Kimberly F Doheny

发表

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Dana C Crawford, Yuki Bradford, Mariza de Andrade, 2011, Genetic epidemiology.

Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network

Gerard Tromp, Dana C Crawford, Helena Kuivaniemi, 2015, Genetic epidemiology.

Quality control and quality assurance in genotypic data for genome‐wide association studies

Peter Kraft, Thomas Lumley, Maria Teresa Landi, 2010, Genetic epidemiology.

Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14

Simon Cawley, Guoying Liu, Laura J Bierut, 2005, BMC Genetics.

Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature.

Cathy C Laurie, Kimberly F Doheny, Daniel B Mirel, 2012, Trends in genetics : TIG.

Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2

Eden R Martin, Karen Marder, Tatiana Foroud, 2012, Annals of neurology.

Common variants in the GDF5-UQCC region are associated with variation in human height

Shah Ebrahim, Debbie A Lawlor, Yoav Ben-Shlomo, 2008, Nature Genetics.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2010, Nature Genetics.

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.

Ying Wang, William Wheeler, Andres Metspalu, 2009, American journal of human genetics.

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.

Chun Li, Kaisa Silander, Soumitra Ghosh, 2004, Diabetes.

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Alan F Scott, Jeffrey C Murray, 2010, Nature Genetics.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Discovery of common and rare genetic risk variants for colorectal cancer

Mathieu Lemire, Steven Gallinger, Michael Wainberg, 2018, Nature Genetics.

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.

Gonçalo R Abecasis, Maria Karayiorgou, Kimberly F Doheny, 2004, American journal of human genetics.

Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database

Randall Pruim, Michael Boehnke, Cristen J Willer, 2006, Genetic epidemiology.

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.

Michael J Ackerman, Joshua C Denny, Dan M Roden, 2016, JAMA.

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Christian Fuchsberger, Tanya M. Teslovich, Johanna Kuusisto, 2012, Nature Genetics.