Rasheed Adebayo Gbadegesin, MBBS

Professor of Pediatrics
Wilburt C. Davison Distinguished Professor
Associate Dean for Physician-Scientist Development
Director of the Office of Physician-Science Development in the School of Medicine
Professor in Medicine
Affiliate of Duke Molecular Physiology Institute
Campus mail Box 3959 Med Ctr, Durham, NC 27710
Phone (919) 684-4246
Email address rasheed.gbadegesin@duke.edu

Molecular genetics of glomerular disease
Genetic risk factors for childhood onset idiopathic nephrotic syndrome

Education and Training

  • Pediatric Nephrology Fellow, Pediatrics, University of Michigan, Ann Arbor, 2004 - 2007
  • Pediatric Resident, Pediatrics, New York Presbyterian Hospital, 2002 - 2004
  • Pediatric Resident, Pediatrics, University of Ibadan, College of Medicine (Nigeria), 1989 - 1995
  • Medical Officer, National Service, University of Ibadan, College of Medicine (Nigeria), 1988 - 1989
  • Intern, Med/Surg/Peds/Ob Gyn, University of Ibadan, College of Medicine (Nigeria), 1987 - 1988
  • M.B.B.S., University of Ibadan, College of Medicine (Nigeria), 1987

Grants

Publications

Bomback, Andrew S., Gerald B. Appel, Debbie S. Gipson, Michelle A. Hladunewich, Richard Lafayette, Carla M. Nester, Samir V. Parikh, et al. “Improving Clinical Trials for Anticomplement Therapies in Complement-Mediated Glomerulopathies: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.” In Am J Kidney Dis, 79:570–81, 2022. https://doi.org/10.1053/j.ajkd.2021.07.025.

PMID
34571062
Full Text

Lane, Brandon M., Megan Chryst-Stangl, Guanghong Wu, Mohamed Shalaby, Sherif El Desoky, Claire C. Middleton, Kinsie Huggins, et al. “Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis.” Jci Insight 7, no. 2 (January 25, 2022). https://doi.org/10.1172/jci.insight.152102.

PMID
34874915
Full Text

Kumar, Reeti, Vahakn Keskinyan, Megan Chryst Stangl, Brandon M. Lane, Anne F. Buckley, Laura Barisoni, David N. Howell, and Rasheed A. Gbadegesin. “Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping.” Front Pediatr 10 (2022): 826330. https://doi.org/10.3389/fped.2022.826330.

PMID
35295700
Full Text

Adeyemo, Adebowale A., Daniel Shriner, Amy R. Bentley, Rasheed A. Gbadegesin, and Charles N. Rotimi. “Evolutionary genetics and acclimatization in nephrology.” Nat Rev Nephrol 17, no. 12 (December 2021): 827–39. https://doi.org/10.1038/s41581-021-00483-7.

PMID
34584272
Full Text

Wine, R., J. Vasilevska-Ristovska, T. Banh, J. Knott, D. Noone, R. Gbadegesin, T. O. Ilori, et al. “Trends in the epidemiology of childhood nephrotic syndrome in Africa: A systematic review.” Global Epidemiology 3 (November 1, 2021). https://doi.org/10.1016/j.gloepi.2021.100061.

Full Text

Shaw, Brian I., Alejandro Ochoa, Cliburn Chan, Chloe Nobuhara, Rasheed Gbadegesin, Annette M. Jackson, and Eileen T. Chambers. “HLA Loci and Recurrence of Focal Segmental Glomerulosclerosis in Pediatric Kidney Transplantation.” Transplant Direct 7, no. 10 (October 2021): e748. https://doi.org/10.1097/TXD.0000000000001201.

PMID
34476293
Full Text

Krissberg, Jill R., Margaret E. Helmuth, Salem Almaani, Yi Cai, Daniel Cattran, Debanjana Chatterjee, Rasheed A. Gbadegesin, et al. “Racial-ethnic differences in health-related quality of life among adults and children with glomerular disease.” Glomerular Dis 1, no. 3 (August 2021): 105–17. https://doi.org/10.1159/000516832.

PMID
34723246
Full Text

Johnson, Kimberly S., Rasheed Gbadegesin, Amanda E. McMillan, Stephanie Molner, L Ebony Boulware, and Laura P. Svetkey. “Diversifying the Research Workforce as a Programmatic Priority for a Career Development Award Program at Duke University.” Acad Med 96, no. 6 (June 1, 2021): 836–41. https://doi.org/10.1097/ACM.0000000000004002.

PMID
34031305
Full Text

McElvaine, Allison T., Jacqueline A. Hawkins-Salsbury, Vineet M. Arora, Mark T. Gladwin, James R. Goldenring, David P. Huston, Deborah Krakow, et al. “Innovations in MD-only physician-scientist training: experiences from the Burroughs Wellcome Fund physician-scientist institutional award initiative.” J Clin Invest 131, no. 10 (May 17, 2021). https://doi.org/10.1172/JCI149948.

PMID
33998594
Full Text

Lane, Brandon M., Susan Murray, Katherine Benson, Agnieszka Bierzynska, Megan Chryst-Stangl, Liming Wang, Guanghong Wu, et al. “A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS.” J Am Soc Nephrol, April 16, 2021. https://doi.org/10.1681/ASN.2020081234.

PMID
33863784
Full Text

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