Yan J, Noltner K, Feng J, Li W, Schroer R, Skinner C, Zeng W, Schwartz CE, Sommer SS (2008). Neurexin 1alpha structural variants associated with autism. Neurosci Lett. 438(3):368-70.

W. Zeng, T.Gillis, M. Flores, L. Djousse, RH. Myers, ME. MacDonald, JF. Gusella (2006) Genetic Analysis of the GRIK2 Modifier Effect in Huntington's Disease.  BMC Neurosci. 7 (62). 1-9

W. Zeng,  H. Gao, G. Goegy, T. Hutchin, MS.Vectory, VE. Shih (2006) Fumarase deficiency caused by homozygous of P131R mutation on partial uniparental isodisomy of Chromosome 1. Am. J. of Med. Genet. Part A 140A:1004-1009

W. Zeng, E. Al-Yamani, JS. Acierno Jr, S. Slaugenhaupt, T. Gillis, ME. MacDonald, PT. Ozand, and JF. Gusella (2005) Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3. Am. J. Hum. Genet. 77, 16-26


This is a partial list. Full publications list available upon request. Information on this page may be self-reported and is subject to change at any time. Last updated: 04/09.