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Nature Genetics|January 19, 2010
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskJosée Dupuis, Claudia Langenberg, Inga Prokopenko, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Addiction Biology|February 18, 2020
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studiesMelissa A Munn-Chernoff, Emma C Johnson, Yi-Ling Chou, et al.Science (New York, N.Y.)|November 6, 2010
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation, Florencia Pereyra, Xiaoming Jia, et al.Nature Genetics|April 5, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementiasCéline Bellenguez, Fahri Küçükali, Iris E Jansen, et al.Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.Plos One|January 13, 2012
A genome-wide association search for type 2 diabetes genes in African AmericansNicholette D Palmer, Caitrin W McDonough, Pamela J Hicks, et al.Science (New York, N.Y.)|March 21, 2020
The genetic architecture of the human cerebral cortexKatrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.Nature Genetics|October 6, 2014
Defining the role of common variation in the genomic and biological architecture of adult human heightAndrew R Wood, Tonu Esko, Jian Yang, et al.Nature Communications|November 2, 2019
Associations of autozygosity with a broad range of human phenotypesDavid W Clark, Yukinori Okada, Kristjan H S Moore, et al.Pageof 46