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Medrxiv : the Preprint Server for Health Sciences
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April 10, 2023
A scalable variational approach to characterize pleiotropic components across thousands of human diseases and complex traits using GWAS summary statistics
Zixuan Zhang, Junghyun Jung, Artem Kim, et al.
Scientific Reports
|
December 3, 2015
High level of inbreeding in final phase of 1000 Genomes Project
Steven Gazal, Mourad Sahbatou, Marie-Claude Babron, et al.
American Journal of Human Genetics
|
October 25, 2023
A scalable approach to characterize pleiotropy across thousands of human diseases and complex traits using GWAS summary statistics
Zixuan Zhang, Junghyun Jung, Artem Kim, et al.
Bioinformatics (Oxford, England)
|
March 18, 2014
FSuite: exploiting inbreeding in dense SNP chip and exome data
Steven Gazal, Mourad Sahbatou, Marie-Claude Babron, et al.
Nature Genetics
|
June 13, 2018
Mixed-model association for biobank-scale datasets
Po-Ru Loh, Gleb Kichaev, Steven Gazal, et al.
Human Heredity
|
July 26, 2014
Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III
Steven Gazal, Mourad Sahbatou, Hervé Perdry, et al.
Nature Genetics
|
April 22, 2020
Liability threshold modeling of case-control status and family history of disease increases association power
Margaux L A Hujoel, Steven Gazal, Po-Ru Loh, et al.
Human Heredity
|
April 19, 2013
Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?
Emmanuelle Génin, Mourad Sahbatou, Steven Gazal, et al.
American Journal of Human Genetics
|
March 10, 2022
Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes
Kathryn S Burch, Kangcheng Hou, Yi Ding, et al.
American Journal of Human Genetics
|
August 13, 2019
Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
Luke J O'Connor, Armin P Schoech, Farhad Hormozdiari, et al.
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of 10
Search research articles
Search
Showing results (11-20 of 98) with videos related to
Sort By:
Page
of 10
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2023
A scalable variational approach to characterize pleiotropic components across thousands of human diseases and complex traits using GWAS summary statistics
Zixuan Zhang, Junghyun Jung, Artem Kim, et al.
Scientific Reports
|
December 3, 2015
High level of inbreeding in final phase of 1000 Genomes Project
Steven Gazal, Mourad Sahbatou, Marie-Claude Babron, et al.
American Journal of Human Genetics
|
October 25, 2023
A scalable approach to characterize pleiotropy across thousands of human diseases and complex traits using GWAS summary statistics
Zixuan Zhang, Junghyun Jung, Artem Kim, et al.
Bioinformatics (Oxford, England)
|
March 18, 2014
FSuite: exploiting inbreeding in dense SNP chip and exome data
Steven Gazal, Mourad Sahbatou, Marie-Claude Babron, et al.
Nature Genetics
|
June 13, 2018
Mixed-model association for biobank-scale datasets
Po-Ru Loh, Gleb Kichaev, Steven Gazal, et al.
Human Heredity
|
July 26, 2014
Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III
Steven Gazal, Mourad Sahbatou, Hervé Perdry, et al.
Nature Genetics
|
April 22, 2020
Liability threshold modeling of case-control status and family history of disease increases association power
Margaux L A Hujoel, Steven Gazal, Po-Ru Loh, et al.
Human Heredity
|
April 19, 2013
Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?
Emmanuelle Génin, Mourad Sahbatou, Steven Gazal, et al.
American Journal of Human Genetics
|
March 10, 2022
Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes
Kathryn S Burch, Kangcheng Hou, Yi Ding, et al.
American Journal of Human Genetics
|
August 13, 2019
Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
Luke J O'Connor, Armin P Schoech, Farhad Hormozdiari, et al.
Page
of 10