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There are 843517 results for: content related to: Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and At-Risk for psychosis

  1. Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions

    Journal of Intellectual Disability Research

    Volume 56, Issue 9, September 2012, Pages: 865–878, V. Shashi, A. Veerapandiyan, K. Schoch, T. Kwapil, M. Keshavan, E. Ip and S. Hooper

    Article first published online : 31 AUG 2011, DOI: 10.1111/j.1365-2788.2011.01477.x

  2. Behavior in preschool children with the 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 94–101, Petra Klaassen, Sasja Duijff, Henriette Swanenburg de Veye, Jacob Vorstman, Frits Beemer and Gerben Sinnema

    Article first published online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35685

  3. You have free access to this content
    Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 1, 5 January 2007, Pages: 27–36, Kathryn Eve Lewandowski, Vandana Shashi, Peggy M. Berry and Thomas R. Kwapil

    Article first published online : 10 OCT 2006, DOI: 10.1002/ajmg.b.30379

  4. Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome

    Journal of Intellectual Disability Research

    Volume 53, Issue 7, July 2009, Pages: 665–676, K. Rockers, O. Ousley, T. Sutton, E. Schoenberg, K. Coleman, E. Walker and J. F. Cubells

    Article first published online : 12 MAY 2009, DOI: 10.1111/j.1365-2788.2009.01178.x

  5. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients

    Human Mutation

    Volume 32, Issue 11, November 2011, Pages: 1278–1289, Tingwei Guo, Donna McDonald-McGinn, Anna Blonska, Alan Shanske, Anne S. Bassett, Eva Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, Maria C. Digilio, Bruno Marino, Bruno Dallapiccola, Courtney Carpenter, Xin Zheng, Jacob Johnson, Jonathan Chung, Anne Marie Higgins, Nicole Philip, Tony J. Simon, Karlene Coleman, Damian Heine-Suner, Jordi Rosell, Wendy Kates, Marcella Devoto, Elizabeth Goldmuntz, Elaine Zackai, Tao Wang, Robert Shprintzen, Beverly Emanuel, Bernice Morrow and The International Chromosome 22q11.2 Consortium

    Article first published online : 16 SEP 2011, DOI: 10.1002/humu.21568

  6. Mathematical learning disabilities in children with 22q11.2 deletion syndrome: A review

    Developmental Disabilities Research Reviews

    Volume 15, Issue 1, 2009, Pages: 4–10, Bert De Smedt, Ann Swillen, Lieven Verschaffel and Pol Ghesquière

    Article first published online : 11 FEB 2009, DOI: 10.1002/ddrr.44

  7. Monitoring of self-generated speech in adolescents with 22q11.2 deletion syndrome

    British Journal of Clinical Psychology

    Volume 49, Issue 3, September 2010, Pages: 373–386, Martin Debbané, Martial Van der Linden, Bronwyn Glaser and Stephan Eliez

    Article first published online : 24 DEC 2010, DOI: 10.1348/014466509X468223

  8. Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning

    Journal of Intellectual Disability Research

    L. E. Campbell, K. L. McCabe, J. L. Melville, P. A. Strutt and U. Schall

    Article first published online : 25 FEB 2015, DOI: 10.1111/jir.12183

  9. Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: A matched control study

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 6, 15 March 2007, Pages: 574–580, P.W. Jansen, S.N. Duijff, F.A. Beemer, J.A.S. Vorstman, P.W.J. Klaassen, M.E.J. Morcus and J.A. Heineman-de Boer

    Article first published online : 22 FEB 2007, DOI: 10.1002/ajmg.a.31623

  10. Clinical Characteristics of an Afrikaner Founder Population Recruited for a Schizophrenia Genetic Study

    Annals of the New York Academy of Sciences

    Volume 1151, Issue 1, January 2009, Pages: 85–101, Johannes Lodewikus Roos, Herman Walter Pretorius and Maria Karayiorgou

    Article first published online : 23 DEC 2008, DOI: 10.1111/j.1749-6632.2008.03453.x

  11. Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome

    Journal of Intellectual Disability Research

    Volume 58, Issue 1, January 2014, Pages: 31–47, T. M. Allen, J. Hersh, K. Schoch, K. Curtiss, S. R. Hooper and V. Shashi

    Article first published online : 7 JUN 2013, DOI: 10.1111/jir.12054

  12. You have free access to this content
    Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

    Developmental Dynamics

    Volume 241, Issue 8, August 2012, Pages: 1310–1324, Subreena Simrick, Dorota Szumska, Jennifer R. Gardiner, Kieran Jones, Karun Sagar, Bernice Morrow, Shoumo Bhattacharya and M. Albert Basson

    Article first published online : 26 JUN 2012, DOI: 10.1002/dvdy.23812

  13. Schizophrenia and 22q11.2 Deletion Syndrome

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    eLS

    Frederick Sundram and Kieran C Murphy

    Published Online : 17 JAN 2011, DOI: 10.1002/9780470015902.a0005229.pub2

  14. Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 2924–2930, Andrea C. Stachon, Berivan Baskin, Adam C. Smith, Andrea Shugar, Cheryl Cytrynbaum, Leona Fishman, Roberto Mendoza-Londono, Regan Klatt, Ahmed Teebi, Peter N. Ray and Rosanna Weksberg

    Article first published online : 14 NOV 2007, DOI: 10.1002/ajmg.a.32101

  15. The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 3, May/June 2013, Pages: 393–403, Irinna Papangeli and Peter Scambler

    Article first published online : 19 JUN 2012, DOI: 10.1002/wdev.75

  16. Clinical features of 78 adults with 22q11 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 138A, Issue 4, 1 November 2005, Pages: 307–313, Anne S. Bassett, Eva W.C. Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D. Webb and Michael A. Gatzoulis

    Article first published online : 5 OCT 2005, DOI: 10.1002/ajmg.a.30984

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    Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia

    Genes, Brain and Behavior

    Volume 7, Issue 1, February 2008, Pages: 61–69, J. Zinkstok, ,, N. Schmitz, T. Van Amelsvoort, M. Moeton, F. Baas and D. Linszen

    Article first published online : 26 MAR 2007, DOI: 10.1111/j.1601-183X.2007.00326.x

  18. Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

    Journal of Intellectual Disability Research

    E. Hidding, H. Swaab, J. A. S. Vorstman, H. van Engeland, M. E. J. Sijmens-Morcus, P. W. J. Klaassen, S. N. Duijff and L. M. J. de Sonneville

    Article first published online : 13 FEB 2015, DOI: 10.1111/jir.12187

  19. Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability

    Journal of Intellectual Disability Research

    Volume 58, Issue 10, October 2014, Pages: 915–925, L. J. M. Evers, T. A. M. J. van Amelsvoort, M. J. J. M. Candel, H. Boer, J. J. M Engelen and L. M. G. Curfs

    Article first published online : 17 FEB 2014, DOI: 10.1111/jir.12117

  20. A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders

    Journal of Intellectual Disability Research

    J. Goodwin, K. Schoch, V. Shashi, S. R. Hooper, O. Morad, M. Zalevsky, D. Gothelf and L. E. Campbell

    Article first published online : 25 JUL 2014, DOI: 10.1111/jir.12151