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

Publications

Hall, G, Lane, BM, Khan, K, Pediaditakis, I, Xiao, J, Wu, G, Wang, L, Kovalik, ME, Chryst-Stangl, M, Davis, EE, Spurney, RF, and Gbadegesin, RA. "The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes." Journal of the American Society of Nephrology : Jasn 29, no. 8 (August 2018): 2110-2122.

PMID
30002222
Full Text

Pelletier, JH, Kumar, KR, Engen, R, Bensimhon, A, Varner, JD, Rheault, MN, Srivastava, T, Straatmann, C, Silva, C, Davis, TK, Wenderfer, SE, Gibson, K, Selewski, D, Barcia, J, Weng, P, Licht, C, Jawa, N, Kallash, M, Foreman, JW, Wigfall, DR, Chua, AN, Chambers, E, Hornik, CP, Brewer, ED, Nagaraj, SK, Greenbaum, LA, and Gbadegesin, RA. "Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings." Pediatric Nephrology (Berlin, Germany) (July 7, 2018).

PMID
29982878
Full Text

Adeyemo, A, Esezobor, C, Solarin, A, Abeyagunawardena, A, Kari, JA, El Desoky, S, Greenbaum, LA, Kamel, M, Kallash, M, Silva, C, Young, A, Hunley, TE, de Jesus-Gonzalez, N, Srivastava, T, and Gbadegesin, R. "HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome." American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation 71, no. 3 (March 2018): 399-406.

PMID
29277510
Full Text

Pelletier, J, Gbadegesin, R, and Staples, B. "Renal Tubular Acidosis." Pediatrics in Review 38, no. 11 (November 2017): 537-539.

Full Text

Karp, AM, and Gbadegesin, RA. "Genetics of childhood steroid-sensitive nephrotic syndrome." Pediatric Nephrology (Berlin, Germany) 32, no. 9 (September 2017): 1481-1488. (Review)

PMID
27470160
Full Text

Pelletier, JH, Nagaraj, S, Gbadegesin, R, Wigfall, D, McGann, KA, and Foreman, J. "Neutropenic enterocolitis (typhlitis) in a pediatric renal transplant patient. A case report and review of the literature." Pediatric transplantation 21, no. 6 (September 2017).

PMID
28664544
Full Text

Selewski, DT, Troost, JP, Cummings, D, Massengill, SF, Gbadegesin, RA, Greenbaum, LA, Shatat, IF, Cai, Y, Kapur, G, Hebert, D, Somers, MJ, Trachtman, H, Pais, P, Seifert, ME, Goebel, J, Sethna, CB, Mahan, JD, Gross, HE, Herreshoff, E, Liu, Y, Carlozzi, NE, Reeve, BB, DeWalt, DA, and Gipson, DS. "Responsiveness of the PROMIS® measures to changes in disease status among pediatric nephrotic syndrome patients: a Midwest pediatric nephrology consortium study." Health and Quality of Life Outcomes 15, no. 1 (August 23, 2017): 166-null.

PMID
28835233
Full Text

Hall, G, Routh, JC, and Gbadegesin, RA. "Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype." American journal of kidney diseases : the official journal of the National Kidney Foundation 70, no. 1 (July 2017): 8-10.

PMID
28456345
Full Text

Tokhmafshan, F, Brophy, PD, Gbadegesin, RA, and Gupta, IR. "Vesicoureteral reflux and the extracellular matrix connection." Pediatric nephrology (Berlin, Germany) 32, no. 4 (April 2017): 565-576. (Review)

PMID
27139901
Full Text

Hall, G, Lane, B, Chryst-Ladd, M, Wu, G, Lin, J-J, Qin, X, Hauser, ER, and Gbadegesin, R. "Dysregulation of WTI (-KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation." Scientific Reports 7 (January 6, 2017): 39933-null.

PMID
28059119
Full Text

Pages