Showing results (841-850 of 873) with videos related to
Sort By:
Pageof 88
Molecular Psychiatry|October 9, 2019
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestryTim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, et al.Nature|June 18, 2013
Mutational heterogeneity in cancer and the search for new cancer-associated genesMichael S Lawrence, Petar Stojanov, Paz Polak, et al.Nature Genetics|June 5, 2019
Publisher Correction: 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.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.Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.Nature|April 21, 2006
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineageMichael C Zody, Manuel Garber, David J Adams, et al.Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.Diabetes|August 26, 2017
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 DiabetesJosep M Mercader, Rachel G Liao, Avery D Bell, et al.Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.Pageof 88