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American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Genetics
|
August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Nature Genetics
|
March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
Elsa Leitão, Amandine Santini, Benjamin Cogne, et al.
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Search research articles
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Showing results (101-110 of 105) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 105 results.
American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Genetics
|
August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Nature Genetics
|
March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
Elsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Page
of 11