Mark J. Rieder

Nature Genetics · 2004–2012

A researcher in the Science corpus: 11 papers; trusts 0 researchers and is trusted by 2 researchers here, as inferred from the citation graph.

Whom Mark J. Rieder trusts overall

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

1. Matthew Stephens

Who trusts Mark J. Rieder overall

1. Reedik Mägi
2. David J. Balding

Papers from Mark J. Rieder's perspective

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

1. Linkage disequilibrium in humans: models and data. (American Journal of Human Genetics)
2. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
3. Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
4. Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
5. Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
6. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
7. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (Science)
8. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
9. Base-calling of automated sequencer traces using phred. II. Error probabilities.
10. The Structure of Haplotype Blocks in the Human Genome (Science)

Their papers

• Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
• Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (2004) — 1,649 citations
• Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. (2012) — 1,064 citations
• Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations (2012) — 2,200 citations
• Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era (2012) — 137 citations
• Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (2011) — 1,162 citations
• Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome (2010) — 1,398 citations
• Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations
• Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans (2008) — 1,459 citations
• Use of Pharmacogenetic and Clinical Factors to Predict the Therapeutic Dose of Warfarin (2008) — 866 citations
• Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose. (2005) — 1,436 citations