Original Articles

Leckman, J.F., Pauls, D.L. , Zhang, H., Rosario-Campos, M.C., Katsovich, L., Kidd, K.K., Pakstis, A.J., Alsobrook, J.P., Robertson, M.M., McMahon, W.M., Walkup, J.T., van de Wetering, B.J.M., King, R.A., Cohen, D.J., and the Tourette Syndrome Association International Consortium for Genetics. (2003). Obsessive-compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics). 116B(1): 60-68.

Kaplan, D.E., Gayan, J., Ahn, J., Won, T.W., Pauls, D. , Olson, R.K., DeFries, J.C., Wood, F., Pennington, B.F., Page, G.P., Smith, S.D., and Gruen, J.R. (2002). Evidence for linkage and association with reading disability, on 6p21.3-22. American Journal of Human Genetics. 70(5):1287-1298.

Zhang, H., Leckman, J.F., Pauls, D.L. , Tsai, C.P., Kidd, K.K., Campos, M.R., and Tourette Syndrome Association International Consortium for Genetics. (2002). Genome wide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome. American Journal of Human Genetics. 70(4):896-904.

Alsobrook II, J.P. and Pauls, D.L. (2002). A factor analysis of tic symptoms in Gilles de la Tourette's syndrome. American Journal of Psychiatry, 159(2):291-296.

Alsobrook II, J.P., Zohar, A.H., Leboyer, M., Chabane, N., Ebstein, R.P., and Pauls, D.L. (2002). Association between the COMT locus and Obsessive Compulsive Disorder in females but not males. American Journal of Medical Genetics (Neuropsychiatric Genetics), 114:116-120.

International Molecular Genetic Study of Autism Consortium (IMGSAC) (2001). Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Human Molecular Genetics, 10(9):973-982.

Grigorenko, E.L., Wood, F.B., Meyer, M.S., Pauls, J.E.D., Hart, L.A., and Pauls, D.L. (2001). Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p. American Journal of Medical Genetics (Neuropsychiatric Genetics), 105(1):120-129.

The Tourette Syndrome Association International Consortium for Genetics [Walkup, J.T., LaBuda, M.C., Guliano, J., Singer, H.S., Riddle, M.A., Robertson, M.M., Hebebrand, J., Klug, B., Remschmidt, H., Weber, J.L., Hiner, B.C., Spindler, M., Pauls, D.L. , Hurst, C.R., Zovko, E., Alsobrook II, J.P., King, R.A., Cohen, D.J., Leckman, J.F., Pakstis, A.J., Kidd, J.R., Kidd, K.K., Kurlan, R., Siderowf, A., Como, P., Palumbo, D., van de Wetering, B.J.M., Heutink, P., Hottenga, J.J., Sandkuijl, A., Oostra, B.A., McMahon, W., Leppert, M., Achilles, J., Sandor, P., Spence, W., Barr, C.L.] (1999). A complete genome screen in sib-pairs affected with the Gilles de la Tourette syndrome. American Journal of Human Genetics, 65:1428-1436.