Stephen J. Chanock

Molecular Biology · 2000–2021

A researcher in the Science corpus: 31 papers; trusts 1 researcher and is trusted by 3 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 140 citations into it

Whom Stephen J. Chanock trusts overall

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

1. Heng Li
2. N. Risch

Who trusts Stephen J. Chanock overall

1. John P. A. Ioannidis
2. L. Duncan
3. Matthew C. Keller
4. Evangelos Evangelou
5. Bríd Ryan
6. Nicholas J. Schork

Papers from Stephen J. Chanock's perspective

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

1. Principal components analysis corrects for stratification in genome-wide association studies
2. Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
3. A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
4. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
5. Complement Factor H Polymorphism in Age-Related Macular Degeneration (Science)
6. Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration (Science)
7. Defining the role of common variation in the genomic and biological architecture of adult human height
8. Genome-partitioning of genetic variation for complex traits using common SNPs (Nature Genetics)
9. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
10. Estimating Effects and Making Predictions from Genome-Wide Marker Data

Their papers

• Assessing the Probability That a Positive Report is False: An Approach for Molecular Epidemiology Studies (2004) — 765 citations
• Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. (2004) — 1,133 citations
• Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. (2005) — 738 citations
• Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
• Replicating genotype–phenotype associations (2007) — 1,394 citations
• LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants (2015) — 1,846 citations
• A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer (2007) — 1,516 citations
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
• A common coding variant in CASP8 is associated with breast cancer risk (2007) — 597 citations
• Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women (2021) — 858 citations
• Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer (2009) — 695 citations
• Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) — 797 citations
• LDlinkR: An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations (2020) — 369 citations
• Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
• Evidence for single-dose protection by the bivalent HPV vaccine—review of the Costa Rica HPV Vaccine Trial and future research studies (2018) — 133 citations
• Genetic evidence of assortative mating in humans (2017) — 288 citations
• Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes (2017) — 623 citations
• Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States (2016) — 328 citations
• Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
• Supplementary Material 7 (2014)