Literature DB >> 14981713

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio.

Lina M Moreno1, Mauricio Arcos-Burgos, Mary L Marazita, Katherine Krahn, Brion S Maher, Margaret E Cooper, Consuelo R Valencia-Ramirez, Andrew C Lidral.   

Abstract

Non-syndromic cleft lip with or without cleft palate (CL/P) is a genetically complex birth defect, with a prevalence from 1/500 to 1/1,000 live births. Evidence from linkage and linkage disequilibrium studies is contradictory suggesting that heterogeneity between study populations may exist. A recent report of a genome widescan in 92 sib pairs from the United Kingdom revealed suggestive linkage to 10 loci [Prescott et al., 2000]. The purpose of this study is to replicate those results and evaluate additional candidate genes in 49 Colombian and 13 Ohio families. Genotypes were obtained for STRPs at 1p36, 2p13 (TGFA), 4p16 (MSX1), 6p23-25, 6q25-27, 8q23-24, 11p12-q13, 12q13, 14q24 (TGFB3), 16q22-24, 17q12-21 (RARA), and Xcen-q21. Linkage was performed using parametric (dominant and recessive models) and non-parametric (GenehunterNPL and SimIBD) analyses. In addition, heterogeneity was analyzed using GenehunterHLOD, and association determined by the TDT. The Colombian families showed significant SimIBD results for 11p12-q13 (P = 0.034), 12q13 (P = 0.015), 16q22-24 (0.01), and 17q12-21 (0.009), while the Ohio families showed significant SimIBD results for 1p36 (P = 0.02), TGFA (P = 0.005), 6p23 (P = 0.004), 11p12-q13 (P = 0.048) and significant NPL results for TGFA (NPL = 3.01, P = 0.009), 4p16 (MNPL = 2.07, P = 0.03) and 12q13 (SNPL = 3.55, P = 0.007). Significant association results were obtained only for the Colombian families in the regions 1p36 (P = 0.046), 6p23-25 (P = 0.020), and 12q13 (P = 0.046). In addition several families yielded LOD scores ranging from 1.09 to 1.73, for loci at 4p16, 6p23-25, 16q22-24, and 17q13. These results confirm previous reports for these loci. However, the differences between the two populations suggest that population specific locus heterogeneity exists. This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299/suppmat/index.html. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 14981713     DOI: 10.1002/ajmg.a.20425

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  21 in total

1.  Retinoic acid, GABA-ergic, and TGF-beta signaling systems are involved in human cleft palate fibroblast phenotype.

Authors:  Tiziano Baroni; Catia Bellucci; Cinzia Lilli; Furio Pezzetti; Francesco Carinci; Ennio Becchetti; Paolo Carinci; Giordano Stabellini; Mario Calvitti; Eleonora Lumare; Maria Bodo
Journal:  Mol Med       Date:  2006 Sep-Oct       Impact factor: 6.354

2.  MSX1 and orofacial clefting with and without tooth agenesis.

Authors:  A Modesto; L M Moreno; K Krahn; S King; A C Lidral
Journal:  J Dent Res       Date:  2006-06       Impact factor: 6.116

Review 3.  Wnt/beta-catenin signaling in oral tissue development and disease.

Authors:  F Liu; S E Millar
Journal:  J Dent Res       Date:  2010-03-03       Impact factor: 6.116

4.  [Associations among PRDM16 polymorphisms, environmental exposure factors during mother's pregnancy, and nonsyndromic cleft lip with or without cleft palate].

Authors:  Bin Yin; Bing Shi; Zhong-Lin Jia
Journal:  Hua Xi Kou Qiang Yi Xue Za Zhi       Date:  2018-10-01

Review 5.  Progress toward discerning the genetics of cleft lip.

Authors:  Andrew C Lidral; Lina M Moreno
Journal:  Curr Opin Pediatr       Date:  2005-12       Impact factor: 2.856

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

Authors:  Lina M Moreno; Maria Adela Mansilla; Steve A Bullard; Margaret E Cooper; Tamara D Busch; Junichiro Machida; Marla K Johnson; David Brauer; Katherine Krahn; Sandy Daack-Hirsch; Jamie L'heureux; Consuelo Valencia-Ramirez; Dora Rivera; Ana Maria López; Manuel A Moreno; Anne Hing; Edward J Lammer; Marilyn Jones; Kaare Christensen; Rolv T Lie; Astanand Jugessur; Allen J Wilcox; Peter Chines; Elizabeth Pugh; Kim Doheny; Mauricio Arcos-Burgos; Mary L Marazita; Jeffrey C Murray; Andrew C Lidral
Journal:  Hum Mol Genet       Date:  2009-09-24       Impact factor: 6.150

7.  Genetic Factors and Orofacial Clefting.

Authors:  Andrew C Lidral; Lina M Moreno; Steven A Bullard
Journal:  Semin Orthod       Date:  2008-06       Impact factor: 0.970

8.  TFAP2A mutations result in branchio-oculo-facial syndrome.

Authors:  Jeff M Milunsky; Tom A Maher; Geping Zhao; Amy E Roberts; Heather J Stalker; Roberto T Zori; Michelle N Burch; Michele Clemens; John B Mulliken; Rosemarie Smith; Angela E Lin
Journal:  Am J Hum Genet       Date:  2008-05       Impact factor: 11.025

9.  Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice.

Authors:  Yu Lan; Rosemary C Ryan; Zunyi Zhang; Steven A Bullard; Jeffrey O Bush; Kathleen M Maltby; Andrew C Lidral; Rulang Jiang
Journal:  Dev Dyn       Date:  2006-05       Impact factor: 3.780

10.  The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts.

Authors:  Marie-José H van den Boogaard; Dominique de Costa; Ingrid P C Krapels; Fan Liu; Cock van Duijn; Richard J Sinke; Dick Lindhout; Régine P M Steegers-Theunissen
Journal:  Hum Genet       Date:  2008-10-19       Impact factor: 4.132

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