Selected Publications 

Chang BS, Lowenstein DH. Epilepsy. N Engl J Med 2003;349:1257-66. 

Chang BS, Piao X, Bodell A, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Grant PE, Barkovich AJ, Walsh CA. Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Ann Neurol 2003;53:596-606. 

Chang BS, Ly J, Appignani B, Bodell A, Apse KA, Ravenscroft RS, Sheen VL, Doherty MJ, 
Hackney DB, O'Connor M, Galaburda AM, Walsh CA. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology 2005;64:799-803. 

Chang BS, Katzir T, Liu T, Corriveau K, Barzillai M, Apse KA, Bodell A, Hackney D, Alsop D, Wong ST, Walsh CA (equal contributions from first two authors). A structural basis for reading fluency: white matter defects in a genetic brain malformation. Neurology 2007;69:2146-54. 

Selvitelli MF, Krishnamurthy KB, Herzog AG, Schomer DL, Chang BS. Sleep spindle alterations in patients with malformations of cortical development. Brain Dev 2009;31:163-8. 

Walker LM, Poduri A, Chang BS. Cerebral volumetric analysis over time in children with malformations of cortical development: a quantitative investigation. J Child Neurol 2011;26:171-8. 

Felker MV, Walker LM, Sokol DK, Edwards-Brown M, Chang BS. Early cognitive and behavioral problems in children with nodular heterotopia. Epilepsy Behav 2011;22:523-6.