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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 3
2006 4
2007 7
2008 5
2009 7
2010 4
2011 6
2012 1
2013 2
2014 1
2015 3
2016 2
2017 7
2018 4
2019 9
2020 7
2021 3
2022 5
2023 1
2024 0

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70 results

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Page 1
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: doyle b. 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.
A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS.
Lane BM, Murray S, Benson K, Bierzynska A, Chryst-Stangl M, Wang L, Wu G, Cavalleri G, Doyle B, Fennelly N, Dorman A, Conlon S, Vega-Warner V, Fermin D, Vijayan P, Qureshi MA, Shril S, Barua M, Hildebrandt F, Pollak M, Howell D, Sampson MG, Saleem M, Conlon PJ, Spurney R, Gbadegesin R. Lane BM, et al. Among authors: doyle b. J Am Soc Nephrol. 2021 Jul;32(7):1682-1695. doi: 10.1681/ASN.2020081234. Epub 2021 Apr 16. J Am Soc Nephrol. 2021. PMID: 33863784 Free PMC article.
Solitary renal mass in Waldenström macroglobulinemia.
Hamill M, Doyle B, Quinn J. Hamill M, et al. Among authors: doyle b. Clin Nephrol. 2021 Apr;95(4):221-223. doi: 10.5414/CN109945. Clin Nephrol. 2021. PMID: 33560218 No abstract available.
70 results