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Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2008
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's diseaseAleksandar Rakovic, Barbara Stiller, Ana Djarmati, et al.
Arthritis and Rheumatism|April 1, 2011
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility lociJan Freudenberg, Hye-Soon Lee, Bok-Ghee Han, et al.
Annals of the Rheumatic Diseases|January 12, 2012
Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-GMichelle M A Fernando, Jan Freudenberg, Annette Lee, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Disease variants in genomes of 44 centenariansYun Freudenberg-Hua, Jan Freudenberg, Vladimir Vacic, et al.
Human Molecular Genetics|May 15, 2010
Refining the association of MHC with multiple sclerosis in African AmericansJoseph P McElroy, Bruce A C Cree, Stacy J Caillier, et al.
Human Mutation|January 30, 2009
A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeatsBoi-Dinh Chung, Hülya Kayserili, Minrong Ai, et al.
The Journal of Investigative Dermatology|August 7, 2022
Comparison of the Inflammatory Circuits in Psoriasis Vulgaris, Non‒Pustular Palmoplantar Psoriasis, and Palmoplantar Pustular PsoriasisClaire Q Wang, Sokol Haxhinasto, Sandra Garcet, et al.
Nature Genetics|January 31, 2012
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritisSoumya Raychaudhuri, Cynthia Sandor, Eli A Stahl, et al.
Investigative Ophthalmology & Visual Science|November 2, 2021
ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 CarriersSahar Gelfman, Dominique Monnet, Ann J Ligocki, et al.
American Journal of Human Genetics|November 18, 2003
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the diseaseAnn Van Den Bogaert, Johannes Schumacher, Thomas G Schulze, et al.
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