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Journal Abstract Search

621 related items for PubMed ID: 24124047

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  • 2. Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
    Ludwig KU, Ahmed ST, Böhmer AC, Sangani NB, Varghese S, Klamt J, Schuenke H, Gültepe P, Hofmann A, Rubini M, Aldhorae KA, Steegers-Theunissen RP, Rojas-Martinez A, Reiter R, Borck G, Knapp M, Nakatomi M, Graf D, Mangold E, Peters H.
    PLoS Genet; 2016 Mar; 12(3):e1005914. PubMed ID: 26968009
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  • 4. Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
    Carlson JC, Standley J, Petrin A, Shaffer JR, Butali A, Buxó CJ, Castilla E, Christensen K, Deleyiannis FW, Hecht JT, Field LL, Garidkhuu A, Moreno Uribe LM, Nagato N, Orioli IM, Padilla C, Poletta F, Suzuki S, Vieira AR, Wehby GL, Weinberg SM, Beaty TH, Feingold E, Murray JC, Marazita ML, Leslie EJ.
    Genet Epidemiol; 2017 Dec; 41(8):887-897. PubMed ID: 29124805
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  • 5. 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. PubMed ID: 28425186
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  • 8. 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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  • 9. Orofacial Clefts: Genetics of Cleft Lip and Palate.
    Babai A, Irving M.
    Genes (Basel); 2023 Aug 09; 14(8):. PubMed ID: 37628654
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  • 11. Studies with Wnt genes and nonsyndromic cleft lip and palate.
    Menezes R, Letra A, Kim AH, Küchler EC, Day A, Tannure PN, Gomes da Motta L, Paiva KB, Granjeiro JM, Vieira AR.
    Birth Defects Res A Clin Mol Teratol; 2010 Nov 09; 88(11):995-1000. PubMed ID: 20890934
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  • 14. Using Whole Exome Sequencing to Identify Candidate Genes With Rare Variants In Nonsyndromic Cleft Lip and Palate.
    Aylward A, Cai Y, Lee A, Blue E, Rabinowitz D, Haddad J, University of Washington Center for Mendelian Genomics.
    Genet Epidemiol; 2016 Jul 09; 40(5):432-41. PubMed ID: 27229527
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  • 17. Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
    Ludwig KU, Wahle P, Reutter H, Paredes-Zenteno M, Muñoz-Jimenez SG, Ortiz-Lopez R, Böhmer AC, Tessmann P, Nowak S, Nöthen MM, Knapp M, Rojas-Martinez A, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2014 Jan 09; 100(1):43-7. PubMed ID: 24382704
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  • 18. Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.
    Lansdon LA, Dickinson A, Arlis S, Liu H, Hlas A, Hahn A, Bonde G, Long A, Standley J, Tyryshkina A, Wehby G, Lee NR, Daack-Hirsch S, Mohlke K, Girirajan S, Darbro BW, Cornell RA, Houston DW, Murray JC, Manak JR.
    Am J Hum Genet; 2023 Jan 05; 110(1):71-91. PubMed ID: 36493769
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  • 20. Identification of Causative Variants Contributing to Nonsyndromic Orofacial Clefts Using Whole-Exome Sequencing in a Saudi Family.
    Al Mahdi HB, Edris S, Bahieldin A, Al-Aama JY, Elango R, Jamalalail BA, Sabbagh HJ.
    Genet Test Mol Biomarkers; 2020 Nov 05; 24(11):723-731. PubMed ID: 33121284
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