Center-Authored Papers

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Specimen Processing Core Facility
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J'an, Kutalik Z et al..  2014.  Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract
Scientific Imaging Core Facility
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J'an, Kutalik Z et al..  2014.  Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract
Public Health Sciences Division
Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. Abstract
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
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
Kho AN, Hayes GM, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei W-Q et al..  2012.  Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.. Journal of the American Medical Informatics Association : JAMIA. 19(22):212-218. 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
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
November 2011
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
May 2012
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
February 2013
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
December 2011
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
Kho AN, Hayes GM, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei W-Q et al..  2012.  Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.. Journal of the American Medical Informatics Association : JAMIA. 19(22):212-218. Abstract
Center-Authored Paper
Kho AN, Hayes GM, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei W-Q et al..  2012.  Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.. Journal of the American Medical Informatics Association : JAMIA. 19(22):212-218. 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
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
August 2014
Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. Abstract
258
Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. Abstract
2014
Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. Abstract
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J'an, Kutalik Z et al..  2014.  Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract
2013
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
2012
Kho AN, Hayes GM, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei W-Q et al..  2012.  Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.. Journal of the American Medical Informatics Association : JAMIA. 19(22):212-218. 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
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
2011
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