Mulin Jun Li
Nature Genetics · 2015–2021
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom Mulin Jun Li trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Gerd Kempermann (in Biomedical Engineering)
Papers from Mulin Jun Li's perspective
Ordered by how strongly the researchers Mulin Jun Li trusts endorse each paper. Same corpus, a different order for every researcher.
- The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 (Nucleic Acids Res.)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (Nature Genetics)
- The DisGeNET knowledge platform for disease genomics: 2019 update (Nucleic Acids Res.)
- Medical Subject Headings (MeSH). (Bulletin of the Medical Library Association)
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (bioRxiv)
- Faculty Opinions recommendation of Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.
- Opportunities and challenges for transcriptome-wide association studies (Nature Genetics)
- ClinVar: public archive of interpretations of clinically relevant variants
Their papers
- The support of human genetic evidence for approved drug indications (2015) — 1,489 citations
- webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study (2021) — 337 citations