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Page 1
Monogenic causes of chronic kidney disease in adults.
Connaughton DM, Kennedy C, Shril S, Mann N, Murray SL, Williams PA, Conlon E, Nakayama M, van der Ven AT, Ityel H, Kause F, Kolvenbach CM, Dai R, Vivante A, Braun DA, Schneider R, Kitzler TM, Moloney B, Moran CP, Smyth JS, Kennedy A, Benson K, Stapleton C, Denton M, Magee C, O'Seaghdha CM, Plant WD, Griffin MD, Awan A, Sweeney C, Mane SM, Lifton RP, Griffin B, Leavey S, Casserly L, de Freitas DG, Holian J, Dorman A, Doyle B, Lavin PJ, Little MA, Conlon PJ, Hildebrandt F. Connaughton DM, et al. Among authors: dorman a. Kidney Int. 2019 Apr;95(4):914-928. doi: 10.1016/j.kint.2018.10.031. Epub 2019 Feb 14. Kidney Int. 2019. PMID: 30773290 Free PMC article.
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. Nephron. 2018;139(1):63-69. doi: 10.1159/000486018. Epub 2018 Jan 19. Nephron. 2018. PMID: 29402819
Utility of Genomic Testing after Renal Biopsy.
Murray SL, Dorman A, Benson KA, Connaughton DM, Stapleton CP, Fennelly NK, Kennedy C, McDonnell CA, Kidd K, Cormican SM, Ryan LA, Lavin P, Little MA, Bleyer AJ, Doyle B, Cavalleri GL, Hildebrandt F, Conlon PJ. Murray SL, et al. Among authors: dorman a. Am J Nephrol. 2020;51(1):43-53. doi: 10.1159/000504869. Epub 2019 Dec 10. Am J Nephrol. 2020. PMID: 31822006 Free PMC article.
The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project.
Elhassan EAE, Murray SL, Connaughton DM, Kennedy C, Cormican S, Cowhig C, Stapleton C, Little MA, Kidd K, Bleyer AJ, Živná M, Kmoch S, Fennelly NK, Doyle B, Dorman A, Griffin MD, Casserly L, Harris PC, Hildebrandt F, Cavalleri GL, Benson KA, Conlon PJ. Elhassan EAE, et al. Among authors: dorman a. J Nephrol. 2022 Jul;35(6):1655-1665. doi: 10.1007/s40620-021-01236-2. Epub 2022 Jan 31. J Nephrol. 2022. PMID: 35099770 Free PMC article.
Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland.
Cormican S, Connaughton DM, Kennedy C, Murray S, Živná M, Kmoch S, Fennelly NK, O'Kelly P, Benson KA, Conlon ET, Cavalleri G, Foley C, Doyle B, Dorman A, Little MA, Lavin P, Kidd K, Bleyer AJ, Conlon PJ. Cormican S, et al. Among authors: dorman a. Ren Fail. 2019 Nov;41(1):832-841. doi: 10.1080/0886022X.2019.1655452. Ren Fail. 2019. PMID: 31509055 Free PMC article.
Kidney transplant outcomes in familial C3 glomerulopathy.
Wong L, Moran S, Lavin PJ, Dorman AM, Conlon PJ. Wong L, et al. Clin Kidney J. 2016 Jun;9(3):403-7. doi: 10.1093/ckj/sfw020. Epub 2016 Apr 14. Clin Kidney J. 2016. PMID: 27274824 Free PMC article.
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. Nephron. 2020;144(2):72-83. doi: 10.1159/000503564. Epub 2019 Dec 19. Nephron. 2020. PMID: 31865346
Diagnostic utility of genetic testing in patients undergoing renal biopsy.
Benson KA, Murray SL, Doyle R, Doyle B, Dorman AM, Sadlier D, Brennan E, Large M, Cavalleri GL, Godson C, Conlon PJ. Benson KA, et al. Among authors: dorman am. Cold Spring Harb Mol Case Stud. 2020 Oct 7;6(5):a005462. doi: 10.1101/mcs.a005462. Print 2020 Oct. Cold Spring Harb Mol Case Stud. 2020. PMID: 32723786 Free PMC article.
106 results