201 related articles for article (PubMed ID: 22978696)
1. 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]
2. 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]
3. Identification of susceptibility genes in non-syndromic cleft lip with or without cleft palate using whole-exome sequencing.
Liu YP; Xu LF; Wang Q; Zhou XL; Zhou JL; Pan C; Zhang JP; Wu QR; Li YQ; Xia YJ; Peng X; Zhang MR; Yu HM; Xu LC
Med Oral Patol Oral Cir Bucal; 2015 Nov; 20(6):e763-70. PubMed ID: 26449438
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Expression Quantitative Trait Locus Study of Non-Syndromic Cleft Lip with or without Cleft Palate GWAS Variants in Lip Tissues.
Li X; Tian Y; Qiu L; Lou S; Zhu G; Gao Y; Ma L; Pan Y
Cells; 2022 Oct; 11(20):. PubMed ID: 36291147
[TBL] [Abstract][Full Text] [Related]
6. Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.
Mangold E; Reutter H; León-Cachón RB; Ludwig KU; Herms S; Chacón-Camacho Ó; Ortiz-López R; Paredes-Zenteno M; Arizpe-Cantú A; Muñoz-Jiménez SG; Nowak S; Kramer FJ; Wienker TF; Nöthen MM; Knapp M; Rojas-Martínez A
Eur J Oral Sci; 2012 Oct; 120(5):373-7. PubMed ID: 22984993
[TBL] [Abstract][Full Text] [Related]
7. Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate.
Yu Y; Alvarado R; Petty LE; Bohlender RJ; Shaw DM; Below JE; Bejar N; Ruiz OE; Tandon B; Eisenhoffer GT; Kiss DL; Huff CD; Letra A; Hecht JT
Hum Mol Genet; 2022 Jul; 31(14):2348-2357. PubMed ID: 35147171
[TBL] [Abstract][Full Text] [Related]
8. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
Leslie EJ; Mansilla MA; Biggs LC; Schuette K; Bullard S; Cooper M; Dunnwald M; Lidral AC; Marazita ML; Beaty TH; Murray JC
Birth Defects Res A Clin Mol Teratol; 2012 Nov; 94(11):934-42. PubMed ID: 23008150
[TBL] [Abstract][Full Text] [Related]
9. Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of
Zieger HK; Weinhold L; Schmidt A; Holtgrewe M; Juranek SA; Siewert A; Scheer AB; Thieme F; Mangold E; Ishorst N; Brand FU; Welzenbach J; Beule D; Paeschke K; Krawitz PM; Ludwig KU
HGG Adv; 2023 Jan; 4(1):100166. PubMed ID: 36589413
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Using whole exome sequencing to identify susceptibility genes associated with nonsyndromic cleft lip with or without cleft palate.
Fu Z; Yue J; Xue L; Xu Y; Ding Q; Xiao W
Mol Genet Genomics; 2023 Jan; 298(1):107-118. PubMed ID: 36322204
[TBL] [Abstract][Full Text] [Related]
12. [Exploring the association between
Chen X; Wang SY; Xue EC; Wang XH; Peng HX; Fan M; Wang MY; Wu YQ; Qin XY; Li J; Wu T; Zhu HP; Li J; Zhou ZB; Chen DF; Hu YH
Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 54(3):387-393. PubMed ID: 35701113
[TBL] [Abstract][Full Text] [Related]
13. Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
Savastano CP; Brito LA; Faria ÁC; Setó-Salvia N; Peskett E; Musso CM; Alvizi L; Ezquina SA; James C; GOSgene ; Beales P; Lees M; Moore GE; Stanier P; Passos-Bueno MR
Clin Genet; 2017 May; 91(5):683-689. PubMed ID: 27350171
[TBL] [Abstract][Full Text] [Related]
14. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
Ishorst N; Henschel L; Thieme F; Drichel D; Sivalingam S; Mehrem SL; Fechtner AC; Fazaal J; Welzenbach J; Heimbach A; Maj C; Borisov O; Hausen J; Raff R; Hoischen A; Dixon M; Rada-Iglesias A; Bartusel M; Rojas-Martinez A; Aldhorae K; Braumann B; Kruse T; Kirschneck C; Spanier G; Reutter H; Nowak S; Gölz L; Knapp M; Buness A; Krawitz P; Nöthen MM; Nothnagel M; Becker T; Ludwig KU; Mangold E
Mol Genet Genomic Med; 2023 Mar; 11(3):e2109. PubMed ID: 36468602
[TBL] [Abstract][Full Text] [Related]
15. Three GLI2 mutations combined potentially underlie non-syndromic cleft lip with or without cleft palate in a Chinese pedigree.
Meng P; Zhao H; Huang W; Zhang Y; Zhong W; Zhang M; Jia P; Zhou Z; Maimaitili G; Chen F; Zhang J; Lin J
Mol Genet Genomic Med; 2019 Sep; 7(9):e714. PubMed ID: 31386309
[TBL] [Abstract][Full Text] [Related]
16. Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population.
Mostowska A; Hozyasz KK; Wójcicki P; Żukowski K; Dąbrowska A; Lasota A; Zadurska M; Radomska A; Dunin-Wilczyńska I; Jagodziński PP
Birth Defects Res A Clin Mol Teratol; 2015 Oct; 103(10):847-56. PubMed ID: 26043427
[TBL] [Abstract][Full Text] [Related]
17. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.
Vieira AR; Avila JR; Daack-Hirsch S; Dragan E; Félix TM; Rahimov F; Harrington J; Schultz RR; Watanabe Y; Johnson M; Fang J; O'Brien SE; Orioli IM; Castilla EE; Fitzpatrick DR; Jiang R; Marazita ML; Murray JC
PLoS Genet; 2005 Dec; 1(6):e64. PubMed ID: 16327884
[TBL] [Abstract][Full Text] [Related]
18. Gene-gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non-syndromic cleft lip with or without cleft palate in Chinese case-parent trios.
Liu D; Wang H; Schwender H; Marazita ML; Wang Z; Yuan Y; Wang P; Liang KY; Wu-Chou YH; Wang M; Shi B; Zhu H; Wu T; Beaty TH
Am J Med Genet A; 2017 Jun; 173(6):1489-1494. PubMed ID: 28402597
[TBL] [Abstract][Full Text] [Related]
19. Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis.
Imani MM; Lopez-Jornet P; Pons-Fuster López E; Sadeghi M
Int J Environ Res Public Health; 2019 Aug; 16(15):. PubMed ID: 31387249
[No Abstract] [Full Text] [Related]
20. MTHFR, TGFB3, and TGFA polymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China.
Zhu J; Hao L; Li S; Bailey LB; Tian Y; Li Z
Am J Med Genet A; 2010 Feb; 152A(2):291-8. PubMed ID: 20082468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
