Works matching IS 13594184 AND DT 2006 AND VI 11 AND IP 2

Results: 18

Homocysteine, methylenetetrahydrofolate reductase and risk of schizophrenia: a meta-analysis.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 143, doi. 10.1038/sj.mp.4001746

By:

Muntjewerff, J. W.;
Kahn, R. S.;
Blom, H. J.;
den Heijer, M.

Publication type:

Article

DCNP1: a novel candidate gene for major depression.

Published in:

2006

By:

Willis-Owen, S. A. G.;
Shifman, S.;
Copley, R. R.;
Flint, J.

Publication type:

Letter

First in vivo evidence of an NMDA receptor deficit in medication-free schizophrenic patients.

Published in:

2006

By:

Pilowsky, L. S.;
Bressan, R. A.;
Stone, J. M.;
Erlandsson, K.;
Mulligan, R. S.;
Krystal, J. H.;
Ell, P. J.

Publication type:

Letter

The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 119, doi. 10.1038/sj.mp.4001752

By:

Amann, D.;
Avidan, N.;
Kanyas, K.;
Kohn, Y.;
Hamdan, A.;
Ben-Asher, E.;
Macciardi, F.;
Beckmann, J. S.;
Lancet, D.;
Lerer, B.

Publication type:

Article

Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 214, doi. 10.1038/sj.mp.4001753

By:

Chen, G. K.;
Kono, N.;
Geschwind, D. H.;
Cantor, R. M.

Publication type:

Article

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 206, doi. 10.1038/sj.mp.4001756

By:

Gauthier, J.;
Joober, R.;
Dubé, M. -P.;
St-Onge, J.;
Bonnel, A.;
Gariépy, D.;
Laurent, S.;
Najafee, R.;
Lacasse, H.;
St-Charles, L.;
Fombonne, É.;
Mottron, L.;
Rouleau, G. A.

Publication type:

Article

Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 134, doi. 10.1038/sj.mp.4001759

By:

McQuillin, A.;
Bass, N. J.;
Kalsi, G.;
Lawrence, J.;
Puri, V.;
Choudhury, K.;
Detera-Wadleigh, S. D.;
Curtis, D.;
Gurling, H. M. D.

Publication type:

Article

A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 196, doi. 10.1038/sj.mp.4001761

By:

Hebebrand, J.;
Dempfle, A.;
Saar, K.;
Thiele, H.;
Herpertz-Dahlmann, B.;
Linder, M.;
Kiefl, H.;
Remschmidt, H.;
Hemminger, U.;
Warnke, A.;
Knölker, U.;
Heiser, P.;
Friedel, S.;
Hinney, A.;
Schäfer, H.;
Nürnberg, P.;
Konrad, K.

Publication type:

Article

Procholinergic and memory enhancing properties of the selective norepinephrine uptake inhibitor atomoxetine.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 187, doi. 10.1038/sj.mp.4001763

By:

Tzavara, E. T.;
Bymaster, F. P.;
Overshiner, C. D.;
Davis, R. J.;
Perry, K. W.;
Wolff, M.;
McKinzie, D. L.;
Witkin, J. M.;
Nomikos, G. G.

Publication type:

Article

Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 125, doi. 10.1038/sj.mp.4001764

By:

Greenwood, T. A.;
Schork, N. J.;
Eskin, E.;
Kelsoe, J. R.

Publication type:

Article

Illness-specific association of val66met BDNF polymorphism with performance on Wisconsin Card Sorting Test in bipolar mood disorder.

Published in:

2006

By:

Rybakowski, J. K.;
Borkowska, A.;
Skibinska, M.;
Hauser, J.

Publication type:

Letter

A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val<sup>158</sup>Met genotype.

Published in:

2006

By:

Tunbridge, E. M.;
Weinberger, D. R.;
Harrison, P. J.

Publication type:

Letter

Mapping of hippocampal gene clusters regulated by the amygdala to nonlinkage sites for schizophrenia.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 158, doi. 10.1038/sj.mp.4001769

By:

Burke, R. E.;
Walsh, J.;
Matzilevich, D.;
Benes, F. M.

Publication type:

Article

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.

Published in:

2006

By:

Sheehan, K.;
Lowe, N.;
Kirley, A.;
Mullins, C.;
Fitzgerald, M.;
Gill, M.;
Hawi, Z.

Publication type:

Correction Notice

Genome scan on Swedish Alzheimer's disease families.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 182, doi. 10.1038/sj.mp.4001772

By:

Sillén, A.;
Forsell, C.;
Lilius, L.;
Axelman, K.;
Björk, B. F.;
Onkamo, P.;
Kere, J.;
Winblad, B.;
Graff, C.

Publication type:

Article

Inhibition of cyclooxygenase as potential novel therapeutic strategy in N141I presenilin-2 familial Alzheimer's disease.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 172, doi. 10.1038/sj.mp.4001773

By:

Qin, W.;
Peng, Y.;
Ksiezak-Reding, H.;
Ho, L.;
Stetka, B.;
Lovati, E.;
Pasinetti, G. M.

Publication type:

Article

Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 115, doi. 10.1038/sj.mp.4001795

By:

Greenwood, T. A.;
Schork, N. J.;
Eskin, E.;
Kelsoe, J. R.

Publication type:

Article

Serine racemase binds to PICK1: potential relevance to schizophrenia.

Published in:

Molecular Psychiatry, 2006, v. 11, n. 2, p. 150, doi. 10.1038/sj.mp.4001776

By:

Fujii, K.;
Maeda, K.;
Hikida, T.;
Mustafa, A. K.;
Balkissoon, R.;
Xia, J.;
Yamada, T.;
Ozeki, Y.;
Kawahara, R.;
Okawa, M.;
Huganir, R. L.;
Ujike, H.;
Snyder, S. H.;
Sawa, A.

Publication type:

Article