Center-Authored Papers

Filters: Author is Doheny, Kimberly F  [Clear All Filters]
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Machiela MJ, Zhou W, Sampson JN, Dean MC, Jacobs KB, Black A, Brinton LA, Chang I-S, Chen C, Chen C et al..  2015.  Characterization of large structural genetic mosaicism in human autosomes.. American journal of human genetics. 96(3):487-97. Abstract
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Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C et al..  2012.  Detectable clonal mosaicism from birth to old age and its relationship to cancer.. Nature genetics. 44(6):642-50. Abstract
Huyghe JR, Bien SA, Harrison TA, Kang HM, Chen S, Schmit SL, Conti DV, Qu C, Jeon J, Edlund CK et al..  2018.  Discovery of common and rare genetic risk variants for colorectal cancer.. Nature genetics. Abstract
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Marosy BA, Craig BD, Hetrick KN, Witmer DP, Ling H, Griffith SM, Myers B, Ostrander EA, Stanford JL, Brody LC et al..  2017.  Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing.. Current protocols in human genetics. 92:18.10.1-18.10.25. Abstract
Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF et al..  2012.  Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.. Human genetics. 131(4):639-652. Abstract
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E et al..  2013.  Genetic variation associated with circulating monocyte count in the eMERGE Network.. Human molecular genetics. 22(10):2119-2127. Abstract
Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M et al..  2009.  A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.. American journal of human genetics. 85(5):679-91. Abstract
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Phelan CM, Kuchenbaecker KB, Tyrer JP, Kar SP, Lawrenson K, Winham SJ, Dennis J, Pirie A, Riggan MJ, Chornokur G et al..  2017.  Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.. Nature genetics. Abstract
Bookman EB, Din-Lovinescu C, Worrall BB, Manolio TA, Bennett SN, Laurie C, Mirel DB, Doheny KF, Anderson GL, Wehr K et al..  2013.  Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).. Genome medicine. 5(1):7. Abstract
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Zuvich RL, Armstrong LL, Bielinski SJ, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL et al..  2011.  Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.. Genetic epidemiology. 35(8):887-98. Abstract
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Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G et al..  2011.  Quality control procedures for genome-wide association studies.. Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.]. Chapter 1:Unit1.19. Abstract