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Genetic testing for kidney disease of unknown etiology.
Hays T, Groopman EE, Gharavi AG. Hays T, et al. Among authors: gharavi ag. Kidney Int. 2020 Sep;98(3):590-600. doi: 10.1016/j.kint.2020.03.031. Epub 2020 Apr 24. Kidney Int. 2020. PMID: 32739203 Free PMC article. Review.
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.
Sanna-Cherchi S, Burgess KE, Nees SN, Caridi G, Weng PL, Dagnino M, Bodria M, Carrea A, Allegretta MA, Kim HR, Perry BJ, Gigante M, Clark LN, Kisselev S, Cusi D, Gesualdo L, Allegri L, Scolari F, D'Agati V, Shapiro LS, Pecoraro C, Palomero T, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: gharavi ag. Kidney Int. 2011 Aug;80(4):389-96. doi: 10.1038/ki.2011.148. Epub 2011 Jun 22. Kidney Int. 2011. PMID: 21697813 Free article.
Diagnosing kidney disease in the genetic era.
Prakash S, Gharavi AG. Prakash S, et al. Among authors: gharavi ag. Curr Opin Nephrol Hypertens. 2015 Jul;24(4):380-7. doi: 10.1097/MNH.0000000000000139. Curr Opin Nephrol Hypertens. 2015. PMID: 26050126 Review.
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, Rasouly H, Mitrotti A, Westland R, Verbitsky M, Nestor J, Slater LM, D'Agati V, Zaniew M, Materna-Kiryluk A, Lugani F, Caridi G, Rampoldi L, Mattoo A, Newton CA, Rao MK, Radhakrishnan J, Ahn W, Canetta PA, Bomback AS, Appel GB, Antignac C, Markowitz GS, Garcia CK, Kiryluk K, Sanna-Cherchi S, Gharavi AG. Lata S, et al. Among authors: gharavi ag. Ann Intern Med. 2018 Jan 16;168(2):100-109. doi: 10.7326/M17-1319. Epub 2017 Dec 5. Ann Intern Med. 2018. PMID: 29204651 Free PMC article.
165 results