Joseph K. Pickrell

Genetics · 2009–2019

A researcher in the Science corpus: 15 papers; trusts 20 researchers and is trusted by 49 researchers here, as inferred from the citation graph.

Subfields

Genetics — 283 citations into it; #183 of 6,854 by trust here, #216 by citations
Molecular Biology — 235 citations into it; #6,596 of 17,773 by trust here, #2,612 by citations
Computational Biology & Bioinformatics — 17 citations into it
Cell Biology — 16 citations into it
Statistics and Probability — 13 citations into it
Epidemiology — 12 citations into it
Surgery — 11 citations into it
Paleontology — 7 citations into it

Whom Joseph K. Pickrell trusts overall

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

Who trusts Joseph K. Pickrell overall

Papers from Joseph K. Pickrell's perspective

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

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
Defining the role of common variation in the genomic and biological architecture of adult human height
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
A Draft Sequence of the Neandertal Genome (Science)
Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Inference of Population Structure using Dense Haplotype Data

Their papers

Understanding mechanisms underlying human gene expression variation with RNA sequencing (2010) — 1,311 citations
A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
Signals of recent positive selection in a worldwide sample of human populations. (2009) — 768 citations
Approximately independent linkage disequilibrium blocks in human populations (2015) — 536 citations
DNaseI sensitivity QTLs are a major determinant of human expression variation (2012) — 674 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
Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) — 986 citations
Detection and interpretation of shared genetic influences on 42 human traits (2016) — 1,123 citations
The complete genome sequence of a Neandertal from the Altai Mountains (2013) — 1,650 citations
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (2013) — 573 citations
Inference of Population Splits and Mixtures from Genome-Wide Allele Frequency Data (2012) — 2,606 citations
The Genetics of Human Adaptation: Hard Sweeps, Soft Sweeps, and Polygenic Adaptation (2010) — 928 citations
Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data (2009) — 527 citations