American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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

15 February 2004

Volume 125B, Issue 1

Pages 1–130

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. Nongenetic pathologic developments of brain-wave patterns in monozygotic twins discordant and concordant for schizophrenia (pages 1–9)

      M. Weisbrod, H. Hill, H. Sauer, R. Niethammer, S. Guggenbühl, D. Hell and H.H. Stassen

      Version of Record online: 25 AUG 2003 | DOI: 10.1002/ajmg.b.20080

    2. No evidence of association or linkage disequilibrium between polymorphisms in the 5′ upstream and coding regions of the dopamine D4 receptor gene and schizophrenia in a Portuguese population (pages 20–24)

      Alda M. Ambrósio, James L. Kennedy, Fabio Macciardi, Cathy Barr, Maria J. Soares, Catarina R. Oliveira and Carlos N. Pato

      Version of Record online: 20 AUG 2003 | DOI: 10.1002/ajmg.b.20084

    3. CALCYON gene variation, schizophrenia, and cocaine dependence (pages 25–30)

      Xingguang Luo, Henry Kranzler, Jaakko Lappalainen, Robert Rosenheck, Dennis Charney, Lingjun Zuo, Joseph Erdos, Daniel P. van Kammen and Joel Gelernter

      Version of Record online: 2 SEP 2003 | DOI: 10.1002/ajmg.b.20092

    4. Is the WKL1 gene associated with schizophrenia? (pages 31–37)

      M. Kaganovich, A. Peretz, M. Ritsner, U. Bening Abu-Shach, B. Attali and R. Navon

      Version of Record online: 19 SEP 2003 | DOI: 10.1002/ajmg.b.20115

    5. Polymorphisms in the dopamine D5 receptor (DRD5) gene and ADHD (pages 38–42)

      Jonathan Mill, Sarah Curran, Sandra Richards, Eric Taylor and Philip Asherson

      Version of Record online: 10 SEP 2003 | DOI: 10.1002/ajmg.b.20127

    6. Confirming RGS4 as a susceptibility gene for schizophrenia (pages 50–53)

      Derek W. Morris, Alana Rodgers, Kevin A. McGhee, Siobhan Schwaiger, Paul Scully, John Quinn, David Meagher, John L. Waddington, Michael Gill and Aiden P. Corvin

      Version of Record online: 5 SEP 2003 | DOI: 10.1002/ajmg.b.20109

  2. Brief Research Communications

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism (pages 54–56)

      John B. Vincent, Sandy Thevarkunnel, Debbie Kolozsvari, Andrew D. Paterson, Wendy Roberts and Stephen W. Scherer

      Version of Record online: 12 AUG 2003 | DOI: 10.1002/ajmg.b.20088

  3. Brief Research Communication

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. No association between the APOE gene and autism (pages 57–60)

      K.L. Raiford, Y. Shao, I.C. Allen, E.R. Martin, M.M. Menold, H.H. Wright, R.K. Abramson, G. Worley, G.R. DeLong, J.M. Vance, M.L. Cuccaro, J.R. Gilbert and M.A. Pericak-Vance

      Version of Record online: 5 SEP 2003 | DOI: 10.1002/ajmg.b.20104

  4. Letters to the Editor

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. Notch4 gene polymorphisms are not associated with autism in Japanese population (pages 61–62)

      Shinko Koishi, Kosuke Yamazaki, Kenji Yamamoto, Seiji Koishi, Youichi Enseki, Yuri Nakamura, Akitoshi Oya, Mitsuaki Yasueda, Arata Asakura, Yutaka Aoki, Mariko Atsumi, Jyoji Inomata, Hidetoshi Inoko and Hideo Matsumoto

      Version of Record online: 29 AUG 2003 | DOI: 10.1002/ajmg.b.20113

  5. Research Articles

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. Association of tryptophan 2,3 dioxygenase gene polymorphism with autism (pages 63–68)

      Rafiqun Nabi, Fatema J. Serajee, Diane C. Chugani, Hailang Zhong and A.H.M. Mahbubul Huq

      Version of Record online: 24 SEP 2003 | DOI: 10.1002/ajmg.b.20147

    2. Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: A family based association study (pages 69–78)

      Ayman H. Fanous, M.C. Neale, R.E. Straub, B.T. Webb, A.F. O'Neill, D. Walsh and K.S. Kendler

      Version of Record online: 29 SEP 2003 | DOI: 10.1002/ajmg.b.20103

    3. Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation (pages 79–82)

      Stuart Pickering-Brown, Matt Baker, Thomas Bird, John Trojanowski, Virginia Lee, Huw Morris, Martin Rossor, John C. Janssen, David Neary, David Craufurd, Anna Richardson, Julie Snowden, John Hardy, David Mann and Mike Hutton

      Version of Record online: 25 AUG 2003 | DOI: 10.1002/ajmg.b.20083

  6. Brief Research Communications

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33 (pages 83–86)

      Kyung Sue Hong, L. Alison McInnes, Susan K. Service, Terry Song, Jennifer Lucas, Sandra Silva, Eduardo Fournier, Pedro León, Julio Molina, Victor I. Reus, Lodewijk A. Sandkuijl and Nelson B. Freimer

      Version of Record online: 25 AUG 2003 | DOI: 10.1002/ajmg.b.20091

  7. Research Articles

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    4. Brief Research Communication
    5. Letters to the Editor
    6. Research Articles
    7. Brief Research Communications
    8. Research Articles
    1. No association between the insulin degrading enzyme gene and Alzheimer's disease in a Japanese population (pages 87–91)

      Ayumu Sakai, Hiroshi Ujike, Kenji Nakata, Yasushi Takehisa, Takaki Imamura, Naohiko Uchida, Akihiro Kanzaki, Mitsutoshi Yamamoto, Yoshikatsu Fujisawa, Kazuya Okumura and Shigetoshi Kuroda

      Version of Record online: 29 AUG 2003 | DOI: 10.1002/ajmg.b.20106

    2. The gender effect in juvenile Huntington disease patients of Italian origin (pages 92–98)

      Milena Cannella, Cinzia Gellera, Vittorio Maglione, Patrizia Giallonardo, Giuliana Cislaghi, Maria Muglia, Aldo Quattrone, Francesco Pierelli, Stefano Di Donato and Ferdinando Squitieri

      Version of Record online: 2 SEP 2003 | DOI: 10.1002/ajmg.b.20110

    3. An investigation into sub-telomeric deletions of chromosome 22 and pervasive developmental disorders (pages 99–104)

      Kumudini Nair-Miranda, Ashleigh Murch, Beverly Petterson, Wayne Hill, Amelia Nikolova-Hill, Linda Bradley, Sandy Jackson and Joachim Hallmayer

      Version of Record online: 19 SEP 2003 | DOI: 10.1002/ajmg.b.20101

    4. Association of adverse childhood experiences, age of menarche, and adult reproductive behavior: Does the androgen receptor gene play a role? (pages 105–111)

      Anthony F. Jorm, Helen Christensen, Bryan Rodgers, Patricia A. Jacomb and Simon Easteal

      Version of Record online: 2 SEP 2003 | DOI: 10.1002/ajmg.b.20114

    5. A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5 (pages 112–119)

      Ging-Yuek R. Hsiung, Bonnie J. Kaplan, Tracey L. Petryshen, Shao Lu and L. Leigh Field

      Version of Record online: 25 AUG 2003 | DOI: 10.1002/ajmg.b.20082

    6. Haplotypes of the monoamine oxidase genes and the risk for substance use disorders (pages 120–125)

      Michael M. Vanyukov, Brion S. Maher, Bernie Devlin, Ralph E. Tarter, Galina P. Kirillova, Ling-Mei Yu and Robert E. Ferrell

      Version of Record online: 5 SEP 2003 | DOI: 10.1002/ajmg.b.20105

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