Ethan M. Lange

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Rare variant contribution to the heritability of coronary artery disease

A methylation risk score for chronic kidney disease: a HyperGEN study

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

Mendelian randomization study of diabetes and dementia in the Million Veteran Program

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Protein prediction for trait mapping in diverse populations

A Diabetes Genetic Risk Score Is Associated With All-Cause Dementia and Clinically Diagnosed Vascular Dementia in the Million Veteran Program

Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci

DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies

Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome‐wide analysis in African Americans

Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans

Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Rare coding variants and X-linked loci associated with age at menarche

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

Germline Mutations in <i>HOXB13</i> and Prostate-Cancer Risk

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

Soluble CD14