331 related articles for article (PubMed ID: 36493769)
1. Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.
Lansdon LA; Dickinson A; Arlis S; Liu H; Hlas A; Hahn A; Bonde G; Long A; Standley J; Tyryshkina A; Wehby G; Lee NR; Daack-Hirsch S; Mohlke K; Girirajan S; Darbro BW; Cornell RA; Houston DW; Murray JC; Manak JR
Am J Hum Genet; 2023 Jan; 110(1):71-91. PubMed ID: 36493769
[TBL] [Abstract][Full Text] [Related]
2. Identification of
Lansdon LA; Darbro BW; Petrin AL; Hulstrand AM; Standley JM; Brouillette RB; Long A; Mansilla MA; Cornell RA; Murray JC; Houston DW; Manak JR
Genetics; 2018 Jan; 208(1):283-296. PubMed ID: 29162626
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk.
Younkin SG; Scharpf RB; Schwender H; Parker MM; Scott AF; Marazita ML; Beaty TH; Ruczinski I
BMC Genet; 2014 Feb; 15():24. PubMed ID: 24528994
[TBL] [Abstract][Full Text] [Related]
5. Application of high resolution SNP arrays in patients with congenital oral clefts in south China.
Lei TY; Wang HT; Li F; Cui YQ; Fu F; Li R; Liao C
J Genet; 2016 Dec; 95(4):801-809. PubMed ID: 27994178
[TBL] [Abstract][Full Text] [Related]
6. A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Leslie EJ; 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; Lidral AC; Valencia-Ramirez LC; Lopez-Palacio AM; Valencia DR; Arcos-Burgos M; Czeizel AE; Field LL; Padilla CD; Cutiongco-de la Paz EM; Deleyiannis F; Christensen K; Munger RG; Lie RT; Wilcox A; Romitti PA; 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; Abate F; Koruyucu M; Seymen F; Ma L; de Salamanca JE; Weinberg SM; Moreno L; Murray JC; Marazita ML
Hum Mol Genet; 2016 Jul; 25(13):2862-2872. PubMed ID: 27033726
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
Jezewski PA; Vieira AR; Nishimura C; Ludwig B; Johnson M; O'Brien SE; Daack-Hirsch S; Schultz RE; Weber A; Nepomucena B; Romitti PA; Christensen K; Orioli IM; Castilla EE; Machida J; Natsume N; Murray JC
J Med Genet; 2003 Jun; 40(6):399-407. PubMed ID: 12807959
[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. 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;
B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
[TBL] [Abstract][Full Text] [Related]
11. Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
Stanier P; Moore GE
Hum Mol Genet; 2004 Apr; 13 Spec No 1():R73-81. PubMed ID: 14722155
[TBL] [Abstract][Full Text] [Related]
12. Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.
Conte F; Oti M; Dixon J; Carels CE; Rubini M; Zhou H
Hum Genet; 2016 Jan; 135(1):41-59. PubMed ID: 26561393
[TBL] [Abstract][Full Text] [Related]
13. Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate.
Leslie EJ; Murray JC
Clin Genet; 2013 Nov; 84(5):496-500. PubMed ID: 22978696
[TBL] [Abstract][Full Text] [Related]
14. Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate.
Mohamad Shah NS; Sulong S; Wan Sulaiman WA; Halim AS
Mol Genet Genomic Med; 2019 May; 7(5):e635. PubMed ID: 30924295
[TBL] [Abstract][Full Text] [Related]
15. Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Ludwig KU; Böhmer AC; Bowes J; Nikolic M; Ishorst N; Wyatt N; Hammond NL; Gölz L; Thieme F; Barth S; Schuenke H; Klamt J; Spielmann M; Aldhorae K; Rojas-Martinez A; Nöthen MM; Rada-Iglesias A; Dixon MJ; Knapp M; Mangold E
Hum Mol Genet; 2017 Feb; 26(4):829-842. PubMed ID: 28087736
[TBL] [Abstract][Full Text] [Related]
16. Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.
Simioni M; Araujo TK; Monlleo IL; Maurer-Morelli CV; Gil-da-Silva-Lopes VL
J Hum Genet; 2015 Jan; 60(1):17-25. PubMed ID: 25391604
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. CHD7 gene and non-syndromic cleft lip and palate.
Félix TM; Hanshaw BC; Mueller R; Bitoun P; Murray JC
Am J Med Genet A; 2006 Oct; 140(19):2110-4. PubMed ID: 16763960
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genetic evidence for the role of loci at 19q13 in cleft lip and palate.
Warrington A; Vieira AR; Christensen K; Orioli IM; Castilla EE; Romitti PA; Murray JC
J Med Genet; 2006 Jun; 43(6):e26. PubMed ID: 16740910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]