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Eclinicalmedicine|September 7, 2021
Increased risk of severe clinical course of COVID-19 in carriers of HLA-C*04:01January Weiner, Phillip Suwalski, Manuel Holtgrewe, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Fine-mapping genomic loci refines bipolar disorder risk genesMaria Koromina, Ashvin Ravi, Georgia Panagiotaropoulou, et al.
Brain : a Journal of Neurology|November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementiaCornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 10, 2014
Common genetic variants associated with cognitive performance identified using the proxy-phenotype methodCornelius A Rietveld, Tõnu Esko, Gail Davies, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Nature Genetics|February 28, 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionAntonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
International Journal of Epidemiology|August 20, 2015
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritisS Hong Lee, Enda M Byrne, Christina M Hultman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed PopulationsMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
Molecular Psychiatry|November 13, 2019
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depressionAndreas J Forstner, Swapnil Awasthi, Christiane Wolf, et al.
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