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Number of Publications: 130

Title
Year
Publication
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways
2020
Kidney International
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease
2020
Journal of the American College of Cardiology
Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis
2020
JAMA cardiology
A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
2020
Genetics in Medicine: Official Journal of the American College of Medical Genetics
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
2020
Nature Genetics
Lack of pathogenic germline DICER1 variants in males with testicular germ-cell tumors
2020
Cancer Genetics
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
2020
Circulation
SARS-CoV-2 seroprevalence among parturient women in Philadelphia
2020
Science Immunology
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study
2020
PLoS medicine
Research on COVID-19 through patient-reported data: a survey for observational studies in the COVID-19 pandemic
2020
Journal of Clinical and Translational Science
Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis
2020
Kidney International
Carnival: A Graph-Based Data Integration and Query Tool to Support Patient Cohort Generation for Clinical Research
2019
Studies in Health Technology and Informatics
A regression framework to uncover pleiotropy in large-scale electronic health record data
2019
Journal of the American Medical Informatics Association: JAMIA
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment
2019
Neurology. Genetics
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry
2019
JAMA
Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell Tumors
2019
JAMA oncology
FBN1 Coding Variants and Nonsyndromic Aortic Disease
2019
Circulation. Genomic and Precision Medicine
Soluble FMS-Like Tyrosine Kinase-1 Is a Circulating Biomarker Associated With Calcific Aortic Stenosis
2019
Journal of the American College of Cardiology
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
2019
Nature Communications
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants
2019
Circulation
The ADP/ATP translocase drives mitophagy independent of nucleotide exchange
2019
Nature
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
2018
The New England Journal of Medicine
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
2018
Nature Communications
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
2018
Nature Genetics
Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization
2018
Circulation. Genomic and Precision Medicine
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
2017
Nature Genetics
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
2017
Nature Genetics
Cost and yield considerations when expanding recruitment for genetic studies: the primary open-angle African American glaucoma genetics study
2017
BMC medical research methodology
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
2017
The New England Journal of Medicine
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
2017
Nature Genetics
101 - 130 of 130 Records

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