David Altshuler

Genetics · 2000–2017

A researcher in the Science corpus: 71 papers; trusts 16 researchers and is trusted by 24 researchers here, as inferred from the citation graph.

Subfields

Genetics — 683 citations into it; #665 of 6,854 by trust here, #6 by citations
Molecular Biology — 491 citations into it; #5,076 of 17,773 by trust here, #75 by citations
Surgery — 126 citations into it
Plant Science — 75 citations into it
Rheumatology — 41 citations into it
Pediatrics, Perinatology and Child Health — 15 citations into it

Whom David Altshuler trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

Who trusts David Altshuler overall

Papers from David Altshuler's perspective

Ordered by how strongly the researchers David Altshuler trusts endorse each paper. Same corpus, a different order for every researcher.

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Defining the role of common variation in the genomic and biological architecture of adult human height
A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Measuring inconsistency in meta-analyses (British medical journal)
Detection of large-scale variation in the human genome (Nature Genetics)

Their papers

A global reference for human genetic variation (2015) — 16,925 citations
A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
An SNP map of the human genome generated by reduced representation shotgun sequencing (2000) — 773 citations
Positive Natural Selection in the Human Lineage (2006) — 1,133 citations
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (2001) — 2,947 citations
PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (2003) — 8,321 citations
The Structure of Haplotype Blocks in the Human Genome (2002) — 5,956 citations
Genetic Mapping in Human Disease (2008) — 1,496 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
Errα and Gabpa/b specify PGC-1α-dependent oxidative phosphorylation gene expression that is altered in diabetic muscle (2004) — 656 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
Whole population, genome-wide mapping of hidden relatedness. (2009) — 464 citations
Multiple regions within 8q24 independently affect risk for prostate cancer (2007) — 676 citations
Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) — 2,928 citations
Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men (2006) — 623 citations
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
Replicating genotype–phenotype associations (2007) — 1,394 citations