<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Clay S</submitter><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>US Department of Defense</funding><funding>NIH</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>809-820</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10939893</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>153(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Most genetic studies of asthma and allergy have focused on common variation in individuals primarily of European ancestry. Studying the role of rare variation in quantitative phenotypes and in asthma phenotypes in populations of diverse ancestries can provide additional, important insights into the development of these traits.&lt;h4>Objective&lt;/h4>We sought to examine the contribution of rare variants to different asthma- or allergy-associated quantitative traits in children with diverse ancestries and explore their role in asthma phenotypes.&lt;h4>Methods&lt;/h4>We examined whole-genome sequencing data from children participants in longitudinal studies of asthma (n = 1035; parent-identified as 67% Black and 25% Hispanic) to identify rare variants (minor allele frequency &lt; 0.01). </pubmed_abstract><journal>The Journal of allergy and clinical immunology</journal><pubmed_title>Gene-based association study of rare variants in children of diverse ancestries implicates TNFRSF21 in the development of allergic asthma.</pubmed_title><pmcid>PMC10939893</pmcid><funding_grant_id>UL1 TR000075</funding_grant_id><funding_grant_id>M01 RR000052</funding_grant_id><funding_grant_id>UL1 TR000150</funding_grant_id><funding_grant_id>M01 RR000071</funding_grant_id><funding_grant_id>R01 CA287257</funding_grant_id><funding_grant_id>UL1 TR001422</funding_grant_id><funding_grant_id>P30 ES005605</funding_grant_id><funding_grant_id>UL1 TR000451</funding_grant_id><funding_grant_id>UL1 TR000077</funding_grant_id><funding_grant_id>UL1 TR001105</funding_grant_id><funding_grant_id>HHSN272201000052I</funding_grant_id><funding_grant_id>UM1 AI160040</funding_grant_id><funding_grant_id>KL2 TR002542</funding_grant_id><funding_grant_id>HHSN272200900052C</funding_grant_id><funding_grant_id>P30 DK054759</funding_grant_id><funding_grant_id>TL1 TR002388</funding_grant_id><funding_grant_id>M01 RR000533</funding_grant_id><funding_grant_id>UM1 AI114271</funding_grant_id><funding_grant_id>UG3 OD035521</funding_grant_id><funding_grant_id>U19 AI162310</funding_grant_id><funding_grant_id>UL1 RR025780</funding_grant_id><funding_grant_id>UM2 AI117870</funding_grant_id><funding_grant_id>T32 HL007605</funding_grant_id><funding_grant_id>UL1 TR000040</funding_grant_id><funding_grant_id>DP2 CA247831</funding_grant_id><funding_grant_id>UL1 TR001873</funding_grant_id><funding_grant_id>UL1 TR001079</funding_grant_id><funding_grant_id>UL1 TR001430</funding_grant_id><funding_grant_id>UG3 OD023282</funding_grant_id><funding_grant_id>T32 GM007197</funding_grant_id><funding_grant_id>UH3 OD023282</funding_grant_id><funding_grant_id>R01 HL104608</funding_grant_id><funding_grant_id>UH2 AI144434</funding_grant_id><funding_grant_id>UL1 RR025771</funding_grant_id><funding_grant_id>U01 AI178772</funding_grant_id><pubmed_authors>Clay S</pubmed_authors><pubmed_authors>Cohen RT</pubmed_authors><pubmed_authors>Bacharier LB</pubmed_authors><pubmed_authors>Kim H</pubmed_authors><pubmed_authors>O'Connor GT</pubmed_authors><pubmed_authors>Busse WW</pubmed_authors><pubmed_authors>Gern JE</pubmed_authors><pubmed_authors>Wood RA</pubmed_authors><pubmed_authors>Jackson DJ</pubmed_authors><pubmed_authors>Smith NP</pubmed_authors><pubmed_authors>Dapas M</pubmed_authors><pubmed_authors>Khurana Hershey GK</pubmed_authors><pubmed_authors>Gill MA</pubmed_authors><pubmed_authors>Villani AC</pubmed_authors><pubmed_authors>Cho JL</pubmed_authors><pubmed_authors>Ober C</pubmed_authors><pubmed_authors>Liu AH</pubmed_authors><pubmed_authors>Gergen PJ</pubmed_authors><pubmed_authors>Visness CM</pubmed_authors><pubmed_authors>Kattan M</pubmed_authors><pubmed_authors>Kercsmar CM</pubmed_authors><pubmed_authors>Rastogi D</pubmed_authors><pubmed_authors>Medoff BD</pubmed_authors><pubmed_authors>Rivera-Spoljaric K</pubmed_authors><pubmed_authors>Gruchalla RS</pubmed_authors><pubmed_authors>Robison RG</pubmed_authors><pubmed_authors>Alladina J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene-based association study of rare variants in children of diverse ancestries implicates TNFRSF21 in the development of allergic asthma.</name><description>&lt;h4>Background&lt;/h4>Most genetic studies of asthma and allergy have focused on common variation in individuals primarily of European ancestry. Studying the role of rare variation in quantitative phenotypes and in asthma phenotypes in populations of diverse ancestries can provide additional, important insights into the development of these traits.&lt;h4>Objective&lt;/h4>We sought to examine the contribution of rare variants to different asthma- or allergy-associated quantitative traits in children with diverse ancestries and explore their role in asthma phenotypes.&lt;h4>Methods&lt;/h4>We examined whole-genome sequencing data from children participants in longitudinal studies of asthma (n = 1035; parent-identified as 67% Black and 25% Hispanic) to identify rare variants (minor allele frequency &lt; 0.01). </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-03T01:39:15.503Z</modification><creation>2024-11-19T23:32:34.225Z</creation></dates><accession>S-EPMC10939893</accession><cross_references><pubmed>37944567</pubmed><doi>10.1016/j.jaci.2023.10.023</doi></cross_references></HashMap>