American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 159B Issue 3

April 2012

Volume 159B, Issue 3

Pages 255–360

  1. Rapid Publications

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Errata
    5. Addendum
    1. Genome-wide supported psychosis risk variant in ZNF804A gene and impact on cortico–limbic WM integrity in schizophrenia (pages 255–262)

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

      Version of Record online: 10 FEB 2012 | DOI: 10.1002/ajmg.b.32032

    2. Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample (pages 263–273)

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

      Version of Record online: 17 FEB 2012 | DOI: 10.1002/ajmg.b.32034

  2. Research Articles

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Errata
    5. Addendum
    1. Multivariate analysis of anxiety disorders yields further evidence of linkage to chromosomes 4q21 and 7p in panic disorder families (pages 274–280)

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

      Version of Record online: 17 JAN 2012 | DOI: 10.1002/ajmg.b.32024

    2. Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity (pages 281–288)

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

      Version of Record online: 18 JAN 2012 | DOI: 10.1002/ajmg.b.32025

    3. Maternal smoking during pregnancy and child emotional problems: The relevance of maternal and child 5-HTTLPR genotype (pages 289–297)

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

      Version of Record online: 18 JAN 2012 | DOI: 10.1002/ajmg.b.32026

    4. Moderation of adult depression by the serotonin transporter promoter variant (5-HTTLPR), childhood abuse and adult traumatic events in a general population sample (pages 298–309)

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

      Version of Record online: 10 FEB 2012 | DOI: 10.1002/ajmg.b.32027

    5. Lack of association of the 5-HT3A receptor with schizophrenia (pages 310–315)

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

      Version of Record online: 10 FEB 2012 | DOI: 10.1002/ajmg.b.32028

    6. Support for involvement of glutamate decarboxylase 1 and neuropeptide y in anxiety susceptibility (pages 316–327)

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

      Version of Record online: 10 FEB 2012 | DOI: 10.1002/ajmg.b.32029

    7. 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 (pages 328–335)

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

      Version of Record online: 10 FEB 2012 | DOI: 10.1002/ajmg.b.32030

    8. Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia (pages 343–353)

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

      Version of Record online: 15 FEB 2012 | DOI: 10.1002/ajmg.b.32035

    9. Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders (pages 354–358)

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

      Version of Record online: 15 FEB 2012 | DOI: 10.1002/ajmg.b.32036

  3. Errata

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Errata
    5. Addendum
    1. You have free access to this content
      Erratum: Neuropsychological intra-individual variability explains unique genetic variance of adhd and shows suggestive linkage to chromosomes 12, 13, and 17 (page 359)

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

      Version of Record online: 15 FEB 2012 | DOI: 10.1002/ajmg.b.32031

  4. Addendum

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Errata
    5. Addendum
    1. You have free access to this content

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