Ali G. Gharavi

Andover Eye Associates — United States

Medicine · Health Sciences

71h-index26.3kcitations319works3.32yr avg
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Research Topics

Renal Diseases and Glomerulopathies(149), Renal and related cancers(65), Genomics and Rare Diseases(44), Chronic Kidney Disease and Diabetes(39), Celiac Disease Research and Management(25)

Publications303 total

Interstitial cystitis: a phenotype and rare variant exome sequencing study
EBioMedicine·2026Open Access
Polygenic risk and rare variants in endotypes of idiopathic pulmonary fibrosis: a genetic analysis of population-based and case–control cohorts
The Lancet Respiratory Medicine·2026· 1 citedOpen Access
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral reflux
JCI Insight·2025Open Access
Atlas of Glomerular Disease-Specific Genetic Effects on Gene Regulation in Blood Empowers New Gene Discovery Studies
Journal of the American Society of Nephrology·2025
Genome-Wide Association Study for Idiopathic Nephrotic Syndrome Identifies Susceptibility Loci Across the Lifespan, Response to Therapy, and Genetic Ancestry
Journal of the American Society of Nephrology·2025
Dysregulation of the Th17 T-Follicular-Like Helper Cell: Naïve B Cell Interactions Enhance the Generation of IgA in IgAN
Journal of the American Society of Nephrology·2025
Analysis of the Coding Regions of 33,894 Individuals Identifies Known and Novel Gene Associations for Idiopathic Nephrotic Syndrome
Journal of the American Society of Nephrology·2025
CureGN Network's Return of Results Study: Participants' Experiences
Journal of the American Society of Nephrology·2025
Impact of Polygenic Scores on Kidney Failure Risk Prediction Models in IgAN
Journal of the American Society of Nephrology·2025
Genome-Wide Association Study (GWAS) of Serum Galactose-Deficient IgA1 Uncovers Shared Genetic Determinants with IgAN
Journal of the American Society of Nephrology·2025
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome
2025· 1 citedOpen Access
Polygenic Risk Score Predicts IgA Nephropathy Recurrence and Graft Failure in Kidney Transplant Recipients
American Journal of Transplantation·2025
CAKUT variants in <i>PRPF8, DYRK2</i> , and <i>CEP78</i> : implications for splicing and ciliogenesis
2025· 1 citedOpen Access
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Journal of Clinical Investigation·2025· 10 citedOpen Access
Family History in the Context of CKD
Journal of the American Society of Nephrology·2025· 3 cited
Interstitial Cystitis: a phenotype and rare variant exome sequencing study
2025Open Access
The paradox of eGFR trends and kidney failure incidence in patients without monogenic kidney disorders. Reply.
Journal of Clinical Investigation·2024Open Access
Genome-wide studies define new genetic mechanisms of IgA vasculitis
2024· 4 citedOpen Access
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy
Journal of the American Society of Nephrology·2024· 12 citedOpen Access
Enhanced Diagnostic Precision in APOL1-Mediated Kidney Disease with the p.N264K M1 Protective Variant
Journal of the American Society of Nephrology·2024
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Frequent Co-authors

Krzysztof Kiryluk(25), Jan Novák(16), Simone Sanna‐Cherchi(15), Francesco Scolari(14), Bruce A. Julian(14), Richard P. Lifton(13), Gian Marco Ghiggeri(12), Vivette D. D’Agati(12), Robert Wyatt(11), Yifu Li(9), Hitoshi Suzuki(8), Maddalena Marasà(8), Claudia Izzi(8), Loreto Gesualdo(8), Zina Moldoveanu(7), Pietro A. Canetta(7), Gerald B. Appel(7), Monica Bodria(7), Miguel Verbitsky(7), David Fasel(6)