Dale R. Nyholt

Genetics · 2004–2019

A researcher in the Science corpus: 18 papers; trusts 8 researchers and is trusted by 21 researchers here, as inferred from the citation graph.

Subfields

Genetics — 374 citations into it; #539 of 6,854 by trust here, #211 by citations
Molecular Biology — 235 citations into it
Cell Biology — 12 citations into it
Plant Science — 12 citations into it
Evaluation & Benchmarks — 7 citations into it

Whom Dale R. Nyholt trusts overall

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

Who trusts Dale R. Nyholt overall

Papers from Dale R. Nyholt's perspective

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

Estimating Effects and Making Predictions from Genome-Wide Marker Data
Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
Controlling the false discovery rate: a practical and powerful approach to multiple testing
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
General and abdominal adiposity and risk of death in Europe. (New England Journal of Medicine)
Comparison of abdominal adiposity and overall obesity in predicting risk of type 2 diabetes among men. (American Journal of Clinical Nutrition)
Acquired and inherited lipodystrophies. (New England Journal of Medicine)

Their papers

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. (2004) — 1,758 citations
A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) — 629 citations
Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
Genetic evidence of assortative mating in humans (2017) — 288 citations
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2017) — 2,735 citations
Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) — 874 citations
Identification of seven loci affecting mean telomere length and their association with disease (2013) — 909 citations
Common SNPs explain a large proportion of heritability for human height (2010) — 4,447 citations
A versatile gene-based test for genome-wide association studies. (2010) — 843 citations
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) — 973 citations
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations (2009) — 658 citations