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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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

5 January 2007

Volume 144B, Issue 1

Pages 1–128

  1. Editorials

    1. Top of page
    2. Editorials
    3. Research Articles
    4. Brief Research Communications
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      Persistence problem in schizophrenia and mitochondrial DNA (pages 1–4)

      Nagafumi Doi and Yoko Hoshi

      Version of Record online: 10 OCT 2006 | DOI: 10.1002/ajmg.b.30348

  2. Research Articles

    1. Top of page
    2. Editorials
    3. Research Articles
    4. Brief Research Communications
    1. You have free access to this content
      The Palau early psychosis study: Distribution of cases by level of genetic risk (pages 5–9)

      Marina Myles-Worsley, Francisca Blailes, Lisa M. Ord, Starla Weaver, Gregory Dever and Stephen V. Faraone

      Version of Record online: 10 OCT 2006 | DOI: 10.1002/ajmg.b.30362

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      Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy (pages 10–13)

      Susanne Lorenz, Armin Heils, Johannes M. Kasper and Thomas Sander

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30369

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      Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects (pages 14–19)

      Jun Li, Yufeng Wang, Rulun Zhou, Haobo Zhang, Li Yang, Bing Wang and Stephen V. Faraone

      Version of Record online: 29 AUG 2006 | DOI: 10.1002/ajmg.b.30373

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      Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome (pages 27–36)

      Kathryn Eve Lewandowski, Vandana Shashi, Peggy M. Berry and Thomas R. Kwapil

      Version of Record online: 10 OCT 2006 | DOI: 10.1002/ajmg.b.30379

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      Further evidence of MAO-A gene variants associated with bipolar disorder (pages 37–40)

      Daniel J. Müller, Alessandro Serretti, Tricia Sicard, Subi Tharmalingam, Nicole King, Paola Artioli, Laura Mandelli, Cristina Lorenzi and James L. Kennedy

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30380

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      Recurrence risk to offspring in extended multiplex schizophrenia pedigrees from a pacific island isolate (pages 41–44)

      Marina Myles-Worsley, Josepha Tiobech, Francisca Blailes, Victor M. Yano and Stephen V. Faraone

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30384

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      Positive association of schizophrenia to JARID2 gene (pages 45–51)

      Erika Pedrosa, Kenny Ye, Karen A. Nolan, Lauren Morrell, Jeffrey M. Okun, Adam D. Persky, Takuya Saito and Herbert M. Lachman

      Version of Record online: 11 SEP 2006 | DOI: 10.1002/ajmg.b.30386

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      Perceived parenting behavior in the childhood of cocaine users: Relationship with genotype and personality traits (pages 52–57)

      G. Gerra, A. Zaimovic, L. Garofano, F. Ciusa, G. Moi, P. Avanzini, E. Talarico, F. Gardini, F. Brambilla, M. Manfredini and C. Donnini

      Version of Record online: 13 SEP 2006 | DOI: 10.1002/ajmg.b.30388

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      The role of RELN in lissencephaly and neuropsychiatric disease (pages 58–63)

      Bernard S. Chang, Fusun Duzcan, Seonhee Kim, Mine Cinbis, Abha Aggarwal, Kira A. Apse, Osman Ozdel, Munevver Atmaca, Sevil Zencir, Huseyin Bagci and Christopher A. Walsh

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30392

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      Schizotypal dimensions: An intermediate phenotype associated with the COMT high activity allele (pages 64–68)

      Franck Schürhoff, Andrei Szöke, Fabien Chevalier, Isabelle Roy, Alexandre Méary, Frank Bellivier, Bruno Giros and Marion Leboyer

      Version of Record online: 10 OCT 2006 | DOI: 10.1002/ajmg.b.30395

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      Serotonin genes and attention deficit/hyperactivity disorder in a Brazilian sample: Preferential transmission of the HTR2A 452His allele to affected boys (pages 69–73)

      Ana Paula M. Guimarães, Cristian Zeni, Guilherme V. Polanczyk, Julia P. Genro, Tatiana Roman, Luis A. Rohde and Mara H. Hutz

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30400

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      Autistic-spectrum disorders in down syndrome: Further delineation and distinction from other behavioral abnormalities (pages 87–94)

      John C. Carter, George T. Capone, Robert M. Gray, Christiane S. Cox and Walter E. Kaufmann

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30407

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      Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins (pages 95–100)

      M. Luciano, E. Hine, M.J. Wright, D.L. Duffy, J. MacMillan and N.G. Martin

      Version of Record online: 11 SEP 2006 | DOI: 10.1002/ajmg.b.30413

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      Serotonin transporter mRNA levels are associated with the methylation of an upstream CpG island (pages 101–105)

      Robert Philibert, Anup Madan, Allan Andersen, Remi Cadoret, Hans Packer and Harinder Sandhu

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30414

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      Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR-CGG-repeat-allele effect on autism (pages 106–112)

      Shruti Dutta, Subhrangshu Guhathakurta, Swagata Sinha, Anindita Chatterjee, Shabina Ahmed, Saurabh Ghosh, Prasanta K. Gangopadhyay, Manoranjan Singh and Rajamma Usha

      Version of Record online: 29 AUG 2006 | DOI: 10.1002/ajmg.b.30419

  3. Brief Research Communications

    1. Top of page
    2. Editorials
    3. Research Articles
    4. Brief Research Communications
    1. You have free access to this content
      Schizophrenia is not associated with the functional candidate gene ERBB3: Results from a case-control study (pages 113–116)

      Tetsufumi Kanazawa, Stephen J. Glatt, Atsushi Tsutsumi, Hiroki Kikuyama, Jun Koh, Hiroshi Yoneda and Ming T. Tsuang

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30367

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      IGF1, growth pathway polymorphisms and schizophrenia: A pooling study (pages 117–120)

      D. Gunnell, S. Lewis, J. Wilkinson, L. Georgieva, G. Smith Davey, I.N.M. Day, J.M.P. Holly, M.C. O'Donovan, M.J. Owen, G. Kirov and S. Zammit

      Version of Record online: 16 OCT 2006 | DOI: 10.1002/ajmg.b.30396

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      The serotonin receptor HTR1B: Gene polymorphisms in attention deficit hyperactivity disorder (pages 121–125)

      Abel Ickowicz, Yu Feng, Karen Wigg, Jennifer Quist, Tejasawe Pathare, Wendy Roberts, Molly Malone, Russell Schachar, Rosemary Tannock, James L. Kennedy and Catyh L. Barr

      Version of Record online: 6 SEP 2006 | DOI: 10.1002/ajmg.b.30398

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      Analysis of the 5HT-2A T102C receptor polymorphism and psychotic symptoms in Alzheimer's disease (pages 126–128)

      David Craig, Caroline Donnelly, Dominic Hart, Robyn Carson and Peter Passmore

      Version of Record online: 11 SEP 2006 | DOI: 10.1002/ajmg.b.30409

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