American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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

15 May 2003

Volume 119B, Issue 1

Pages 1–130

  1. Editor's Note

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
    9. Brief Research Communication
    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
    1. Editor's note (page 1)

      Stephen V. Faraone

      Version of Record online: 14 MAR 2003 | DOI: 10.1002/ajmg.b.20027

  2. Rapid Publication

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
    9. Brief Research Communication
    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
    1. Reduced expression of the muscarinic 1 receptor cortical subtype in schizophrenia (pages 2–6)

      D. Mancama, MJ. Arranz, S. Landau and R. Kerwin

      Version of Record online: 5 MAR 2003 | DOI: 10.1002/ajmg.b.20020

  3. Brief Research Communication

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
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    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
  4. Research Articles

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
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    10. Research Articles
    11. Brief Research Communication
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    13. Research Articles
    1. 5HTTLPR polymorphism in schizophrenic patients: Further support for association with violent suicide attempts (pages 13–17)

      F.J. Bayle, S. Leroy, D. Gourion, B. Millet, J.P. Olié, M.F. Poirier and M.O. Krebs

      Version of Record online: 7 MAR 2003 | DOI: 10.1002/ajmg.b.10037

    2. Apolipoprotein E in schizophrenia: A French association study and meta-analysis (pages 18–23)

      Franck Schürhoff, Marie-Odile Krebs, Andrei Szöke, Jean-Yves Loze, Céline Goldberger, Valérie Quignon, Jean Tignol, Frédéric Rouillon, Jean-Louis Laplanche and Marion Leboyer

      Version of Record online: 28 JAN 2003 | DOI: 10.1002/ajmg.b.20007

  5. Brief Research Communications

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
    9. Brief Research Communication
    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
    1. N-methyl-d-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case-control analyses (pages 24–27)

      Livia Martucci, Albert H.C. Wong, Joseph Trakalo, Tasha Cate-Carter, Gregory W.H. Wong, Fabio M. Macciardi and James L. Kennedy

      Version of Record online: 7 MAR 2003 | DOI: 10.1002/ajmg.b.20014

  6. Research Articles

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
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    10. Research Articles
    11. Brief Research Communication
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    13. Research Articles
    1. Dopamine D2 receptor gene Ser311Cys variant and schizophrenia: association study and meta-analysis (pages 28–34)

      Erik G Jönsson, Anna Sillén, Maria Vares, Birgit Ekholm, Lars Terenius and Göran C Sedvall

      Version of Record online: 22 JAN 2003 | DOI: 10.1002/ajmg.b.20004

    2. Family-based and case–control study of catechol-O-methyltransferase in schizophrenia among Palestinian Arabs (pages 35–39)

      I. Kremer, M. Pinto, I. Murad, M. Muhaheed, I. Bannoura, D.J. Muller, T.G. Schulze, A. Reshef, M. Blanaru, S. Gathas, R. Goichman, M. Rietschel, M. Dobrusin, R. Bachner-Melman, L. Nemanov, R.H. Belmaker, W. Maier and R.P. Ebstein

      Version of Record online: 28 JAN 2003 | DOI: 10.1002/ajmg.b.20008

  7. Brief Research Communications

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
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    8. Brief Research Communications
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    10. Research Articles
    11. Brief Research Communication
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    13. Research Articles
    1. Depression in Alzheimer's disease: The effect of serotonin receptor gene variation (pages 40–43)

      Clive Holmes, Maria Arranz, David Collier, John Powell and Simon Lovestone

      Version of Record online: 28 JAN 2003 | DOI: 10.1002/ajmg.b.10068

  8. Brief Research Communication

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
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    13. Research Articles
    1. Specific BACE1 genotypes provide additional risk for late-onset alzheimer disease in APOE ε4 carriers (pages 44–47)

      Gabriel Gold, Jean-Louis Blouin, François R. Herrmann, Agnès Michon, Reinhild Mulligan, Geneviève Duriaux Saïl, Constantin Bouras, Prof. Panteleimon Giannakopoulos and Prof. Stylianos E. Antonarakis

      Version of Record online: 4 MAR 2003 | DOI: 10.1002/ajmg.b.10010

  9. Research Articles

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
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    1. Association of HFE mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with APOE (pages 48–53)

      Joseph F. Pulliam, C. Darrell Jennings, Richard J. Kryscio, Daron G. Davis, Dianne Wilson, Thomas J. Montine, Frederick A. Schmitt and William R. Markesbery

      Version of Record online: 19 FEB 2003 | DOI: 10.1002/ajmg.b.10069

    2. Evaluation of the genes for the adrenergic receptors α2A and α1C and Gilles de la Tourette Syndrome (pages 54–59)

      Chun Xu, Fatih Ozbay, Karen Wigg, Rayzie Shulman, Eda Tahir, Yanki Yazgan, Paul Sandor and Cathy L. Barr

      Version of Record online: 28 JAN 2003 | DOI: 10.1002/ajmg.b.20001

  10. Brief Research Communication

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
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    13. Research Articles
    1. HLA-DRB genotyping in Gilles de la Tourette patients and their parents (pages 60–64)

      Sarah Schoenian, Inke König, Wolfgang Oertel, Helmut Remschmidt, Andreas Ziegler, Johannes Hebebrand and Oliver Bandmann

      Version of Record online: 22 JAN 2003 | DOI: 10.1002/ajmg.b.20003

  11. Brief Research Communications

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
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    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
  12. Research Articles

    1. Top of page
    2. Editor's Note
    3. Rapid Publication
    4. Brief Research Communication
    5. Research Articles
    6. Brief Research Communications
    7. Research Articles
    8. Brief Research Communications
    9. Brief Research Communication
    10. Research Articles
    11. Brief Research Communication
    12. Brief Research Communications
    13. Research Articles
    1. Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X (pages 69–76)

      Peter P. Zandi, Virginia L. Willour, Yuqing Huo, Jennifer Chellis, James B. Potash, Dean F. MacKinnon, Sylvia G. Simpson, Francis J. McMahon, Elliot Gershon, Theodore Reich, Tatiana Foroud, John Nurnberger Jr., J. Raymond DePaulo Jr. and Melvin G. McInnis

      Version of Record online: 7 FEB 2003 | DOI: 10.1002/ajmg.b.10063

    2. Association of the dopamine beta hydroxylase gene with attention deficit hyperactivity disorder: Genetic analysis of the Milwaukee longitudinal study (pages 77–85)

      Karen Müller Smith, Mark Daly, Mariellen Fischer, Constantin T. Yiannoutsos, Lorri Bauer, Russell Barkley and Bradford A. Navia

      Version of Record online: 19 FEB 2003 | DOI: 10.1002/ajmg.b.20005

    3. CHIP: Defining a dimension of the vulnerability to attention deficit hyperactivity disorder (ADHD) using sibling and individual data of children in a community-based sample (pages 86–97)

      Sarah Curran, Fruhling Rijsdijk, Neilson Martin, Katja Marusic, Philip Asherson, Eric Taylor and Pak Sham

      Version of Record online: 24 FEB 2003 | DOI: 10.1002/ajmg.b.20002

    4. No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21-q22 and autism (pages 98–101)

      Rafiqun Nabi, Hailang Zhong, Fatema J Serajee and AHM Mahbubul Huq

      Version of Record online: 14 MAR 2003 | DOI: 10.1002/ajmg.b.10012

    5. Study of MECP2 gene in Rett syndrome variants and autistic girls (pages 102–107)

      Michele Zappella, Ilaria Meloni, Ilaria Longo, Roberto Canitano, Giuseppe Hayek, Lucia Rosaia, Francesca Mari and Alessandra Renieri

      Version of Record online: 6 JAN 2003 | DOI: 10.1002/ajmg.b.10070

    6. Wolfram syndrome and suicide: Evidence for a role of WFS1 in suicidal and impulsive behavior (pages 108–113)

      Adolfo Sequeira, Caroline Kim, Monique Seguin, Alain Lesage, Nadia Chawky, Alex Desautels, Michel Tousignant, Claude Vanier, Olivier Lipp, Chawki Benkelfat, Guy Rouleau and Gustavo Turecki

      Version of Record online: 7 MAR 2003 | DOI: 10.1002/ajmg.b.20011

    7. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation (pages 114–117)

      Lucie Maréchal, Grégory Raux, Cécile Dumanchin, Guillaume Lefebvre, Emmanuelle Deslandre, Carole Girard, Dominique Campion, Dominique Parain, Thierry Frebourg and Didier Hannequin

      Version of Record online: 7 MAR 2003 | DOI: 10.1002/ajmg.b.10062

    8. Genetics of recurrent early-onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies (pages 118–130)

      Douglas F. Levinson, George S. Zubenko, Raymond R. Crowe, Raymond J. DePaulo, William S. Scheftner, Myrna M. Weissman, Peter Holmans, Wendy N. Zubenko, Sandra Boutelle, Kathleen Murphy-Eberenz, Dean MacKinnon, Melvin G. McInnis, Diana H. Marta, Philip Adams, Stephanie Sassoon, James A. Knowles, Jo Thomas and Jennifer Chellis

      Version of Record online: 28 JAN 2003 | DOI: 10.1002/ajmg.b.20009

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