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Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation. 2013 Apr 2;127(13):1377-85
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High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Clin Transl Sci. 2012 Oct;5(5):394-9
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Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network.
J Am Med Inform Assoc. 2013 Jun;20(e1):e147-54
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Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.
G3 (Bethesda). 2013 Jul;3(7):1061-8
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Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.
Invest Ophthalmol Vis Sci. 2013;54(9):6248-54
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Fine Mapping and Identification of BMI Loci in African Americans.
Am J Hum Genet. 2013 Oct 3;93(4):661-71
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Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
Pac Symp Biocomput. 2014;:253-64
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Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
Gut. 2014 May;63(5):800-7
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Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.
J Invest Dermatol. 2014 Jul;134(7):2049-52
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Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.
Ann Hum Genet. 2013 Jul;77(4):321-32
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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
PLoS Genet. 2014 Aug;10(8):e1004517
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Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.
PLoS One. 2014;9(12):e111301
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Leveraging Epidemiologic and Clinical Collections for Genomic Studies of Complex Traits.
Hum Hered. 2015;79(3-4):137-46
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Causes and prevalence of visual impairment among adults in the United States.
Arch Ophthalmol. 2004 Apr;122(4):477-85
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Prevalence of open-angle glaucoma among adults in the United States.
Arch Ophthalmol. 2004 Apr;122(4):532-8
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Racial differences in the prevalence of age-related macular degeneration: the Baltimore Eye Survey.
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Global data on visual impairment in the year 2002.
Bull World Health Organ. 2004 Nov;82(11):844-51
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
Am J Hum Genet. 2007 Sep;81(3):559-75
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Development of a large-scale de-identified DNA biobank to enable personalized medicine.
Clin Pharmacol Ther. 2008 Sep;84(3):362-9
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Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.
Am J Hum Genet. 2010 Apr 9;86(4):560-72
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Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.
Circulation. 2010 Nov 16;122(20):2016-21
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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
BMC Med Genomics. 2011;4:13
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Electronic medical records for genetic research: results of the eMERGE consortium.
Sci Transl Med. 2011 Apr 20;3(79):79re1
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Using electronic health records to drive discovery in disease genomics.
Nat Rev Genet. 2011 Jun;12(6):417-28
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Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
Nat Genet. 2011 Jun;43(6):574-8
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Differences in rates of glaucoma among Asian Americans and other racial groups, and among various Asian ethnic groups.
Ophthalmology. 2011 Jun;118(6):1031-7
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The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study.
Am J Epidemiol. 2011 Oct 1;174(7):849-59
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Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am J Hum Genet. 2011 Oct 7;89(4):529-42
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Predicting clopidogrel response using DNA samples linked to an electronic health record.
Clin Pharmacol Ther. 2012 Feb;91(2):257-63
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Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
J Am Med Inform Assoc. 2012 Mar-Apr;19(2):212-8
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Importance of multi-modal approaches to effectively identify cataract cases from electronic health records.
J Am Med Inform Assoc. 2012 Mar-Apr;19(2):225-34
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Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.
Pharmacogenomics. 2012 Mar;13(4):407-18
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Projected clinical outcomes of glaucoma screening in African American individuals.
Arch Ophthalmol. 2012 Mar;130(3):365-72
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Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Hum Genet. 2012 Apr;131(4):639-52
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Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.
PLoS One. 2012;7(3):e33389
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Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet. 2012;8(4):e1002654
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A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
Hum Mol Genet. 2012 Jun 15;21(12):2836-42
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The changing face of primary open-angle glaucoma in the United States: demographic and geographic changes from 2011 to 2050.
Am J Ophthalmol. 2012 Aug;154(2):303-314.e3
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The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet. 2012;8(8):e1002793
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Genetic variation associated with circulating monocyte count in the eMERGE Network.
Hum Mol Genet. 2013 May 15;22(10):2119-27
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