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

Year Number of Results
1996 1
1998 1
1999 2
2000 1
2001 1
2002 5
2003 2
2004 6
2005 3
2006 2
2007 1
2008 3
2009 1
2010 2
2011 1
2012 5
2013 2
2014 2
2015 7
2016 6
2017 7
2018 2
2019 4
2020 9
2021 11
2022 6
2023 6
2024 7
2025 6
2026 0

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98 results

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Page 1
Diagnosis of monogenic chronic kidney diseases.
Armstrong ME, Thomas CP. Armstrong ME, et al. Among authors: thomas cp. Curr Opin Nephrol Hypertens. 2019 Mar;28(2):183-194. doi: 10.1097/MNH.0000000000000486. Curr Opin Nephrol Hypertens. 2019. PMID: 30601180 Review.
Educating the Next-Generation Expert in Nephrology Genetics.
Lanktree MB, Shurrab S, Ejaz R, McNiven V, Brick L, Selvathesan N, Margetts P, Gangji A, Pigeyre M, Chang A, Thomas CP, Lemaire M. Lanktree MB, et al. Among authors: thomas cp. Semin Nephrol. 2025 Sep;45(5):151648. doi: 10.1016/j.semnephrol.2025.151648. Epub 2025 Jul 15. Semin Nephrol. 2025. PMID: 40670224 Free article. Review.
Managing the Costs of Routine Follow-up Care After Living Kidney Donation: a Review and Survey of Contemporary Experience, Practices, and Challenges.
Lentine KL, Sarabu N, McNatt G, Howey R, Hays R, Thomas CP, Lebron-Banks U, Ohler L, Wooley C, Wisniewski A, Xiao H, Tietjen A. Lentine KL, et al. Among authors: thomas cp. Curr Transplant Rep. 2022;9(4):328-335. doi: 10.1007/s40472-022-00379-w. Epub 2022 Sep 22. Curr Transplant Rep. 2022. PMID: 36187071 Free PMC article. Review.
Evaluation for genetic disease in kidney transplant candidates: A practice resource.
Ames EG, Anand PM, Bekheirnia MR, Doshi MD, El Ters M, Freese ME, Gbadegesin RA, Guay-Woodford LM, Java A, Ranch D, Rodig NM, Wang X, Thomas CP. Ames EG, et al. Among authors: thomas cp. Am J Transplant. 2025 Feb;25(2):237-249. doi: 10.1016/j.ajt.2024.10.019. Epub 2024 Oct 31. Am J Transplant. 2025. PMID: 39488252 Free article. Review.
Suspected Autosomal Recessive Polycystic Kidney Disease but Cerebellar Vermis Hypoplasia, Oligophrenia Ataxia, Coloboma, and Hepatic Fibrosis (COACH) Syndrome in Retrospect, A Delayed Diagnosis Aided by Genotyping and Reverse Phenotyping: A Case Report and A Review of the Literature.
Sambharia M, Freese ME, Donato F, Bathla G, Abukhiran IMM, Dantuma MI, Mansilla MA, Thomas CP. Sambharia M, et al. Among authors: thomas cp. Nephron. 2024;148(4):264-272. doi: 10.1159/000527991. Epub 2023 Jan 6. Nephron. 2024. PMID: 36617405 Review.
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma.
Ma M, Ganapathi M, Zheng Y, Tan KL, Kanca O, Bove KE, Quintanilla N, Sag SO, Temel SG, LeDuc CA, McPartland AJ, Pereira EM, Shen Y, Hagen J, Thomas CP, Nguyen Galván NT, Pan X, Lu S, Rosenfeld JA, Calame DG, Wangler MF, Lupski JR, Pehlivan D, Hertel PM, Chung WK, Bellen HJ. Ma M, et al. Among authors: thomas cp. Genet Med. 2024 Jul;26(7):101125. doi: 10.1016/j.gim.2024.101125. Epub 2024 Mar 21. Genet Med. 2024. PMID: 38522068 Free PMC article.
98 results