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Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.Proteomics. Clinical Applications|November 2, 2016
Sample preparation method considerations for integrated transcriptomic and proteomic analysis of tumorsAnupama Rajan Bhat, Manoj Kumar Gupta, Priya Krithivasan, et al.JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.Journal of the Endocrine Society|June 8, 2026
Genome sequencing identifies monogenic causes in adults with metabolic diseasesVolkan Okur, Amanda Marcus, John N Falcone, et al.The New England Journal of Medicine|December 27, 2018
Diagnostic Utility of Exome Sequencing for Kidney DiseaseEmily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, et al.Nature Communications|November 11, 2022
Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traitsLili Liu, Atlas Khan, Elena Sanchez-Rodriguez, et al.American Journal of Human Genetics|November 4, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.Journal of the American Society of Nephrology : JASN|February 18, 2021
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral RefluxMiguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, 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.Pageof 2