Association between the oxytocin receptor (OXTR) gene and children's social cognition at 18 months von Wade, M., Hoffmann, T. J., Wigg, K., Jenkins, J. M.

Volltext

Support for EKN1 as the susceptibility locus for dyslexia on 15q21 von WIGG, K. G, COUTO, J. M, FENG, Y, ANDERSON, B, CATE-CARTER, T. D, MACCIARDI, F, TANNOCK, R, LOVETT, M. W, HUMPHRIES, T. W, BARR, C. L

Volltext

Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation von Bisceglia, R., Jenkins, J. M., Wigg, K. G., O’Connor, T. G., Moran, G., Barr, C. L.

Volltext

A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1 von Tran, C., Gagnon, F., Wigg, K.G., Feng, Y., Gomez, L., Cate-Carter, T.D., Kerr, E.N., Field, L.L., Kaplan, B.J., Lovett, M.W., Barr, C.L.

Volltext

Association of the ROBO1 gene with reading disabilities in a family‐based analysis von Tran, C., Wigg, K. G., Zhang, K., Cate‐Carter, T. D., Kerr, E., Field, L. L., Kaplan, B. J., Lovett, M. W., Barr, C. L.

Volltext

Association of the KCNJ5 gene with Tourette Syndrome and Attention‐Deficit/Hyperactivity Disorder von Gomez, L., Wigg, K., Zhang, K., Lopez, L., Sandor, P., Malone, M., Barr, C. L.

Volltext

Association of the glutamate receptor subunit gene GRIN2B with attention‐deficit/hyperactivity disorder von Dorval, K. M., Wigg, K. G., Crosbie, J., Tannock, R., Kennedy, J. L., Ickowicz, A., Pathare, T., Malone, M., Schachar, R., Barr, C. L.

Volltext

Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems von LUCA, P, LAURIN, N, MISENER, V. L, WIGG, K. G, ANDERSON, B, CATE-CARTER, T, TANNOCK, R, HUMPHRIES, T, LOVETT, M. W, BARR, C. L

Volltext

Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder von BARR, C. L, FENG, Y, WIGG, K, BLOOM, S, ROBERTS, W, MALONE, M, SCHACHAR, R, TANNOCK, R, KENNEDY, J. L

Volltext

Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders von Misener, V L, Gomez, L, Wigg, K G, Luca, P, King, N, Kiss, E, Daróczi, G, Kapornai, K, Tamas, Z, Mayer, L, Gádoros, J, Baji, I, Kennedy, J L, Kovacs, M, Vetró, A, Barr, C L

Volltext

Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor von BARR, C. L, WIGG, K. G, FENG, Y, ZAI, G, MALONE, M, ROBERTS, W, SCHACHAR, R, TANNOCK, R, KENNEDY, J. L

Volltext

Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention- deficit/hyperactivity disorder in the 16p13 region von ADAMS, J, CROSBIE, J, BARR, C. L, WIGG, K, ICKOWICZ, A, PATHARE, T, ROBERTS, W, MALONE, M, SCHACHAR, R, TANNOCK, R, KENNEDY, J. L

Volltext

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region von Wigg, K. G., Feng, Y., Crosbie, J., Tannock, R., Kennedy, J. L., Ickowicz, A., Malone, M., Schachar, R., Barr, C. L.

Volltext

Genome scan for linkage to Gilles de la Tourette syndrome von Barr, Cathy L., Wigg, Karen G., Pakstis, Andrew J., Kurlan, Roger, Pauls, David, Kidd, Kenneth K., Tsui, Lap-Chee, Sandor, Paul

Volltext

Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD) von Mill, J., Wigg, K., Burcescu, I., Vetró, Á., Kiss, E., Kapornai, K., Tamás, Z., Baji, I., Gádoros, J., Kennedy, J.L., Kovacs, M., Barr, C.L.

Volltext

Association study between gilles de la tourette syndrome and two genes in the robo-slit pathway located in the chromosome 11q24 linked/associated region von Miranda, D.M., Wigg, K., Feng, Y., Sandor, P., Barr, C.L.

Volltext

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder von FENG, Y, CROSBIE, J, KENNEDY, J. L, BARR, C. L, WIGG, K, PATHARE, T, ICKOWICZ, A, SCHACHAR, R, TANNOCK, R, ROBERTS, W, MALONE, M, SWANSON, J

Volltext

Catechol-O-methyltransferase and Gilles de la Tourette syndrome von BARR, C. L, WIGG, K. G, SANDOR, P

Volltext

Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder von Barr, Cathy L., Wigg, Karen G., Wu, Jie, Zai, Clement, Bloom, Stacey, Tannock, Rosemary, Roberts, Wendy, Malone, Molly, Schachar, Russell, Kennedy, James L.

Volltext

Association study of CREB1 and childhood-onset mood disorders von Burcescu, I., Wigg, K., King, N., Vetró, Á., Kiss, E., Katay, L., Kennedy, J.L., Kovacs, M., Barr, C.L.

Volltext