Benjamin F. Voight
Genetics · 2005–2020
A researcher in the Science corpus: 25 papers; trusts 7 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 388 citations into it; #1,844 of 6,854 by trust here, #60 by citations
- Molecular Biology — 237 citations into it
- Rheumatology — 14 citations into it
Whom Benjamin F. Voight trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthew Stephens
- Paul Scheet
- W. James Kent
- J. K. Pritchard
- Na Li
- N. Risch
- Michael Olivier
- Paul D. Thomas
- Chung-I Wu
- Julian P. T. Higgins
Who trusts Benjamin F. Voight overall
- James R. Brown
- Zachary A. Szpiech
- J. Stinchcombe
- Carl T. Bergstrom
- J. K. Pritchard
- Mathieu Gautier
- Yi-Fei Huang
- Stephen Burgess
- Joseph K. Pickrell
- Matthew D. Rasmussen
Papers from Benjamin F. Voight's perspective
Ordered by how strongly the researchers Benjamin F. Voight trusts endorse each paper. Same corpus, a different order for every researcher.
- A global reference for human genetic variation
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- The PANTHER database of protein families, subfamilies, functions and pathways (Nucleic Acids Res.)
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (Nature Genetics)
- PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification (Nucleic Acids Res.)
- Principal components analysis corrects for stratification in genome-wide association studies
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- Testing for an Unusual Distribution of Rare Variants (2011) — 617 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) — 2,928 citations
- Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ethnic meta-analysis (2020) — 622 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Guidelines for investigating causality of sequence variants in human disease (2014) — 1,235 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) — 2,232 citations
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) — 841 citations
- Large-scale association analyses identifies 13 new susceptibility loci for coronary artery disease (2011) — 1,948 citations
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations