Ali G. Gharavi

Ali G. Gharavi

Nephrology

1150 St. Nicholas Avenue
New York, NY 10032

Last Updated: 09/26/2026

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Found 164 publications

Critically Ill Children Frequently Receive Medications with Established but Unused Pharmacogenomic Guidelines: Actionable Findings from an Integrated Electronic Medical Record and Exome Sequencing Study.

Critically Ill Children Frequently Receive Medications with Established but Unused Pharmacogenomic Guidelines: Actionable Findings from an Integrated Electronic Medical Record and Exome Sequencing Study.

Journal: medRxiv : the preprint server for health sciences

Published: July 29, 2026

Mapping Genetic Susceptibility to Urinary Tract Infection from Kidney Papilla to Bladder.

Mapping Genetic Susceptibility to Urinary Tract Infection from Kidney Papilla to Bladder.

Journal: medRxiv : the preprint server for health sciences

Published: July 17, 2026

Inherited Susceptibility to Urinary Tract Infections from Kidney Papilla to Bladder.

Inherited Susceptibility to Urinary Tract Infections from Kidney Papilla to Bladder.

Journal: medRxiv : the preprint server for health sciences

Published: July 17, 2026

Atlas of glomerular disease-specific genetic effects on blood transcriptome.

Atlas of glomerular disease-specific genetic effects on blood transcriptome.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy.

Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy.

Journal: The Journal of clinical investigation

Published: June 15, 2026

Primary Glomerular Diseases in the Elderly: Clinical Features, Treatment Patterns, and Outcomes in the CureGN Cohort.

Primary Glomerular Diseases in the Elderly: Clinical Features, Treatment Patterns, and Outcomes in the CureGN Cohort.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: March 26, 2026

Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant.

Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant.

Journal: JAMA network open

Published: March 11, 2026

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Journal: Nature communications

Published: October 09, 2025

Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome.

Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: September 19, 2025

Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral reflux.

Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral reflux.

Journal: JCI insight

Published: September 02, 2025

CAKUT variants in PRPF8, DYRK2, and CEP78: implications for splicing and ciliogenesis.

CAKUT variants in PRPF8, DYRK2, and CEP78: implications for splicing and ciliogenesis.

Journal: bioRxiv : the preprint server for biology

Published: August 08, 2025

Interstitial cystitis: a phenotype and rare variant exome sequencing study.

Interstitial cystitis: a phenotype and rare variant exome sequencing study.

Journal: EBioMedicine

Published: August 06, 2025

Showing 1-12 of 164

Last Updated: 09/26/2026