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Medrxiv : the Preprint Server for Health Sciences|August 14, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney diseaseYask Gupta, David J Friedman, Michelle McNulty, et al.Nature Genetics|December 23, 2018
The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.Nature Genetics|March 1, 2019
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.Nature Communications|August 7, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.Nature Communications|April 2, 2020
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosisJingyuan Xie, Lili Liu, Nikol Mladkova, et al.Nature Genetics|June 19, 2023
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathyKrzysztof Kiryluk, Elena Sanchez-Rodriguez, Xu-Jie Zhou, et al.Pageof 4