Cathryn M. Lewis

Genetics · 2001–2021

A researcher in the Science corpus: 17 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

• Genetics — 238 citations into it; #6,831 of 6,854 by trust here, #141 by citations

Whom Cathryn M. Lewis trusts overall

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

1. Frank Dudbridge
2. Christopher C. Chang

Who trusts Cathryn M. Lewis overall

1. Elias Zintzaras
2. Tian Ge
3. Timothy Shin Heng Mak

Papers from Cathryn M. Lewis's perspective

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

1. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
2. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
3. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
4. Approximately independent linkage disequilibrium blocks in human populations (bioRxiv)
5. Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
6. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
7. The support of human genetic evidence for approved drug indications (Nature Genetics)
8. FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
9. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
10. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (The Lancet)

Their papers

• Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease (2003) — 860 citations
• Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) — 604 citations
• Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2019) — 2,238 citations
• A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
• Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
• Polygenic risk scores: from research tools to clinical instruments (2020) — 1,117 citations
• Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
• Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
• An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis. (2017) — 201 citations
• Meta-analysis of the Association Between the Level of Cannabis Use and Risk of Psychosis. (2016) — 777 citations
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
• PRSice: Polygenic Risk Score software (2014) — 1,232 citations
• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations
• Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn disease susceptibility (2007) — 1,239 citations
• Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. (2003) — 1,198 citations
• The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. (2002) — 709 citations
• Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. (2001) — 1,135 citations