Deborah A. Nickerson

Genetics · 2001–2019

A researcher in the Science corpus: 27 papers; trusts 8 researchers and is trusted by 16 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 347 citations into it; #962 of 6,854 by trust here, #33 by citations
• Molecular Biology — 260 citations into it; #3,618 of 17,773 by trust here, #616 by citations

Whom Deborah A. Nickerson trusts overall

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

1. Matthew Stephens

Who trusts Deborah A. Nickerson overall

1. Michael Olivier
2. Jay Shendure
3. Phillip A. Morin
4. Reedik Mägi
5. Devon E. Pearse

Papers from Deborah A. Nickerson's perspective

Ordered by how strongly the researchers Deborah A. Nickerson trusts endorse each paper. Same corpus, a different order for every researcher.

1. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
2. The Human Gene Mutation Database: 2008 update
3. Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
4. Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
5. Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (American Journal of Human Genetics)
6. Exome sequencing as a tool for Mendelian disease gene discovery
7. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
8. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
9. Next-generation genotype imputation service and methods (Nature Genetics)
10. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)

Their papers

• A global reference for human genetic variation (2015) — 16,925 citations
• The utility of single nucleotide polymorphisms in inferences of population history (2003) — 655 citations
• Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
• Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
• Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
• Exome sequencing identifies the cause of a Mendelian disorder (2009) — 2,093 citations
• Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (2004) — 1,649 citations
• Variation is the spice of life (2001) — 998 citations
• Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
• Single-nucleotide evolutionary constraint scores highlight disease-causing mutations (2010) — 208 citations
• Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders (2012) — 1,254 citations
• Insights into genetics, human biology and disease gleaned from family based genomic studies (2019) — 179 citations
• Mendelian Gene Discovery: Fast and Furious with No End in Sight. (2019) — 210 citations
• Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
• The contribution of de novo coding mutations to autism spectrum disorder (2014) — 2,476 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
• An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
• Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era (2012) — 137 citations
• Copy number variation detection and genotyping from exome sequence data (2012) — 660 citations