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Paper Details

Identifying genetically driven clinical phenotypes using linear mixed models.
Nat Commun
11
2016
/, C6orf10, HLA, HLA SNP, HLA SNP variation, HLA-DQA1, HLA-DQB1, Illumina Exome Beadchip, Type I diabetes, human, human leukocyte antigen, human leukocyte antigen (HLA) region, hypothyroidism, polymyalgia rheumatica, rs6906021, rs6910071, single-nucleotide polymorphism
Author NameAffiliation
Jonathan D MosleyVanderbilt University
John S WitteUniversity of California san francisco
Lisa BastaracheVanderbilt University
Lisa BastaracheVanderbilt University
Christian M ShafferVanderbilt University
Jason H KarnesVanderbilt University
Charles M SteinVanderbilt University
Elizabeth J PhillipsVanderbilt University
Scott J HebbringCenter for Human Genetics, Marshfield Clinic Research Foundation
Murray H BrilliantCenter for Human Genetics, Marshfield Clinic Research Foundation
Dan M RodenVanderbilt University
Joshua C DennyVanderbilt University
Joshua C DennyVanderbilt University
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