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There are 290662 results for: content related to: Evidence of normal hearing laterality in familial schizophrenic patients and their relatives

  1. Substantial genetic link between iq and working memory: Implications for molecular genetic studies on schizophrenia. the european twin study of schizophrenia (EUTwinsS)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 413–418, Ximena Goldberg, Silvia Alemany, Araceli Rosa, Marco Picchioni, Igor Nenadic, Sheena F. Owens, Fruhling Rijsdijk, Irene Rebollo, Heinrich Sauer, Robin M. Murray, Lourdes Fañanás and Timothea Toulopoulou

    Article first published online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32158

  2. Heritability of neurocognitive traits in familial schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 6, 5 September 2009, Pages: 845–853, Janice A. Husted, Sooyeol Lim, Eva W.C. Chow, Celia Greenwood and Anne S. Bassett

    Article first published online : 29 JAN 2009, DOI: 10.1002/ajmg.b.30907

  3. PRODH gene is associated with executive function in schizophrenic families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 5, 5 July 2008, Pages: 654–657, Tao Li, Xiaohong Ma, Xun Hu, Yingcheng Wang, Chengying Yan, Huaqing Meng, Xiehe Liu, Timothea Toulopoulou, Robin M. Murray and David A. Collier

    Article first published online : 28 DEC 2007, DOI: 10.1002/ajmg.b.30648

  4. Executive function and genetic predisposition to schizophrenia—the Maudsley family study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 3, 5 April 2008, Pages: 285–293, P. Birkett, T. Sigmundsson, T. Sharma, T. Toulopoulou, T.D. Griffiths, A. Reveley and R. Murray

    Article first published online : 12 SEP 2007, DOI: 10.1002/ajmg.b.30594

  5. Neurocognitive deficits in first-episode schizophrenic patients and their first-degree relatives

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 4, 5 June 2007, Pages: 407–416, Xiaohong Ma, Qiang Wang, Pak C. Sham, Xiehe Liu, Sophia Rabe-Hesketh, Xueli Sun, Junmei Hu, Huaqing Meng, Wai Chen, Eric Y.H. Chen, Wei Deng, Raymond C.K. Chan, Robin M. Murray, David A. Collier and Tao Li

    Article first published online : 17 APR 2007, DOI: 10.1002/ajmg.b.30330

  6. Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 3, April 2012, Pages: 263–273, Franziska Degenhardt, Lutz Priebe, Stefan Herms, Manuel Mattheisen, Thomas W. Mühleisen, Sandra Meier, Susanne Moebus, Jana Strohmaier, Magdalena Groß, René Breuer, Christoph Lange, Per Hoffmann, Andreas Meyer-Lindenberg, Andreas Heinz, Henrik Walter, Susanne Lucae, Christiane Wolf, Bertram Müller-Myhsok, Florian Holsboer, Wolfgang Maier, Marcella Rietschel, Markus M. Nöthen and Sven Cichon

    Article first published online : 17 FEB 2012, DOI: 10.1002/ajmg.b.32034

  7. Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 7, October 2012, Pages: 812–822, Maarten J. Van Den Bossche, Mandy Johnstone, Mojca Strazisar, Benjamin S. Pickard, Dirk Goossens, An-Sofie Lenaerts, Sonia De Zutter, Annelie Nordin, Karl-Fredrik Norrback, Julien Mendlewicz, Daniel Souery, Peter De Rijk, Bernard G. Sabbe, Rolf Adolfsson, Douglas Blackwood and Jurgen Del-Favero

    Article first published online : 22 AUG 2012, DOI: 10.1002/ajmg.b.32088

  8. You have free access to this content
    A genome-wide supported psychiatric risk variant in NCAN influences brain function and cognitive performance in healthy subjects

    Human Brain Mapping

    Volume 36, Issue 1, January 2015, Pages: 378–390, Heidelore Raum, Bruno Dietsche, Arne Nagels, Stephanie H. Witt, Marcella Rietschel, Tilo Kircher and Axel Krug

    Article first published online : 12 SEP 2014, DOI: 10.1002/hbm.22635

  9. Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: A combined twin and family study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 5, 5 July 2008, Pages: 619–627, Mei-Hua Hall, Katja Schulze, Pak Sham, Sridevi Kalidindi, Colm McDonald, Elvira Bramon, Deborah L. Levy, Robin M. Murray and Frühling Rijsdijk

    Article first published online : 11 JAN 2008, DOI: 10.1002/ajmg.b.30653

  10. Association between BDNF val66 met genotype and episodic memory

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 134B, Issue 1, 5 April 2005, Pages: 73–75, Emma Dempster, Timothea Toulopoulou, Colm McDonald, Elvira Bramon, Muriel Walshe, Francesca Filbey, Harvey Wickham, Pak C. Sham, Robin M. Murray and David A. Collier

    Article first published online : 17 FEB 2005, DOI: 10.1002/ajmg.b.30150

  11. BDNF gene variants and brain morphology in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 5, 5 July 2006, Pages: 513–523, Ingrid Agartz, Göran C. Sedvall, Lars Terenius, Bettina Kulle, Arnoldo Frigessi, Håkan Hall and Erik G. Jönsson

    Article first published online : 1 JUN 2006, DOI: 10.1002/ajmg.b.30338

  12. You have free access to this content
    Not really identical: Epigenetic differences in monozygotic twins and implications for twin studies in psychiatry

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 151C, Issue 2, 15 May 2009, Pages: 136–141, F. Nipa Haque, Irving I. Gottesman and Albert H.C. Wong

    Article first published online : 17 APR 2009, DOI: 10.1002/ajmg.c.30206

  13. Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 2, March 2011, Pages: 204–214, Tod Fullston, Bronte Gabb, David Callen, Reinhard Ullmann, Erica Woollatt, Sharon Bain, Hilger H. Ropers, Matt Cooper, David Chandler, Kim Carter, Assen Jablensky, Luba Kalaydjieva and Jozef Gecz

    Article first published online : 13 JAN 2011, DOI: 10.1002/ajmg.b.31157

  14. Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 3, April 2012, Pages: 343–353, Heather C. Whalley, Jessika E. Sussmann, Mandy Johnstone, Liana Romaniuk, Holly Redpath, Goultchira Chakirova, Prerona Mukherjee, Jeremy Hall, Eve C. Johnstone, Stephen M. Lawrie and Andrew M. McIntosh

    Article first published online : 15 FEB 2012, DOI: 10.1002/ajmg.b.32035

  15. Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 4, 5 June 2008, Pages: 459–462, Araceli Rosa, Marco M. Picchioni, Sridevi Kalidindi, Caroline S. Loat, Joanne Knight, Timothea Toulopoulou, Ronald Vonk, Astrid C. van der Schot, Willem Nolen, René S. Kahn, Peter McGuffin, Robin M. Murray and Ian W. Craig

    Article first published online : 22 OCT 2007, DOI: 10.1002/ajmg.b.30616

  16. Disease and genetic contributions toward local tissue volume disturbances in schizophrenia: A tensor-based morphometry study

    Human Brain Mapping

    Volume 33, Issue 9, September 2012, Pages: 2081–2091, Yaling Yang, Keith H. Nuechterlein, Owen R. Phillips, Boris Gutman, Florian Kurth, Ivo Dinov, Paul M. Thompson, Robert F Asarnow, Arthur W. Toga and Katherine L. Narr

    Article first published online : 30 AUG 2011, DOI: 10.1002/hbm.21349

  17. You have free access to this content
    No association of Disrupted-in-Schizophrenia-1 variation with prefrontal function in patients with schizophrenia and bipolar disorder

    Genes, Brain and Behavior

    Volume 10, Issue 3, April 2011, Pages: 276–285, D. P. Prata, A. Mechelli, M. Picchioni, C. H. Y. Fu, F. Kane, S. Kalidindi, C. McDonald, E. Kravariti, T. Toulopoulou, E. Bramon, M. Walshe, R. Murray, D. A. Collier and P. K. McGuire

    Article first published online : 16 DEC 2010, DOI: 10.1111/j.1601-183X.2010.00665.x

  18. Semantic but not phonological verbal fluency associated with BDNF Val66Met polymorphism in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 3, 5 April 2009, Pages: 441–442, O. Kebir, F. Mouaffak, M. Chayet, S. Leroy, S. Tordjman, I. Amado and M.O. Krebs

    Article first published online : 5 JUN 2008, DOI: 10.1002/ajmg.b.30794

  19. Association study of neuregulin 1 gene polymorphisms with auditory p300 in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 4, June 2012, Pages: 422–428, ChuanYuan Kang, XiaoBin Yang, XiuFeng Xu, Hua Liu, Ping Su and JianZhong Yang

    Article first published online : 29 MAR 2012, DOI: 10.1002/ajmg.b.32045

  20. Selectivity of verbal memory deficit in schizophrenic patients and their relatives

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 116B, Issue 1, 1 January 2003, Pages: 1–7, Timothea Toulopoulou, Robin G. Morris, Sophia Rabe-Hesketh and Robin M. Murray

    Article first published online : 1 NOV 2002, DOI: 10.1002/ajmg.b.10027