Mark J Rieder

发表

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

Dolores Corella, Olle Melander, Thomas Hedner, 2008, Nature Genetics.

High-throughput genotyping of intermediate-size structural variation.

Deborah A Nickerson, Andrew J Sharp, Evan E Eichler, 2006, Human molecular genetics.

Evidence for substantial fine-scale variation in recombination rates across the human genome

Dana C Crawford, Matthew Stephens, Deborah A Nickerson, 2004, Nature Genetics.

Pattern of sequence variation across 213 environmental response genes.

Sivakumar Gowrisankar, Dana C Crawford, Deborah A Nickerson, 2004, Genome research.

Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era

Deborah A Nickerson, Stephan Züchner, Eden Martin, 2012, Circulation. Cardiovascular genetics.

Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

Yusuke Nakamura, Dan M Roden, Matthew Oetjens, 2013, The Lancet.

Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes

Deborah A Nickerson, Leonid Kruglyak, Mark D Shriver, 2004, PLoS biology.

Genomic regions exhibiting positive selection identified from dense genotype data.

Deborah A Nickerson, Michael A Eberle, C. Carlson, 2005, Genome research.

Variation in the 3-Hydroxyl-3-Methylglutaryl Coenzyme A Reductase Gene Is Associated With Racial Differences in Low-Density Lipoprotein Cholesterol Response to Simvastatin Treatment

Deborah A Nickerson, David Waters, Xiuqing Guo, 2008, Circulation.

Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose.

Deborah A Nickerson, Howard L McLeod, David L Veenstra, 2005, The New England journal of medicine.

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Jay Shendure, Deborah A Nickerson, Choli Lee, 2012, Nature Genetics.

VKORC1 polymorphisms, haplotypes and haplotype groups on warfarin dose among African-Americans and European-Americans.

Nianjun Liu, T Mark Beasley, Donna K Arnett, 2008, Pharmacogenomics.

Renin-angiotensin system haplotypes and the risk of myocardial infarction and stroke in pharmacologically treated hypertensive patients.

Thomas Lumley, Bruce M Psaty, Charles Kooperberg, 2007, American journal of epidemiology.

Cryptic transmission of SARS-CoV-2 in Washington state

Trevor Bedford, Deborah A Nickerson, Michael Famulare, 2020, Science.

Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes.

Deborah A Nickerson, M. Rieder, D. Nickerson, 2005, Human molecular genetics.

Functional polymorphism in human CYP4F2 decreases 20-HETE production.

M. Rieder, R. Roman, D. Stec, 2007, Physiological genomics.

Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome

Deborah A Nickerson, Leonid Kruglyak, Michael A Eberle, 2006, PLoS genetics.

Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations.

Dana C Crawford, Deborah A Nickerson, Leonid Kruglyak, 2004, American journal of human genetics.

Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis

Francesca Antonacci, Heather C Mefford, Evan E Eichler, 2010, American journal of medical genetics. Part A.

Soluble P-Selectin, SELP Polymorphisms, and Atherosclerotic Risk in European-American and African-African Young Adults: The Coronary Artery Risk Development in Young Adults (CARDIA) Study

Deborah A Nickerson, Bharat Thyagarajan, C. Carlson, 2008, Arteriosclerosis, thrombosis, and vascular biology.

Identifying the genotype behind the phenotype: a role model found in VKORC1 and its association with warfarin dosing.

Dana C Crawford, Marylyn D Ritchie, M. Rieder, 2007, Pharmacogenomics.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

Deborah A Nickerson, Stephan Züchner, Eden Martin, 2011, American journal of human genetics.