American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 150B Issue 2

5 March 2009

Volume 150B, Issue 2

Pages 155–307

  1. Rapid Publications

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Brief Research Communication
    5. Brief Research Communications
    6. Erratum
    1. You have free access to this content
      Convergent functional genomics of genome-wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms (pages 155–181)

      H. Le-Niculescu, S.D. Patel, M. Bhat, R. Kuczenski, S.V. Faraone, M.T. Tsuang, F.J. McMahon, N.J. Schork, J.I. Nurnberger Jr. and A.B. Niculescu III

      Version of Record online: 21 NOV 2008 | DOI: 10.1002/ajmg.b.30887

    2. Convergent genome wide association results for bipolar disorder and substance dependence (pages 182–190)

      Catherine Johnson, Tomas Drgon, Francis J. McMahon and George R. Uhl

      Version of Record online: 6 JAN 2009 | DOI: 10.1002/ajmg.b.30900

  2. Research Articles

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Brief Research Communication
    5. Brief Research Communications
    6. Erratum
    1. Bipolar disorder in the Bulgarian Gypsies: Genetic heterogeneity in a young founder population (pages 191–201)

      Radka Kaneva, Vihra Milanova, Dora Angelicheva, Stuart MacGregor, Christian Kostov, Rositza Vladimirova, Spiridon Aleksiev, Mina Angelova, Vessela Stoyanova, Angeline Loh, Joachim Hallmayer, Luba Kalaydjieva and Assen Jablensky

      Version of Record online: 28 APR 2008 | DOI: 10.1002/ajmg.b.30775

    2. The tryptophan hydroxylase-1 A218C polymorphism is associated with diagnosis, but not suicidal behavior, in borderline personality disorder (pages 202–208)

      Scott T. Wilson, Barbara Stanley, David A. Brent, Maria A. Oquendo, Yung-yu Huang and J. John Mann

      Version of Record online: 27 MAY 2008 | DOI: 10.1002/ajmg.b.30788

    3. Emotional symptoms in children: The effect of maternal depression, life events, and COMT genotype (pages 209–218)

      Jonathan Evans, Ke Xu, Jon Heron, Mary-Anne Enoch, Ricardo Araya, Glyn Lewis, Nic Timpson, Simon Davies, David Nutt and David Goldman

      Version of Record online: 5 JUN 2008 | DOI: 10.1002/ajmg.b.30789

    4. Methionine sulfoxide reductase: A novel schizophrenia candidate gene (pages 219–225)

      Consuelo Walss-Bass, Maria Clara Soto-Bernardini, Teresa Johnson-Pais, Robin J. Leach, Alfonso Ontiveros, Humberto Nicolini, Ricardo Mendoza, Alvaro Jerez, Albana Dassori, Ivan Chavarria-Siles, Michael A. Escamilla and Henriette Raventos

      Version of Record online: 27 MAY 2008 | DOI: 10.1002/ajmg.b.30791

    5. Association study between the PIK4CA gene and methamphetamine use disorder in a Japanese population (pages 233–238)

      Nobuhisa Kanahara, Ryosuke Miyatake, Yoshimoto Sekine, Toshiya Inada, Norio Ozaki, Nakao Iwata, Mutsuo Harano, Tokutaro Komiyama, Mitsuhiko Yamada, Ichiro Sora, Hiroshi Ujike, Masaomi Iyo and Kenji Hashimoto

      Version of Record online: 2 JUN 2008 | DOI: 10.1002/ajmg.b.30797

    6. Analysis of genetic variations in the RGS9 gene and antipsychotic-induced tardive dyskinesia in schizophrenia (pages 239–242)

      Ying-Jay Liou, Mao-Liang Chen, Ying-Chieh Wang, Jen-Yeu Chen, Ding-Lieh Liao, Ya-Mei Bai, Chao-Cheng Lin, Tzu-Ting Chen, Geng-Han Mo and I-Ching Lai

      Version of Record online: 11 JUN 2008 | DOI: 10.1002/ajmg.b.30796

    7. Mitochondrial DNA haplogroup analysis in patients with bipolar disorder (pages 243–247)

      An-a Kazuno, Kae Munakata, Kanako Mori, Shinichiro Nanko, Hiroshi Kunugi, Kazuhiko Nakamura, Norio Mori, Kazuo Yamada, Takeo Yoshikawa, Nobumasa Kato and Tadafumi Kato

      Version of Record online: 10 JUN 2008 | DOI: 10.1002/ajmg.b.30804

    8. A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; Extra-short alleles and accumulated allele homozygosity (pages 248–253)

      Y. Heshmati, A. Mirabzadeh, G. Feizzade, M. Gilanipour, M.R. Etminan, H.R. Khoram Khorshid, K. Kamali, M. Fakhri, N. Moghimi, H. Najmabadi and M. Ohadi

      Version of Record online: 16 JUN 2008 | DOI: 10.1002/ajmg.b.30805

    9. The impact of genetic variation in DRD2 and SLC6A3 on smoking cessation in a cohort of participants 1 year after enrollment in a lung cancer screening study (pages 254–261)

      Mindi A. Styn, Tomoko Nukui, Marjorie Romkes, Kenneth Perkins, Stephanie R. Land and Joel L. Weissfeld

      Version of Record online: 18 JUN 2008 | DOI: 10.1002/ajmg.b.30801

    10. Risk of cognitive impairment in female premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models (pages 262–270)

      Mónica Mínguez, Berta Ibáñez, Maria-Pilar Ribate, Feliciano Ramos, Eva García-Alegría, Aránzazu Fernández-Rivas, Eduardo Ruiz-Parra, Marisa Poch, Angel Alonso, Cristina Martinez-Bouzas, Elena Beristain and Maria-Isabel Tejada

      Version of Record online: 18 JUN 2008 | DOI: 10.1002/ajmg.b.30803

    11. 5-HTTLPR genotype and anxiety-related personality traits: A meta-analysis and new data (pages 271–281)

      Marcus R. Munafò, Nelson B. Freimer, Whitney Ng, Roel Ophoff, Juha Veijola, Jouko Miettunen, Marjo-Riitta Järvelin, Anja Taanila and Jonathan Flint

      Version of Record online: 10 JUN 2008 | DOI: 10.1002/ajmg.b.30808

    12. Dopamine transporter polymorphism modulates oculomotor function and DAT1 mRNA expression in schizophrenia (pages 282–289)

      Ikwunga Wonodi, L. Elliot Hong, O. Colin Stine, Braxton D. Mitchell, Amie Elliott, Rosalinda C. Roberts, Robert R. Conley, Robert P. McMahon and Gunvant K. Thaker

      Version of Record online: 13 JUN 2008 | DOI: 10.1002/ajmg.b.30811

  3. Brief Research Communication

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Brief Research Communication
    5. Brief Research Communications
    6. Erratum
    1. Angiotensin I-converting enzyme I/D polymorphism and suicidal behaviors (pages 290–294)

      D. Larry Sparks, John C. Hunsaker III, Philippe Amouyel, Alain Malafosse, Franck Bellivier, Marion Leboyer, Philippe Courtet and Nicole Helbecque

      Version of Record online: 2 JUN 2008 | DOI: 10.1002/ajmg.b.30793

    2. Association between depression and the Gln460Arg polymorphism of P2RX7 Gene: A dimensional approach (pages 295–299)

      Krisztina Hejjas, Anna Szekely, Eszter Domotor, Zsuzsa Halmai, Gabriella Balogh, Boglarka Schilling, Andrea Sarosi, Gabor Faludi, Maria Sasvari-Szekely and Zsofia Nemoda

      Version of Record online: 9 JUN 2008 | DOI: 10.1002/ajmg.b.30799

  4. Brief Research Communications

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Brief Research Communication
    5. Brief Research Communications
    6. Erratum
    1. Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios (pages 300–306)

      Hyo-Won Kim, Soo-Churl Cho, Jae-Won Kim, In Hee Cho, Soon Ae Kim, Mira Park, Eun Jeong Cho and Hee-Jeong Yoo

      Version of Record online: 18 JUN 2008 | DOI: 10.1002/ajmg.b.30798

  5. Erratum

    1. Top of page
    2. Rapid Publications
    3. Research Articles
    4. Brief Research Communication
    5. Brief Research Communications
    6. Erratum
    1. You have free access to this content
      No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder (page 307)

      X. Xu, E. A. Duman, R. Anney, K. Brookes, B. Franke, K. Zhou, C. Buschgens, W. Chen, H. Christiansen, J. Eisenberg, I. Gabriëls, I. Manor, R. Marco, U.C. Müller, A. Mulligan, N. Rommelse, M. Thompson, H. Uebel, T. Banaschewski, J. Buitelaar, R. Ebstein, M. Gill, A. Miranda, F. Mulas, R.D. Oades, H. Roeyers, A. Rothenberger, J. Sergeant, E. Sonuga-Barke, H.-C. Steinhausen, E. Taylor, S.V. Faraone and P. Asherson

      Version of Record online: 3 FEB 2009 | DOI: 10.1002/ajmg.b.30921

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