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Plos One|October 3, 2012
Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palateAriadne Letra, Walid Fakhouri, Renata F Fonseca, et al.
American Journal of Human Genetics|December 9, 2022
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genesLisa A Lansdon, Amanda Dickinson, Sydney Arlis, et al.
The New England Journal of Medicine|May 7, 2015
Between-hospital variation in treatment and outcomes in extremely preterm infantsMatthew A Rysavy, Lei Li, Edward F Bell, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 7, 2010
CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palateAriadne Letra, Renato Menezes, Margaret E Cooper, et al.
American Journal of Human Genetics|June 28, 2011
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial cleftingIrfan Saadi, Fowzan S Alkuraya, Stephen S Gisselbrecht, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Research Square|March 11, 2024
Rare Variants Analyses Suggest Novel Cleft Genes in the African PopulationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Pediatrics|June 5, 2013
Ten-year review of major birth defects in VLBW infantsIra Adams-Chapman, Nellie I Hansen, Seetha Shankaran, et al.
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