Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 May-Jun;35(3):423-424.
doi: 10.25259/IJN_802_2024. Epub 2025 Mar 11.

Clinical Application of Genetic Testing in Nephrology

Gladwin Jeemon  1 , J K Jayram  1 , Kartik Ganesh  1 , Jithin S Kumar  1 , Sunita Simon  1 , M Abi Abraham  1
Affiliations

Clinical Application of Genetic Testing in Nephrology

Gladwin Jeemon et al. Indian J Nephrol. 2025 May-Jun.
No abstract available

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest.

References

    1. Carminatti M, Tedesco-Silva H, Silva Fernandes N, Sanders-Pinheiro H. Chronic kidney disease progression in kidney transplant recipients: A focus on traditional risk factors. Nephrology (Carlton) 2019;24:141–7. doi: 10.1111/nep.13483. - DOI - PubMed
    1. Devarajan P, Chertow G, Susztak K, Levin A, Agarwal R, Stenvinkel P, et al. Emerging role of clinical genetics in CKD. Kidney Med. 2022;4:100435. doi: 10.1016/j.xkme.2022.100435. - DOI - PMC - PubMed
    1. Gast C, Pengelly R, Lyon M, Bunyan D, Seaby E, Graham N, et al. Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis. Nephrol Dial Transplant. 2016;31:961–70. doi: 10.1093/ndt/gfv325. - DOI - PubMed
    1. Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, et al. Whole-exome sequencing in adults with chronic kidney disease a pilot study. Ann Intern Med. 2018;168:100–9. doi: 10.7326/M17-1319. - DOI - PMC - PubMed
    1. Cameron-Christie S, Wolock C, Groopman E, Petrovski S, Kamalakaran S, Povysil G, et al. Exome-Based rare-Variant analyses in CKD. J Am Soc Nephrol. 2019;30:1109–22. doi: 10.1681/ASN.2018090909. - DOI - PMC - PubMed

LinkOut - more resources