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Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
GWAS Meta-analysis Identifies Novel Associated Loci and Points to Causal Tissues in Central Serous ChorioretinopathyLiyin Chen, Soo Hyun Kim, Buu Truong, et al.Nature Genetics|October 5, 2001
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn diseaseJ D Rioux, M J Daly, M S Silverberg, et al.Nature Communications|July 23, 2024
Complex trait susceptibilities and population diversity in a sample of 4,145 RussiansDmitrii Usoltsev, Nikita Kolosov, Oxana Rotar, et al.Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucomaJoel T Rämö, Bryan Gorman, Lu-Chen Weng, et al.Nature Neuroscience|March 18, 2018
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.Cancer Research|June 22, 2017
Phosphoproteomic Profiling Reveals ALK and MET as Novel Actionable Targets across Synovial Sarcoma SubtypesEmmy D G Fleuren, Myrella Vlenterie, Winette T A van der Graaf, et al.Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.Genome Medicine|March 19, 2020
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disordersDennis Lal, Patrick May, Eduardo Perez-Palma, et al.Proceedings of the National Academy of Sciences of the United States of America|April 7, 2007
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupusRobert R Graham, Chieko Kyogoku, Snaevar Sigurdsson, et al.Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.Pageof 163