<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen H</submitter><funding>NCATS NIH HHS</funding><funding>Swiss National Science Foundation</funding><funding>NIDDK NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIAMS NIH HHS</funding><pagination>391-401</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5854957</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>58(3)</volume><pubmed_abstract>Obstructive sleep apnea (OSA) is a common heritable disorder displaying marked sexual dimorphism in disease prevalence and progression. Previous genetic association studies have identified a few genetic loci associated with OSA and related quantitative traits, but they have only focused on single ethnic groups, and a large proportion of the heritability remains unexplained. The apnea-hypopnea index (AHI) is a commonly used quantitative measure characterizing OSA severity. Because OSA differs by sex, and the pathophysiology of obstructive events differ in rapid eye movement (REM) and non-REM (NREM) sleep, we hypothesized that additional genetic association signals would be identified by analyzing the NREM/REM-specific AHI and by conducting sex-specific analyses in multiethnic samples. 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SA</pubmed_authors><pubmed_authors>Warby SC</pubmed_authors><pubmed_authors>Liang J</pubmed_authors><pubmed_authors>Patel SR</pubmed_authors><pubmed_authors>Tranah GJ</pubmed_authors><pubmed_authors>Ewert R</pubmed_authors><pubmed_authors>Palmer LJ</pubmed_authors><pubmed_authors>Bell GI</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Arens R</pubmed_authors><pubmed_authors>Below JE</pubmed_authors><pubmed_authors>Gharib SA</pubmed_authors><pubmed_authors>Loredo JS</pubmed_authors><pubmed_authors>Redline S</pubmed_authors><pubmed_authors>Sul JH</pubmed_authors><pubmed_authors>Mukherjee S</pubmed_authors><pubmed_authors>Tafti M</pubmed_authors><pubmed_authors>Haba-Rubio J</pubmed_authors><pubmed_authors>Frazier-Wood AC</pubmed_authors><pubmed_authors>Ancoli-Israel S</pubmed_authors><pubmed_authors>Kutalik Z</pubmed_authors><pubmed_authors>Saxena R</pubmed_authors><pubmed_authors>Lane JM</pubmed_authors><pubmed_authors>Hagen EW</pubmed_authors><pubmed_authors>Azarbarzin A</pubmed_authors><pubmed_authors>Chun S</pubmed_authors><pubmed_authors>Shah NA</pubmed_authors><pubmed_authors>Conomos MP</pubmed_authors><pubmed_authors>Sofer T</pubmed_authors><pubmed_authors>Hillman DR</pubmed_authors><pubmed_authors>Post WS</pubmed_authors><pubmed_authors>Peppard PE</pubmed_authors><pubmed_authors>Gottlieb DJ</pubmed_authors><pubmed_authors>Johnson WC</pubmed_authors><pubmed_authors>Lee SK</pubmed_authors><pubmed_authors>Taylor KD</pubmed_authors><pubmed_authors>Bjonnes AC</pubmed_authors><pubmed_authors>Stilp AM</pubmed_authors><pubmed_authors>Stone KL</pubmed_authors><pubmed_authors>Laurie CC</pubmed_authors><pubmed_authors>Wellman DA</pubmed_authors><pubmed_authors>Shin C</pubmed_authors><pubmed_authors>Thornton TA</pubmed_authors><pubmed_authors>Cade BE</pubmed_authors><pubmed_authors>Penzel T</pubmed_authors><pubmed_authors>Heinzer R</pubmed_authors><pubmed_authors>Teumer A</pubmed_authors><pubmed_authors>Zhu X</pubmed_authors><pubmed_authors>Stubbe B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.</name><description>Obstructive sleep apnea (OSA) is a common heritable disorder displaying marked sexual dimorphism in disease prevalence and progression. Previous genetic association studies have identified a few genetic loci associated with OSA and related quantitative traits, but they have only focused on single ethnic groups, and a large proportion of the heritability remains unexplained. The apnea-hypopnea index (AHI) is a commonly used quantitative measure characterizing OSA severity. Because OSA differs by sex, and the pathophysiology of obstructive events differ in rapid eye movement (REM) and non-REM (NREM) sleep, we hypothesized that additional genetic association signals would be identified by analyzing the NREM/REM-specific AHI and by conducting sex-specific analyses in multiethnic samples. We pe</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-26T00:18:38.339Z</modification><creation>2019-06-06T19:08:37Z</creation></dates><accession>S-EPMC5854957</accession><cross_references><pubmed>29077507</pubmed><doi>10.1165/rcmb.2017-0237OC</doi><doi>10.1165/rcmb.2017-0237oc</doi></cross_references></HashMap>