Benjamin M. Neale

Genetics · 2004–2022

A researcher in the Science corpus: 55 papers; trusts 20 researchers and is trusted by 12 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 1,200 citations into it; #1,255 of 6,854 by trust here, #18 by citations
• Molecular Biology — 635 citations into it; #11,614 of 17,773 by trust here, #370 by citations
• Computational Biology & Bioinformatics — 115 citations into it; #616 of 660 by trust here, #82 by citations
• Cognitive Neuroscience — 82 citations into it
• Evaluation & Benchmarks — 20 citations into it

Whom Benjamin M. Neale trusts overall

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

1. Yoav Benjamini
2. J. K. Pritchard
3. John D. Storey
4. Alkes L Price
5. Y. Hochberg
6. Daniel J. Schaid
7. Dmitri V. Zaykin
8. David Reich
9. Robert Tibshirani
10. Pauline Crystal Ng

Who trusts Benjamin M. Neale overall

1. D. Curtis
2. Gibran Hemani
3. Jian Yang
4. Peter M. Visscher
5. Seunggeun Lee
6. Yun Li
7. Brian L. Browning
8. Jiabo Wang
9. Gonçalo R. Abecasis
10. Naomi R. Wray

Papers from Benjamin M. Neale's perspective

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

1. Controlling the false discovery rate: a practical and powerful approach to multiple testing
2. Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
3. Searching for genetic determinants in the new millennium (Nature)
4. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
5. High-resolution haplotype structure in the human genome (Nature Genetics)
6. A comprehensive review of genetic association studies (Genetics in Medicine)
7. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
8. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
9. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
10. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)

Their papers

• A synthetic-diploid benchmark for accurate variant calling evaluation (2018) — 209 citations
• PLINK: a tool set for whole-genome association and population-based linkage analyses. (2007) — 32,716 citations
• The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
• Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
• A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations
• Testing for an Unusual Distribution of Rare Variants (2011) — 617 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
• The genetic architecture of type 2 diabetes (2016) — 1,066 citations
• Regional missense constraint improves variant deleteriousness prediction (2017) — 358 citations
• The future of association studies: gene-based analysis and replication. (2004) — 641 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
• Searching for missing heritability: Designing rare variant association studies (2014) — 633 citations
• Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes (2019) — 1,088 citations
• A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
• Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) — 257 citations
• Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
• Linkage disequilibrium dependent architecture of human complex traits reveals action of negative selection (2016) — 192 citations
• A global overview of pleiotropy and genetic architecture in complex traits (2019) — 1,107 citations
• Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis (2013) — 2,591 citations