Jordan W. Smoller
Genetics · 2003–2022
A researcher in the Science corpus: 30 papers; trusts 13 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 595 citations into it; #6,642 of 6,854 by trust here, #140 by citations
- Molecular Biology — 359 citations into it
- Statistics and Probability — 35 citations into it
- Artificial Intelligence — 20 citations into it
Whom Jordan W. Smoller trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Jordan W. Smoller overall
Papers from Jordan W. Smoller's perspective
Ordered by how strongly the researchers Jordan W. Smoller trusts endorse each paper. Same corpus, a different order for every researcher.
- 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)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- GCTA: a tool for genome-wide complex trait analysis. (American Journal of Human Genetics)
- MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
- Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (Nature Neuroscience)
Their papers
- The Evaluation of Tools Used to Predict the Impact of Missense Variants Is Hindered by Two Types of Circularity (2015) — 342 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
- Common genetic variants influence human subcortical brain structures (2015) — 868 citations
- Largest GWAS of PTSD (N=20,070) Yields Genetic Overlap with Schizophrenia and Sex Differences in Heritability (2017) — 392 citations
- Pleiotropy in complex traits: challenges and strategies (2013) — 1,050 citations
- A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
- Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis (2013) — 2,591 citations
- The genetic architecture of the human cerebral cortex (2020) — 777 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Genome-wide association studies in ancestrally diverse populations: opportunities, methods, pitfalls, and recommendations. (2019) — 634 citations
- The “All of Us” Research Program (2019) — 1,731 citations
- Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study (2019) — 625 citations
- Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders (2019) — 648 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
- Polygenic prediction via Bayesian regression and continuous shrinkage priors (2018) — 1,656 citations
- Psychiatric Genomics: An Update and an Agenda (2017) — 635 citations