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Nature|April 13, 2012
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutationsBrian J O'Roak, Laura Vives, Santhosh Girirajan, et al.Science (New York, N.Y.)|May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomesJacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.Genome Research|June 22, 2021
Deep sequencing of 1320 genes reveals the landscape of protein-truncating variants and their contribution to psoriasis in 19,973 Chinese individualsHuixin Xu, Qi Zhen, Mingzhou Bai, et al.Science (New York, N.Y.)|February 26, 2016
The phenotypic legacy of admixture between modern humans and NeandertalsCorinne N Simonti, Benjamin Vernot, Lisa Bastarache, et al.Human Genomics|July 12, 2005
Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variationMark D Shriver, Rui Mei, Esteban J Parra, et al.Biorxiv : the Preprint Server for Biology|September 26, 2025
Metadomain and metaloop genome interactions in mammalian T cellsGabriel Dolsten, Zhong-Mig Wang, Xiao Huang, et al.Cell Reports|May 9, 2026
Metadomain and metaloop genome interactions in mammalian T cellsGabriel Dolsten, Zhong-Min Wang, Xiao Huang, et al.Science (New York, N.Y.)|November 20, 2012
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersBrian J O'Roak, Laura Vives, Wenqing Fu, et al.Nature|August 4, 2016
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibilityXander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, et al.Nature|September 8, 2012
An expansive human regulatory lexicon encoded in transcription factor footprintsShane Neph, Jeff Vierstra, Andrew B Stergachis, et al.Pageof 13