Reith RM, McKenna J, Wu H, Hashmi SS, Cho SH, Dash PK, Gambello MJ.  Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex. Neurobiology of Disease. 2013 Mar;51:93-103.

Sen S, Kundu BK, Wu HC, Hashmi SS, Guthrie P, Locke LW, Roy RJ, Matherne GP, Berr SS, Terwelp M, Scott B, Carranza S, Frazier OH, Glover DK, Dillman WH, Gambello MJ, Entman ML, Taegtmeyer H. Glucose regulation of load-induced mTOR signaling and ER stress in mammalian heart. J Am Heart Assoc. 2013 May 17;2(3):e004796.

Barnes AM, Duncan G, Weis M, Paton W, Cabral WA, Mertz EL, Makareeva E, Gambello MJ, Lacbawan FL, Leikin S, Fertala A, Eyre DR, Bale SJ, Marini JC.  Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations. Hum Mutat. 2013 Sep;34(9):1279-88.

Carter RD, Raia M, Ewing-Cobbs L, Gambello M, Hashmi SS, Peterson SK, Robbins-Furman P, Potocki L.  Stress and well-being among parents of children with Potocki-Lupski syndrome. J Genet Couns. 2013 Oct;22(5):633-42.

Mietzsch U, McKenna J 3rd, Reith RM, Way SW, Gambello MJ. Comparative analysis of Tsc1 and Tsc2 single and double radial glial cell mutants. J Comp Neurol. 2013 Nov. 521(16):3817-31.


Way SW, Rozas NS, Wu HC, McKenna J 3rd, Reith RM, Hashmi SS, Dash PK, Gambello MJ.  The differential effects of prenatal and/or postnatal rapamycin on neurodevelopmental defects and cognition in a neuroglial mouse model of tuberous sclerosis complex. Human Molecular Genetics. 2012 Jul 15;21(14):3226-36.


Reith RM, Way S, McKenna J 3rd, Haines K, Gambello MJ.  Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration. Neurobiology of Disease. 2011 Jul;43(1):113-22.


Way SW, McKenna J 3rd, Mietzsch U, Reith RM, Wu HC, Gambello MJ.  Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse.  Human Molecular Genetics. 2009 Apr 1; 18(7):1252-65.


Hernandez O, Way S, McKenna J 3rd, Gambello MJ.  Generation of a conditional disruption of the Tsc2 gene. Genesis. 2007 Feb; 45(2):101-6.