Joel Hirschhorn

Genetics · 2000–2021

A researcher in the Science corpus: 38 papers; trusts 7 researchers and is trusted by 31 researchers here, as inferred from the citation graph.

Subfields

Genetics — 519 citations into it; #326 of 6,854 by trust here, #43 by citations

Whom Joel Hirschhorn trusts overall

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

Who trusts Joel Hirschhorn overall

Papers from Joel Hirschhorn's perspective

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

Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
High-resolution haplotype structure in the human genome (Nature Genetics)
Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (Science)
Principal components analysis corrects for stratification in genome-wide association studies
Next-generation genotype imputation service and methods (Nature Genetics)
Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Haplotype tagging for the identification of common disease genes (Nature Genetics)
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)

Their papers

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (2003) — 8,321 citations
Genome-wide association studies for complex traits: consensus, uncertainty and challenges (2008) — 3,055 citations
Biological interpretation of genome-wide association studies using predicted gene functions (2015) — 821 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
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015) — 4,590 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
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
Replicating genotype–phenotype associations (2007) — 1,394 citations
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (2000) — 1,189 citations
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases (2020) — 305 citations
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry (2018) — 1,022 citations
Meta-analysis of genome-wide association studies for height and body mass index in ∼700,000 individuals of European ancestry (2018) — 1,929 citations
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies (2018) — 30 citations
Genetic evidence of assortative mating in humans (2017) — 288 citations
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015)
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations