Yang I Li
Molecular Biology · 2016–2017
A researcher in the Science corpus: 3 papers; trusts 4 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 55 citations into it
- Genetics — 48 citations into it
Whom Yang I Li trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Henrik Kaessmann
- Matthew Stephens
- Simon Anders
- Joseph K. Pickrell
- Brendan K. Bulik-Sullivan
- Hilary K Finucane
- Michael Olivier
- Steven H. Strogatz
- Alejandro Reyes
Who trusts Yang I Li overall
Papers from Yang I Li's perspective
Ordered by how strongly the researchers Yang I Li 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)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (bioRxiv)
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (Human Molecular Genetics)
- Detecting differential usage of exons from RNA-seq data (Genome Research)
- False discovery rates: a new deal (bioRxiv)
- Common genetic variation and human traits. (New England Journal of Medicine)
- Chromatin marks identify critical cell types for fine mapping complex trait variants (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies (Nature Genetics)
Their papers
- Annotation-free quantification of RNA splicing using LeafCutter (2017) — 647 citations
- RNA splicing is a primary link between genetic variation and disease (2016) — 634 citations
- An expanded view of complex traits: from polygenic to omnigenic (2017) — 2,673 citations