{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,29]],"date-time":"2025-05-29T09:52:33Z","timestamp":1748512353904,"version":"3.40.5"},"reference-count":45,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2022,8,2]],"date-time":"2022-08-02T00:00:00Z","timestamp":1659398400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100005150","name":"Chinese Academy of Medical Sciences","doi-asserted-by":"publisher","award":["2020\u2010PT310\u2010007"],"award-info":[{"award-number":["2020\u2010PT310\u2010007"]}],"id":[{"id":"10.13039\/501100005150","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81870288","82170353"],"award-info":[{"award-number":["81870288","82170353"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Genetics"],"published-print":{"date-parts":[[2022,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease. Highly penetrant copy number variants (CNVs) and genes related to the etiology of TOF likely exist with differences among populations. We aimed to identify CNV contributions to sporadic TOF cases in Han Chinese. Genomic DNA was extracted from peripheral blood in 605 subjects (303 sporadic TOF and 302 unaffected Han Chinese [Control] from cardiac centers in China) and analyzed by genome\u2010wide association study (GWAS). The GWAS results were compared with existing Database of Genetic Variants. These CNVs were further validated by qPCR. Bioinformatics analyses were performed with protein\u2013protein interaction (PPI) network and KEGG pathway enrichment. Across all chromosomes 119 novel \u201cTOF\u2010specific CNVs\u201d were identified with prevalence of CNVs of 21.5% in chromosomes 1\u201020 and 37.0% including Chr21\/22. In chromosomes 1\u201020, CNVs on 11q25 (encompasses genes <jats:italic>ACAD8<\/jats:italic>, <jats:italic>B3GAT1<\/jats:italic>, <jats:italic>GLB1L2<\/jats:italic>, <jats:italic>GLB1L3<\/jats:italic>, <jats:italic>IGSF9B<\/jats:italic>, <jats:italic>JAM3<\/jats:italic>, <jats:italic>LOC100128239<\/jats:italic>, <jats:italic>LOC283177<\/jats:italic>, <jats:italic>MIR4697<\/jats:italic>, <jats:italic>MIR4697HG<\/jats:italic>, <jats:italic>NCAPD3<\/jats:italic>, <jats:italic>OPCML<\/jats:italic>, <jats:italic>SPATA19<\/jats:italic>, <jats:italic>THYN1<\/jats:italic>, and <jats:italic>VPS26B)<\/jats:italic> and 14q32.33 (encompasses genes <jats:italic>THYN1<\/jats:italic>, <jats:italic>OPCML<\/jats:italic>, and <jats:italic>NCAPD3<\/jats:italic>) encompass genes most likely to be associated with TOF. Specific CNVs found on the chromosome 21 <jats:bold>(<\/jats:bold>6.3%) and 22(11.9%) were also identified in details. PPI network analysis identified the genes covering the specific CNVs related to TOF and the signaling pathways. This study for first time identified novel TOF\u2010specific CNVs in the Han Chinese with higher frequency than in Caucasians and with 11q25 and 14q32.33 not reported in TOF of Caucasians. These novel CNVs identify new candidate genes for TOF and provide new insights into genetic basis of TOF.<\/jats:p>","DOI":"10.1111\/cge.14201","type":"journal-article","created":{"date-parts":[[2022,7,27]],"date-time":"2022-07-27T02:34:45Z","timestamp":1658889285000},"page":"391-403","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications"],"prefix":"10.1111","volume":"102","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6497-876X","authenticated-orcid":false,"given":"Guo\u2010Wei","family":"He","sequence":"first","affiliation":[{"name":"Institute of Cardiovascular Diseases &amp; Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital Tianjin University &amp; Chinese Academy of Medical Sciences  Tianjin China"},{"name":"Department of Surgery Oregon Health and Science University  Portland Oregon USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cheryl L.","family":"Maslen","sequence":"additional","affiliation":[{"name":"Knight Cardiovascular Institute Oregon Health &amp; Science University  Portland Oregon USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huan\u2010Xin","family":"Chen","sequence":"additional","affiliation":[{"name":"Institute of Cardiovascular Diseases &amp; Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital Tianjin University &amp; Chinese Academy of Medical Sciences  Tianjin China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hai\u2010Tao","family":"Hou","sequence":"additional","affiliation":[{"name":"Institute of Cardiovascular Diseases &amp; Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital Tianjin University &amp; Chinese Academy of Medical Sciences  Tianjin 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