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International Journal of Cancer|August 14, 2009
Loss of STARD10 expression identifies a group of poor prognosis breast cancers independent of HER2/Neu and triple negative statusNiamh C Murphy, Andrew V Biankin, Ewan K A Millar, et al.
Nature Genetics|September 29, 2015
Partitioning heritability by functional annotation using genome-wide association summary statisticsHilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Nature Genetics|December 6, 2023
Inferring compound heterozygosity from large-scale exome sequencing dataMichael H Guo, Laurent C Francioli, Sarah L Stenton, et al.
Gut|July 12, 2020
Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBDShixian Hu, Arnau Vich Vila, Ranko Gacesa, et al.
Neurobiology of Aging|November 8, 2011
A genome-wide scan for common variants affecting the rate of age-related cognitive declinePhilip L De Jager, Joshua M Shulman, Lori B Chibnik, et al.
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