M. Emond
Genetics · 1998–2012
A researcher in the Science corpus: 5 papers; trusts 4 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 39 citations into it
- Molecular Biology — 21 citations into it
Whom M. Emond trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts M. Emond overall
Papers from M. Emond's perspective
Ordered by how strongly the researchers M. Emond trusts endorse each paper. Same corpus, a different order for every researcher.
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
- Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (American Journal of Human Genetics)
- Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
- A method and server for predicting damaging missense mutations
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic (PLoS Genetics)
- Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect against Type 1 Diabetes (Science)
- Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma (Proceedings of the National Academy of Sciences of the United States of America)
Their papers
- Extension of Murine Life Span by Overexpression of Catalase Targeted to Mitochondria (2005) — 1,745 citations
- Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. (2012) — 1,064 citations
- Exome sequencing as a tool for Mendelian disease gene discovery (2011) — 1,755 citations
- Influence of a diet very high in vegetables, fruit, and fiber and low in fat on prognosis following treatment for breast cancer: the Women's Healthy Eating and Living (WHEL) randomized trial. (2007) — 760 citations
- I-PpoI and I-CreI homing site sequence degeneracy determined by random mutagenesis and sequential in vitro enrichment. (1998)