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  1. 1
    Mathilde Nizon, Joris Andrieux, Caroline Rooryck, Marie-Christine de Blois, Emilie Bourel-Ponchel, Béatrice Bourgois, Odile Boute, Albert David, Bruno Delobel, Bénédicte Duban-Bedu, Fabienne Giuliano, Alice Goldenberg, Sarah Grotto, Delphine Héron, Houda Karmous-Benailly, Boris Keren, Didier Lacombe, Jean-Michel Lapierre, Cédric Le Caignec, Eric Le Galloudec, Martine Le Merrer, Anne-Gaëlle Le Moing, Michèle Mathieu-Dramard, Sylvie Nusbaum, Olivier Pichon, Lucile Pinson, Odile Raoul, Marlène Rio, Serge Romana, Agnès Roubertie, Laurence Colleaux, Catherine Turleau, Michel Vekemans, Rima Nabbout, Valérie Malan, Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature, American Journal of Medical Genetics Part A, 2015, 167, 1
  2. 2
    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
  3. 3
    Toshiyuki Yamamoto, Keiko Shimojima, Shino Shimada, Kenji Yokochi, Shinsaku Yoshitomi, Keiko Yanagihara, Katsumi Imai, Nobuhiko Okamoto, Clinical impacts of genomic copy number gains at Xq28, Human Genome Variation, 2014, 1, 14001

    CrossRef

  4. 4
    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

  5. 5
    Nathalie Fieremans, Marijke Bauters, Stefanie Belet, Jelle Verbeeck, Anna C. Jansen, Sara Seneca, Filip Roelens, Elfride De Baere, Peter Marynen, Guy Froyen, De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation, Human Genetics, 2014, 133, 11, 1359

    CrossRef

  6. 6
    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, 23, 5, 405

    CrossRef

  7. 7
    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, 5
  8. 8
    P. Martin, N. Bohnert, Epileptologische Behandlung von Menschen mit schwerer geistiger Behinderung, Zeitschrift für Epileptologie, 2014,

    CrossRef

  9. 9
    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, 39, 8, 1946

    CrossRef

  10. You have free access to this content10
    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
  11. 11
    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, 18, 4, 475

    CrossRef

  12. 12
    Daniel W. Bellott, Jennifer F. Hughes, Helen Skaletsky, Laura G. Brown, Tatyana Pyntikova, Ting-Jan Cho, Natalia Koutseva, Sara Zaghlul, Tina Graves, Susie Rock, Colin Kremitzki, Robert S. Fulton, Shannon Dugan, Yan Ding, Donna Morton, Ziad Khan, Lora Lewis, Christian Buhay, Qiaoyan Wang, Jennifer Watt, Michael Holder, Sandy Lee, Lynne Nazareth, Steve Rozen, Donna M. Muzny, Wesley C. Warren, Richard A. Gibbs, Richard K. Wilson, David C. Page, Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators, Nature, 2014, 508, 7497, 494

    CrossRef

  13. 13
    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

  14. 14
    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
  15. 15
    Juan Ausió, Alexia Martínez de Paz, Manel Esteller, MeCP2: the long trip from a chromatin protein to neurological disorders, Trends in Molecular Medicine, 2014, 20, 9, 487

    CrossRef

  16. 16
    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, 5
  17. 17
    Fang Fu, Huan-ling Liu, Ru Li, Jin Han, Xin Yang, Pan Min, Li Zhen, Yong-ling Zhang, Gui-e Xie, Ting-ying Lei, Yan Li, Jian Li, Dong-zhi Li, Can Liao, Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region, Gene, 2014, 546, 2, 222

    CrossRef

  18. 18
    Alan Percy, Rett Syndrome: Coming to Terms with Treatment, Advances in Neuroscience, 2014, 2014, 1

    CrossRef

  19. 19
    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

  20. 20
    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, 7
  21. 21
    Ewa Jamroz, Ewa Grzywna-Rozenek, Antoni Pyrkosz, Zespół duplikacji MECP2 – opis przypadku, Pediatria Polska, 2014, 89, 6, 453

    CrossRef

  22. 22
    Adrian Zhubi, Edwin H. Cook, Alessandro Guidotti, Dennis R. Grayson, Epigenetics, 2014,

    CrossRef

  23. 23
    Jeffrey E. Ming, John M. Graham, Stiehm's Immune Deficiencies, 2014,

    CrossRef

  24. 24
    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
  25. 25
    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

  26. 26
    Mark J. Millan, An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy, Neuropharmacology, 2013, 68, 2

    CrossRef

  27. 27
    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

  28. 28
    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

  29. 29
    Sampathkumar Rangasamy, Santosh R. D’Mello, Vinodh Narayanan, Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders, Neurotherapeutics, 2013, 10, 4, 742

    CrossRef

  30. 30
    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

  31. 31
    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

  32. 32
    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

  33. 33
    Laura Ricceri, Bianca De Filippis, Giovanni Laviola, Rett syndrome treatment in mouse models: Searching for effective targets and strategies, Neuropharmacology, 2013, 68, 106

    CrossRef

  34. 34
    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
  35. 35
    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

  36. 36
    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

  37. 37
    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

  38. 38
    Quan Lin, Yi E. Sun, Epigenetic Regulation in the Nervous System, 2013,

    CrossRef

  39. 39
    Kathryn B. Garber, Stephen T. Warren, Jeannie Visootsak, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  40. 40
    S.-J. Kim, M. Lewis, J. Veenstra-VanderWeele, Neural Circuit Development and Function in the Brain, 2013,

    CrossRef

  41. 41
    Timothy W. Yu, Michael Coulter, Maria Chahrour, Christopher A. Walsh, Genomic and Personalized Medicine, 2013,

    CrossRef

  42. 42
    Catalina Betancur, Mary Coleman, The Neuroscience of Autism Spectrum Disorders, 2013,

    CrossRef

  43. 43
    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

  44. 44
    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

  45. 45
    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

  46. 46
    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

  47. You have free access to this content47
    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
  48. 48
    Aglaia Vignoli, Renato Borgatti, Angela Peron, Claudio Zucca, Lucia Ballarati, Clara Bonaglia, Melissa Bellini, Lucio Giordano, Romina Romaniello, Maria Francesca Bedeschi, Roberta Epifanio, Silvia Russo, Rossella Caselli, Daniela Giardino, Francesca Darra, Francesca La Briola, Giuseppe Banderali, Maria Paola Canevini, Electroclinical pattern in MECP2 duplication syndrome: Eight new reported cases and review of literature, Epilepsia, 2012, 53, 7
  49. You have free access to this content49
    Renzo Guerrini, Elena Parrini, Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene–related encephalopathies, Epilepsia, 2012, 53, 12
  50. 50
    Shan S. Tang, Daphin Fernandez, Lazarus P. Lazarou, Rahul Singh, Penny Fallon, MECP2 triplication in 3 brothers – A rarely described cause of familial neurological regression in boys, European Journal of Paediatric Neurology, 2012, 16, 2, 209

    CrossRef

  51. 51
    T. Yang, M. B. Ramocki, J. L. Neul, W. Lu, L. Roberts, J. Knight, C. S. Ward, H. Y. Zoghbi, F. Kheradmand, D. B. Corry, Overexpression of Methyl-CpG Binding Protein 2 Impairs TH1 Responses, Science Translational Medicine, 2012, 4, 163, 163ra158

    CrossRef

  52. 52
    Shozo Honda, Shin Hayashi, Takaya Nakane, Issei Imoto, Kenji Kurosawa, Seiji Mizuno, Nobuhiko Okamoto, Mitsuhiro Kato, Hiroshi Yoshihashi, Takeo Kubota, Eiji Nakagawa, Yu-ichi Goto, Johji Inazawa, The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints, American Journal of Medical Genetics Part A, 2012, 158A, 6
  53. 53
    E.K. Bijlsma, A. Collins, F.T. Papa, M.I. Tejada, P. Wheeler, E.A.J. Peeters, A.C.J. Gijsbers, J.M. van de Kamp, M. Kriek, M. Losekoot, A.J. Broekma, J.A. Crolla, M. Pollazzon, M. Mucciolo, E. Katzaki, V. Disciglio, M.I. Ferreri, A. Marozza, M.A. Mencarelli, C. Castagnini, L. Dosa, F. Ariani, F. Mari, R. Canitano, G. Hayek, M.P. Botella, B. Gener, M. Mínguez, A. Renieri, C.A.L. Ruivenkamp, Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation, European Journal of Medical Genetics, 2012, 55, 6-7, 404

    CrossRef

  54. 54
    Jin S. Hahn, Aminoff's Electrodiagnosis in Clinical Neurology, 2012,

    CrossRef

  55. 55
    B. Peeters, M.A. Benninga, R.C. Hennekam, Childhood constipation; an overview of genetic studies and associated syndromes, Best Practice & Research Clinical Gastroenterology, 2011, 25, 1, 73

    CrossRef

  56. 56
    Kiran P. Maski, Shafali S. Jeste, Sarah J. Spence, Common neurological co-morbidities in autism spectrum disorders, Current Opinion in Pediatrics, 2011, 23, 6, 609

    CrossRef

  57. 57
    Cheryl L Gatto, Kendal Broadie, Drosophila modeling of heritable neurodevelopmental disorders, Current Opinion in Neurobiology, 2011, 21, 6, 834

    CrossRef

  58. 58
    Catalina Betancur, Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting, Brain Research, 2011, 1380, 42

    CrossRef

  59. 59
    Claudia M B Carvalho, Melissa B Ramocki, Davut Pehlivan, Luis M Franco, Claudia Gonzaga-Jauregui, Ping Fang, Alanna McCall, Eniko Karman Pivnick, Stacy Hines-Dowell, Laurie H Seaver, Linda Friehling, Sansan Lee, Rosemarie Smith, Daniela del Gaudio, Marjorie Withers, Pengfei Liu, Sau Wai Cheung, John W Belmont, Huda Y Zoghbi, P J Hastings, James R Lupski, Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome, Nature Genetics, 2011, 43, 11, 1074

    CrossRef

  60. 60
    Amy M Breman, Melissa B Ramocki, Sung-Hae L Kang, Misti Williams, Debra Freedenberg, Ankita Patel, Patricia I Bader, Sau Wai Cheung, MECP2 duplications in six patients with complex sex chromosome rearrangements, European Journal of Human Genetics, 2011, 19, 4, 409

    CrossRef

  61. 61
    Yu Wang, Caroline GL Lee, Role of miR-224 in hepatocellular carcinoma: a tool for possible therapeutic intervention?, Epigenomics, 2011, 3, 2, 235

    CrossRef

  62. 62
    Jacky Guy, Hélène Cheval, Jim Selfridge, Adrian Bird, The Role of MeCP2 in the Brain, Annual Review of Cell and Developmental Biology, 2011, 27, 1, 631

    CrossRef

  63. 63
    Omar S. Khwaja, Mustafa Sahin, Translational research, Current Opinion in Pediatrics, 2011, 23, 6, 633

    CrossRef

  64. 64
    Jun Tohyama, Toshiyuki Yamamoto, Kana Hosoki, Keisuke Nagasaki, Noriyuki Akasaka, Tsukasa Ohashi, Yu Kobayashi, Shinji Saitoh, West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14, American Journal of Medical Genetics Part A, 2011, 155, 10