Or Zuk
Molecular Biology · 2006–2014
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 11 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 89 citations into it; #4,608 of 17,773 by trust here, #1,613 by citations
Whom Or Zuk trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Or Zuk overall
- Seunggeun Lee
- Alex Smola
- Le Song
- David Broadhurst
- Riccardo Bellazzi
- Anne-Claire Haury
- Arthur Gretton
- Gonçalo R. Abecasis
- Markus Ringnér
Papers from Or Zuk's perspective
Ordered by how strongly the researchers Or Zuk 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)
- Sequence variations in PCSK9, low LDL, and protection against coronary heart disease.
- Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9 (Nature Genetics)
- Finding the missing heritability of complex diseases (Nature)
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
- Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (American Journal of Human Genetics)
- On the allelic spectrum of human disease. (Trends in Genetics)
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- Genetics and Analysis of Quantitative Traits.
- A method and server for predicting damaging missense mutations
Their papers
- Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals (2009) — 4,137 citations
- A large intergenic non-coding RNA induced by p53 mediates global gene repression in the p53 response (2010) — 2,069 citations
- The mystery of missing heritability: Genetic interactions create phantom heritability (2012) — 1,592 citations
- Thousands of samples are needed to generate a robust gene list for predicting outcome in cancer. (2006) — 720 citations
- Searching for missing heritability: Designing rare variant association studies (2014) — 633 citations
- A high-resolution map of human evolutionary constraint using 29 mammals (2011) — 867 citations