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This article [doi:10.1038/nn1765] has been cited in the following papers, taken from those publishers and societies that are participating in CrossRef's Cited-by Linking service. The number of citations from this service is usually lower than citation numbers from databases that include more journals.

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  1. EISSN: 10982779 ISSN: 10804013

    Mental Retardation and Developmental Disabilities Research Reviews

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    Ralph-Axel Müller

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    doi:10.1002/mrdd.20141

  2. EISSN: 13652788 ISSN: 09642633

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    Understanding of facial expressions of emotion by children with intellectual disabilities of differing aetiology

    J. G. Wishart, K. R. Cebula, D. S. Willis, T. K. Pitcairn

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    doi:10.1111/j.1365-2788.2006.00947.x

  3. EISSN: 17524571 ISSN: 17524563

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    Evolutionary genomics of human intellectual disability

    Bernard Crespi, Kyle Summers, Steve Dorus

    doi:10.1111/j.1752-4571.2009.00098.x

  4. EISSN: 15392791 ISSN: 15392791

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    7 (3), 2009, p.195

    doi:10.1007/s12021-009-9052-3

  5. EISSN: 15318249 ISSN: 03645134

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    Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP)

    Doron Gothelf et al.

    63 (1), 2008, p.40

    doi:10.1002/ana.21243

  6. EISSN: 10981004 ISSN: 10597794

    Human Mutation

    Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

    Reinhard Ullmann et al.

    28 (7), 2007, p.674

    doi:10.1002/humu.20546

  7. EISSN: 13652788 ISSN: 09642633

    Journal of Intellectual Disability Research

    Autism spectrum disorders in genetic syndromes: implications for diagnosis, intervention and understanding the wider autism spectrum disorder population

    P. Howlin, J. Moss

    53 (10), 2009, p.852

    doi:10.1111/j.1365-2788.2009.01197.x

  8. EISSN: 10959203 ISSN: 00368075

    Science

    A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice

    K. Tabuchi et al.

    318 (5847), 2007, p.71

    doi:10.1126/science.1146221

  9. EISSN: 13594184 ISSN: 13594184

    Molecular Psychiatry

    Advances in behavioral genetics: mouse models of autism

    S S Moy, J J Nadler

    13 (1), 2008, p.4

    doi:10.1038/sj.mp.4002082

  10. EISSN: 15461718 ISSN: 10614036

    Nature Genetics

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Peter Szatmari et al.

    39 (3), 2007, p.319

    doi:10.1038/ng1985

  11. EISSN: 13594184 ISSN: 13594184

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    Abnormal melatonin synthesis in autism spectrum disorders

    J Melke et al.

    13 (1), 2008, p.90

    doi:10.1038/sj.mp.4002016

  12. EISSN: 10916490 ISSN: 00278424

    Proceedings of the National Academy of Sciences

    Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

    S. Jamain et al.

    105 (5), 2008, p.1710

    doi:10.1073/pnas.0711555105

  13. EISSN: 19393806 ISSN: 19393792

    Autism Research

    The potential role for emergence in autism

    George M. Anderson

    1 (1), 2008, p.18

    doi:10.1002/aur.2

  14. EISSN: 19434456 ISSN: 00917451

    Cold Spring Harbor Symposia on Quantitative Biology

    The Possible Interplay of Synaptic and Clock Genes in Autism Spectrum Disorders

    T. Bourgeron

    72 (1), 2007, p.645

    doi:10.1101/sqb.2007.72.020

  15. EISSN: 15524833 ISSN: 15524825

    American Journal of Medical Genetics Part A

    Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder

    Catalina García-Nonell et al.

    146a (15), 2008, p.1911

    doi:10.1002/ajmg.a.32290

  16. EISSN: 14691825 ISSN: 0140525X

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    Psychosis and autism as diametrical disorders of the social brain

    Bernard Crespi, Christopher Badcock

    31 (3), 2008.

    doi:10.1017/S0140525X08004214

  17. EISSN: 1552485X ISSN: 15524841

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    Anne-Berit Ekström, Louise Hakenäs-Plate, Lena Samuelsson, Már Tulinius, Elisabet Wentz

    147b (6), 2008, p.918

    doi:10.1002/ajmg.b.30698

  18. EISSN: 1469185X ISSN: 14647931

    Biological Reviews

    Genomic imprinting in the development and evolution of psychotic spectrum conditions

    Bernard Crespi

    doi:10.1111/j.1469-185X.2008.00050.x

  19. EISSN: 19393806 ISSN: 19393792

    Autism Research

    Brain function and gaze fixation during facial-emotion processing in fragile X and autism

    Kim M. Dalton, Laura Holsen, Leonard Abbeduto, Richard J. Davidson

    1 (4), 2008, p.231

    doi:10.1002/aur.32

  20. EISSN: 1600079X ISSN: 07423098

    Journal of Pineal Research

    Protective effects of melatonin against oxidative stress in Fmr1 knockout mice: a therapeutic research model for the fragile X syndrome

    Yanina Romero-Zerbo et al.

    46 (2), 2009, p.224

    doi:10.1111/j.1600-079X.2008.00653.x

  21. EISSN: 13652788 ISSN: 09642633

    Journal of Intellectual Disability Research

    Motor abilities of children diagnosed with fragile X syndrome with and without autism

    C. Zingerevich et al.

    53 (1), 2009, p.11

    doi:10.1111/j.1365-2788.2008.01107.x

  22. EISSN: 08937648 ISSN: 08937648

    Molecular Neurobiology

    The Fragile X Mental Retardation Protein in Circadian Rhythmicity and Memory Consolidation

    Cheryl L. Gatto, Kendal Broadie

    39 (2), 2009, p.107

    doi:10.1007/s12035-009-8057-0

  23. EISSN: 14602083 ISSN: 09646906

    Human Molecular Genetics

    Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

    I. Cusco et al.

    18 (10), 2009, p.1795

    doi:10.1093/hmg/ddp092

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