Cristen J. Willer
Genetics · 2007–2021
A researcher in the Science corpus: 28 papers; trusts 10 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 460 citations into it; #880 of 6,854 by trust here, #79 by citations
- Molecular Biology — 289 citations into it
Whom Cristen J. Willer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthew Stephens
- Gonçalo R. Abecasis
- Paul Scheet
- Jonathan Marchini
- David J. Balding
- Wei-Min Chen
- Eleftheria Zeggini
- Shaun Purcell
- Peter Donnelly
- Lon R. Cardon
Who trusts Cristen J. Willer overall
- Heng Li
- Evangelos Evangelou
- Brian L. Browning
- William S. Bush
- Olivier Delaneau
- Gonçalo R. Abecasis
- Yun Li
- Bryan N. Howie
- John P. A. Ioannidis
- Jonathan Marchini
Papers from Cristen J. Willer's perspective
Ordered by how strongly the researchers Cristen J. Willer trusts endorse each paper. Same corpus, a different order for every researcher.
- Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9 (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
- Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
- High-resolution haplotype structure in the human genome (Nature Genetics)
- Genomewide Association Analysis of Coronary Artery Disease (New England Journal of Medicine)
Their papers
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants (2007) — 2,870 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies (2017) — 1,245 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) — 813 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 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
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) — 749 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) — 652 citations
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) — 2,232 citations
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (2010) — 2,056 citations
- METAL: fast and efficient meta-analysis of genomewide association scans (2010) — 5,095 citations