. 2012 Oct; 44(10):1122-5. Jenkins RB, Xiao Y, Sicotte H, Decker PA, Kollmeyer TM, Hansen HM, Kosel ML, Zheng S, Walsh KM, Rice T, Bracci P, McCoy LS, Smirnov I, Patoka JS, Hsuang G, Wiemels JL, Tihan T, Pico AR, Prados MD, Chang SM, Berger MS, Caron AA, Fink SR, Halder C, Rynearson AL, Fridley BL, Buckner JC, O'Neill BP, Giannini C, Lachance DH, Wiencke JK, Eckel-Passow JE, Wrensch MR. PMID: 22922872.
      View in: PubMed   Mentions: 57     Fields:    Translation:HumansCells
    85. Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. BMC Pregnancy Childbirth. 2012 Jun 29; 12:61. Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT. PMID: 22748001.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    86. Cigarette smoking and risk of meningioma: the effect of gender. Cancer Epidemiol Biomarkers Prev. 2012 Jun; 21(6):943-50. Claus EB, Walsh KM, Calvocoressi L, Bondy ML, Schildkraut JM, Wrensch M, Wiemels JL. PMID: 22473761.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    87. Genetic signatures of exceptional longevity in humans. PLoS One. 2012; 7(1):e29848. Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT. PMID: 22279548.
      View in: PubMed   Mentions: 144     Fields:    Translation:Humans
    88. Disease risk prediction with rare and common variants. BMC Proc. 2011 Nov 29; 5 Suppl 9:S61. Wu C, Walsh KM, Dewan AT, Hoh J, Wang Z. PMID: 22373337.
      View in: PubMed   Mentions:
    89. Decreased use of non-steroidal anti-inflammatory drugs for the treatment of juvenile idiopathic arthritis in the era of modern aggressive treatment. Rheumatol Int. 2012 Oct; 32(10):3055-60. Kochar R, Walsh KM, Jain A, Spalding SJ, Hashkes PJ. PMID: 21909947.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    90. Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthma. Hum Hered. 2011; 71(2):97-105. Murk W, Walsh K, Hsu LI, Zhao L, Bracken MB, Dewan AT. PMID: 21734400.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    91. Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis. Genet Med. 2011 May; 13(5):377-84. Walsh KM, Bracken MB. PMID: 21289514.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    92. A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocr Relat Cancer. 2011 Feb; 18(1):171-80. Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, Dewan AT, Hoh J. PMID: 21139019.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    93. Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutat Res. 2010 Aug 07; 690(1-2):89-94. Walsh KM, Bracken MB, Murk WK, Hoh J, Dewan AT. PMID: 20553737.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    94. Origins and prevalence of the American Founder Mutation of MSH2. Cancer Res. 2008 Apr 01; 68(7):2145-53. Clendenning M, Baze ME, Sun S, Walsh K, Liyanarachchi S, Fix D, Schunemann V, Comeras I, Deacon M, Lynch JF, Gong G, Thomas BC, Thibodeau SN, Lynch HT, Hampel H, de la Chapelle A. PMID: 18381419.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells