American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Copyright © 2012 Wiley-Liss, Inc., A Wiley Company

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

June 2010

Volume 153B, Issue 4

Pages 847–982

  1. Editorials

    1. Top of page
    2. Editorials
    3. Rapid Publications
    4. Research Articles
    5. Brief Research Communications
    6. Letters to the Editor
    1. The P-value illusion: How to improve (psychiatric) genetic studies (pages 847–849)

      Alexander B. Niculescu and Helen Le-Niculescu

      Article first published online: 17 MAR 2010 | DOI: 10.1002/ajmg.b.31076

  2. Rapid Publications

    1. Top of page
    2. Editorials
    3. Rapid Publications
    4. Research Articles
    5. Brief Research Communications
    6. Letters to the Editor
    1. You have free access to this content
      Coming to grips with complex disorders: Genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics (pages 850–877)

      S.D. Patel, H. Le-Niculescu, D.L. Koller, S.D. Green, D.K. Lahiri, F.J. McMahon, J.I. Nurnberger Jr and A.B. Niculescu III

      Article first published online: 9 APR 2010 | DOI: 10.1002/ajmg.b.31087

  3. Research Articles

    1. Top of page
    2. Editorials
    3. Rapid Publications
    4. Research Articles
    5. Brief Research Communications
    6. Letters to the Editor
    1. A systematic association mapping on chromosome 6q in bipolar affective disorder—evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder (pages 878–884)

      Rami Abou Jamra, Thomas G. Schulze, Tim Becker, Felix F. Brockschmidt, Elaine Green, Margrieta A. Alblas, Jens R. Wendland, Mazda Adli, Detelina Grozeva, Jana Strohmeier, Alexander Georgi, Nick Craddock, Peter Propping, Marcella Rietschel, Markus M. Nöthen, Sven Cichon and Johannes Schumacher

      Article first published online: 19 NOV 2009 | DOI: 10.1002/ajmg.b.31051

    2. Heritability estimates for cognitive factors and brain white matter integrity as markers of schizophrenia (pages 885–894)

      Hilary Bertisch, Dawei Li, Matthew J. Hoptman and Lynn E. DeLisi

      Article first published online: 5 JAN 2010 | DOI: 10.1002/ajmg.b.31054

    3. A megalin polymorphism associated with promoter activity and Alzheimer's disease risk (pages 895–902)

      Teo Vargas, Maria Jesus Bullido, Ana Martinez-Garcia, Desiree Antequera, Jordi Clarimon, Marcel Rosich-Estrago, Angeles Martin-Requero, Ignacio Mateo, Eloy Rodriguez-Rodriguez, Elisabet Vilella-Cuadrada, Ana Frank, Alberto Lleo, Laura Molina-Porcel, Rafael Blesa, Onofre Combarros, Teresa Gomez-Isla, Felix Bermejo-Pareja, Fernando Valdivieso and Eva Carro

      Article first published online: 5 JAN 2010 | DOI: 10.1002/ajmg.b.31056

    4. High frequency of multiexonic deletion of the GCH1 gene in a Taiwanese cohort of dopa-response dystonia (pages 903–908)

      Yah-Huei Wu-Chou, Tu-Hsueh Yeh, Chuan-Yu Wang, Juei-Jueng Lin, Chin-Chang Huang, Hsiu-Chen Chang, Szu-Chia Lai, Rou-Shayn Chen, Yi-Hsin Weng, Chia-Ling Huang and Chin-Song Lu

      Article first published online: 15 JAN 2010 | DOI: 10.1002/ajmg.b.31058

    5. Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims (pages 909–918)

      Nader Perroud, Elizabeth Neidhart, Brice Petit, Monique Vessaz, Térèse Laforge, Céline Relecom, Romano La Harpe, Alain Malafosse and Michel Guipponi

      Article first published online: 5 JAN 2010 | DOI: 10.1002/ajmg.b.31059

    6. Analysis of whole genome biomarker expression in blood and brain (pages 919–936)

      Brandi Rollins, Maureen V. Martin, Ling Morgan and Marquis P. Vawter

      Article first published online: 2 FEB 2010 | DOI: 10.1002/ajmg.b.31062

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      Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders (pages 937–947)

      Michael S.L. Ching, Yiping Shen, Wen-Hann Tan, Shafali S. Jeste, Eric M. Morrow, Xiaoli Chen, Nahit M. Mukaddes, Seung-Yun Yoo, Ellen Hanson, Rachel Hundley, Christina Austin, Ronald E. Becker, Gerard T. Berry, Katherine Driscoll, Elizabeth C. Engle, Sandra Friedman, James F. Gusella, Fuki M. Hisama, Mira B. Irons, Tina Lafiosca, Elaine LeClair, David T. Miller, Michael Neessen, Jonathan D. Picker, Leonard Rappaport, Cynthia M. Rooney, Dean P. Sarco, Joan M. Stoler, Christopher A. Walsh, Robert R. Wolff, Ting Zhang, Ramzi H. Nasir and Bai-Lin Wu, on behalf of the Children's Hospital Boston Genotype Phenotype Study Group

      Article first published online: 7 APR 2010 | DOI: 10.1002/ajmg.b.31063

    8. Sexually dimorphic interaction between the DRD1 and COMT genes in schizophrenia (pages 948–954)

      Janet Hoenicka, Elena Garrido, Guillermo Ponce, Roberto Rodríguez-Jiménez, Isabel Martínez, Gabriel Rubio, Miguel Ángel Jiménez-Arriero and Tomás Palomo

      Article first published online: 2 FEB 2010 | DOI: 10.1002/ajmg.b.31065

  4. Brief Research Communications

    1. Top of page
    2. Editorials
    3. Rapid Publications
    4. Research Articles
    5. Brief Research Communications
    6. Letters to the Editor
    1. Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease (pages 955–959)

      J.S.K. Kauwe, S. Bertelsen, K. Mayo, C. Cruchaga, R. Abraham, P. Hollingworth, D. Harold, M.J. Owen, J. Williams, S. Lovestone, J.C. Morris and A.M. Goate

      Article first published online: 22 DEC 2009 | DOI: 10.1002/ajmg.b.31053

    2. A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder (pages 960–966)

      Bert van der Zwaag, Wouter G. Staal, Ron Hochstenbach, Martin Poot, Henk A. Spierenburg, Maretha V. de Jonge, Nienke E. Verbeek, Ruben van 't Slot, Michael A. van Es, Frank J. Staal, Christine M. Freitag, Jacobine E. Buizer-Voskamp, Marcel R. Nelen, Leonard H. van den Berg, Hans K. Ploos van Amstel, Herman van Engeland and J. Peter H. Burbach

      Article first published online: 22 DEC 2009 | DOI: 10.1002/ajmg.b.31055

    3. Functional variants of TSPAN8 are associated with bipolar disorder and schizophrenia (pages 967–972)

      Claus-Jürgen Scholz, Christian P. Jacob, Henriette N. Buttenschon, Sarah Kittel-Schneider, Andrea Boreatti-Hümmer, Michael Zimmer, Ulrich Walter, Klaus-Peter Lesch, Ole Mors, Susanne Kneitz, Jürgen Deckert and Andreas Reif

      Article first published online: 5 JAN 2010 | DOI: 10.1002/ajmg.b.31057

    4. SNPs in CAST are associated with Parkinson disease: A confirmation study (pages 973–979)

      Andrew S. Allen and Glen A. Satten

      Article first published online: 2 FEB 2010 | DOI: 10.1002/ajmg.b.31061

  5. Letters to the Editor

    1. Top of page
    2. Editorials
    3. Rapid Publications
    4. Research Articles
    5. Brief Research Communications
    6. Letters to the Editor
    1. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome (pages 980–982)

      Masashi Ikeda, Nigel Williams, Hywel J. Williams, Rhodri Smith, Stephen Monks, Michael J. Owen, Kieran C. Murphy and Michael C. O'Donovan

      Article first published online: 5 JAN 2010 | DOI: 10.1002/ajmg.b.31060

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