These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
197 related articles for article (PubMed ID: 34061439)
1. Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Li M; Olotu J; Buxo-Martinez CJ; Mossey PA; Anand D; Busch T; Alade A; Gowans LJJ; Eshete M; Adeyemo WL; Naicker T; Awotoye WO; Gupta S; Adeleke C; Bravo V; Huang S; Adamson OO; Toraño AM; Bello CA; Soto M; Soto M; Ledesma R; Marquez M; Cordero JF; Lopez-Del Valle LM; Salcedo MI; Debs N; Petrin A; Malloy H; Elhadi K; James O; Ogunlewe MO; Abate F; Hailu A; Mohammed I; Gravem P; Deribew M; Gesses M; Hassan M; Pape J; Obiri-Yeboah S; Arthur FKN; Oti AA; Donkor P; Marazita ML; Lachke SA; Adeyemo AA; Murray JC; Butali A Oral Dis; 2022 Oct; 28(7):1921-1935. PubMed ID: 34061439 [TBL] [Abstract][Full Text] [Related]
2. 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 [TBL] [Abstract][Full Text] [Related]
3. Orofacial Clefts: Genetics of Cleft Lip and Palate. Babai A; Irving M Genes (Basel); 2023 Aug; 14(8):. PubMed ID: 37628654 [TBL] [Abstract][Full Text] [Related]
4. Orofacial clefts embryology, classification, epidemiology, and genetics. Nasreddine G; El Hajj J; Ghassibe-Sabbagh M Mutat Res Rev Mutat Res; 2021; 787():108373. PubMed ID: 34083042 [TBL] [Abstract][Full Text] [Related]
5. A comparison of DNA methylation in newborn blood samples from infants with and without orofacial clefts. Xu Z; Lie RT; Wilcox AJ; Saugstad OD; Taylor JA Clin Epigenetics; 2019 Mar; 11(1):40. PubMed ID: 30832715 [TBL] [Abstract][Full Text] [Related]
6. Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population. Butali A; Mossey P; Adeyemo W; Eshete M; Gaines L; Braimah R; Aregbesola B; Rigdon J; Emeka C; Olutayo J; Ogunlewe O; Ladeinde A; Abate F; Hailu T; Mohammed I; Gravem P; Deribew M; Gesses M; Adeyemo A; Marazita M; Murray J Am J Med Genet A; 2014 Oct; 164A(10):2567-71. PubMed ID: 25081408 [TBL] [Abstract][Full Text] [Related]
7. IRF6 polymorphisms in Brazilian patients with non-syndromic cleft lip with or without palate. Bezerra JF; Silva HPVD; Bortolin RH; Luchessi AD; Ururahy MAG; Loureiro MB; Gil-da-Silva-Lopes VL; Almeida MDG; Amaral VSD; Rezende AA Braz J Otorhinolaryngol; 2020; 86(6):696-702. PubMed ID: 31495697 [TBL] [Abstract][Full Text] [Related]
8. Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Dąbrowska J; Biedziak B; Szponar-Żurowska A; Budner M; Jagodziński PP; Płoski R; Mostowska A Mol Genet Genomics; 2022 Sep; 297(5):1315-1327. PubMed ID: 35778651 [TBL] [Abstract][Full Text] [Related]
9. Genetics of cleft lip and cleft palate. Leslie EJ; Marazita ML Am J Med Genet C Semin Med Genet; 2013 Nov; 163C(4):246-58. PubMed ID: 24124047 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach. Masotti C; Brito LA; Nica AC; Ludwig KU; Nunes K; Savastano CP; Malcher C; Ferreira SG; Kobayashi GS; Bueno DF; Alonso N; Franco D; Rojas-Martinez A; Dos Santos SE; Galante PA; Meyer D; Hünemeier T; Mangold E; Dermitzakis ET; Passos-Bueno MR J Dent Res; 2018 Jan; 97(1):33-40. PubMed ID: 29053389 [TBL] [Abstract][Full Text] [Related]
12. Identification of Causative Variants Contributing to Nonsyndromic Orofacial Clefts Using Whole-Exome Sequencing in a Saudi Family. Al Mahdi HB; Edris S; Bahieldin A; Al-Aama JY; Elango R; Jamalalail BA; Sabbagh HJ Genet Test Mol Biomarkers; 2020 Nov; 24(11):723-731. PubMed ID: 33121284 [No Abstract] [Full Text] [Related]
13. Distinct DNA methylation profiles in subtypes of orofacial cleft. Sharp GC; Ho K; Davies A; Stergiakouli E; Humphries K; McArdle W; Sandy J; Davey Smith G; Lewis SJ; Relton CL Clin Epigenetics; 2017; 9():63. PubMed ID: 28603561 [TBL] [Abstract][Full Text] [Related]
14. Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. Leslie EJ; Carlson JC; Shaffer JR; Buxó CJ; Castilla EE; Christensen K; Deleyiannis FWB; Field LL; Hecht JT; Moreno L; Orioli IM; Padilla C; Vieira AR; Wehby GL; Feingold E; Weinberg SM; Murray JC; Marazita ML Am J Med Genet A; 2017 Jun; 173(6):1531-1538. PubMed ID: 28425186 [TBL] [Abstract][Full Text] [Related]
15. 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; 179(3):467-474. PubMed ID: 30582786 [TBL] [Abstract][Full Text] [Related]
16. Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. Carlson JC; Taub MA; Feingold E; Beaty TH; Murray JC; Marazita ML; Leslie EJ Birth Defects Res; 2017 Jul; 109(13):1030-1038. PubMed ID: 28762674 [TBL] [Abstract][Full Text] [Related]