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Items: 1 to 20 of 96

1.

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. doi: 10.1002/ajmg.a.61002. Epub 2018 Dec 24.

PMID:
30582786
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. doi: 10.1007/s00439-016-1754-7. Epub 2017 Jan 4.

3.

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. doi: 10.1002/ajmg.a.38210. Epub 2017 Apr 19.

4.

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. doi: 10.1177/0022034516657003. Epub 2016 Jul 1.

5.

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 17;109(13):1030-1038. doi: 10.1002/bdr2.23605.

6.

Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population.

Peng HH, Chang NC, Chen KT, Lu JJ, Chang PY, Chang SC, Wu-Chou YH, Chou YT, Phang W, Cheng PJ.

BMC Med Genet. 2016 Aug 15;17(1):59. doi: 10.1186/s12881-016-0322-2.

7.

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. doi: 10.1597/09-227. Epub 2010 Jul 1.

8.

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.

Moreno LM, Mansilla MA, Bullard SA, Cooper ME, Busch TD, Machida J, Johnson MK, Brauer D, Krahn K, Daack-Hirsch S, L'heureux J, Valencia-Ramirez C, Rivera D, López AM, Moreno MA, Hing A, Lammer EJ, Jones M, Christensen K, Lie RT, Jugessur A, Wilcox AJ, Chines P, Pugh E, Doheny K, Arcos-Burgos M, Marazita ML, Murray JC, Lidral AC.

Hum Mol Genet. 2009 Dec 15;18(24):4879-96. doi: 10.1093/hmg/ddp444. Epub 2009 Sep 24.

9.

Whole-genome sequencing in a pair of monozygotic twins with discordant cleft lip and palate subtypes.

Takahashi M, Hosomichi K, Yamaguchi T, Nagahama R, Yoshida H, Maki K, Marazita ML, Weinberg SM, Tajima A.

Oral Dis. 2018 Oct;24(7):1303-1309. doi: 10.1111/odi.12910. Epub 2018 Jul 10.

PMID:
29873870
10.

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 1;25(13):2862-2872. Epub 2016 Mar 30.

11.

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 Jun 8;9:63. doi: 10.1186/s13148-017-0362-2. eCollection 2017.

12.

The Role of Noncoding Genetic Variation in Isolated Orofacial Clefts.

Thieme F, Ludwig KU.

J Dent Res. 2017 Oct;96(11):1238-1247. doi: 10.1177/0022034517720403. Epub 2017 Jul 21. Review.

PMID:
28732180
13.

Maternal occupational cadmium exposure and nonsyndromic orofacial clefts.

Suhl J, Romitti PA, Cao Y, Rocheleau CM, Burns TL, Conway K, Rajaraman P, Agopian AJ, Stewart P; National Birth Defects Prevention Study.

Birth Defects Res. 2018 Apr 17;110(7):603-609. doi: 10.1002/bdr2.1202. Epub 2018 Jan 23.

14.

[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].

Doray B, Badila-Timbolschi D, Schaefer E, Fattori D, Monga B, Dott B, Favre R, Kohler M, Nisand I, Viville B, Kauffmann I, Bruant-Rodier C, Grollemund B, Rinkenbach R, Astruc D, Gasser B, Lindner V, Marcellin L, Flori E, Girard-Lemaire F, Dollfus H.

Arch Pediatr. 2012 Oct;19(10):1021-9. doi: 10.1016/j.arcped.2012.07.002. Epub 2012 Aug 24. French.

PMID:
22925539
15.

Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population.

Liu K, Lu Y, Ai L, Jiao B, Yu J, Zhang B, Liu Q.

Br J Oral Maxillofac Surg. 2015 Oct;53(8):705-10. doi: 10.1016/j.bjoms.2015.05.021. Epub 2015 Jun 19.

PMID:
26100861
16.

Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations.

Lennon CJ, Birkeland AC, Nuñez JA, Su GH, Lanzano P, Guzman E, Celis K, Eisig SB, Hoffman D, Rendon MT, Ostos H, Chung WK, Haddad J Jr.

Laryngoscope. 2012 Sep;122(9):2082-7. doi: 10.1002/lary.23394. Epub 2012 Jul 2.

PMID:
22753311
17.

Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample.

Ishorst N, Francheschelli P, Böhmer AC, Khan MFJ, Heilmann-Heimbach S, Fricker N, Little J, Steegers-Theunissen RPM, Peterlin B, Nowak S, Martini M, Kruse T, Dunsche A, Kreusch T, Gölz L, Aldhorae K, Halboub E, Reutter H, Mossey P, Nöthen MM, Rubini M, Ludwig KU, Knapp M, Mangold E.

Birth Defects Res. 2018 Jun 1;110(10):871-882. doi: 10.1002/bdr2.1213. Epub 2018 Mar 2.

PMID:
29498243
18.

The functional EGF+61 polymorphism and nonsyndromic oral clefts susceptibility in a Brazilian population.

Falagan-Lotsch P, Lopes TS, Küchler EC, Tannure PN, Costa Mde C, Amorim LM, Granjeiro JM.

J Appl Oral Sci. 2015 Jul-Aug;23(4):390-6. doi: 10.1590/1678-775720140517.

19.

Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing.

Khandelwal KD, Ishorst N, Zhou H, Ludwig KU, Venselaar H, Gilissen C, Thonissen M, van Rooij IA, Dreesen K, Steehouwer M, van de Vorst M, Bloemen M, van Beusekom E, Roosenboom J, Borstlap W, Admiraal R, Dormaar T, Schoenaers J, Vander Poorten V, Hens G, Verdonck A, Bergé S, Roeleveldt N, Vriend G, Devriendt K, Brunner HG, Mangold E, Hoischen A, van Bokhoven H, Carels CE.

J Dent Res. 2017 Feb;96(2):179-185. doi: 10.1177/0022034516678829. Epub 2016 Nov 13.

PMID:
27834299
20.

Prediction of liability to orofacial clefting using genetic and craniofacial data from parents.

Mossey PA, Arngrimsson R, McColl J, Vintiner GM, Connor JM.

J Med Genet. 1998 May;35(5):371-8.

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