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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. Epub 2005 Dec 2.


Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families.

Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC.

Am J Med Genet A. 2004 Feb 15;125A(1):17-22.


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.


Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC.

Am J Hum Genet. 1998 Aug;63(2):557-68.


Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations.

Ingersoll RG, Hetmanski J, Park JW, Fallin MD, McIntosh I, Wu-Chou YH, Chen PK, Yeow V, Chong SS, Cheah F, Sull JW, Jee SH, Wang H, Wu T, Murray T, Huang S, Ye X, Jabs EW, Redett R, Raymond G, Scott AF, Beaty TH.

Eur J Hum Genet. 2010 Jun;18(6):726-32. doi: 10.1038/ejhg.2009.228. Epub 2010 Jan 20.


Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.

Salahshourifar I, Halim AS, Wan Sulaiman WA, Zilfalil BA.

J Hum Genet. 2011 Nov;56(11):755-8. doi: 10.1038/jhg.2011.95. Epub 2011 Aug 25.


In a Vietnamese population, MSX1 variants contribute to cleft lip and palate.

Suzuki Y, Jezewski PA, Machida J, Watanabe Y, Shi M, Cooper ME, Viet le T, Nguyen TD, Hai H, Natsume N, Shimozato K, Marazita ML, Murray JC.

Genet Med. 2004 May-Jun;6(3):117-25.


Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate.

Lace B, Vasiljeva I, Dundure I, Barkane B, Akota I, Krumina A.

Stomatologija. 2006;8(1):21-4.


Cleft lip and/or palate with monogenic autosomal recessive transmission in Pyrenees shepherd dogs.

Kemp C, Thiele H, Dankof A, Schmidt G, Lauster C, Fernahl G, Lauster R.

Cleft Palate Craniofac J. 2009 Jan;46(1):81-8. doi: 10.1597/06-229.1. Epub 2008 Mar 5.


Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines.

Lidral AC, Murray JC, Buetow KH, Basart AM, Schearer H, Shiang R, Naval A, Layda E, Magee K, Magee W.

Cleft Palate Craniofac J. 1997 Jan;34(1):1-6.


Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population.

Kim NY, Kim YH, Park JW, Baek SH.

J Korean Med Sci. 2013 Apr;28(4):522-6. doi: 10.3346/jkms.2013.28.4.522. Epub 2013 Mar 27.


MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.

Jagomägi T, Nikopensius T, Krjutskov K, Tammekivi V, Viltrop T, Saag M, Metspalu A.

Eur J Oral Sci. 2010 Jun;118(3):213-20. doi: 10.1111/j.1600-0722.2010.00729.x.


Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).

Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC.

Am J Med Genet A. 2013 May;161A(5):965-72. doi: 10.1002/ajmg.a.35749. Epub 2013 Mar 5.


Contributions of PTCH gene variants to isolated cleft lip and palate.

Mansilla MA, Cooper ME, Goldstein T, Castilla EE, Lopez Camelo JS, Marazita ML, Murray JC.

Cleft Palate Craniofac J. 2006 Jan;43(1):21-9.


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.


MSX1 and TGFB3 contribute to clefting in South America.

Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC.

J Dent Res. 2003 Apr;82(4):289-92.


MSX1 and orofacial clefting with and without tooth agenesis.

Modesto A, Moreno LM, Krahn K, King S, Lidral AC.

J Dent Res. 2006 Jun;85(6):542-6.


PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses.

Ichikawa E, Watanabe A, Nakano Y, Akita S, Hirano A, Kinoshita A, Kondo S, Kishino T, Uchiyama T, Niikawa N, Yoshiura K.

J Hum Genet. 2006;51(1):38-46. Epub 2005 Oct 25.


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.


Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate.

Suazo J, Santos JL, Jara L, Blanco R.

Am J Med Genet A. 2010 Aug;152A(8):2011-6. doi: 10.1002/ajmg.a.33528.


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