J. Tung
Genetics · 2010–2021
A researcher in the Science corpus: 17 papers; trusts 3 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 369 citations into it; #5,766 of 6,854 by trust here, #620 by citations
- Molecular Biology — 276 citations into it
- Epidemiology — 22 citations into it
- Immunology — 7 citations into it
- Surgery — 6 citations into it
Whom J. Tung trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts J. Tung overall
Papers from J. Tung's perspective
Ordered by how strongly the researchers J. Tung trusts endorse each paper. Same corpus, a different order for every researcher.
- Genome-wide genetic data on ~500,000 UK Biobank participants (bioRxiv)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. (American Journal of Human Genetics)
- A note on exact tests of Hardy-Weinberg equilibrium. (American Journal of Human Genetics)
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Nature)
- From the Cover: Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
Their papers
- Quantifying penetrance in a dominant disease gene using large population control cohorts (2016) — 400 citations
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) — 813 citations
- Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) — 705 citations
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson’s disease: a meta-genome wide association study (2019) — 1,651 citations
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) — 629 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- Multi-trait analysis of genome-wide association summary statistics using MTAG (2018) — 1,002 citations
- An atlas of genetic influences on osteoporosis in humans and mice (2018) — 681 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- Identification of 15 genetic loci associated with risk of major depression in individuals of European descent (2016) — 756 citations
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) — 129 citations
- Detection and interpretation of shared genetic influences on 42 human traits (2016) — 1,123 citations
- A genetic variant near olfactory receptor genes influences cilantro preference (2012) — 107 citations
- Web-Based, Participant-Driven Studies Yield Novel Genetic Associations for Common Traits (2010) — 464 citations