<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mak ACY</submitter><funding>National Institute of Environmental Health Sciences</funding><funding>Tobacco-Related Disease Research Program</funding><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>NIEHS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>American Asthma Foundation</funding><funding>NHLBI NIH HHS</funding><funding>Gordon and Betty Moore Foundation</funding><funding>National Human Genome Research Institute</funding><funding>National Eye Institute</funding><funding>NHLBI</funding><funding>NIDDK NIH HHS</funding><funding>Alfred P. Sloan Foundation</funding><pagination>869-886</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7337089</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>215(3)</volume><pubmed_abstract>Baseline lung function, quantified as forced expiratory volume in the first second of exhalation (FEV&lt;sub>1&lt;/sub>), is a standard diagnostic criterion used by clinicians to identify and classify lung diseases. Using whole-genome sequencing data from the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine project, we identified a novel genetic association with FEV&lt;sub>1&lt;/sub> on chromosome 12 in 867 African American children with asthma (&lt;i>P&lt;/i> = 1.26 × 10&lt;sup>-8&lt;/sup>, β = 0.302). Conditional analysis within 1 Mb of the tag signal (rs73429450) yielded one major and two other weaker independent signals within this peak. We explored statistical and functional evidence for all variants in linkage disequilibrium with the three independent signals and yielded nine var</pubmed_abstract><journal>Genetics</journal><pubmed_title>Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand &lt;i>KITLG/SCF&lt;/i> and Gene-By-Air-Pollution Interaction.</pubmed_title><pmcid>PMC7337089</pmcid><funding_grant_id>R01 HL-118267</funding_grant_id><funding_grant_id>R01 HL-141485</funding_grant_id><funding_grant_id>R01 HL133433</funding_grant_id><funding_grant_id>P30 ES013508</funding_grant_id><funding_grant_id>3R01 HL-120393-02S1; contract HHSN268201800001I</funding_grant_id><funding_grant_id>R01 AI079139</funding_grant_id><funding_grant_id>R01 HL141845</funding_grant_id><funding_grant_id>GBMF3834</funding_grant_id><funding_grant_id>R01 HL-141992</funding_grant_id><funding_grant_id>HHSN268201600032I</funding_grant_id><funding_grant_id>R01 DK113003</funding_grant_id><funding_grant_id>X01 HL-134589</funding_grant_id><funding_grant_id>1R01 HD-085993-01</funding_grant_id><funding_grant_id>R01 HL-135156-S1</funding_grant_id><funding_grant_id>K01 HL-140218</funding_grant_id><funding_grant_id>R01 ES-015794</funding_grant_id><funding_grant_id>K01 HL140218</funding_grant_id><funding_grant_id>24RT-0025</funding_grant_id><funding_grant_id>R01 HL-133433</funding_grant_id><funding_grant_id>R01 HL141992</funding_grant_id><funding_grant_id>2013-10-27</funding_grant_id><funding_grant_id>R01 HL118267</funding_grant_id><funding_grant_id>3R01 HL-117626-02S1; contract HHSN268201800002I</funding_grant_id><funding_grant_id>3R01 HL-117004-02S3</funding_grant_id><funding_grant_id>P30 ES006694</funding_grant_id><pubmed_authors>Huntsman S</pubmed_authors><pubmed_authors>Martinez FD</pubmed_authors><pubmed_authors>Burchard EG</pubmed_authors><pubmed_authors>Lee EY</pubmed_authors><pubmed_authors>Keys KL</pubmed_authors><pubmed_authors>Ziv E</pubmed_authors><pubmed_authors>Kumar R</pubmed_authors><pubmed_authors>Himes BE</pubmed_authors><pubmed_authors>Joo J</pubmed_authors><pubmed_authors>Salazar S</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>White MJ</pubmed_authors><pubmed_authors>Saef B</pubmed_authors><pubmed_authors>Germer S</pubmed_authors><pubmed_authors>Gui H</pubmed_authors><pubmed_authors>Sleiman PM</pubmed_authors><pubmed_authors>Sajuthi S</pubmed_authors><pubmed_authors>Eng C</pubmed_authors><pubmed_authors>Zody MC</pubmed_authors><pubmed_authors>Kang HM</pubmed_authors><pubmed_authors>Abecasis G</pubmed_authors><pubmed_authors>Gilliland FD</pubmed_authors><pubmed_authors>Lurmann F</pubmed_authors><pubmed_authors>Reeves C</pubmed_authors><pubmed_authors>Nickerson DA</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors><pubmed_authors>Jain D</pubmed_authors><pubmed_authors>Oh SS</pubmed_authors><pubmed_authors>Seibold MA</pubmed_authors><pubmed_authors>Williams LK</pubmed_authors><pubmed_authors>Hu D</pubmed_authors><pubmed_authors>Winterkorn L</pubmed_authors><pubmed_authors>Hakonarson H</pubmed_authors><pubmed_authors>Mak ACY</pubmed_authors><pubmed_authors>Wu AC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand &lt;i>KITLG/SCF&lt;/i> and Gene-By-Air-Pollution Interaction.</name><description>Baseline lung function, quantified as forced expiratory volume in the first second of exhalation (FEV&lt;sub>1&lt;/sub>), is a standard diagnostic criterion used by clinicians to identify and classify lung diseases. Using whole-genome sequencing data from the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine project, we identified a novel genetic association with FEV&lt;sub>1&lt;/sub> on chromosome 12 in 867 African American children with asthma (&lt;i>P&lt;/i> = 1.26 × 10&lt;sup>-8&lt;/sup>, β = 0.302). Conditional analysis within 1 Mb of the tag signal (rs73429450) yielded one major and two other weaker independent signals within this peak. We explored statistical and functional evidence for all variants in linkage disequilibrium with the three independent signals and yielded nine var</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-18T18:10:14.852Z</modification><creation>2021-02-20T04:55:45Z</creation></dates><accession>S-EPMC7337089</accession><cross_references><pubmed>32327564</pubmed><doi>10.1534/genetics.120.303231</doi></cross_references></HashMap>