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Journal Abstract Search

204 related items for PubMed ID: 37676273

  • 21. Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.
    Gowans LJJ, Al Dhaheri N, Li M, Busch T, Obiri-Yeboah S, Oti AA, Sabbah DK, Arthur FKN, Awotoye WO, Alade AA, Twumasi P, Agbenorku P, Plange-Rhule G, Naicker T, Donkor P, Murray JC, Sobreira NLM, Butali A.
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1655. PubMed ID: 33719213
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  • 22. Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts.
    Itai T, Yan F, Liu A, Dai Y, Iwaya C, Curtis SW, Leslie EJ, Simon LM, Jia P, Chen X, Iwata J, Zhao Z.
    HGG Adv; 2024 Jul 18; 5(3):100313. PubMed ID: 38807368
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  • 23. Genome Analysis Using Whole-Exome Sequencing of Non-Syndromic Cleft Lip and/or Palate from Malagasy Trios Identifies Variants Associated with Cilium-Related Pathways and Asian Genetic Ancestry.
    Manojlovic Z, Auslander A, Jin Y, Schmidt RJ, Xu Y, Chang S, Song R, Ingles SA, Nunes A, Vavra KC, Feigelson D, Rakotoarison S, DiBona M, Magee K, Smile O, Ramamonjisoa A, Magee Iii W.
    Genes (Basel); 2023 Mar 07; 14(3):. PubMed ID: 36980938
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  • 24. Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
    Ray D, Venkataraghavan S, Zhang W, Leslie EJ, Hetmanski JB, Weinberg SM, Murray JC, Marazita ML, Ruczinski I, Taub MA, Beaty TH.
    PLoS Genet; 2021 Jul 07; 17(7):e1009584. PubMed ID: 34242216
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  • 28. Genetic models and approaches to study orofacial clefts.
    Leslie EJ.
    Oral Dis; 2022 Jul 07; 28(5):1327-1338. PubMed ID: 34923716
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  • 30. Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.
    Al Chawa T, Ludwig KU, Fier H, Pötzsch B, Reich RH, Schmidt G, Braumann B, Daratsianos N, Böhmer AC, Schuencke H, Alblas M, Fricker N, Hoffmann P, Knapp M, Lange C, Nöthen MM, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2014 Jun 07; 100(6):493-8. PubMed ID: 24706492
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  • 31. Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
    Diaz Perez KK, Chung S, Head ST, Epstein MP, Hecht JT, Wehby GL, Weinberg SM, Murray JC, Marazita ML, Leslie EJ.
    Am J Med Genet A; 2023 Oct 07; 191(10):2558-2570. PubMed ID: 37350193
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  • 32. Exploration of genetic factors determining cleft side in a pair of monozygotic twins with mirror-image cleft lip and palate using whole-genome sequencing and comparison of craniofacial morphology.
    Takahashi M, Hosomichi K, Yamaguchi T, Nagahama R, Yoshida H, Marazita ML, Weinberg SM, Maki K, Tajima A.
    Arch Oral Biol; 2018 Dec 07; 96():33-38. PubMed ID: 30172943
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  • 33. Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate.
    Morris VE, Hashmi SS, Zhu L, Maili L, Urbina C, Blackwell S, Greives MR, Buchanan EP, Mulliken JB, Blanton SH, Zheng WJ, Hecht JT, Letra A.
    Hum Genet; 2020 Oct 07; 139(10):1261-1272. PubMed ID: 32318854
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  • 36. 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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  • 38. Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.
    Simioni M, Araujo TK, Monlleo IL, Maurer-Morelli CV, Gil-da-Silva-Lopes VL.
    J Hum Genet; 2015 Jan 14; 60(1):17-25. PubMed ID: 25391604
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  • 39. Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.
    Conte F, Oti M, Dixon J, Carels CE, Rubini M, Zhou H.
    Hum Genet; 2016 Jan 14; 135(1):41-59. PubMed ID: 26561393
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  • 40. Genetics of cleft lip and cleft palate.
    Leslie EJ, Marazita ML.
    Am J Med Genet C Semin Med Genet; 2013 Nov 14; 163C(4):246-58. PubMed ID: 24124047
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