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Journal Abstract Search

284 related items for PubMed ID: 32574564

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  • 4. Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.
    Garg P, Ludwig KU, Böhmer AC, Rubini M, Steegers-Theunissen R, Mossey PA, Mangold E, Sharp AJ.
    Eur J Hum Genet; 2014 Jun; 22(6):822-30. PubMed ID: 24169523
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  • 9. 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 14; 15():24. PubMed ID: 24528994
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  • 10. Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.
    Xiao Y, Taub MA, Ruczinski I, Begum F, Hetmanski JB, Schwender H, Leslie EJ, Koboldt DC, Murray JC, Marazita ML, Beaty TH.
    Genet Epidemiol; 2017 Apr 14; 41(3):244-250. PubMed ID: 28019042
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  • 11. 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 14; 136(3):275-286. PubMed ID: 28054174
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  • 14. Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.
    Beaty TH, Taub MA, Scott AF, Murray JC, Marazita ML, Schwender H, Parker MM, Hetmanski JB, Balakrishnan P, Mansilla MA, Mangold E, Ludwig KU, Noethen MM, Rubini M, Elcioglu N, Ruczinski I.
    Hum Genet; 2013 Jul 14; 132(7):771-81. PubMed ID: 23512105
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  • 15. Exploring the interaction between FGF Genes and T-box genes among chinese nonsyndromic cleft lip with or without cleft palate case-parent trios.
    Li W, Wang M, Zhou R, Wang S, Zheng H, Liu D, Zhou Z, Zhu H, Wu T, Beaty TH.
    Environ Mol Mutagen; 2019 Aug 14; 60(7):602-606. PubMed ID: 30848863
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  • 16. [Exploring the association between de novo mutations and non-syndromic cleft lip with or without palate based on whole exome sequencing of case-parent trios].
    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 18; 54(3):387-393. PubMed ID: 35701113
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  • 17. Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians.
    Figueiredo JC, Ly S, Raimondi H, Magee K, Baurley JW, Sanchez-Lara PA, Ihenacho U, Yao C, Edlund CK, van den Berg D, Casey G, DeClerk YA, Samet JM, Magee W.
    Am J Med Genet A; 2014 Oct 18; 164A(10):2572-80. PubMed ID: 25099202
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  • 19. Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.
    Jia Z, Leslie EJ, Cooper ME, Butali A, Standley J, Rigdon J, Suzuki S, Gongorjav A, Shonkhuuz TE, Natsume N, Shi B, Marazita ML, Murray JC.
    Am J Med Genet A; 2015 May 18; 167A(5):1054-1060. PubMed ID: 25786657
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