Brendan K. Bulik-Sullivan
Genetics · 2013–2018
A researcher in the Science corpus: 13 papers; trusts 2 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 311 citations into it; #4,662 of 6,854 by trust here, #118 by citations
Whom Brendan K. Bulik-Sullivan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- George Davey Smith
- Jian Yang
- Frank Dudbridge
- J. Stockman
- Joshua D. Angrist
- Peter M. Visscher
- Alkes L Price
- Shaun Purcell
- Joseph K. Pickrell
- Xiaoping Zhou
Who trusts Brendan K. Bulik-Sullivan overall
- Po-Ru Loh
- Evan A. Boyle
- Hilary K Finucane
- Florian Privé
- Joseph K. Pickrell
- Tomaz Berisa
- Alkes L Price
- Steven Gazal
- P. Turley
- Tian Ge
Papers from Brendan K. Bulik-Sullivan's perspective
Ordered by how strongly the researchers Brendan K. Bulik-Sullivan trusts endorse each paper. Same corpus, a different order for every researcher.
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (Human Molecular Genetics)
- MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Their papers
- Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 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
- Linkage disequilibrium dependent architecture of human complex traits reveals action of negative selection (2016) — 192 citations
- Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (2016) — 890 citations
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) — 996 citations
- An Atlas of Genetic Correlations across Human Diseases and Traits (2015) — 4,075 citations
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) — 7,422 citations
- LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies (2014) — 5,156 citations
- Efficient Bayesian mixed model analysis increases association power in large cohorts (2014) — 1,384 citations
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) — 740 citations