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NPJ Digital Medicine|April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studiesNing Shang, Atlas Khan, Fernanda Polubriaginof, et al.Kidney International Reports|September 22, 2025
Rationale and Design of the International Prospective Study of CKD of Uncertain Etiology in Agricultural CommunitiesJill F Lebov, Daniel R Brooks, Anna Aceituno, et al.Clinical Journal of the American Society of Nephrology : CJASN|May 2, 2020
Identifying Outcomes Important to Patients with Glomerular Disease and Their CaregiversSimon A Carter, Talia Gutman, Charlotte Logeman, et al.Kidney International Reports|January 10, 2022
A Focus Group Study of Self-Management in Patients With Glomerular DiseaseSimon A Carter, Claris Teng, Talia Gutman, et al.Nature|January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalitiesLynn M Boyden, Murim Choi, Keith A Choate, et al.Kidney International Reports|March 11, 2020
APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and RationaleBarry I Freedman, Marva M Moxey-Mims, Amir A Alexander, et al.Journal of the American Society of Nephrology : JASN|March 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic DiagnosisDina F Ahram, Tze Y Lim, Juntao Ke, 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 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 43