American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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

5 February 2005

Volume 133B, Issue 1

Pages 1–130

  1. Brief Research Communications

    1. Top of page
    2. Brief Research Communications
    3. Research Articles
    4. Brief Research Communications
    1. Assessing the validity of blood-based gene expression profiles for the classification of schizophrenia and bipolar disorder: A preliminary report (pages 1–5)

      Ming T. Tsuang, Nadine Nossova, Tom Yager, Min-Min Tsuang, Shi-Chin Guo, Kou Ge Shyu, Stephen J. Glatt and C.C. Liew

      Version of Record online: 11 JAN 2005 | DOI: 10.1002/ajmg.b.30161

  2. Research Articles

    1. Top of page
    2. Brief Research Communications
    3. Research Articles
    4. Brief Research Communications
    1. Family history influences age of onset in bipolar I disorder in females but not in males (pages 6–11)

      Maria Grigoroiu-Serbanescu, Markus M. Nöthen, Stephanie Ohlraun, Peter Propping, Wolfgang Maier, Priya Wickramaratne, Marie-Jana Georgescu, Dan Prelipceanu, Mihaela Grimberg, Dorina Sima and Marcella Rietschel

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30133

    2. Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder (pages 12–17)

      Dilberto O. Ferraren, Chunyu Liu, Judith A. Badner, Winston Corona, Azadeh Rezvani, Virginia D. Monje, Elliot S. Gershon, Tom I. Bonner and Sevilla D. Detera-Wadleigh

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30121

    3. Joint multi-population analysis for genetic linkage of bipolar disorder or “wellness” to chromosome 4p (pages 18–24)

      P.M. Visscher, C.S. Haley, H. Ewald, O. Mors, J. Egeland, B. Thiel, E. Ginns, W. Muir and D.H. Blackwood

      Version of Record online: 23 NOV 2004 | DOI: 10.1002/ajmg.b.30108

    4. A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder (pages 25–30)

      H. Ewald, F.P. Wikman, B.M. Teruel, H.N. Buttenschön, M. Torralba, T.D. Als, A. El Daoud, T.J. Flint, T.H. Jorgensen, L. Blanco, T.A. Kruse, T.F. Orntoft and O. Mors

      Version of Record online: 22 NOV 2004 | DOI: 10.1002/ajmg.b.30106

    5. Familial aggregation of schizophrenia-spectrum disorders and obsessive-compulsive associated disorders in schizophrenia probands with and without OCD (pages 31–36)

      Michael Poyurovsky, Victoria Kriss, Gregory Weisman, Sarit Faragian, Michael Schneidman, Camil Fuchs, Abraham Weizman and Ronit Weizman

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30148

    6. Familial cognitive deficits in schizophrenia (pages 43–49)

      Anne L. Hoff, Christine Svetina, Andrea M. Maurizio, Timothy J. Crow, Kate Spokes and Lynn E. DeLisi

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30120

    7. Structural variants in the retinoid receptor genes in patients with schizophrenia and other psychiatric diseases (pages 50–53)

      Jinong Feng, Jiesheng Chen, Jin Yan, Ian R. Jones, Nick Craddock, Edwin H. Cook Jr., David Goldman, Leonard L. Heston and Steve S. Sommer

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30113

    8. Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): Increased prevalence of the 2-repeat allele (pages 54–56)

      Patrick W.L. Leung, C.C. Lee, S.F. Hung, T.P. Ho, C.P. Tang, S.L. Kwong, S.Y. Leung, S.T. Yuen, F. Lieh-Mak, Jaap Oosterlaan, Deborah Grady, Ante Harxhi, Y.C. Ding, H.C. Chi, Pamela Flodman, Sabrina Schuck, M. Anne Spence, Robert Moyzis and James Swanson

      Version of Record online: 2 DEC 2004 | DOI: 10.1002/ajmg.b.30129

    9. Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder (pages 57–63)

      Karen Müller Smith, Lorri Bauer, Mariellen Fischer, Russell Barkley and Bradford A. Navia

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30127

    10. A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) (pages 64–67)

      D. Turic, H. Williams, K. Langley, M. Owen, A. Thapar and M.C. O'Donovan

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30123

    11. Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B (pages 68–73)

      Jonathan Mill, Xiaohui Xu, Angelica Ronald, Sarah Curran, Tom Price, Jo Knight, Ian Craig, Pak Sham, Robert Plomin and Philip Asherson

      Version of Record online: 2 DEC 2004 | DOI: 10.1002/ajmg.b.30107

    12. Serotonin transporter promoter polymorphism and monoamine oxidase type A VNTR allelic variants together influence alcohol binge drinking risk in young women (pages 74–78)

      Aryeh I. Herman, Kristi M. Kaiss, Rui Ma, John W. Philbeck, Asfar Hasan, Humza Dasti and Paolo B. DePetrillo

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30135

    13. GRIN1 locus may modify the susceptibility to seizures during alcohol withdrawal (pages 85–87)

      D. Rujescu, M. Soyka, N. Dahmen, U. Preuß, A.M. Hartmann, I. Giegling, G. Koller, B. Bondy, H.-J. Möller and A. Szegedi

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30112

    14. Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease (pages 88–92)

      Anna Håkansson, Lars Westberg, Staffan Nilsson, Silvia Buervenich, Andrea Carmine, Björn Holmberg, Olof Sydow, Lars Olson, Bo Johnels, Elias Eriksson and Hans Nissbrandt

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30136

    15. Serotonin transporter intron 2 polymorphism associated with rigid-compulsive behaviors in Dutch individuals with pervasive developmental disorder (pages 93–96)

      Erik J. Mulder, George M. Anderson, Ido P. Kema, Astrid M. Brugman, Cees E.J. Ketelaars, Annelies de Bildt, Natasja D.J. van Lang, Johan A. den Boer and Ruud B. Minderaa

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30122

    16. Clozapine-induced weight gain associated with the 5HT2C receptor −759C/T polymorphism (pages 97–100)

      Del D. Miller, Vicki L. Ellingrod, Timothy L. Holman, Peter F. Buckley and Stephan Arndt

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30115

    17. The 3111T/C polymorphism of hClock is associated with evening preference and delayed sleep timing in a Japanese population sample (pages 101–104)

      Kazuo Mishima, Takuma Tozawa, Kohtoku Satoh, Hidetomo Saitoh and Yumiko Mishima

      Version of Record online: 2 DEC 2004 | DOI: 10.1002/ajmg.b.30110

    18. Novel exonic μ-opioid receptor gene (OPRM1) polymorphisms not associated with opioid dependence (pages 105–109)

      Rachel J. Smith, Glenn A. Doyle, Angela M. Han, James J. Crowley, David W. Oslin, Ashwin A. Patkar, Paolo Mannelli, Peter A. DeMaria Jr., Charles P. O'Brien and Wade H. Berrettini

      Version of Record online: 22 NOV 2004 | DOI: 10.1002/ajmg.b.30105

    19. Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders (pages 110–115)

      Jessica A. Lasky-Su, Stephen V. Faraone, Stephen J. Glatt and Ming T. Tsuang

      Version of Record online: 2 DEC 2004 | DOI: 10.1002/ajmg.b.30104

    20. Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease (pages 120–123)

      Jordi Clarimon, Janel Johnson, Okan Dogu, Wagner Horta, Naheed Khan, Andrew J. Lees, John Hardy and Andrew Singleton

      Version of Record online: 5 JAN 2005 | DOI: 10.1002/ajmg.b.30119

    21. Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus (pages 124–126)

      Quasar Saleem Padiath, Achal Kumar Srivastava, Sanghmitra Roy, Satish Jain and Samir Kumar Brahmachari

      Version of Record online: 29 SEP 2004 | DOI: 10.1002/ajmg.b.30088

  3. Brief Research Communications

    1. Top of page
    2. Brief Research Communications
    3. Research Articles
    4. Brief Research Communications
    1. New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts (pages 127–130)

      Milena Cannella, Vittorio Maglione, Tiziana Martino, Maria Simonelli, Giuseppe Ragona and Ferdinando Squitieri

      Version of Record online: 15 NOV 2004 | DOI: 10.1002/ajmg.b.30125

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