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Journal Abstract Search

195 related items for PubMed ID: 37330696

  • 1. Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
    Diaz Perez KK, Curtis SW, Sanchis-Juan A, Zhao X, Head T, Ho S, Carter B, McHenry T, Bishop MR, Valencia-Ramirez LC, Restrepo C, Hecht JT, Uribe LM, Wehby G, Weinberg SM, Beaty TH, Murray JC, Feingold E, Marazita ML, Cutler DJ, Epstein MP, Brand H, Leslie EJ.
    Genet Med; 2023 Oct; 25(10):100918. PubMed ID: 37330696
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  • 2. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.
    Leslie EJ, Koboldt DC, Kang CJ, Ma L, Hecht JT, Wehby GL, Christensen K, Czeizel AE, Deleyiannis FW, Fulton RS, Wilson RK, Beaty TH, Schutte BC, Murray JC, Marazita ML.
    Clin Genet; 2016 Jul; 90(1):28-34. PubMed ID: 26346622
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  • 3. Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
    Leslie EJ, Carlson JC, Shaffer JR, Butali A, Buxó CJ, Castilla EE, Christensen K, Deleyiannis FW, Leigh Field L, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Feingold E, Weinberg SM, Murray JC, Beaty TH, Marazita ML.
    Hum Genet; 2017 Mar; 136(3):275-286. PubMed ID: 28054174
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  • 4. Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
    Diaz Perez KK, Chung S, Head ST, Epstein MP, Hecht JT, Wehby GL, Weinberg SM, Murray JC, Marazita ML, Leslie EJ.
    Am J Med Genet A; 2023 Oct; 191(10):2558-2570. PubMed ID: 37350193
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  • 9. Orofacial clefting: update on the role of genetics.
    Ghassibe M, Bayet B, Revencu N, Desmyter L, Verellen-Dumoulin C, Gillerot Y, Deggouj N, Vanwijck R, Vikkula M, CL/P Study Group.
    B-ENT; 2006 Oct; 2 Suppl 4():20-4. PubMed ID: 17366841
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  • 10. A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22.
    Slavec L, Geršak K, Eberlinc A, Hovnik T, Lovrečić L, Mlinarič-Raščan I, Karas Kuželički N.
    Int J Mol Sci; 2023 Feb 21; 24(5):. PubMed ID: 36901693
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  • 12. Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
    Shaffer JR, LeClair J, Carlson JC, Feingold E, Buxó CJ, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Murray JC, Weinberg SM, Marazita ML, Leslie EJ.
    Am J Med Genet A; 2019 Mar 21; 179(3):467-474. PubMed ID: 30582786
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  • 14. Gene×environment associations in orofacial clefting.
    Marazita ML.
    Curr Top Dev Biol; 2023 Mar 21; 152():169-192. PubMed ID: 36707211
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  • 15. Orofacial clefts embryology, classification, epidemiology, and genetics.
    Nasreddine G, El Hajj J, Ghassibe-Sabbagh M.
    Mutat Res Rev Mutat Res; 2021 Mar 21; 787():108373. PubMed ID: 34083042
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  • 16. IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population.
    Gurramkonda VB, Syed AH, Murthy J, Lakkakula BVKS.
    Braz J Otorhinolaryngol; 2018 Mar 21; 84(4):473-477. PubMed ID: 28712851
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  • 17. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
    Charzewska A, Obersztyn E, Hoffman-Zacharska D, Lenart J, Poznański J, Bal J.
    Cleft Palate Craniofac J; 2015 Sep 21; 52(5):e161-7. PubMed ID: 25489771
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  • 18. Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population.
    Salahshourifar I, Sulaiman WA, Zilfalil BA, Halim AS.
    Am J Med Genet A; 2011 Sep 21; 155A(9):2302-7. PubMed ID: 21834040
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