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Nature|September 8, 2012
The accessible chromatin landscape of the human genomeRobert E Thurman, Eric Rynes, Richard Humbert, et al.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 MenHan 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 scaleXihao Li, Zilin Li, Hufeng Zhou, et al.Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon 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 ChallengeCatherine 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 encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.Physical Review Letters|March 28, 2015
Joint analysis of BICEP2/keck array and Planck DataP A R Ade, N Aghanim, Z Ahmed, et al.Pageof 11