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Breast Cancer Research : BCR|November 6, 2016
Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicitiesSara Lindström, Akweley Ablorh, Brad Chapman, et al.Plos Genetics|January 4, 2014
Quantifying missing heritability at known GWAS lociAlexander Gusev, Gaurav Bhatia, Noah Zaitlen, et al.Nature|July 12, 2018
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterationsPo-Ru Loh, Giulio Genovese, Robert E Handsaker, et al.Nature Genetics|June 27, 2018
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traitsFarhad Hormozdiari, Steven Gazal, Bryce van de Geijn, et al.Nature Genetics|February 26, 2013
Using population admixture to help complete maps of the human genomeGiulio Genovese, Robert E Handsaker, Heng Li, et al.Nature Communications|February 4, 2026
scLong: a billion-parameter foundation model for capturing long-range gene context in single-cell transcriptomicsDing Bai, Shentong Mo, Ruiyi Zhang, et al.American Journal of Human Genetics|November 20, 2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesPier Francesco Palamara, Laurent C Francioli, Peter R Wilton, et al.Nature Genetics|June 6, 2022
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicitySteven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.Research Square|January 3, 2024
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selectionMartin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.Medrxiv : the Preprint Server for Health Sciences|December 18, 2023
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selectionMartin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.Pageof 19