Jian Yang

Genetics · Nature Genetics · 2010–2021

A researcher in the Science corpus: 42 papers; trusts 20 researchers and is trusted by 34 researchers here, as inferred from the citation graph.

Subfields

Genetics — 875 citations into it; #355 of 6,854 by trust here, #54 by citations
Molecular Biology — 501 citations into it; #15,319 of 17,773 by trust here, #2,498 by citations
Computational Biology & Bioinformatics — 85 citations into it
Plant Science — 51 citations into it
Artificial Intelligence — 15 citations into it

Whom Jian Yang trusts overall

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

Who trusts Jian Yang overall

Papers from Jian Yang's perspective

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

Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Principal components analysis corrects for stratification in genome-wide association studies
Regression Shrinkage and Selection via the Lasso
Accuracy of Predicting the Genetic Risk of Disease Using a Genome-Wide Approach (PLoS ONE)
The support of human genetic evidence for approved drug indications (Nature Genetics)
Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
The Elements of Statistical Learning
Pitfalls of predicting complex traits from SNPs
Genomic selection: prediction of accuracy and maximisation of long term response (Genetica)
Increased accuracy of artificial selection by using the realized relationship matrix. (Genetics Research)

Their papers

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (2016) — 2,949 citations
10 Years of GWAS Discovery: Biology, Function, and Translation. (2017) — 3,277 citations
Biological interpretation of genome-wide association studies using predicted gene functions (2015) — 821 citations
The transcriptional landscape of age in human peripheral blood (2015) — 654 citations
The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) — 511 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
The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
A generalized linear mixed model association tool for biobank-scale data (2021) — 578 citations
Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
Recovery of trait heritability from whole genome sequence data (2019) — 222 citations
Improved polygenic prediction by Bayesian multiple regression on summary statistics (2019) — 484 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
Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
A resource-efficient tool for mixed model association analysis of large-scale data (2019) — 483 citations
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry (2018) — 1,022 citations
Meta-analysis of genome-wide association studies for height and body mass index in ∼700,000 individuals of European ancestry (2018) — 1,929 citations
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) — 707 citations
Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits (2018) — 613 citations