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Journal Abstract Search

172 related items for PubMed ID: 38807368

  • 1. 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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  • 2. 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 18; 136(3):275-286. PubMed ID: 28054174
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  • 3. Distinct DNA methylation profiles in subtypes of orofacial cleft.
    Sharp GC, Ho K, Davies A, Stergiakouli E, Humphries K, McArdle W, Sandy J, Davey Smith G, Lewis SJ, Relton CL.
    Clin Epigenetics; 2017 Mar 18; 9():63. PubMed ID: 28603561
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  • 4. Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
    Shaffer JR, LeClair J, Carlson JC, Feingold E, Buxó CJ, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Murray JC, Weinberg SM, Marazita ML, Leslie EJ.
    Am J Med Genet A; 2019 Mar 18; 179(3):467-474. PubMed ID: 30582786
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  • 5. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
    Ishorst N, Henschel L, Thieme F, Drichel D, Sivalingam S, Mehrem SL, Fechtner AC, Fazaal J, Welzenbach J, Heimbach A, Maj C, Borisov O, Hausen J, Raff R, Hoischen A, Dixon M, Rada-Iglesias A, Bartusel M, Rojas-Martinez A, Aldhorae K, Braumann B, Kruse T, Kirschneck C, Spanier G, Reutter H, Nowak S, Gölz L, Knapp M, Buness A, Krawitz P, Nöthen MM, Nothnagel M, Becker T, Ludwig KU, Mangold E.
    Mol Genet Genomic Med; 2023 Mar 18; 11(3):e2109. PubMed ID: 36468602
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  • 8. A comparison of DNA methylation in newborn blood samples from infants with and without orofacial clefts.
    Xu Z, Lie RT, Wilcox AJ, Saugstad OD, Taylor JA.
    Clin Epigenetics; 2019 Mar 04; 11(1):40. PubMed ID: 30832715
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  • 9. Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.
    Carlson JC, Taub MA, Feingold E, Beaty TH, Murray JC, Marazita ML, Leslie EJ.
    Birth Defects Res; 2017 Jul 17; 109(13):1030-1038. PubMed ID: 28762674
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  • 12. Gene×environment associations in orofacial clefting.
    Marazita ML.
    Curr Top Dev Biol; 2023 Jul 17; 152():169-192. PubMed ID: 36707211
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  • 14. 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 17; 191(10):2558-2570. PubMed ID: 37350193
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  • 16. Comprehensive analysis of differentially expressed profiles of non‑coding RNAs in peripheral blood and ceRNA regulatory networks in non‑syndromic orofacial clefts.
    Gao Y, Zang Q, Song H, Fu S, Sun W, Zhang W, Wang X, Li Y, Jiao X.
    Mol Med Rep; 2019 Jul 17; 20(1):513-528. PubMed ID: 31115538
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  • 17. 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 17; 17(7):e1009584. PubMed ID: 34242216
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  • 18. Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
    Cox LL, Cox TC, Moreno Uribe LM, Zhu Y, Richter CT, Nidey N, Standley JM, Deng M, Blue E, Chong JX, Yang Y, Carstens RP, Anand D, Lachke SA, Smith JD, Dorschner MO, Bedell B, Kirk E, Hing AV, Venselaar H, Valencia-Ramirez LC, Bamshad MJ, Glass IA, Cooper JA, Haan E, Nickerson DA, van Bokhoven H, Zhou H, Krahn KN, Buckley MF, Murray JC, Lidral AC, Roscioli T.
    Am J Hum Genet; 2018 Jun 07; 102(6):1143-1157. PubMed ID: 29805042
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