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Medrxiv : the Preprint Server for Health Sciences
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March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Nature Genetics
|
April 5, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementias
Céline Bellenguez, Fahri Küçükali, Iris E Jansen, et al.
Nature
|
February 2, 2017
Rare and low-frequency coding variants alter human adult height
Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Nature Genetics
|
August 13, 2013
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
, S Hong Lee, Stephan Ripke, et al.
Plos One
|
January 13, 2012
A genome-wide association search for type 2 diabetes genes in African Americans
Nicholette 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 cortex
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
Nature
|
April 9, 2022
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Vassily Trubetskoy, Antonio F Pardiñas, Ting Qi, et al.
Nature Communications
|
November 2, 2019
Associations of autozygosity with a broad range of human phenotypes
David W Clark, Yukinori Okada, Kristjan H S Moore, et al.
Plos Genetics
|
April 6, 2012
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Zari Dastani, Marie-France Hivert, Nicholas Timpson, et al.
Science (New York, N.Y.)
|
June 23, 2018
Analysis of shared heritability in common disorders of the brain
, Verneri Anttila, Brendan Bulik-Sullivan, et al.
Page
of 25
Search research articles
Search
Showing results (231-240 of 242) with videos related to
Sort By:
Page
of 25
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 subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Nature Genetics
|
April 5, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementias
Céline Bellenguez, Fahri Küçükali, Iris E Jansen, et al.
Nature
|
February 2, 2017
Rare and low-frequency coding variants alter human adult height
Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Nature Genetics
|
August 13, 2013
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
, S Hong Lee, Stephan Ripke, et al.
Plos One
|
January 13, 2012
A genome-wide association search for type 2 diabetes genes in African Americans
Nicholette 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 cortex
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
Nature
|
April 9, 2022
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Vassily Trubetskoy, Antonio F Pardiñas, Ting Qi, et al.
Nature Communications
|
November 2, 2019
Associations of autozygosity with a broad range of human phenotypes
David W Clark, Yukinori Okada, Kristjan H S Moore, et al.
Plos Genetics
|
April 6, 2012
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Zari Dastani, Marie-France Hivert, Nicholas Timpson, et al.
Science (New York, N.Y.)
|
June 23, 2018
Analysis of shared heritability in common disorders of the brain
, Verneri Anttila, Brendan Bulik-Sullivan, et al.
Page
of 25