American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

December 2012

Volume 159B, Issue 8

Pages 885–1012

  1. Review Article

    1. Top of page
    2. Review Article
    3. Research Articles
    4. Letter to the Letter
    5. Letter to Editor
    1. You have free access to this content
  2. Research Articles

    1. Top of page
    2. Review Article
    3. Research Articles
    4. Letter to the Letter
    5. Letter to Editor
    1. Rare variants in TMEM132D in a case–control sample for panic disorder (pages 896–907)

      Carina Quast, Andre Altmann, Peter Weber, Janine Arloth, Daniel Bader, Angela Heck, Hildegard Pfister, Bertram Müller-Myhsok, Angelika Erhardt and Elisabeth B. Binder

      Version of Record online: 22 AUG 2012 | DOI: 10.1002/ajmg.b.32096

    2. An association and haplotype analysis of porcine maternal infanticide: A model for human puerperal psychosis? (pages 908–927)

      C.R. Quilter, C.A. Sargent, J. Bauer, M. R. Bagga, C. P. Reiter, E. L. Hutchinson, O. I. Southwood, G. Evans, A. Mileham, D.K. Griffin and N.A. Affara

      Version of Record online: 13 SEP 2012 | DOI: 10.1002/ajmg.b.32097

    3. Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: Relevance for major depression (pages 928–940)

      Dorottya Pap, Xenia Gonda, Eszter Molnar, Judit Lazary, Anita Benko, Darragh Downey, Emma Thomas, Diana Chase, Zoltan G. Toth, Krisztina Mekli, Hazel Platt, Antony Payton, Rebecca Elliott, Ian M. Anderson, J.F. William Deakin, Gyorgy Bagdy and Gabriella Juhasz

      Version of Record online: 24 SEP 2012 | DOI: 10.1002/ajmg.b.32098

    4. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, ift27 and parvalbumin (pages 941–950)

      Stephanie Nissen, Sherri Liang, Tatyana Shehktman, John R. Kelsoe and the Bipolar Genome Study (BiGS)

      Version of Record online: 4 OCT 2012 | DOI: 10.1002/ajmg.b.32099

    5. CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy (pages 951–957)

      Jun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, Koichiro Higasa, Jun Yoshimura, Taro L. Saito, Budrul Ahsan, Yuji Takahashi, Jun Goto, Atsushi Iwata, Yuki Niimi, Yuuichi Riku, Yoji Goto, Kazuo Mano, Mari Yoshida, Shinichi Morishita and Shoji Tsuji

      Version of Record online: 4 OCT 2012 | DOI: 10.1002/ajmg.b.32100

    6. Association of KIBRA with episodic and working memory: A meta-analysis (pages 958–969)

      Annette Milnik, Angela Heck, Christian Vogler, Hans-Jochen Heinze, Dominique J.-F. de Quervain and Andreas Papassotiropoulos

      Version of Record online: 12 OCT 2012 | DOI: 10.1002/ajmg.b.32101

    7. Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta-analysis (pages 970–976)

      Li Zou, Wei Chen, Shanshan Shao, Zhao Sun, Rong Zhong, Junxin Shi, Xiaoping Miao and Ranran Song

      Version of Record online: 12 OCT 2012 | DOI: 10.1002/ajmg.b.32102

    8. Gene expression changes in peripheral blood from chinese han patients with tourette syndrome (pages 977–980)

      Jing Lei, Hongbo Xu, Hui Liang, Linyan Su, Jie Zhang, Xian Huang, Zhi Song, Weidong Le and Hao Deng

      Version of Record online: 17 OCT 2012 | DOI: 10.1002/ajmg.b.32103

    9. You have full text access to this OnlineOpen article
      Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: No consistent evidence for an association in the nordic population (pages 981–986)

      Peter Saetre, Jakob Grove, Anders D. Børglum, Ole Mors, Thomas Werge, Ole A. Andreassen, Maria Vares, Ingrid Agartz, Lars Terenius and Erik G. Jönsson

      Version of Record online: 17 OCT 2012 | DOI: 10.1002/ajmg.b.32104

    10. Effectiveness of a web-based protocol for the screening and phenotyping of individuals with tourette syndrome for genetic studies (pages 987–996)

      Crystelle A. Egan, Susan E. Marakovitz, Julia A. O'Rourke, Lisa Osiecki, Cornelia Illmann, Lauren Barton, Elizabeth McLaughlin, Rachel Proujansky, Justin Royal, Heather Cowley, Martha Rangel-Lugo, David L. Pauls, Jeremiah M. Scharf, Carol A. Mathews and for the Tourette Syndrome Association International Consortium for Genetics

      Version of Record online: 22 OCT 2012 | DOI: 10.1002/ajmg.b.32107

    11. ANK3 as a risk gene for schizophrenia: New data in han Chinese and meta analysis (pages 997–1005)

      Aihua Yuan, Zhenghui Yi, Qiang Wang, Jinhua Sun, Zhiqiang Li, Yasong Du, Chen Zhang, Tao Yu, Juan Fan, Huafang Li and Shunying Yu

      Version of Record online: 25 OCT 2012 | DOI: 10.1002/ajmg.b.32112

  3. Letter to the Letter

    1. Top of page
    2. Review Article
    3. Research Articles
    4. Letter to the Letter
    5. Letter to Editor
    1. Genetic studies indicate a potential target 5-HTR3B for Drug Therapy in Schizophrenia Patients (pages 1006–1008)

      Meenal Gupta, Sanjeev Jain, Nagaraj S. Moily, Harpreet Kaur, Ajay Jajodia, Meera Purushottam and Ritushree Kukreti

      Version of Record online: 17 OCT 2012 | DOI: 10.1002/ajmg.b.32105

  4. Letter to Editor

    1. Top of page
    2. Review Article
    3. Research Articles
    4. Letter to the Letter
    5. Letter to Editor
    1. Maternal prenatal smoking and offspring emotional problems: No moderating effect of maternal or child 5-HTTLPR genotype (pages 1009–1012)

      Lot M. Geels, Maria M. Groen-Blokhuis, Catharina E.M. van Beijsterveldt, Jacqueline M. Vink, Christel M. Middeldorp, Meike Bartels, Kelly A. Nelson, Patricia E. Huizenga, Gareth E. Davies and Dorret I. Boomsma

      Version of Record online: 22 OCT 2012 | DOI: 10.1002/ajmg.b.32110

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