The contribution of alternative splicing to genetic risk for psychiatric disorders von Reble, E., Dineen, A., Barr, C. L.

Volltext

Decoding the non‐coding genome: elucidating genetic risk outside the coding genome von Barr, C. L., Misener, V. L.

Volltext

Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample von Strauss, J, Barr, C L, George, C J, Devlin, B, Vetró, Á, Kiss, E, Baji, I, King, N, Shaikh, S, Lanktree, M, Kovacs, M, Kennedy, J 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

The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder von Quist, J F, Barr, C L, Schachar, R, Roberts, W, Malone, M, Tannock, R, Basile, V S, Beitchman, J, Kennedy, J L

Volltext

Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder von Misener, V L, Luca, P, Azeke, O, Crosbie, J, Waldman, I, Tannock, R, Roberts, W, Malone, M, Schachar, R, Ickowicz, A, Kennedy, J L, 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

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

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

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 study of brain-derived neurotrophic factor in adults with a history of childhood onset mood disorder von Strauss, J., Barr, C.L., George, C.J., King, N., Shaikh, S., Devlin, B., Kovacs, M., Kennedy, J.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

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, Wigg, K, Ickowicz, A, Pathare, T, Roberts, W, Malone, M, Schachar, R, Tannock, R, Kennedy, J L, Barr, C L

Volltext

Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD) von QUIST, J. F, BARR, C. L, SCHACHAR, R, ROBERTS, W, MALONE, M, TANNOCK, R, BASILE, V. S, BEITCHMAN, J, KENNEDY, J. L

Volltext

Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region von Paschou, P., Feng, Y., Pakstis, A.J., Speed, W.C., DeMille, M.M., Kidd, J.R., Jaghori, B., Kurlan, R., Pauls, D.L., Sandor, P., Barr, C.L., Kidd, K.K.

Volltext

Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder von Laurin, N, Misener, V L, Crosbie, J, Ickowicz, A, Pathare, T, Roberts, W, Malone, M, Tannock, R, Schachar, R, Kennedy, J L, Barr, C L

Volltext

Association of the GABRD gene and childhood‐onset mood disorders von Feng, Y., Kapornai, K., Kiss, E., Tamás, Z., Mayer, L., Baji, I., Daróczi, G., Benák, I., Kothencné, V. O., Dombovári, E., Kaczvinszk, E., Besnyő, M., Gádoros, J., Székely, J., Kovacs, M., Vetró, Á., Kennedy, J. L., Barr, C. 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