American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 156 Issue 2

March 2011

Volume 156, Issue 2

Pages 115–245

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Letters to Editor
    5. Letters to the Editor
    1. Copy number variation characteristics in subpopulations of patients with autism spectrum disorders (pages 115–124)

      Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Åsa Uppströmer, Britt-Marie Anderlid, Magnus Nordenskjöld and Jacqueline Schoumans

      Version of Record online: 8 DEC 2010 | DOI: 10.1002/ajmg.b.31142

    2. Parent-of-origin effects of the serotonin transporter gene associated with autism (pages 139–144)

      Emily Kistner-Griffin, Camille W. Brune, Lea K. Davis, James S. Sutcliffe, Nancy J. Cox and Edwin H. Cook Jr

      Version of Record online: 8 DEC 2010 | DOI: 10.1002/ajmg.b.31146

    3. You have full text access to this OnlineOpen article
      The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects (pages 145–157)

      Thais S. Rizzi, Alejandro Arias-Vasquez, Nanda Rommelse, Jonna Kuntsi, Richard Anney, Philip Asherson, Jan Buitelaar, Tobias Banaschewski, Richard Ebstein, Dina Ruano, Sophie Van der Sluis, Christina A. Markunas, Melanie E. Garrett, Allison E. Ashley-Koch, Scott H. Kollins, Arthur D. Anastopoulos, Narelle K. Hansell, Margaret J. Wright, Grant W. Montgomery, Nicholas G. Martin, Sarah E. Harris, Gail Davies, Albert Tenesa, David J. Porteous, John M. Starr, Ian J. Deary, Beate St. Pourcain, George Davey Smith, Nicholas J. Timpson, David M. Evans, Michael Gill, Ana Miranda, Fernando Mulas, Robert D. Oades, Herbert Roeyers, Aribert Rothenberger, Joseph Sergeant, Edmund Sonuga-Barke, Hans Christoph Steinhausen, Eric Taylor, Stephen V. Faraone, Barbara Franke and Danielle Posthuma

      Version of Record online: 16 DEC 2010 | DOI: 10.1002/ajmg.b.31149

    4. You have full text access to this OnlineOpen article
    5. Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q (pages 168–176)

      Haiyan Xu, Rong Cheng, Suh-Hang Juo, Jianjun Liu, Jo Ellen Loth, Jean Endicott, Conrad Gilliam and Miron Baron

      Version of Record online: 16 DEC 2010 | DOI: 10.1002/ajmg.b.31151

    6. Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder (pages 177–187)

      Ana C. Parente Pereira, Andrew McQuillin, Vinay Puri, Adebayo Anjorin, Nicholas Bass, Radhika Kandaswamy, Jacob Lawrence, David Curtis, Pamela Sklar, Shaun M. Purcell and Hugh M.D. Gurling

      Version of Record online: 13 JAN 2011 | DOI: 10.1002/ajmg.b.31153

    7. Linkage and association on 8p21.2-p21.1 in schizophrenia (pages 188–197)

      M. Daniele Fallin, Virginia K. Lasseter, Yaping Liu, Dimitrios Avramopoulos, John McGrath, Paula S. Wolyniec, Gerald Nestadt, Kung-Yee Liang, Pei-Lung Chen, David Valle and Ann E. Pulver

      Version of Record online: 28 DEC 2010 | DOI: 10.1002/ajmg.b.31154

    8. Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia (pages 204–214)

      Tod Fullston, Bronte Gabb, David Callen, Reinhard Ullmann, Erica Woollatt, Sharon Bain, Hilger H. Ropers, Matt Cooper, David Chandler, Kim Carter, Assen Jablensky, Luba Kalaydjieva and Jozef Gecz

      Version of Record online: 13 JAN 2011 | DOI: 10.1002/ajmg.b.31157

    9. Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and age of onset in schizophrenia: A combined analysis of independent samples (pages 215–224)

      Peter Saetre, Maria Vares, Thomas Werge, Ole A. Andreassen, Tadao Arinami, Hiroki Ishiguro, Shinichiro Nanko, Ene Choo Tan, Doug Hyun Han, Joshua L. Roffman, Jan-Willem Muntjewerff, Pawel P. Jagodzinski, Bartosz Kempisty, Joanna Hauser, Elisabet Vilella, Elitza Betcheva, Yusuke Nakamura, Björn Regland, Ingrid Agartz, Håkan Hall, Lars Terenius and Erik G. Jönsson

      Version of Record online: 13 JAN 2011 | DOI: 10.1002/ajmg.b.31160

  2. Brief Research Communications

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Letters to Editor
    5. Letters to the Editor
    1. Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family (pages 225–232)

      Yiping Shen, Xiaoli Chen, Liwen Wang, Jin Guo, Jianliang Shen, Yu An, Haitao Zhu, Yanli Zhu, Ruolei Xin, Yihua Bao, James F. Gusella, Ting Zhang and Bai-Lin Wu

      Version of Record online: 28 DEC 2010 | DOI: 10.1002/ajmg.b.31147

    2. Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders (pages 233–239)

      Shun-Chiao Chang, David L. Pauls, Christoph Lange, Roksana Sasanfar and Susan L. Santangelo

      Version of Record online: 16 DEC 2010 | DOI: 10.1002/ajmg.b.31148

  3. Letters to Editor

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Letters to Editor
    5. Letters to the Editor
    1. Genome-wide association study of hoarding traits (pages 240–242)

      Nader Perroud, Michel Guipponi, Alberto Pertusa, Miguel Angel Fullana, Alessandra C. Iervolino, Lynn Cherkas, Tim Spector, David Collier and David Mataix-Cols

      Version of Record online: 28 DEC 2010 | DOI: 10.1002/ajmg.b.31152

  4. Letters to the Editor

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Letters to Editor
    5. Letters to the Editor
    1. Narrowing the critical deletion region for autism spectrum disorders on 16p11.2 (pages 243–245)

      An Crepel, Jean Steyaert, Wouter De la Marche, Veerle De Wolf, Jean-Pierre Fryns, Ilse Noens, Koen Devriendt and Hilde Peeters

      Version of Record online: 11 JAN 2011 | DOI: 10.1002/ajmg.b.31163

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