SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Daisuke Fukushi, Kenichiro Yamada, Noriko Nomura, Misako Naiki, Reiko Kimura, Yasukazu Yamada, Toshiyuki Kumagai, Kumiko Yamaguchi, Yoshishige Miyake, Nobuaki Wakamatsu, Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2, American Journal of Medical Genetics Part A, 2014, 164, 4
  2. 2
    Dar-Shong Lin, Tzu-Po Chuang, Ming-Fu Chiang, Che-Sheng Ho, Chung-Der Hsiao, Yu-Wen Huang, Tsu-Yen Wu, Jer-Yuarn Wu, Yuan-Tsong Chen, Tsai-Chuan Chen, Ling-Hui Li, De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay, Gene, 2014, 533, 1, 78

    CrossRef

  3. 3
    Fabio A. Nascimento, Hanna Faghfoury, Timo Krings, Anfal Ali, Jonathan D. Fridhandler, Andres Lozano, Richard Wennberg, Danielle M. Andrade, Deep brain stimulation for the management of seizures in MECP2 duplication syndrome, Seizure, 2014,

    CrossRef

  4. 4
    Lu-Yao Ma, Chen Wu, Yu Jin, Ming Gao, Guo-Hui Li, Dharshaun Turner, Jian-Xin Shen, Shi-Jiang Zhang, Vinodh Narayanan, Garilyn Jentarra, Jie Wu, Electrophysiological Phenotypes of MeCP2 A140V Mutant Mouse Model, CNS Neuroscience & Therapeutics, 2014, 20, 4
  5. 5
    Elisa S Na, Michael J Morris, Erika D Nelson, Lisa M Monteggia, GABAA Receptor Antagonism Ameliorates Behavioral and Synaptic Impairments Associated with MeCP2 Overexpression, Neuropsychopharmacology, 2014,

    CrossRef

  6. You have free access to this content6
    Wen-Hann Tan, Lynne M. Bird, Ronald L. Thibert, Charles A. Williams, If not Angelman, what is it? a review of Angelman-like syndromes, American Journal of Medical Genetics Part A, 2014, 164, 4
  7. 7
    Roseline Caumes, Odile Boespflug-Tanguy, Nathalie Villeneuve, Laetitia Lambert, Catherine Delanoe, Bruno Leheup, Nadia Bahi-Buisson, Stéphane Auvin, Late onset epileptic spasms is frequent in MECP2 gene duplication: Electroclinical features and long-term follow-up of 8 epilepsy patients, European Journal of Paediatric Neurology, 2014,

    CrossRef

  8. 8
    Francesca Novara, Alessandro Simonati, Federico Sicca, Roberta Battini, Simona Fiori, Annarita Contaldo, Lucia Criscuolo, Orsetta Zuffardi, Roberto Ciccone, MECP2 duplication phenotype in symptomatic females: report of three further cases, Molecular Cytogenetics, 2014, 7, 1, 10

    CrossRef

  9. 9
    Jessica Scott Schwoerer, Jennifer Laffin, Joanne Haun, Gordana Raca, Michael J. Friez, Philip F. Giampietro, MECP2 duplication: Possible cause of severe phenotype in females, American Journal of Medical Genetics Part A, 2014, 164, 4
  10. 10
    Martesa Tantra, Christian Hammer, Anne Kästner, Liane Dahm, Martin Begemann, Chiranjeevi Bodda, Kurt Hammerschmidt, Ina Giegling, Beata Stepniak, Aracely Castillo Venzor, Bettina Konte, Begun Erbaba, Annette Hartmann, Asieh Tarami, Walter Schulz-Schaeffer, Dan Rujescu, Ashraf U Mannan, Hannelore Ehrenreich, Mild expression differences of MECP2 influencing aggressive social behavior, EMBO Molecular Medicine, 2014, 6, 4
  11. 11
    Alan Percy, Rett Syndrome: Coming to Terms with Treatment, Advances in Neuroscience, 2014, 2014, 1

    CrossRef

  12. 12
    R. S. Møller, L. R. Jensen, S. M. Maas, J. Filmus, M. Capurro, C. Hansen, C. L. M. Marcelis, K. Ravn, J. Andrieux, M. Mathieu, M. Kirchhoff, O. K. Rødningen, N. de Leeuw, H. G. Yntema, G. Froyen, J. Vandewalle, K. Ballon, E. Klopocki, S. Joss, J. Tolmie, A. C. Knegt, A. M. Lund, H. Hjalgrim, A. W. Kuss, N. Tommerup, R. Ullmann, A. P. M. de Brouwer, P. Strømme, S. Kjaergaard, Z. Tümer, T. Kleefstra, X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome, Human Genetics, 2014, 133, 5, 625

    CrossRef

  13. 13
    Erica F. Andersen, Erin E. Baldwin, Sara Ellingwood, Rosemarie Smith, Allen N. Lamb, Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability, American Journal of Medical Genetics Part A, 2014, 164, 5
  14. 14
    Malgorzata I. Srebniak, Lisanne Mout, Diane Van Opstal, Robert-Jan H. Galjaard, 0.5 Mb Array as a First-Line Prenatal Cytogenetic Test in Cases without Ultrasound Abnormalities and Its Implementation in Clinical Practice, Human Mutation, 2013, 34, 9
  15. 15
    Daniel H. Ebert, Harrison W. Gabel, Nathaniel D. Robinson, Nathaniel R. Kastan, Linda S. Hu, Sonia Cohen, Adrija J. Navarro, Matthew J. Lyst, Robert Ekiert, Adrian P. Bird, Michael E. Greenberg, Activity-dependent phosphorylation of MECP2 threonine 308 regulates interaction with NcoR, Nature, 2013,

    CrossRef

  16. 16
    Mark J. Millan, An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy, Neuropharmacology, 2013, 68, 2

    CrossRef

  17. 17
    Vivian Alejandra Neira, Pavel Romero-Espinoza, Augusto Rojas-Martínez, Rocío Ortiz-López, Carlos Córdova-Fletes, Alberto Plaja, Patricio Barros-Núñez, De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features, Gene, 2013, 524, 2, 381

    CrossRef

  18. 18
    Bess M. Flashner, Mark E. Russo, Jenine E. Boileau, Derek W. Leong, G. Ian Gallicano, Epigenetic Factors and Autism Spectrum Disorders, NeuroMolecular Medicine, 2013, 15, 2, 339

    CrossRef

  19. 19
    Sampathkumar Rangasamy, Santosh R. D’Mello, Vinodh Narayanan, Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders, Neurotherapeutics, 2013, 10, 4, 742

    CrossRef

  20. 20
    Travis M Kerr, Christopher L Muller, Mahfuzur Miah, Christopher S Jetter, Rita Pfeiffer, Charisma Shah, Nicole Baganz, George M Anderson, Jacqueline N Crawley, James S Sutcliffe, Randy D Blakely, Jeremy Veenstra-VanderWeele, Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice, Molecular Autism, 2013, 4, 1, 35

    CrossRef

  21. 21
    Shino Shimada, Nobuhiko Okamoto, Masahiro Ito, Yasuhiro Arai, Ken Momosaki, Masami Togawa, Yoshihiro Maegaki, Midori Sugawara, Keiko Shimojima, Makiko Osawa, Toshiyuki Yamamoto, MECP2 duplication syndrome in both genders, Brain and Development, 2013, 35, 5, 411

    CrossRef

  22. 22
    Chiranjeevi Bodda, Martesa Tantra, Rustam Mollajew, Jayamuruga P. Arunachalam, Franco A. Laccone, Karolina Can, Albert Rosenberger, Sergej L. Mironov, Hannelore Ehrenreich, Ashraf U. Mannan, Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures, The American Journal of Pathology, 2013, 183, 1, 195

    CrossRef

  23. 23
    Laura Ricceri, Bianca De Filippis, Giovanni Laviola, Rett syndrome treatment in mouse models: Searching for effective targets and strategies, Neuropharmacology, 2013, 68, 106

    CrossRef

  24. You have free access to this content24
    Sarika U. Peters, Rachel J. Hundley, Amy K. Wilson, Zachary Warren, Alison Vehorn, Claudia M.B. Carvalho, James R. Lupski, Melissa B. Ramocki, The Behavioral Phenotype in MECP2 Duplication Syndrome: A Comparison With Idiopathic Autism, Autism Research, 2013, 6, 1
  25. 25
    Elisa S Na, Erika D Nelson, Ege T Kavalali, Lisa M Monteggia, The Impact of MeCP2 Loss- or Gain-of-Function on Synaptic Plasticity, Neuropsychopharmacology, 2013, 38, 1, 212

    CrossRef

  26. 26
    Covadonga Huidobro, Agustin F. Fernandez, Mario F. Fraga, The role of genetics in the establishment and maintenance of the epigenome, Cellular and Molecular Life Sciences, 2013, 70, 9, 1543

    CrossRef

  27. 27
    J T Plummer, O V Evgrafov, M Y Bergman, M Friez, C A Haiman, P Levitt, K A Aldinger, Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome, Translational Psychiatry, 2013, 3, 10, e316

    CrossRef

  28. 28
    Quan Lin, Yi E. Sun, Epigenetic Regulation in the Nervous System, 2013,

    CrossRef

  29. 29
    Kathryn B. Garber, Stephen T. Warren, Jeannie Visootsak, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  30. 30
    S.-J. Kim, M. Lewis, J. Veenstra-VanderWeele, Neural Circuit Development and Function in the Brain, 2013,

    CrossRef

  31. 31
    Timothy W. Yu, Michael Coulter, Maria Chahrour, Christopher A. Walsh, Genomic and Personalized Medicine, 2013,

    CrossRef

  32. 32
    Catalina Betancur, Mary Coleman, The Neuroscience of Autism Spectrum Disorders, 2013,

    CrossRef

  33. 33
    Xiu Xu, Qiong Xu, Ying Zhang, Xiaodi Zhang, Tianlin Cheng, Bingbing Wu, Yanhua Ding, Ping Lu, Jingjing Zheng, Min Zhang, Zilong Qiu, Xiang Yu, A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections, BMC Medical Genetics, 2012, 13, 1, 75

    CrossRef

  34. 34
    Inesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, Abir Gmidène, Soumaya Mougou, Najla Soyah, Moez Gribaa, Damien Sanlaville, Hatem Elghezal, Ali Saad, Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia, European Journal of Medical Genetics, 2012, 55, 8-9, 461

    CrossRef

  35. 35
    Grace J. Noh, Y. Jane Tavyev Asher, John M. Graham, Clinical review of genetic epileptic encephalopathies, European Journal of Medical Genetics, 2012, 55, 5, 281

    CrossRef

  36. 36
    Shozo Honda, Shigeko Satomura, Shin Hayashi, Issei Imoto, Eiji Nakagawa, Yu-ichi Goto, Johji Inazawa, Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation, Journal of Human Genetics, 2012, 57, 1, 73

    CrossRef

  37. You have free access to this content37
    Nicole de Leeuw, Trijnie Dijkhuizen, Jayne Y. Hehir-Kwa, Nigel P. Carter, Lars Feuk, Helen V. Firth, Robert M. Kuhn, David H. Ledbetter, Christa Lese Martin, Conny M. A. van Ravenswaaij-Arts, Steven W. Scherer, Soheil Shams, Steven Van Vooren, Rolf Sijmons, Morris Swertz, Ros Hastings, Diagnostic interpretation of array data using public databases and internet sources, Human Mutation, 2012, 33, 6
  38. 38
    Aglaia Vignoli, Renato Borgatti, An