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An Exome Sequencing Study of 10 Families with IgA Nephropathy.
Stapleton CP, Kennedy C, Fennelly NK, Murray SL, Connaughton DM, Dorman AM, Doyle B, Cavalleri GL, Conlon PJ. Stapleton CP, et al. Among authors: connaughton dm. Nephron. 2020;144(2):72-83. doi: 10.1159/000503564. Epub 2019 Dec 19. Nephron. 2020. PMID: 31865346
Home haemodialysis in Ireland.
Connaughton DM, Jamal A, McWilliams J, O'Kelly P, Ormond J, Butler A, McEntee N, Tierney E, Lambe G, Denton M, Magee C, Conlon PJ. Connaughton DM, et al. Ir J Med Sci. 2013 Mar;182(1):91-6. doi: 10.1007/s11845-012-0835-4. Epub 2012 Jun 3. Ir J Med Sci. 2013. PMID: 22661098
Home haemodialysis in Ireland.
Kennedy C, Connaughton DM, Murray S, Ormond J, Butler A, Phelan E, Young J, Durack L, Flavin J, O'Grady M, O'Kelly P, Lavin P, Leavey S, Lappin D, Giblin L, Casserly L, Plant WD, Conlon PJ. Kennedy C, et al. Among authors: connaughton dm. QJM. 2018 Apr 1;111(4):225-229. doi: 10.1093/qjmed/hcx249. QJM. 2018. PMID: 29272506
Clinical Heterogeneity in Familial IgA Nephropathy.
Fennelly NK, Kennedy C, Jenkinson AC, Connaughton DM, Stapleton C, Dorman AM, Doyle B, Conlon PJ. Fennelly NK, et al. Among authors: connaughton dm. Nephron. 2018;139(1):63-69. doi: 10.1159/000486018. Epub 2018 Jan 19. Nephron. 2018. PMID: 29402819
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease.
Živná M, Kidd K, Přistoupilová A, Barešová V, DeFelice M, Blumenstiel B, Harden M, Conlon P, Lavin P, Connaughton DM, Hartmannová H, Hodaňová K, Stránecký V, Vrbacká A, Vyleťal P, Živný J, Votruba M, Sovová J, Hůlková H, Robins V, Perry R, Wenzel A, Beck BB, Seeman T, Viklický O, Rajnochová-Bloudíčková S, Papagregoriou G, Deltas CC, Alper SL, Greka A, Bleyer AJ, Kmoch S. Živná M, et al. Among authors: connaughton dm. J Am Soc Nephrol. 2018 Sep;29(9):2418-2431. doi: 10.1681/ASN.2018020180. Epub 2018 Jul 2. J Am Soc Nephrol. 2018. PMID: 29967284 Free PMC article.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F. van der Ven AT, et al. Among authors: connaughton dm. J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24. J Am Soc Nephrol. 2018. PMID: 30143558 Free PMC article.
45 results