Steven A. McCarroll

Genetics · 2003–2022

A researcher in the Science corpus: 55 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.

Subfields

Genetics — 893 citations into it; #5,851 of 6,854 by trust here, #16 by citations
Molecular Biology — 792 citations into it; #15,242 of 17,773 by trust here, #449 by citations
Plant Science — 112 citations into it

Whom Steven A. McCarroll trusts overall

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

Who trusts Steven A. McCarroll overall

Papers from Steven A. McCarroll's perspective

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

Detection of large-scale variation in the human genome (Nature Genetics)
Large-Scale Copy Number Polymorphism in the Human Genome (Science)
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
Diet and the evolution of human amylase gene copy number variation (Nature Genetics)
The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility (Science)
Segmental duplications and copy-number variation in the human genome. (American Journal of Human Genetics)
A tiling resolution DNA microarray with complete coverage of the human genome (Nature Genetics)
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn’s disease (Nature Genetics)

Their papers

A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
COMPREHENSIVE CLASSIFICATION OF RETINAL BIPOLAR NEURONS BY SINGLE-CELL TRANSCRIPTOMICS (2016) — 1,065 citations
Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets (2015) — 6,545 citations
Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain (2018) — 1,389 citations
Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans (2003) — 2,285 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
De novo mutations in schizophrenia implicate synaptic networks (2014) — 1,622 citations
A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 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
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
A Single-Cell Atlas of Cell Types, States, and Other Transcriptional Patterns from Nine Regions of the Adult Mouse Brain (2018) — 27 citations
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (2017) — 984 citations
Comparative cellular analysis of motor cortex in human, marmoset and mouse (2021) — 639 citations
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) — 577 citations
Quantifying penetrance in a dominant disease gene using large population control cohorts (2016) — 400 citations
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations