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Medicine

D-Index
73
Citations
22071
World Ranking
19604
National Ranking
9761

Overview

Ali G. Gharavi is affiliated with Columbia University in the United States. Their research primarily focuses on medicine, with significant contributions in biochemistry, genetics, and molecular biology.

The scientist's work spans several key subfields, including genetics, nephrology, molecular biology, immunology, and pediatrics, perinatology, and child health. Their main topics of study concentrate on renal diseases and glomerulopathies, genomics and rare diseases, renal and related cancers, chronic kidney disease and diabetes, BRCA gene mutations in cancer, celiac disease research and management, and genetic associations and epidemiology.

Recent notable publications by Ali G. Gharavi include:

  • Kidney Biopsy Findings in Patients with COVID-19 (2020) in the Journal of the American Society of Nephrology
  • Presentation and Outcomes of Patients with ESKD and COVID-19 (2020) in the Journal of the American Society of Nephrology
  • The All of Us Research Program: Data quality, utility, and diversity (2022) in Patterns
  • Acute Kidney Injury Due to Collapsing Glomerulopathy Following COVID-19 Infection (2020) in Kidney International Reports
  • Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference (2022) in Kidney International

The scientist frequently collaborates with several co-authors, including:

  • Krzysztof Kiryluk
  • Simone Sanna-Cherchi
  • Maddalena Marasà
  • Atlas Khan
  • Hila Milo Rasouly

Ali G. Gharavi's research appears regularly in specific publication venues, with the highest number of publications in the Journal of the American Society of Nephrology. Other frequent venues include bioRxiv (Cold Spring Harbor Laboratory), Kidney International Reports, American Journal of Kidney Diseases, and Genetics in Medicine.

Best Publications

  • Molecular Mechanisms of Human Hypertension

    Richard P. Lifton;Ali G. Gharavi;Ali G. Gharavi;David S. Geller

  • Genetic studies of body mass index yield new insights for obesity biology

    Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice

  • The Pathophysiology of IgA Nephropathy

    Hitoshi Suzuki;Krzysztof Kiryluk;Jan Novak;Zina Moldoveanu

  • Diagnostic Utility of Exome Sequencing for Kidney Disease

    Emily E Groopman;Maddalena Marasa;Sophia Cameron-Christie;Slavé Petrovski

  • Genome-wide association study identifies susceptibility loci for IgA nephropathy

    Ali G Gharavi;Krzysztof Kiryluk;Murim Choi;Yifu Li

  • Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

    Krzysztof Kiryluk;Yifu Li;Francesco Scolari;Simone Sanna-Cherchi

  • Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

    Lynn M. Boyden;Murim Choi;Keith A. Choate;Carol J. Nelson-Williams

  • IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

    Ali G. Gharavi;Ali G. Gharavi;Yan Yan;Francesco Scolari;F. Paolo Schena

  • Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis

    Krzysztof Kiryluk;Yifu Li;Simone Sanna-Cherchi;Simone Sanna-Cherchi;Mersedeh Rohanizadegan

  • Kidney Biopsy Findings in Patients with COVID-19.

    Satoru Kudose;Ibrahim Batal;Dominick Santoriello;Katherine Xu

  • Current Understanding of the Role of Complement in IgA Nephropathy

    Nicolas Maillard;Nicolas Maillard;Robert J. Wyatt;Bruce A. Julian;Krzysztof Kiryluk

  • Presentation and Outcomes of Patients with ESKD and COVID-19.

    Anthony M Valeri;Shelief Y Robbins-Juarez;Jacob S Stevens;Wooin Ahn

  • Aberrant IgA1 Glycosylation Is Inherited in Familial and Sporadic IgA Nephropathy

    Ali G. Gharavi;Zina Moldoveanu;Robert J. Wyatt;Catherine V. Barker

  • Mutations in SEC63 cause autosomal dominant polycystic liver disease.

    Sonia Davila;Sonia Davila;Laszlo Furu;Ali G Gharavi;Xin Tian

  • Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch–Schönlein purpura nephritis

    Krzysztof Kiryluk;Zina Moldoveanu;John T. Sanders;John T. Sanders;T. Matthew Eison;T. Matthew Eison

  • The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression

    Na Zhao;Ping Hou;Jicheng Lv;Zina Moldoveanu

  • Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

    Simone Sanna-Cherchi;Krzysztof Kiryluk;Katelyn E. Burgess;Monica Bodria

  • Acute Kidney Injury Due to Collapsing Glomerulopathy Following COVID-19 Infection.

    Yonatan Peleg;Satoru Kudose;Vivette D’Agati;Eric Siddall

  • The copy number variation landscape of congenital anomalies of the kidney and urinary tract

    Miguel Verbitsky;Rik Westland;Alejandra Perez;Krzysztof Kiryluk

  • Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.

    Sneh Lata;Maddalena Marasa;Yifu Li;David A Fasel

Frequent Co-Authors

Jan Novak
Jan Novak University of Alabama at Birmingham
Bruce A. Julian
Bruce A. Julian University of Alabama at Birmingham
Richard P. Lifton
Richard P. Lifton Rockefeller University
Vivette D. D'Agati
Vivette D. D'Agati Columbia University
Gian Marco Ghiggeri
Gian Marco Ghiggeri Istituto Giannina Gaslini
Chunhua Weng
Chunhua Weng Columbia University
David Goldstein
David Goldstein University of New South Wales
Loreto Gesualdo
Loreto Gesualdo University of Bari Aldo Moro
Zina Moldoveanu
Zina Moldoveanu University of Alabama at Birmingham
Wendy K. Chung
Wendy K. Chung Columbia University

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