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Rasheed Adebayo Gbadegesin, MBBS

Professor of Pediatrics
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 at 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

Selected Grants and Awards

Publications

Tokhmafshan, Fatima, Jasmine El Andalousi, Vasikar Murugapoopathy, Marie-Lyne Fillion, Sarah Campillo, John-Paul Capolicchio, Roman Jednak, et al. “Children with vesico-ureteric reflux have joint hypermobility and occasional TNXB sequence variants.” Can Urol Assoc J, November 5, 2019. https://doi.org/10.5489/cuaj.6068.

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Sood, S., A. O. Ojo, D. Adu, K. Kannan, A. Ghassabian, T. Koshy, S. M. Vento, et al. “Association Between Perfluoroalkyl Substance Exposure and Renal Function in Children With CKD Enrolled in H3Africa Kidney Disease Research Network.” Kidney International Reports 4, no. 11 (November 1, 2019): 1641–45. https://doi.org/10.1016/j.ekir.2019.07.017.

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Bensimhon, Adam R., Anna E. Williams, and Rasheed A. Gbadegesin. “Treatment of steroid-resistant nephrotic syndrome in the genomic era.” Pediatr Nephrol 34, no. 11 (November 2019): 2279–93. https://doi.org/10.1007/s00467-018-4093-1.

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Chambers, Eileen Tsai, and Rasheed A. Gbadegesin. “Aberrant IgM on T cells: biomarker or pathogenic factor in childhood nephrotic syndrome?” Kidney Int 96, no. 4 (October 2019): 818–20. https://doi.org/10.1016/j.kint.2019.05.031.

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Blew, Kathryn H., Annabelle Chua, John Foreman, Rasheed Gbadegesin, Annette Jackson, Shashi Nagaraj, Rebecca Sadun, Del Wigfall, Allan D. Kirk, and Eileen T. Chambers. “Tailored use of belatacept in adolescent kidney transplantation.” Am J Transplant, September 24, 2019. https://doi.org/10.1111/ajt.15611.

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Hurst, Jillian H., Katherine J. Barrett, Matthew S. Kelly, Betty B. Staples, Kathleen A. McGann, Coleen K. Cunningham, Ann M. Reed, Rasheed A. Gbadegesin, and Sallie R. Permar. “Cultivating Research Skills During Clinical Training to Promote Pediatric-Scientist Development.” Pediatrics 144, no. 2 (August 2019). https://doi.org/10.1542/peds.2019-0745.

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Dufek, Stephanie, Chris Cheshire, Adam P. Levine, Richard S. Trompeter, Naomi Issler, Matthew Stubbs, Monika Mozere, et al. “Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.” J Am Soc Nephrol 30, no. 8 (August 2019): 1375–84. https://doi.org/10.1681/ASN.2018101054.

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Zahr, Rima S., Marianne E. Yee, Jack Weaver, Katherine Twombley, Raed Bou Matar, Diego Aviles, Rajasree Sreedharan, et al. “Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study.” Pediatr Nephrol 34, no. 8 (August 2019): 1435–45. https://doi.org/10.1007/s00467-019-04237-3.

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Hall, Gentzon, Sidharth K. Sethi, Brandon M. Lane, Matthew G. Sampson, Olivia G. Gregory, Maria E. Kovalik, Megan Chryst-Stangl, et al. “A NOVEL HETEROZYGOUS MISSENSE MUTATION OF WILMS' TUMOR 1 MAY CAUSE FSGS THROUGH DYSREGULATED EXPRESSION OF ARHGAP24.” In Nephrology Dialysis Transplantation, Vol. 34. OXFORD UNIV PRESS, 2019.

Scholars@Duke

Hall, Gentzon, G Michelle Ducasa, Brandon M. Lane, Max Lagas, Maria E. Kovalik, Olivia G. Gregory, Guanghong Wu, et al. “THE LMX1 beta R246Q MUTATION INDUCES PODOCYTE INJURY THROUGH DYSREGULATION OF CHOLESTEROL TRANSPORT GENE EXPRESSION.” In Nephrology Dialysis Transplantation, Vol. 34. OXFORD UNIV PRESS, 2019.

Scholars@Duke

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