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There are 16894 results for: content related to: A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1

  1. Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 970–976, Li Zou, Wei Chen, Shanshan Shao, Zhao Sun, Rong Zhong, Junxin Shi, Xiaoping Miao and Ranran Song

    Version of Record online : 12 OCT 2012, DOI: 10.1002/ajmg.b.32102

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    Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region

    Genes, Brain and Behavior

    Volume 7, Issue 8, November 2008, Pages: 877–886, K. G. Wigg, Y. Feng, J. Crosbie, R. Tannock, J. L. Kennedy, A. Ickowicz, M. Malone, R. Schachar and C. L. Barr

    Version of Record online : 24 JUL 2008, DOI: 10.1111/j.1601-183X.2008.00425.x

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    Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1

    Genes, Brain and Behavior

    Volume 10, Issue 2, March 2011, Pages: 244–252, C. E. Szalkowski, J. R. Hinman, S. W. Threlkeld, Y. Wang, A. LePack, G. D. Rosen, J. J. Chrobak, J. J. LoTurco and R. H. Fitch

    Version of Record online : 25 NOV 2010, DOI: 10.1111/j.1601-183X.2010.00662.x

  4. You have full text access to this OnlineOpen article
    Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

    Genes, Brain and Behavior

    Volume 10, Issue 2, March 2011, Pages: 158–165, S. Paracchini, Q. W. Ang, F. J. Stanley, A. P. Monaco, C. E. Pennell and A. J. O. Whitehouse

    Version of Record online : 19 OCT 2010, DOI: 10.1111/j.1601-183X.2010.00651.x

  5. A review of association and linkage studies for genetical analyses of learning disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 7, 5 October 2007, Pages: 923–943, Emrah Caylak

    Version of Record online : 17 MAY 2007, DOI: 10.1002/ajmg.b.30537

  6. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 4, 5 June 2007, Pages: 556–560, Zoran Brkanac, Nicola H. Chapman, Mark M. Matsushita, Lani Chun, Kathleen Nielsen, Elizabeth Cochrane, Virginia W. Berninger, Ellen M. Wijsman and Wendy H. Raskind

    Version of Record online : 20 APR 2007, DOI: 10.1002/ajmg.b.30471

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    Association of short-term memory with a variant within DYX1C1 in developmental dyslexia

    Genes, Brain and Behavior

    Volume 6, Issue 7, October 2007, Pages: 640–646, C. Marino, ,, A. Citterio, R. Giorda, A. Facoetti, , G. Menozzi, L. Vanzin, M. L. Lorusso, M. Nobile and M. Molteni

    Version of Record online : 15 NOV 2006, DOI: 10.1111/j.1601-183X.2006.00291.x

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    Molecular Genetics of Dyslexia: An Overview

    Dyslexia

    Volume 19, Issue 4, November 2013, Pages: 214–240, Amaia Carrion-Castillo, Barbara Franke and Simon E. Fisher

    Version of Record online : 17 OCT 2013, DOI: 10.1002/dys.1464

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    An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes

    Genes, Brain and Behavior

    Volume 12, Issue 1, February 2013, Pages: 47–55, S. Mascheretti, A. Bureau, M. Battaglia, D. Simone, E. Quadrelli, J. Croteau, M. R. Cellino, R. Giorda, S. Beri, M. Maziade and C. Marino

    Version of Record online : 24 NOV 2012, DOI: 10.1111/gbb.12000

  10. Molecular Genetics of Dyslexia

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    Silvia Paracchini

    Published Online : 15 MAR 2009, DOI: 10.1002/9780470015902.a0021474

  11. Molecular genetics and molecular biology of dyslexia

    Wiley Interdisciplinary Reviews: Cognitive Science

    Volume 2, Issue 4, July/August 2011, Pages: 441–448, Juha Kere

    Version of Record online : 3 FEB 2011, DOI: 10.1002/wcs.138

  12. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 1, 5 January 2009, Pages: 140–147, G. Poelmans, J.J.M. Engelen, J. Van Lent-Albrechts, H.J. Smeets, E. Schoenmakers, B. Franke, J.K. Buitelaar, M. Wuisman-Frerker, W. Erens, J. Steyaert and C. Schrander-Stumpel

    Version of Record online : 2 JUN 2008, DOI: 10.1002/ajmg.b.30787

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    Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice

    Genes, Brain and Behavior

    Volume 10, Issue 8, November 2011, Pages: 868–875, L. A. Gabel, I. Marin, J. J. LoTurco, A. Che, C. Murphy, M. Manglani and S. Kass

    Version of Record online : 19 OCT 2011, DOI: 10.1111/j.1601-183X.2011.00727.x

  14. Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability

    Genes, Brain and Behavior

    Volume 13, Issue 8, November 2014, Pages: 802–811, D. T. Truong, A. Che, A. R. Rendall, C. E. Szalkowski, J. J. LoTurco, A. M. Galaburda and R. Holly Fitch

    Version of Record online : 3 SEP 2014, DOI: 10.1111/gbb.12170

  15. Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 3, 5 April 2008, Pages: 294–300, Carolien G.F. de Kovel, Barbara Franke, Frans A. Hol, Jérémie J.P. Lebrec, Ben Maassen, Han Brunner, George W. Padberg, Jill Platko and David Pauls

    Version of Record online : 20 SEP 2007, DOI: 10.1002/ajmg.b.30598

  16. Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples

    Journal of Child Psychology and Psychiatry

    Sara Mascheretti, Vittoria Trezzi, Roberto Giorda, Michel Boivin, Vickie Plourde, Frank Vitaro, Mara Brendgen, Ginette Dionne and Cecilia Marino

    Version of Record online : 8 AUG 2016, DOI: 10.1111/jcpp.12612

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    A genome-wide association study for reading and language abilities in two population cohorts

    Genes, Brain and Behavior

    Volume 12, Issue 6, August 2013, Pages: 645–652, M. Luciano, D. M. Evans, N. K. Hansell, S. E. Medland, G. W. Montgomery, N. G. Martin, M. J. Wright and T. C. Bates

    Version of Record online : 20 JUN 2013, DOI: 10.1111/gbb.12053

  18. Genetics of Language Disorders

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    Katalin Csiszar and Adam Szalontai

    Published Online : 15 JUL 2014, DOI: 10.1002/9780470015902.a0025707

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    The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains

    Genes, Brain and Behavior

    Volume 14, Issue 4, April 2015, Pages: 377–385, J. D. Eicher, C. M. Stein, F. Deng, A. A. Ciesla, N. R. Powers, R. Boada, S. D. Smith, B. F. Pennington, S. K. Iyengar, B. A. Lewis and J. R. Gruen

    Version of Record online : 8 APR 2015, DOI: 10.1111/gbb.12214

  20. Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 1, 5 January 2006, Pages: 15–27, Robert P. Igo Jr, Nicola H. Chapman, Virginia W. Berninger, Mark Matsushita, Zoran Brkanac, Joseph H. Rothstein, Ted Holzman, Kathleen Nielsen, Wendy H. Raskind and Ellen M. Wijsman

    Version of Record online : 5 DEC 2005, DOI: 10.1002/ajmg.b.30245