Stephen S. Rich

发表

Results of NOTCH3 Sequencing in Siblings with Ischemic Stroke Study Probands

Owen A. Ross, Alexandra I. Soto-Ortolaza, Christophe Verbeeck, 2011 .

Genome-Wide Interaction with Selected Type 2 Diabetes Loci Reveals Novel Loci for Type 2 Diabetes in African Americans

James G. Wilson, Donald W. Bowden, Barry I. Freedman, 2017, PSB.

Robust relationship inference in genome-wide association studies

Josyf Mychaleckyj, Wei-Min Chen, Stephen S. Rich, 2010, Bioinform..

A Genome-Wide Scan for Type 2 Diabetes in African-American Families Reveals Evidence for a Locus on Chromosome 6 q

Donald W. Bowden, Barry I. Freedman, Carl D. Langefeld, 2004 .

The landscape of recombination in African Americans

Xiaofeng Zhu, Alex P. Reiner, Jasmin Divers, 2011, Nature.

Mendelian randomization of blood lipids for coronary heart disease

Alex P. Reiner, Tom R. Gaunt, Fotios Drenos, 2014, European heart journal.

Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction

Harlan M. Krumholz, Ryan L. Collins, Stephen S. Rich, 2019, Circulation.

Population Structure of Hispanics in the United States: The Multi-Ethnic Study of Atherosclerosis

Jasmin Divers, Wei-Min Chen, Walter Palmas, 2012, PLoS genetics.

Discovery and Refinement Supplementary

Christian Gieger, Cisca Wijmenga, Inês Barroso, 2015 .

Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes

Stephen S. Rich, Lucia Mirea, Shelley B. Bull, 2009, Diabetes.

Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425))

Suzette J. Bielinski, Christian Gieger, Ingo Ruczinski, 2012 .

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

An open resource of structural variation for medical and population genetics

Grace Tiao, Daniel G. MacArthur, Ryan L. Collins, 2019 .

Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens

Buhm Han, Wei-Min Chen, Stephen S. Rich, 2013, PloS one.

A genome-wide search for asthma susceptibility loci in ethnically diverse populations

Farhad Imani, Alan R. Leff, James L. Weber, 1997, Nature Genetics.

Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy

Stephen S. Rich, Josyf C. Mychaleckyj, G. David Poznik, 2009, Diabetes.

Directional dominance on stature and cognition in diverse human populations

Laura J. Scott, Claude Bouchard, Christian Gieger, 2015, Nature.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

David M. Herrington, Adam Kiezun, Peter Donnelly, 2014, Nature.

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Sarah Edkins, Cisca Wijmenga, Lude Franke, 2011, Nature Genetics.

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Scott T. Weiss, Hemant K. Tiwari, Donald W. Bowden, 2019, bioRxiv.

Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project

Donald W. Bowden, Eric Boerwinkle, Christopher A. Haiman, 2011, PLoS genetics.

Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Sanghoon Moon, Cheng Hu, Xu Lin, 2017, Human molecular genetics.

Fine-Scale Patterns of Population Stratification Confound Rare Variant Association Tests

Adam Kiezun, Michael Bamshad, Joshua M. Akey, 2013, PloS one.

Genetics of Type 1 Diabetes: What's Next?

John A. Todd, Concepcion R. Nierras, Stephen S. Rich, 2010, Diabetes.

Genome-wide association study and meta-analysis finds over 40 loci affect risk of type 1 diabetes

Helen Schuilenburg, Neil M. Walker, John A. Todd, 2009, Nature Genetics.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Association of the Estrogen Receptor-α Gene With the Metabolic Syndrome and Its Component Traits in African-American Families

Donald W. Bowden, Carl D. Langefeld, Stephen S. Rich, 2007, Diabetes.

Publisher Correction: Functional aspects of meningeal lymphatics in ageing and Alzheimer’s disease

Scott T. Acton, Christopher C. Overall, Andrea Vaccari, 2018, Nature.

Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis

Sampath Prahalad, Carl D. Langefeld, Wei-Min Chen, 2013, Nature Genetics.

Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium

Eric Boerwinkle, Vilmundur Gudnason, Lenore J. Launer, 2013, PloS one.

Functional aspects of meningeal lymphatics in aging and Alzheimer’s disease

Scott T. Acton, Christopher C. Overall, Andrea Vaccari, 2018, Nature.

Pervasive Sharing of Genetic Effects in Autoimmune Disease

Kasper Lage, Gonçalo R. Abecasis, John A. Todd, 2011, PLoS genetics.