Works matching IS 15524841 AND DT 2012 AND VI 159B AND IP 3

Results: 14

Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 343, doi. 10.1002/ajmg.b.32035

By:

Whalley, Heather C.;
Sussmann, Jessika E.;
Johnstone, Mandy;
Romaniuk, Liana;
Redpath, Holly;
Chakirova, Goultchira;
Mukherjee, Prerona;
Hall, Jeremy;
Johnstone, Eve C.;
Lawrie, Stephen M.;
McIntosh, Andrew M.

Publication type:

Article

Erratum: Neuropsychological intra-individual variability explains unique genetic variance of adhd and shows suggestive linkage to chromosomes 12, 13, and 17.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 359, doi. 10.1002/ajmg.b.32031

By:

Frazier-Wood, Alexis C.;
Bralten, Janita;
Arias-Vasquez, Alejandro;
Luman, Marjolein;
Oosterlaan, Jaap;
Sergeant, Joseph;
Faraone, Stephen V.;
Buitelaar, Jan;
Franke, Barbara;
Kuntsi, Jonna;
Rommelse, Nanda N.J.

Publication type:

Article

Multivariate analysis of anxiety disorders yields further evidence of linkage to chromosomes 4q21 and 7p in panic disorder families.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 274, doi. 10.1002/ajmg.b.32024

By:

Logue, Mark W.;
Bauver, Sarah R.;
Knowles, James A.;
Gameroff, Marc J.;
Weissman, Myrna M.;
Crowe, Raymond R.;
Fyer, Abby J.;
Hamilton, Steven P.

Publication type:

Article

Lack of association of the 5-HT<sub>3A</sub> receptor with schizophrenia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 310, doi. 10.1002/ajmg.b.32028

By:

Nothdurfter, Caroline;
Giegling, Ina;
Konte, Bettina;
Hartmann, Annette M.;
Konnerth, Heike;
Friedl, Marion;
Rammes, Gerhard;
Rupprecht, Rainer;
Rujescu, Dan

Publication type:

Article

Addendum: Novel pathogenic mutations and copy number variations in the VPS13A gene in patients with chorea-acanthocytosis. A. Tomiyasu, M. Nakamura, M. Ichiba, S. Ueno, S. Saiki, M. Morimoto, J. Kobal, Y. Kageyama, T. Inui, K. Wakabayashi, T. Yamada, Y. Kanemori, H. Jung, H. Tanaka, S. Orimo, Z. Afawi, I. Blatt, J. Aasly, H. Ujike, D. Babovic-Vuksanovic, K. A. Josephs, R. Tohge, G. R. Rodrigues, N. Dupré, H. Yamada, F. Yokochi, K. Kotschet, T. Takei, M. Rudzinska, A. Szczudlik, S. Penco, M. Fujiwara, K. Tojo, and A. Sano.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 360, doi. 10.1002/ajmg.b.32039
Publication type:: Article

Sequencing of the ANKYRIN 3 gene ( ANK3) encoding ankyrin G in bipolar disorder reveals a non-conservative amino acid change in a short isoform of ankyrin G.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 328, doi. 10.1002/ajmg.b.32030

By:

Dedman, Alexandra;
McQuillin, Andrew;
Kandaswamy, Radhika;
Sharp, Sally;
Anjorin, Adebayo;
Gurling, Hugh

Publication type:

Article

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 263, doi. 10.1002/ajmg.b.32034

By:

Degenhardt, Franziska;
Priebe, Lutz;
Herms, Stefan;
Mattheisen, Manuel;
Mühleisen, Thomas W.;
Meier, Sandra;
Moebus, Susanne;
Strohmaier, Jana;
Groß, Magdalena;
Breuer, René;
Lange, Christoph;
Hoffmann, Per;
Meyer-Lindenberg, Andreas;
Heinz, Andreas;
Walter, Henrik;
Lucae, Susanne;
Wolf, Christiane;
Müller-Myhsok, Bertram;
Holsboer, Florian;
Maier, Wolfgang

Publication type:

Article

Moderation of adult depression by the serotonin transporter promoter variant (5-HTTLPR), childhood abuse and adult traumatic events in a general population sample.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 298, doi. 10.1002/ajmg.b.32027

By:

Grabe, Hans Jörgen;
Schwahn, Christian;
Mahler, Jessie;
Schulz, Andrea;
Spitzer, Carsten;
Fenske, Kristin;
Appel, Katja;
Barnow, Sven;
Nauck, Matthias;
Schomerus, Georg;
Biffar, Reiner;
Rosskopf, Dieter;
John, Ulrich;
Völzke, Henry;
Freyberger, Harald Jürgen

Publication type:

Article

A study of the combined effects of the EHD3 and FREM3 genes in patients with major depressive disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 336, doi. 10.1002/ajmg.b.32033

By:

Shi, Cuijuan;
Zhang, Kerang;
Wang, Xuan;
Shen, Yan;
Xu, Qi

Publication type:

Article

Maternal smoking during pregnancy and child emotional problems: The relevance of maternal and child 5-HTTLPR genotype.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 289, doi. 10.1002/ajmg.b.32026

By:

Cents, Rolieke A.M.;
Tiemeier, Henning;
Velders, Fleur P.;
Jaddoe, Vincent W.V.;
Hofman, Albert;
Verhulst, Frank C.;
Lambregtse-van den Berg, Mijke P.;
Hudziak, James J.

Publication type:

Article

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 354, doi. 10.1002/ajmg.b.32036

By:

Duong, Linh;
Klitten, Laura L.;
Møller, Rikke S.;
Ingason, Andrés;
Jakobsen, Klaus D.;
Skjødt, Celina;
Didriksen, Michael;
Hjalgrim, Helle;
Werge, Thomas;
Tommerup, Niels

Publication type:

Article

Support for involvement of glutamate decarboxylase 1 and neuropeptide y in anxiety susceptibility.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 316, doi. 10.1002/ajmg.b.32029

By:

Donner, Jonas;
Sipilä, Tessa;
Ripatti, Samuli;
Kananen, Laura;
Chen, Xiangning;
Kendler, Kenneth S.;
Lönnqvist, Jouko;
Pirkola, Sami;
Hettema, John M.;
Hovatta, Iiris

Publication type:

Article

Genome-wide supported psychosis risk variant in ZNF804A gene and impact on cortico-limbic WM integrity in schizophrenia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 255, doi. 10.1002/ajmg.b.32032

By:

Kuswanto, Carissa Nadia;
Woon, Puay-San;
Zheng, Xue Bin;
Qiu, Anqi;
Sitoh, Yih-Yian;
Chan, Yiong Huak;
Liu, Jianjun;
Williams, Hywel;
Ong, Wei Yi;
Sim, Kang

Publication type:

Article

Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 281, doi. 10.1002/ajmg.b.32025

By:

Varga, Gabor;
Szekely, Anna;
Antal, Peter;
Sarkozy, Peter;
Nemoda, Zsofia;
Demetrovics, Zsolt;
Sasvari-Szekely, Maria

Publication type:

Article