Sarah S. Murray
Genetics · 2006–2015
A researcher in the Science corpus: 6 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 119 citations into it
- Molecular Biology — 84 citations into it
Whom Sarah S. Murray trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Sarah S. Murray's perspective
Ordered by how strongly the researchers Sarah S. Murray trusts endorse each paper. Same corpus, a different order for every researcher.
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Nature Genetics)
- Detection of large-scale variation in the human genome (Nature Genetics)
- Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion (Nature Genetics)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- Large-Scale Copy Number Polymorphism in the Human Genome (Science)
- Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
- On the allelic spectrum of human disease. (Trends in Genetics)
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
Their papers
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Family Income, Parental Education and Brain Structure in Children and Adolescents (2015) — 1,261 citations
- Common vs. Rare Allele Hypotheses for Complex Diseases (2009) — 694 citations
- Evaluation of next generation sequencing platforms for population targeted sequencing studies (2009) — 658 citations
- Human genetic variation and its contribution to complex traits (2009) — 1,127 citations
- A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006) — 810 citations