Deborah A. Nickerson

发表

Characterizing reduced coverage regions through comparison of exome and genome sequencing data across ten centers

Mahdi Sarmady, Rashesh V. Sanghvi, Christian J. Buhay, 2017, Genetics in Medicine.

PRIMUS: improving pedigree reconstruction using mitochondrial and Y haplotypes

James G. Wilson, Deborah A. Nickerson, Jeffrey Staples, 2016, Bioinform..

SNPing in the human genome

Deborah A. Nickerson, D. Nickerson, 2004, RECOMB.

The contribution of de novo coding mutations to autism spectrum disorder

Boris Yamrom, Kenny Q. Ye, Michael C. Schatz, 2014, Nature.

denovo-db: a compendium of human de novo variants

Raphael A. Bernier, Qian Yi, Deborah A. Nickerson, 2016, Nucleic Acids Res..

Targeted interrogation of copy number variation using SCIMMkit

Gregory M. Cooper, Deborah A. Nickerson, Evan E. Eichler, 2009, Bioinform..

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network

Marylyn D. Ritchie, Andrea Hartzler, James Ralston, 2015, Genome Medicine.

The NIST SQL Database Loader: STEP Working Form to SQL. National PDES Testbed Report Series

Deborah A. Nickerson, 1990 .

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

Yun Li, Goo Jun, Dana C. Crawford, 2013, Bioinform..

Cryptic transmission of SARS-CoV-2 in Washington state

Trevor Bedford, Jeffrey S. Duchin, Deborah A. Nickerson, 2020, Science.

Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study

Deborah A. Nickerson, Carlos Iribarren, Alexander P. Reiner, 2007, Human Genetics.

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

Deborah A. Nickerson, Leonid Kruglyak, Mark J. Rieder, 2003, Nature Genetics.

Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies

Mark I. McCarthy, Deborah A. Nickerson, Xiaowu Gai, 2008, PloS one.

Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multi-Center Pilot for Pre-Emptive Pharmacogenomics in Electronic Health Record Systems

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, Clinical pharmacology and therapeutics.

Genome-Wide Association of Lipid-Lowering Response to Statins in Combined Study Populations

Paul T. Williams, Russell A. Wilke, Matthew Stephens, 2010, PloS one.

Massively parallel sequencing: the new frontier of hematologic genomics.

Alex P. Reiner, Deborah A. Nickerson, A. Reiner, 2013, Blood.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

David M. Herrington, Adam Kiezun, Peter Donnelly, 2014, Nature.

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Matti Pirinen, David M. Herrington, Alex Doney, 2014, Nature Communications.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers

Stephen J. Salipante, Deborah A. Nickerson, Jay Shendure, 2011, Proceedings of the National Academy of Sciences.

Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue

Christopher D. Brown, Gregory M. Cooper, Deborah A. Nickerson, 2011, PLoS genetics.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

Andrew G. Clark, Deborah A. Nickerson, Stephanie M. Fullerton, 2004, Human Genetics.

Efficient selection of tagging single-nucleotide polymorphisms in multiple populations

Deborah A. Nickerson, Mark J. Rieder, C. Carlson, 2006, Human Genetics.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Genetic ancestry in lung-function predictions.

Alex P. Reiner, Deborah A. Nickerson, Paul Enright, 2010, The New England journal of medicine.

A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration

Rajiv Raman, Ronnie George, Lingam Vijaya, 2011, PloS one.