Lionel A.C., Tammimies K., Vaags A.K., Rosenfeld J.A., Ahn J.W., Merico D., Noor A., Runke C.K., Pillalamarri V.K., Carter M.T., Gazzellone M.J., Thiruvahindrapuram B., Fagerberg C., Laulund L.W., Pellecchia G., Lamoureux S., Deshpande C., Clayton-Smith J., White A.C., Leather S., Trounce J., Melanie Bedford H., Hatchwell E., Eis P.S., Yuen R.K., Walker S., Uddin M., Geraghty M.T., Nikkel S.M., Tomiak E.M., Fernandez B.A., Soreni N., Crosbie J., Arnold P.D., Schachar R.J., Roberts W., Paterson A.D. et al. Disruption of the ASTN2/TRIM32 locus at 9q331 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Human Molecular Genetics, 2013, 23(10), pp.2752-2768
Davis L.K., Yu D., Keenan C.L., Gamazon E.R., Konkashbaev A.I., Derks E.M., Neale B.M., Yang J., Lee S.H., Evans P., Barr C.L., Bellodi L., Benarroch F., Berrio G.B., ... Shugart Y.Y., Miguel E.C., McMahon W., Wagner M., Nicolini H., Posthuma D., Hanna G.L., Heutink P., Denys D., Arnold P.D., Oostra B.A., Nestadt G., Freimer N.B., Pauls D.L., Wray N.R., Stewart S.E., Mathews C.A., Knowles J.A., Cox N.J., Scharf J.M. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS genetics, 2013, 9(10)
Stewart S.E., Mayerfeld C., Arnold P.D., Crane J.R., O'Dushlaine C., Fagerness J.A., Yu D., Scharf J.M., Chan E., Kassam F., Moya P.R., Wendland J.R., Delorme R., Richter M.A., Kennedy J.L., Veenstra-VanderWeele J., Samuels J., Greenberg B.D., McCracken J.T., Knowles J.A., Fyer A.J., Rauch S.L., Riddle M.A., Grados M.A., Bienvenu O.J., Cullen B., Wang Y., Shugart Y.Y., Piacentini J., Rasmussen S., Nestadt G., Murphy D.L., Jenike M.A., Cook E.H., Pauls D.L., Hanna G.L., Mathews C.A. Meta‐analysis of association between obsessive‐compulsive disorder and the 3′ region of neuronal glutamate transporter gene SLC1A1. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2013, 162(4), pp.367-379