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3. Novel IRF6 variant in orofacial cleft patients from Durban, South Africa. Naicker T; Alade A; Adeleke C; Mossey PA; Awotoye WA; Busch T; Li M; Olotu J; Aldous C; Butali A Mol Genet Genomic Med; 2023 May; 11(5):e2138. PubMed ID: 36811272 [TBL] [Abstract][Full Text] [Related]
4. Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population. He M; Bian Z PLoS One; 2016; 11(7):e0159940. PubMed ID: 27459192 [TBL] [Abstract][Full Text] [Related]
5. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Wang Y; Sun Y; Huang Y; Pan Y; Jia Z; Ma L; Ma L; Lan F; Zhou Y; Shi J; Yang X; Zhang L; Jiang H; Jiang M; Yin A; Cheng J; Wang L; Yang Y; Shi B Gene; 2016 Aug; 588(1):69-73. PubMed ID: 27129939 [TBL] [Abstract][Full Text] [Related]
6. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. Mangold E; Böhmer AC; Ishorst N; Hoebel AK; Gültepe P; Schuenke H; Klamt J; Hofmann A; Gölz L; Raff R; Tessmann P; Nowak S; Reutter H; Hemprich A; Kreusch T; Kramer FJ; Braumann B; Reich R; Schmidt G; Jäger A; Reiter R; Brosch S; Stavusis J; Ishida M; Seselgyte R; Moore GE; Nöthen MM; Borck G; Aldhorae KA; Lace B; Stanier P; Knapp M; Ludwig KU Am J Hum Genet; 2016 Apr; 98(4):755-62. PubMed ID: 27018475 [TBL] [Abstract][Full Text] [Related]
7. Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of non-syndromic oral clefts in the Brazilian population. Azevedo CMS; Machado RA; Martelli-Júnior H; Reis SRA; Persuhn DC; Coletta RD; Rangel ALCA Oral Dis; 2020 Jan; 26(1):145-151. PubMed ID: 31564061 [TBL] [Abstract][Full Text] [Related]
8. Two rare variants reveal the significance of Grainyhead-like 3 Arginine 391 underlying non-syndromic cleft palate only. Huang W; He Q; Li M; Ding Y; Liang W; Li W; Lin J; Zhao H; Chen F Oral Dis; 2023 May; 29(4):1632-1643. PubMed ID: 35189007 [TBL] [Abstract][Full Text] [Related]
10. CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate. Letra A; Menezes R; Cooper ME; Fonseca RF; Tropp S; Govil M; Granjeiro JM; Imoehl SR; Mansilla MA; Murray JC; Castilla EE; Orioli IM; Czeizel AE; Ma L; Chiquet BT; Hecht JT; Vieira AR; Marazita ML Cleft Palate Craniofac J; 2011 Jul; 48(4):363-70. PubMed ID: 20815724 [TBL] [Abstract][Full Text] [Related]
11. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes. Basha M; Demeer B; Revencu N; Helaers R; Theys S; Bou Saba S; Boute O; Devauchelle B; Francois G; Bayet B; Vikkula M J Med Genet; 2018 Jul; 55(7):449-458. PubMed ID: 29500247 [TBL] [Abstract][Full Text] [Related]
12. A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. Leslie EJ; Liu H; Carlson JC; Shaffer JR; Feingold E; Wehby G; Laurie CA; Jain D; Laurie CC; Doheny KF; McHenry T; Resick J; Sanchez C; Jacobs J; Emanuele B; Vieira AR; Neiswanger K; Standley J; Czeizel AE; Deleyiannis F; Christensen K; Munger RG; Lie RT; Wilcox A; Romitti PA; Field LL; Padilla CD; Cutiongco-de la Paz EM; Lidral AC; Valencia-Ramirez LC; Lopez-Palacio AM; Valencia DR; Arcos-Burgos M; Castilla EE; Mereb JC; Poletta FA; Orioli IM; Carvalho FM; Hecht JT; Blanton SH; Buxó CJ; Butali A; Mossey PA; Adeyemo WL; James O; Braimah RO; Aregbesola BS; Eshete MA; Deribew M; Koruyucu M; Seymen F; Ma L; de Salamanca JE; Weinberg SM; Moreno L; Cornell RA; Murray JC; Marazita ML Am J Hum Genet; 2016 Apr; 98(4):744-54. PubMed ID: 27018472 [TBL] [Abstract][Full Text] [Related]
13. Irf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate. Liu H; Leslie EJ; Jia Z; Smith T; Eshete M; Butali A; Dunnwald M; Murray J; Cornell RA Hum Mol Genet; 2016 Feb; 25(4):766-76. PubMed ID: 26692521 [TBL] [Abstract][Full Text] [Related]
14. Association analysis of SNPs in GRHL3, FAF1, and KCNJ2 with NSCPO sub-phenotypes in Han Chinese. Sun JL; Shi JY; Yin B; Lin YS; Shi B; Jia ZL Oral Dis; 2022 Nov; 28(8):2204-2214. PubMed ID: 34255421 [TBL] [Abstract][Full Text] [Related]
15. Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations. Gowans LJ; Adeyemo WL; Eshete M; Mossey PA; Busch T; Aregbesola B; Donkor P; Arthur FK; Bello SA; Martinez A; Li M; Augustine-Akpan EA; Deressa W; Twumasi P; Olutayo J; Deribew M; Agbenorku P; Oti AA; Braimah R; Plange-Rhule G; Gesses M; Obiri-Yeboah S; Oseni GO; Olaitan PB; Abdur-Rahman L; Abate F; Hailu T; Gravem P; Ogunlewe MO; Buxó CJ; Marazita ML; Adeyemo AA; Murray JC; Butali A J Dent Res; 2016 Oct; 95(11):1245-56. PubMed ID: 27369588 [TBL] [Abstract][Full Text] [Related]
16. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. Peyrard-Janvid M; Leslie EJ; Kousa YA; Smith TL; Dunnwald M; Magnusson M; Lentz BA; Unneberg P; Fransson I; Koillinen HK; Rautio J; Pegelow M; Karsten A; Basel-Vanagaite L; Gordon W; Andersen B; Svensson T; Murray JC; Cornell RA; Kere J; Schutte BC Am J Hum Genet; 2014 Jan; 94(1):23-32. PubMed ID: 24360809 [TBL] [Abstract][Full Text] [Related]
17. Screening of Transforming Growth Factor Beta 3 and Jagged2 Genes in the Malay Population With Nonsyndromic Cleft Lip With or Without Cleft Palate. Ghazali N; Rahman NA; Kannan TP; Jaafar S Cleft Palate Craniofac J; 2015 Jul; 52(4):e88-94. PubMed ID: 26151095 [TBL] [Abstract][Full Text] [Related]
18. Association of Nucleotide Variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 Genes with Nonsyndromic Cleft Lip With/Without Cleft Palate in Multigenerational Families: A Retrospective Study. Neela PK; Gosla SR; Husain A; Mohan V; Thumoju S; Rajeshwari BV Contemp Clin Dent; 2021; 12(2):138-142. PubMed ID: 34220153 [TBL] [Abstract][Full Text] [Related]
19. 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; 84(4):473-477. PubMed ID: 28712851 [TBL] [Abstract][Full Text] [Related]
20. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. Zucchero TM; Cooper ME; Maher BS; Daack-Hirsch S; Nepomuceno B; Ribeiro L; Caprau D; Christensen K; Suzuki Y; Machida J; Natsume N; Yoshiura K; Vieira AR; Orioli IM; Castilla EE; Moreno L; Arcos-Burgos M; Lidral AC; Field LL; Liu YE; Ray A; Goldstein TH; Schultz RE; Shi M; Johnson MK; Kondo S; Schutte BC; Marazita ML; Murray JC N Engl J Med; 2004 Aug; 351(8):769-80. PubMed ID: 15317890 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]