Education and Training
- Nephrology Fellowship, Medicine, Duke University School of Medicine, 2011 - 2015
- Internal Medicine Residency, Medicine, Duke University School of Medicine, 2007 - 2010
- MD./PhD., University of Maryland - Baltimore, 2007
Gbadegesin, RA, Hall, G, Adeyemo, A, Hanke, N, Tossidou, I, Burchette, J, Wu, G, Homstad, A, Sparks, MA, Gomez, J, Jiang, R, Alonso, A, Lavin, P, Conlon, P, Korstanje, R, Stander, MC, Shamsan, G, Barua, M, Spurney, R, Singhal, PC, Kopp, JB, Haller, H, Howell, D, Pollak, MR, Shaw, AS, Schiffer, M, and Winn, MP. "Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS." Journal of the American Society of Nephrology : Jasn 25, no. 9 (September 2014): 1991-2002.
Hall, G, Rowell, J, Farinelli, F, Gbadegesin, RA, Lavin, P, Wu, G, Homstad, A, Malone, A, Lindsey, T, Jiang, R, Spurney, R, Tomaselli, GF, Kass, DA, and Winn, MP. "Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity." American Journal of Physiology Renal Physiology 306, no. 12 (June 2014): F1442-F1450.
Malone, AF, Phelan, PJ, Hall, G, Cetincelik, U, Homstad, A, Alonso, AS, Jiang, R, Lindsey, TB, Wu, G, Sparks, MA, Smith, SR, Webb, NJA, Kalra, PA, Adeyemo, AA, Shaw, AS, Conlon, PJ, Jennette, JC, Howell, DN, Winn, MP, and Gbadegesin, RA. "Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis." Kidney International 86, no. 6 (January 1, 2014): 1253-1259.
Gbadegesin, RA, Brophy, PD, Adeyemo, A, Hall, G, Gupta, IR, Hains, D, Bartkowiak, B, Rabinovich, CE, Chandrasekharappa, S, Homstad, A, Westreich, K, Wu, G, Liu, Y, Holanda, D, Clarke, J, Lavin, P, Selim, A, Miller, S, Wiener, JS, Ross, SS, Foreman, J, Rotimi, C, and Winn, MP. "TNXB mutations can cause vesicoureteral reflux." J Am Soc Nephrol 24, no. 8 (July 2013): 1313-1322.
"CORRECTION." Journal of the American Society of Nephrology 24, no. 1 (January 1, 2013): 160-160.
Gbadegesin, RA, Lavin, PJ, Hall, G, Bartkowiak, B, Homstad, A, Jiang, R, Wu, G, Byrd, A, Lynn, K, Wolfish, N, Ottati, C, Stevens, P, Howell, D, Conlon, P, and Winn, MP. "Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis." Kidney International 81, no. 1 (January 2012): 94-99.
Luo, X, Hall, G, Li, S, Bird, A, Lavin, PJ, Winn, MP, Kemper, AR, Brown, TT, and Koeberl, DD. "Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector." Molecular Therapy : the Journal of the American Society of Gene Therapy 19, no. 11 (November 2011): 1961-1970.
Eckel, J, Lavin, PJ, Finch, EA, Mukerji, N, Burch, J, Gbadegesin, R, Wu, G, Bowling, B, Byrd, A, Hall, G, Sparks, M, Zhang, ZS, Homstad, A, Barisoni, L, Birbaumer, L, Rosenberg, P, and Winn, MP. "TRPC6 enhances angiotensin II-induced albuminuria." J Am Soc Nephrol 22, no. 3 (March 2011): 526-535.
Rogers, TB, Pati, S, Gaa, S, Riley, D, Khakoo, AY, Patel, S, Wardlow, RD, Frederick, CA, Hall, G, He, L-P, and Lederer, WJ. "Mesenchymal stem cells stimulate protective genetic reprogramming of injured cardiac ventricular myocytes." Journal of molecular and cellular cardiology 50, no. 2 (February 2011): 346-356.
Hall, G, Hasday, JD, and Rogers, TB. "Regulating the regulator: NF-kappaB signaling in heart." Journal of Molecular and Cellular Cardiology 41, no. 4 (October 2006): 580-591. (Review)