Patrick F. Sullivan
Genetics · 2003–2021
A researcher in the Science corpus: 40 papers; trusts 2 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 826 citations into it; #4,252 of 6,854 by trust here, #71 by citations
Whom Patrick F. Sullivan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Patrick F. Sullivan overall
Papers from Patrick F. Sullivan's perspective
Ordered by how strongly the researchers Patrick F. Sullivan trusts endorse each paper. Same corpus, a different order for every researcher.
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. (The Lancet)
- Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (The Lancet)
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease
- Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
Their papers
- Integrative approaches for large-scale transcriptome-wide association studies (2015) — 2,212 citations
- Meta-analysis of the heritability of human traits based on fifty years of twin studies (2015) — 2,080 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
- Genetic identification of brain cell types underlying schizophrenia (2017) — 638 citations
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2019) — 2,238 citations
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) — 511 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
- Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) — 740 citations
- Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia (2017) — 413 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Microduplications of 16p11.2 are Associated with Schizophrenia (2009) — 730 citations
- Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) — 577 citations
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) — 1,862 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs (2013) — 310 citations
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) — 2,006 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations