Suzanne M. Leal
Genetics · 2001–2014
A researcher in the Science corpus: 7 papers; trusts 1 researcher and is trusted by 70 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 111 citations into it; #131 of 6,854 by trust here, #193 by citations
Whom Suzanne M. Leal trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Suzanne M. Leal overall
- Rachel B. Brem
- Daniel Nettle
- S. Franks
- S. Fevolden
- Seunggeun Lee
- E. Saillant
- Meghan Larivee
- Michael Lynch
- J. Merilä
- Matthew A. Barbour
Papers from Suzanne M. Leal's perspective
Ordered by how strongly the researchers Suzanne M. Leal trusts endorse each paper. Same corpus, a different order for every researcher.
- Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
- Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (Nature Genetics)
- Data and Theory Point to Mainly Additive Genetic Variance for Complex Traits (PLoS Genetics)
- Heritability in the genomics era — concepts and misconceptions (Nature reviews genetics)
- Large-Scale Copy Number Polymorphism in the Human Genome (Science)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
- Population analysis of large copy number variants and hotspots of human genetic disease. (American Journal of Human Genetics)
- Genome-wide genetic association of complex traits in heterogeneous stock mice (Nature Genetics)
- Human genetic variation and its contribution to complex traits
Their papers
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
- Guidelines for investigating causality of sequence variants in human disease (2014) — 1,235 citations
- Missing heritability and strategies for finding the underlying causes of complex disease (2010) — 1,739 citations
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (2008) — 1,578 citations
- Genetics and Analysis of Quantitative Traits (2001) — 1,214 citations