SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Brian Hon-Yin Chung, Victoria Qinchen Tao, Winnie Wan-Yee Tso, Copy number variation and autism: New insights and clinical implications, Journal of the Formosan Medical Association, 2014, 113, 7, 400

    CrossRef

  2. 2
    Borislav Dejanovic, Dennis Lal, Claudia B. Catarino, Sita Arjune, Abdel A. Belaidi, Holger Trucks, Christian Vollmar, Rainer Surges, Wolfram S. Kunz, Susanne Motameny, Janine Altmüller, Anna Köhler, Bernd A. Neubauer, EPICURE Consortium, Peter Nürnberg, Soheyl Noachtar, Günter Schwarz, Thomas Sander, Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy, Neurobiology of Disease, 2014, 67, 88

    CrossRef

  3. 3
    Josep-Antoni Ramos-Quiroga, Cristina Sánchez-Mora, Miguel Casas, Iris Garcia-Martínez, Rosa Bosch, Mariana Nogueira, Montse Corrales, Gloria Palomar, Raquel Vidal, Mireia Coll-Tané, Mònica Bayés, Bru Cormand, Marta Ribasés, Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder, Journal of Psychiatric Research, 2014, 49, 60

    CrossRef

  4. 4
    Fabiola Ceroni, Nuala H Simpson, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Ann Clark, Patrick F Bolton, Elizabeth R Hennessy, Peter Donnelly, David R Bentley, Hilary Martin, Jeremy Parr, Alistair T Pagnamenta, Elena Maestrini, Elena Bacchelli, Simon E Fisher, Dianne F Newbury, Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment, European Journal of Human Genetics, 2014, 22, 10, 1165

    CrossRef

  5. 5
    Robert M. Kirkpatrick, Matt McGue, William G. Iacono, Michael B. Miller, Saonli Basu, Nathan Pankratz, Low-frequency copy-number variants and general cognitive ability: No evidence of association, Intelligence, 2014, 42, 98

    CrossRef

  6. 6
    Elena Bonora, Claudio Graziano, Fiorella Minopoli, Elena Bacchelli, Pamela Magini, Chiara Diquigiovanni, Silvia Lomartire, Francesca Bianco, Manuela Vargiolu, Piero Parchi, Elena Marasco, Vilma Mantovani, Luca Rampoldi, Matteo Trudu, Antonia Parmeggiani, Agatino Battaglia, Luigi Mazzone, Giada Tortora, Elena Maestrini, Marco Seri, Giovanni Romeo, Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients, EMBO Molecular Medicine, 2014, 6, 6
  7. 7
    Michelle B Polan, Matthew T Pastore, Katherine Steingass, Sayaka Hashimoto, Devon L Thrush, Robert Pyatt, Shalini Reshmi, Julie M Gastier-Foster, Caroline Astbury, Kim L McBride, Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster, European Journal of Human Genetics, 2014, 22, 1, 105

    CrossRef

  8. 8
    Michael M. Halassa, Zhe Chen, Ralf D. Wimmer, Philip M. Brunetti, Shengli Zhao, Basilis Zikopoulos, Fan Wang, Emery N. Brown, Matthew A. Wilson, State-Dependent Architecture of Thalamic Reticular Subnetworks, Cell, 2014, 158, 4, 808

    CrossRef

  9. 9
    Mehmet Seven, Bahadir Batar, Selin Unal, Gozde Yesil, Adnan Yuksel, Mehmet Guven, The Effect of Genetic Polymorphisms of Cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on Drug-Resistant Epilepsy in Turkish Children, Molecular Diagnosis & Therapy, 2014, 18, 2, 229

    CrossRef

  10. 10
    Rasim O Rosti, Abdelrahim A Sadek, Keith K Vaux, Joseph G Gleeson, The genetic landscape of autism spectrum disorders, Developmental Medicine & Child Neurology, 2014, 56, 1
  11. 11
    Guia Guffanti, Simona Gaudi, James H. Fallon, Janet Sobell, Steven G. Potkin, Carlos Pato, Fabio Macciardi, Transposable elements and psychiatric disorders, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2014, 165, 3
  12. 12
    B Chilian, H Abdollahpour, T Bierhals, I Haltrich, G Fekete, I Nagel, G Rosenberger, K Kutsche, Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci, Clinical Genetics, 2013, 84, 6
  13. 13
    Harumitsu Murohashi, Editorial: Cognitive science approach to developmental disorders: From “discrete diagnostic” to “dimensional”, Japanese Psychological Research, 2013, 55, 2
  14. You have free access to this content14
    Rikke S. Møller, Yvonne G. Weber, Laura L. Klitten, Holger Trucks, Hiltrud Muhle, Wolfram S. Kunz, Heather C. Mefford, Andre Franke, Monika Kautza, Peter Wolf, Dieter Dennig, Stefan Schreiber, Ina-Maria Rückert, H.-Erich Wichmann, Jan P. Ernst, Claudia Schurmann, Hans J. Grabe, Niels Tommerup, Ulrich Stephani, Holger Lerche, Helle Hjalgrim, Ingo Helbig, Thomas Sander, Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy, Epilepsia, 2013, 54, 2
  15. 15
    Christelle Golzio, Nicholas Katsanis, Genetic architecture of reciprocal CNVs, Current Opinion in Genetics & Development, 2013, 23, 3, 240

    CrossRef

  16. 16
    S. Girirajan, R. L. Johnson, F. Tassone, J. Balciuniene, N. Katiyar, K. Fox, C. Baker, A. Srikanth, K. H. Yeoh, S. J. Khoo, T. B. Nauth, R. Hansen, M. Ritchie, I. Hertz-Picciotto, E. E. Eichler, I. N. Pessah, S. B. Selleck, Global increases in both common and rare copy number load associated with autism, Human Molecular Genetics, 2013, 22, 14, 2870

    CrossRef

  17. You have free access to this content17
    Dennis Lal, Holger Trucks, Rikke S. Møller, Helle Hjalgrim, Bobby P. C. Koeleman, Carolien G. F. Kovel, Frank Visscher, Yvonne G. Weber, Holger Lerche, Felicitas Becker, Christoph J. Schankin, Bernd A. Neubauer, Rainer Surges, Wolfram S. Kunz, Fritz Zimprich, Andre Franke, Thomas Illig, Janina S. Ried, Costin Leu, Peter Nürnberg, Thomas Sander, Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy, Epilepsia, 2013, 54, 2
  18. 18
    Andrew Dauber, Christelle Golzio, Cécile Guenot, Francine M. Jodelka, Maria Kibaek, Susanne Kjaergaard, Bruno Leheup, Danielle Martinet, Malgorzata J.M. Nowaczyk, Jill A. Rosenfeld, Susan Zeesman, Janice Zunich, Jacques S. Beckmann, Joel N. Hirschhorn, Michelle L. Hastings, Sebastien Jacquemont, Nicholas Katsanis, SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant, The American Journal of Human Genetics, 2013, 93, 5, 798

    CrossRef

  19. 19
    Saiqa Yasmeen, Linea Melchior, Birgitte Bertelsen, Liselotte Skov, Nanette Mol Debes, Zeynep Tümer, Sequence analysis of SLITRK1 for var321 in Danish patients with Tourette syndrome and review of the literature, Psychiatric Genetics, 2013, 23, 3, 130

    CrossRef

  20. 20
    Thomas A Lanz, Edward Guilmette, Mark M Gosink, James E Fischer, Lawrence W Fitzgerald, Diane T Stephenson, Mathew T Pletcher, Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of action, Molecular Autism, 2013, 4, 1, 45

    CrossRef

  21. 21
    Alexander E. Urban, A Role of Genomic Copy Number Variation in the Complex Behavioral Phenotype of Alcohol Dependence: A Commentary, Alcoholism: Clinical and Experimental Research, 2012, 36, 9
  22. 22
    Lesley Hart, Mark O'Driscoll, Causes and Consequences of Structural Genomic Alterations in the Human Genome, eLS,