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Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
Genetics|June 21, 2015
Automated Assay of Telomere Length Measurement and Informatics for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) CohortKyle Lapham, Mark N Kvale, Jue Lin, et al.
Genetics|June 21, 2015
Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) CohortYambazi Banda, Mark N Kvale, Thomas J Hoffmann, et al.
Nature Communications|February 1, 2017
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancerThomas J Hoffmann, Michael N Passarelli, Rebecca E Graff, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
JAMA Psychiatry|February 14, 2014
Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigreesScott C Fears, Susan K Service, Barbara Kremeyer, et al.
Cancer Discovery|June 3, 2015
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differencesThomas J Hoffmann, Stephen K Van Den Eeden, Lori C Sakoda, et al.
Genetics|June 21, 2015
Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) CohortMark N Kvale, Stephanie Hesselson, Thomas J Hoffmann, et al.
American Journal of Human Genetics|September 8, 2018
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved PopulationsLaura M Amendola, Jonathan S Berg, Carol R Horowitz, et al.
Genomics|May 14, 2011
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP arrayThomas J Hoffmann, Mark N Kvale, Stephanie E Hesselson, et al.
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