{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T04:39:35Z","timestamp":1777523975288,"version":"3.51.4"},"reference-count":36,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2025,1,22]],"date-time":"2025-01-22T00:00:00Z","timestamp":1737504000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"funder":[{"DOI":"10.13039\/100012542","name":"Sichuan Provincial Science and Technology Support Program","doi-asserted-by":"publisher","award":["2024NSFSC0649"],"award-info":[{"award-number":["2024NSFSC0649"]}],"id":[{"id":"10.13039\/100012542","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81271118"],"award-info":[{"award-number":["81271118"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81600849"],"award-info":[{"award-number":["81600849"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"name":"the Research and Develop Program, West China Hospital of Stomatology Sichuan University","award":["RD-03-202301"],"award-info":[{"award-number":["RD-03-202301"]}]}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["The Cleft Palate Craniofacial Journal"],"published-print":{"date-parts":[[2026,4]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>Orofacial cleft (OC) can be classified into syndromic orofacial cleft (SOC) and non-syndromic orofacial cleft (NSOC), depending on whether there are other congenital deformities. Craniosynostosis, the premature closure of cranial sutures, is a common phenotype of SOC resulting in abnormal ossification of skull and brain development disorders. Its correlation with OC offers a promising approach to identify susceptibility genes for NSOC by examining causative genes of SOCs with craniosynostosis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and Methods<\/jats:title>\n                    <jats:p>This study included 2556 patients with NSOC and 2255 normal controls from western Han Chinese with their genomic DNA samples. We selected 31 causative genes of 34 syndromes with both craniosynostosis and OC as candidate genes and performed quality control. Allelic and genotypic association analyses and haplotype analysis were performed to identify statistically significant single nucleotide polymorphisms (SNPs).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In allelic association analysis performed with 1265 qualified SNPs in 20 genes, only rs2239936, located in\n                      <jats:italic toggle=\"yes\">MYH3<\/jats:italic>\n                      gene, was statistically associated with non-syndromic cleft lip only (NSCLO) (\n                      <jats:italic toggle=\"yes\">P\u2009<\/jats:italic>\n                      =\u20091.70\u00d710\n                      <jats:sup>\u221207<\/jats:sup>\n                      , OR\n                      <jats:italic toggle=\"yes\">\u2009<\/jats:italic>\n                      =\n                      <jats:italic toggle=\"yes\">\u2009<\/jats:italic>\n                      1.33, 95%CI: 1.17-1.52) and non-syndromic cleft palate only (NSCPO) (\n                      <jats:italic toggle=\"yes\">P\u2009<\/jats:italic>\n                      =\u20096.43\u00d710\n                      <jats:sup>\u221205<\/jats:sup>\n                      , OR\n                      <jats:italic toggle=\"yes\">\u2009<\/jats:italic>\n                      =\n                      <jats:italic toggle=\"yes\">\u2009<\/jats:italic>\n                      1.33, 95%CI: 1.16-1.52). The higher frequency of allele G in NSCPO suggesting that minor allele G at rs2239936 will result in an elevated risk of NSCPO. However, rs2239936 only exhibited a statistical association with NSCPO in genotypic association analysis (\n                      <jats:italic toggle=\"yes\">P\u2009<\/jats:italic>\n                      =\u20098.06\u00d710\n                      <jats:sup>\u221206<\/jats:sup>\n                      ) and haplotype analysis (\n                      <jats:italic toggle=\"yes\">P\u2009<\/jats:italic>\n                      =\u20091.43\u00d710\n                      <jats:sup>\u221205<\/jats:sup>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      This study identified that allele G at rs2239936 in\n                      <jats:italic toggle=\"yes\">MYH3<\/jats:italic>\n                      gene was significantly associated with NSCPO as a risk factor and\n                      <jats:italic toggle=\"yes\">MYH3<\/jats:italic>\n                      was a new susceptibility gene for NSCPO in western Han Chinese population.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/10556656251313842","type":"journal-article","created":{"date-parts":[[2025,1,22]],"date-time":"2025-01-22T03:36:47Z","timestamp":1737517007000},"page":"745-752","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":2,"title":["Identifying New Susceptibility Genes of Non-Syndromic Orofacial Cleft Based on Syndromes Accompanied With Craniosynostosis"],"prefix":"10.1177","volume":"63","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3337-5250","authenticated-orcid":false,"given":"Si-Di","family":"Zhang","sequence":"first","affiliation":[{"name":"Sichuan University"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0866-0893","authenticated-orcid":false,"given":"Yan-Song","family":"Lin","sequence":"additional","affiliation":[{"name":"Sichuan University"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bing","family":"Shi","sequence":"additional","affiliation":[{"name":"Sichuan University"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0129-0367","authenticated-orcid":false,"given":"Zhong-Lin","family":"Jia","sequence":"additional","affiliation":[{"name":"Sichuan University"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2025,1,22]]},"reference":[{"key":"e_1_3_3_2_2","doi-asserted-by":"publisher","DOI":"10.1597\/10-178"},{"key":"e_1_3_3_3_2","doi-asserted-by":"publisher","DOI":"10.1177\/10556656211059966"},{"key":"e_1_3_3_4_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.bjps.2023.06.019"},{"key":"e_1_3_3_5_2","doi-asserted-by":"publisher","DOI":"10.1097\/01.JAA.0000721644.06681.06"},{"key":"e_1_3_3_6_2","doi-asserted-by":"publisher","DOI":"10.18632\/oncotarget.24238"},{"key":"e_1_3_3_7_2","doi-asserted-by":"publisher","DOI":"10.1038\/s41415-023-6000-9"},{"key":"e_1_3_3_8_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.c.31381"},{"key":"e_1_3_3_9_2","doi-asserted-by":"publisher","DOI":"10.1080\/15384101.2015.1120928"},{"key":"e_1_3_3_10_2","doi-asserted-by":"publisher","DOI":"10.1038\/s41576-019-0127-1"},{"key":"e_1_3_3_11_2","doi-asserted-by":"publisher","DOI":"10.1038\/78119"},{"key":"e_1_3_3_12_2","doi-asserted-by":"publisher","DOI":"10.1038\/ng740"},{"issue":"1","key":"e_1_3_3_13_2","article-title":"Genetics of cleft lip and palate: Syndromic genes contribute to the incidence of non-syndromic clefts","volume":"13","author":"Stanier P","year":"2004","unstructured":"Stanier P, Moore GE. 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