• Skip to main content
  • Skip to header right navigation
  • Skip to site footer
  • Member Portal
  • Find a Nephrologist
IgA Nephropathy Foundation Logo
  • IgA Nephropathy Foundation Logo
  • About Us
        • MM About

          • About Us
          • Leadership Team
          • Board of Directors
          • Medical & Scientific Advisory Board
          • IgAN Go Global Network
        • MM About 2

          • Latest News, Media, and Tips
          • Our Partners
          • IgAN Ambassadors
          • Join The Newsletter
  • Events
        • Events

          • Calendar of Events
          • SPARK 2025
          • IgA Nephropathy Day
          • Rare Disease Day
  • Resources
        • MM – Resource 1

          • What is IgAN
          • Diagnosis
          • Understanding Your Lab Results
          • Understanding Your Biopsy
          • Understanding blood pressure and your kidneys
          • Treatment Options
        • MM – Resource 2

          • IgAN Info
          • Faces of IgAN
          • IgAN Risk Quiz
          • Asian IgAN Awareness Initiative
          • IgAN Cookbook
          • IgAN FAQs
        • MM – Resource 3

          • Support Options
          • Patient Aid
          • IgANCare Program
          • Learn About Insurance
          • Patient + Care Partner Support
          • The IgA Nephropathy Foundation Ambassador Program
          • Caregiver Resources
          • Pregnancy and Family Planning
        • MM – Resource 4

          • Learning & Resources
          • IgAN+ App
          • Tools & Resources
          • Mental Health
          • Podcasts
          • IgAN Nutrition
          • IgAN Recipes
          • The Foundation Pop-Up Store is Here — for 3 Weeks Only!
          • HCP Library
  • Research
        • MM Research

          • IgA Nephropathy Studies
          • IgA Nephropathy Research
          • Published Research Articles
        • MM Research 2

          • Clinical Trials
          • Considering a Clinical Trial?
          • View All Clinical Trials
  • Join
        • MM – Join 1

          • Become a Member
          • The IgA Nephropathy Foundation Ambassador Program
          • Ways to Give
          • Advocacy for IgAN
        • MM – Join 2

          • Join Our Newsletter
          • Patient Registry
  • Donate
  • IgANCare Program

History of IgAN

Written by: The IgAN Team
  • 58Share on Facebook
  • 13Share on Twitter
  • 51Share on Pinterest
  • 30Share on Reddit
  • 16Share on LinkedIn
  • 35Share on Email

Dr. Bruce Julian, Professor Emeritus at University of Alabama

BIO

Dr. Bruce A. Julian is Professor Emeritus in the Division of Nephrology, Department of Medicine, at the University of Alabama at Birmingham (UAB). His research interest in IgA nephropathy (IgAN) started in 1979 during his nephrology training at the University of Kentucky with collaborative studies with Dr. Robert J. Wyatt on the role of complement proteins in the disease. In 1980 he entered private practice in Lexington and in 1982 discovered a family with multiple members with biopsy-proven IgAN, indicating that genetic factors are important for development of the disease. He joined the faculty at UAB in 1984 to pursue investigations for the cause and clinical expression of IgAN. During his 36 years at UAB, he has collaborated with many scientists at UAB, University of Tennessee, Memphis, and Columbia University in the US and in the Czech Republic, France, England, Italy, The Netherlands, China, and Japan. The research sought to define the genetic influences in the disease and the unique structural characteristics of the IgA protein in the blood and kidneys of patients with IgAN. Based on the results of these studies, the UAB IgA Nephropathy Research team in 2011 proposed a multi- step process for the development of IgAN that has become the blueprint for testing new approaches for the treatment of the disease.

In 1987 Dr. Julian was a founding member of the IgA Nephropathy Club that later expanded to become the International IgA Nephropathy Network to organize multiple international symposia for researchers to discuss their recent studies and exchange ideas. He was a member of the international group of nephrologists and pathologists that developed the Oxford Classification of the pathology features of IgAN. In 2013 Dr. Julian received the UAB Max Cooper Award for Excellence in Research. In 2015 he co-founded Reliant Glycosciences, LLC, a biotechnology company focused on the development of biomarker assays for IgAN. Dr. Julian has published 145 papers and 18 book chapters on IgAN.

SESSION DESCRIPTION

History of discovery, research and treatment of IgA Nephropathy

  • 58Share on Facebook
  • 13Share on Twitter
  • 51Share on Pinterest
  • 30Share on Reddit
  • 16Share on LinkedIn
  • 35Share on Email
Category: Resources

Return to The Blog

About The IgAN Team

Previous Post:Transplant Process & Living With Your Transplant Q&A
Next Post:Thriving Through Food
Donate
  • Facebook
  • Twitter
  • Instagram
  • YouTube

Quick Links

  • About Us
  • Financials
  • Patient Resources
  • Research
  • Contact Us
  • Join Our Efforts
  • Privacy Policy

Contact Us

(848) 298-4618

PO Box 1322 Wall, NJ 07719

© 2025 All Rights Reserved.

IgAN Foundation Newsletter

Subscribe to our newsletter below!

First Name
Last Name
Enter your email address

No thanks, I’m not interested!

References

  • Hall, Y.N., Fuentes, E.F., Chertow, G.M. et al. Race/ethnicity and disease severity in IgA nephropathy. BMC Nephrol 5, 10 (2004). https://doi.org/10.1186/1471-2369-5-10
  • Kiryluk K, Li Y, Sanna-Cherchi S, Rohanizadegan M, Suzuki H, et al. (2012) Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis. PLoS Genet 8(6): e1002765. doi:10.1371/journal.pgen.1002765