Center-Authored Papers

Filters: Author is de Andrade, Mariza  [Clear All Filters]
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A
Lindor NM, Yang P, Evans I, Schowalter K, de Andrade M, Li J, Jeavons E, Peterson G, Gallinger S, Bapat B et al..  2010.  Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registry.. Molecular genetics and metabolism. 99(2):157-9. Abstract
C
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
D
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
E
McDavid A, Crane PK, Newton KM, Crosslin DR, McCormick W, Weston N, Ehrlich K, Hart E, Harrison R, Kukull WA et al..  2013.  Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.. PloS one. 8(6):e63481. Abstract
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Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y et al..  2016.  Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.. Nature communications. 7:10023. 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
O'Donnell CJ, Kavousi M, Smith AV, Kardia SLR, Feitosa MF, Hwang S-J, Sun YV, Province MA, Aspelund T, Dehghan A et al..  2011.  Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction.. Circulation. 124(25):2855-2864. Abstract
Petersen GM, Amundadottir L, Fuchs CS, Kraft P, Stolzenberg-Solomon RZ, Jacobs KB, Arslan AA, Bueno-de-Mesquita BH, Gallinger S, Gross M et al..  2010.  A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.. Nature genetics. 42(3):224-8. Abstract
Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, Bueno-de-Mesquita BH, Gross M, Helzlsouer K, Jacobs EJ et al..  2009.  Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.. Nature genetics. 41(9):986-90. Abstract
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Schmidt AF, Swerdlow DI, Holmes MV, Patel RS, Fairhurst-Hunter Z, Lyall DM, Hartwig FP, Horta BL, Hyppönen E, Power C et al..  2016.  PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.. The lancet. Diabetes & endocrinology. Abstract
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
Q
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