An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy

Millan, Mark J.·2013·Neuropharmacology

Cites (1,085)

Items 201–400 of 1,085

  1. Autism spectrum disorders-a genetics review
    Miles, Judith H. · 2011 · Genetics in Medicine
  2. W. H. Fox Talbot and the history of photography
    Helmut Gernsheim · 1977 · Endeavour
  3. Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model
    Verne S. Caviness, Takashi Takahashi, Richard S. Nowakowski · 1995 · Trends in Neurosciences
  4. Epigenetics and the environmental regulation of the genome and its function
    Zhang, Tie-Yuan, Meaney, Michael J. · 2010 · Annual Review of Psychology
  5. Dysregulation of mTOR signaling in fragile X syndrome
    Sharma, Ali, Hoeffer, Charles A., Takayasu, Yukihiro, Miyawaki, Takahiro, McBride, Sean M., Klann, Eric, Zukin, R. Suzanne · 2010 · The Journal of Neuroscience
  6. DNA methyltransferase 1, cytosine methylation, and cytosine hydroxymethylation in mammalian mitochondria
    Shock, Lisa S., Thakkar, Prashant V., Peterson, Erica J., Moran, Richard G., Taylor, Shirley M. · 2011 · Proceedings of the National Academy of Sciences
  7. Reelin promoter hypermethylation in schizophrenia
    Grayson, Dennis R., Jia, Xiaomei, Chen, Ying, Sharma, Rajiv P., Mitchell, Colin P., Guidotti, Alessandro, Costa, Erminio · 2005 · Proceedings of the National Academy of Sciences
  8. Resolving the paradox of common, harmful, heritable mental disorders: Which evolutionary genetic models work best?
    Matthew C. Keller, Geoffrey F. Miller · 2006 · Behavioral and Brain Sciences
  9. Monoubiquitination of Human Histone H2B: The Factors Involved and Their Roles in HOX Gene Regulation
    Bing Zhu, Yong Zheng, Anh-Dung Pham, Subhrangsu S. Mandal, Hediye Erdjument‐Bromage, Paul Tempst, Danny Reinberg · 2005 · Molecular Cell
  10. Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome
    Xie, Wei, Barr, Cathy L., Kim, Audrey, Yue, Feng, Lee, Ah Young, Eubanks, James, Dempster, Emma L., Ren, Bing · 2012 · Cell
  11. The DISC locus in psychiatric illness
    Chubb, J E, Bradshaw, N J, Soares, D C, Porteous, D J, Millar, J K · 2008 · Molecular Psychiatry
  12. Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3
    Wang, Xiaoming, McCoy, Portia A., Rodriguiz, Ramona M., Pan, Yanzhen, Je, H. Shawn, Roberts, Adam C., Kim, Caroline J., Berrios, Janet, Colvin, Jennifer S., Bousquet-Moore, Danielle et al. · 2011 · Human Molecular Genetics
  13. Cortical DNA methylation maintains remote memory
    Courtney A. Miller, Cristin F. Gavin, Jason A. White, R. Ryley Parrish, Avinash Honasoge, Christopher R Yancey, Ivonne M Rivera, María Dolores Rubio, Gavin Rumbaugh, J. David Sweatt · 2010 · Nature Neuroscience
  14. Development of the social brain in adolescence
    Sarah‐Jayne Blakemore · 2012 · Journal of the Royal Society of Medicine
  15. Valproic acid in pregnancy: how much are we endangering the embryo and fetus?
    Ornoy, Asher · 2009 · Reproductive Toxicology
  16. Modeling human cortical development in vitro using induced pluripotent stem cells
    Mariani, Jessica, Simonini, Maria Vittoria, Palejev, Dean, Tomasini, Livia, Coppola, Gianfilippo, Szekely, Anna M., Horvath, Tamas L., Vaccarino, Flora M. · 2012 · Proceedings of the National Academy of Sciences
  17. Stochastic epigenetic variation as a driving force of development, evolutionary adaptation, and disease
    Andrew P. Feinberg, Rafael A. Irizarry · 2009 · Proceedings of the National Academy of Sciences
  18. X-linked mental retardation
    Hans‐Hilger Ropers, Ben C.J. Hamel · 2005 · Nature Reviews Genetics
  19. Jarid2 and PRC2, partners in regulating gene expression
    Gang Li, Raphaël Margueron, Manching Ku, Pierre Chambon, B Bernstein, Danny Reinberg · 2010 · Genes & Development
  20. Epigenetic mechanisms mediating the long-term effects of maternal care on development
    Frances A. Champagne, James P. Curley · 2008 · Neuroscience & Biobehavioral Reviews
  21. Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
    Donna M. McDonald‐McGinn, Kathleen E. Sullivan · 2010 · Medicine
  22. Histone arginine methylation
    Alessandra Di Lorenzo, Mark T. Bedford · 2010 · FEBS Letters
  23. CTCF physically links cohesin to chromatin
    Rubio, Eric D., Reiss, David J., Welcsh, Piri L., Disteche, Christine M., Filippova, Galina N., Baliga, Nitin S., Aebersold, Ruedi, Ranish, Jeffrey A., Krumm, Anton · 2008 · Proceedings of the National Academy of Sciences
  24. The Transcription Factor Nerve Growth Factor-Inducible Protein A Mediates Epigenetic Programming: Altering Epigenetic Marks by Immediate-Early Genes
    Weaver, Ian C. G., D'Alessio, Ana C., Brown, Shelley E., Hellstrom, Ian C., Dymov, Sergiy, Sharma, Shakti, Szyf, Moshe, Meaney, Michael J. · 2007 · The Journal of Neuroscience
  25. A Method for Genetically Installing Site-Specific Acetylation in Recombinant Histones Defines the Effects of H3 K56 Acetylation
    Heinz Neumann, Susan M. Hancock, Ruth Buning, Andrew L. Routh, Lynda Chapman, Joanna Somers, Tom Owen‐Hughes, John van Noort, Daniela Rhodes, Jason W. Chin · 2009 · Molecular Cell
  26. MicroRNAs control de novo DNA methylation through regulation of transcriptional repressors in mouse embryonic stem cells
    Lasse Sinkkonen, Tabea Hugenschmidt, Philipp Berninger, Dimos Gaidatzis, Fabio Mohn, Caroline G. Artus-Revel, Mihaela Zavolan, Petr Svoboda, Witold Filipowicz · 2008 · Nature Structural & Molecular Biology
  27. Modulation of synaptic plasticity and memory by Reelin involves differential splicing of the lipoprotein receptor Apoer2
    Beffert, Uwe, Weeber, Edwin J., Durudas, Andre, Qiu, Shenfeng, Masiulis, Irene, Sweatt, J. David, Li, Wei-Ping, Adelmann, Giselind, Frotscher, Michael, Hammer, Robert E. et al. · 2005 · Neuron
  28. A role for glia in the progression of Rett’s syndrome
    Lioy, Daniel T., Garg, Saurabh K., Monaghan, Caitlin E., Raber, Jacob, Foust, Kevin D., Kaspar, Brian K., Hirrlinger, Petra G., Kirchhoff, Frank, Bissonnette, John M., Ballas, Nurit et al. · 2011 · Nature
  29. Cross talk between microRNA and epigenetic regulation in adult neurogenesis
    Szulwach, Keith E., Li, Xuekun, Smrt, Richard D., Li, Yujing, Luo, Yuping, Lin, Li, Santistevan, Nicholas J., Li, Wendi, Zhao, Xinyu, Jin, Peng · 2010 · Journal of Cell Biology
  30. Induced pluripotent stem cells — opportunities for disease modelling and drug discovery
    Marica Grs̆ković, Ashkan Javaherian, Berta Strulovici, George Q. Daley · 2011 · Nature Reviews Drug Discovery
  31. Chronic Pharmacological mGlu5 Inhibition Corrects Fragile X in Adult Mice
    Michalon, Aubin, Sidorov, Michael, Ballard, Theresa M., Ozmen, Laurence, Spooren, Will, Wettstein, Joseph G., Jaeschke, Georg, Bear, Mark F., Lindemann, Lothar · 2012 · Neuron
  32. Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2
    Young, Juan I., Hong, Eugene P., Castle, John C., Crespo-Barreto, Juan, Bowman, Aaron B., Rose, Matthew F., Kang, Dongcheul, Richman, Ron, Johnson, Jason M., Berget, Susan et al. · 2005 · Proceedings of the National Academy of Sciences
  33. Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars
    Benes, Francine M., Lim, Benjamin, Matzilevich, David, Walsh, John P., Subburaju, Sivan, Minns, Martin · 2007 · Proceedings of the National Academy of Sciences
  34. Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism
    Nakatani, Jin, Tamada, Kota, Hatanaka, Fumiyuki, Ise, Satoko, Ohta, Hisashi, Inoue, Kiyoshi, Tomonaga, Shozo, Watanabe, Yasuhito, Chung, Yeun Jun, Banerjee, Ruby et al. · 2009 · Cell
  35. Protein methyltransferases as a target class for drug discovery
    Robert A. Copeland, Michael E. Solomon, Victoria M. Richon · 2009 · Nature Reviews Drug Discovery
  36. The ribosome as a platform for co-translational processing, folding and targeting of newly synthesized proteins
    Günter Krämer, Daniel Boehringer, Nenad Ban, Bernd Bukau · 2009 · Nature Structural & Molecular Biology
  37. Role of Corticotropin-Releasing Factor in Drug Addiction
    Marian L. Logrip, George F. Koob, Eric P. Zorrilla · 2011 · CNS Drugs
  38. Prenatal Famine and Adult Health
    Lambert H. Lumey, Aryeh D. Stein, Ezra Susser · 2011 · Annual Review of Public Health
  39. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR)
    Juan Manuel García‐Martínez, Jennifer Moran, Rosemary G. Clarke, Alex Gray, Sabina C. Cosulich, Christine M. Chresta, Dario R. Alessi · 2009 · Biochemical Journal
  40. Sticky fingers: zinc-fingers as protein-recognition motifs
    Roland Gamsjaeger, C LIEW, Fionna E. Loughlin, Merlin Crossley, Joel P. Mackay · 2007 · Trends in Biochemical Sciences
  41. Non–cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
    Ballas, Nurit, Lioy, Daniel T, Grunseich, Christopher, Mandel, Gail · 2009 · Nature Neuroscience
  42. Sperm-borne microRNA-34c is required for the first cleavage division in mouse
    Weimin Liu, Ronald T.K. Pang, Philip C.N. Chiu, Benancy P.C. Wong, Kaiqin Lao, Ckf Lee, William S.B. Yeung · 2011 · Proceedings of the National Academy of Sciences
  43. Periconceptional Maternal Folic Acid Use of 400 µg per Day Is Related to Increased Methylation of the IGF2 Gene in the Very Young Child
    Régine P.M. Steegers‐Theunissen, Sylvia A Obermann-Borst, Dennis Kremer, Jan Willem Lindemans, Cissy Siebel, Eric A.P. Steegers, P. Eline Slagboom, Bastiaan T. Heijmans · 2009 · PLoS ONE
  44. CREB's control of intrinsic and synaptic plasticity: implications for CREB-dependent memory models
    Eva Benito, Ángel Barco · 2010 · Trends in Neurosciences
  45. The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)
    Phelan, K., McDermid, H.E. · 2011 · Molecular Syndromology
  46. ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner
    Martin J. Law, Karen M. Lower, Hsiao P. J. Voon, Jim R. Hughes, David Garrick, Vip Viprakasit, Matthew Mitson, Marco De Gobbi, Marco A. Marra, Andrew P. Morris et al. · 2010 · Cell
  47. The PHD finger: a versatile epigenome reader
    Roberto Sánchez, Ming‐Ming Zhou · 2011 · Trends in Biochemical Sciences
  48. Chromatin higher-order structures and gene regulation
    Li, Guohong, Reinberg, Danny · 2011 · Current Opinion in Genetics & Development
  49. The Arc of synaptic memory
    Bramham, Clive R., Alme, Maria N., Bittins, Margarethe, Kuipers, Sjoukje D., Nair, Rajeevkumar R., Pai, Balagopal, Panja, Debabrata, Schubert, Manja, Soule, Jonathan, Tiron, Adrian et al. · 2010 · Experimental Brain Research
  50. De novo DNA methylation: a germ cell perspective
    Smallwood, Sébastien A., Kelsey, Gavin · 2012 · Trends in Genetics
  51. Dnmt3a and Dnmt3b Are Transcriptional Repressors That Exhibit Unique Localization Properties to Heterochromatin
    Kurtis E. Bachman, Michael R. Rountree, Stephen B. Baylin · 2001 · Journal of Biological Chemistry
  52. Neurofibromin Regulation of ERK Signaling Modulates GABA Release and Learning
    Yijun Cui, Rui M. Costa, Geoffrey G. Murphy, Ype Elgersma, Yuan Zhu, David H. Gutmann, Luis F. Parada, István Módy, Alcino J. Silva · 2008 · Cell
  53. Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA
    Klein, Matthew E, Lioy, Daniel T, Ma, Lin, Impey, Soren, Mandel, Gail, Goodman, Richard H · 2007 · Nature Neuroscience
  54. RNA nucleotide methylation
    Yuri Motorin, Mark Helm · 2011 · Wiley Interdisciplinary Reviews - RNA
  55. SIRT1 regulates the histone methyl-transferase SUV39H1 during heterochromatin formation.
    Vaquero, Alejandro, Scher, Michael, Erdjument-Bromage, Hediye, Tempst, Paul, Serrano, Lourdes, Reinberg, Danny · 2007 · Nature
  56. Noncoding RNAs and Gene Silencing
    Mikel Zaratiegui, Danielle V. Irvine, Robert A. Martienssen · 2007 · Cell
  57. DNA methylation and histone acetylation work in concert to regulate memory formation and synaptic plasticity
    Courtney A. Miller, Susan L. Campbell, J. David Sweatt · 2007 · Neurobiology of Learning and Memory
  58. Resilience to social stress coincides with functional DNA methylation of the Crf gene in adult mice
    Elliott, Evan, Ezra-Nevo, Gili, Regev, Limor, Neufeld-Cohen, Adi, Chen, Alon · 2010 · Nature Neuroscience
  59. Schizophrenia is associated with an increase in cortical microRNA biogenesis
    Natalie Jane Beveridge, Erin J. Gardiner, Adam P. Carroll, Paul A. Tooney, Murray J. Cairns · 2009 · Molecular Psychiatry
  60. Immune function across generations: integrating mechanism and evolutionary process in maternal antibody transmission
    Jennifer L. Grindstaff, Edmund D. Brodie, Ellen D. Ketterson · 2003 · Proceedings of the Royal Society B Biological Sciences
  61. The Chd family of chromatin remodelers
    Concetta G.A. Marfella, Anthony N. Imbalzano · 2007 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
  62. Long non-coding RNAs in nervous system function and disease
    Irfan Qureshi, John S. Mattick, Mark F. Mehler · 2010 · Brain Research
  63. A MicroRNA Imparts Robustness against Environmental Fluctuation during Development
    Li, Xin, Cassidy, Justin J., Reinke, Catherine A., Fischboeck, Stephen, Carthew, Richard W. · 2009 · Cell
  64. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation
    Anita M. Rauch, Juliane Hoyer, Sabine Guth, Christiane Zweier, Cornelia S. Kraus, Christian Becker, Martin Zenker, Ulrike Hüffmeier, Christian Thomas Thiel, Franz Rüschendorf et al. · 2006 · American Journal of Medical Genetics Part A
  65. The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation
    Mamta Tahiliani, Pinchao Mei, Rui Fang, Thiago Leonor, Michael Scott Rutenberg, Fumiko Shimizu, Jing Li, Anjana Rao, Yujiang Geno Shi · 2007 · Nature
  66. Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
    Guilmatre, Audrey, Dubourg, Christèle, Mosca, Anne-Laure, Legallic, Solenn, Goldenberg, Alice, Drouin-Garraud, Valérie, Layet, Valérie, Rosier, Antoine, Briault, Sylvain, Bonnet-Brilhault, Frédérique et al. · 2009 · Archives of General Psychiatry
  67. Changing numbers of neuronal and non-neuronal cells underlie postnatal brain growth in the rat
    Fabiana Bandeira, Roberto Lent, Suzana Herculano‐Houzel · 2009 · Proceedings of the National Academy of Sciences
  68. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3
    Rodney C. Samaco, Amber Hogart, Janine M. LaSalle · 2004 · Human Molecular Genetics
  69. A survey of small RNAs in human sperm
    Stephen A. Krawetz, Adéle Kruger, Claudia Lalancette, Rebecca Tagett, Ester Antón, Sorin Drăghici, Michael P. Diamond · 2011 · Human Reproduction
  70. Dysregulated Metabotropic Glutamate Receptor-Dependent Translation of AMPA Receptor and Postsynaptic Density-95 mRNAs at Synapses in a Mouse Model of Fragile X Syndrome
    Muddashetty, Ravi S., Kelić, Sofija, Gross, Christina, Xu, Mei, Bassell, Gary J. · 2007 · The Journal of Neuroscience
  71. The Pathophysiology of Fragile X Syndrome
    Penagarikano, Olga, Mulle, Jennifer G., Warren, Stephen T. · 2007 · Annual Review of Genomics and Human Genetics
  72. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
    Christopher J. Klein, Maria Victoria Botuyan, Yanhong Wu, Christopher J. Ward, Garth A. Nicholson, Simon R. Hammans, Kaori Hojo, Hiromitch Yamanishi, Adam R. Karpf, Douglas C. Wallace et al. · 2011 · Nature Genetics
  73. Common genetic variants, acting additively, are a major source of risk for autism
    Klei, Lambertus, Sanders, Stephan J, Murtha, Michael T, Hus, Vanessa, Lowe, Jennifer K, Willsey, A Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel et al. · 2012 · Molecular Autism
  74. Modulation of long-term memory for object recognition via HDAC inhibition
    Daniel P. Stefanko, Ruth M. Barrett, Alexandra R. Ly, Gustavo Kellermann Reolon, Marcelo A. Wood · 2009 · Proceedings of the National Academy of Sciences
  75. The spliceosome as a target of novel antitumour drugs
    Sophie Bonnal, Luisa Vigevani, Juan Valcárcel · 2012 · Nature Reviews Drug Discovery
  76. The HMG-CoA Reductase Inhibitor Lovastatin Reverses the Learning and Attention Deficits in a Mouse Model of Neurofibromatosis Type 1
    Weidong Li, Yijun Cui, Steven A. Kushner, Robert A.M. Brown, James David Jentsch, Paul W. Frankland, Tyrone D. Cannon, Alcino J. Silva · 2005 · Current Biology
  77. Deletion of FMR1 in Purkinje Cells Enhances Parallel Fiber LTD, Enlarges Spines, and Attenuates Cerebellar Eyelid Conditioning in Fragile X Syndrome
    Sebastiaan K. E. Koekkoek, Kazuhiko Yamaguchi, Bogdan A. Milojkovic, Bjorn R. Dortland, Tom J. H. Ruigrok, Reinoud Maex, W. De Graaf, Albertine E. Smit, Frans VanderWerf, C.E. Bakker et al. · 2005 · Neuron
  78. KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
    Golzio, Christelle, Willer, Jason, Talkowski, Michael E., Oh, Edwin C., Taniguchi, Yu, Jacquemont, Sébastien, Reymond, Alexandre, Sun, Mei, Sawa, Akira, Gusella, James F. et al. · 2012 · Nature
  79. Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited
    Judith L. Rapoport, Alexis M. Chavez, DEANNA K. GREENSTEIN, Anjene Musick Addington, Nitin Gogtay · 2008 · Journal of the American Academy of Child & Adolescent Psychiatry
  80. Characterization of Small RNAs in Aplysia Reveals a Role for miR-124 in Constraining Synaptic Plasticity through CREB
    Rajasethupathy, Priyamvada, Fiumara, Ferdinando, Sheridan, Robert, Betel, Doron, Puthanveettil, Sathyanarayanan V., Russo, James J., Sander, Chris, Tuschl, Thomas, Kandel, Eric · 2009 · Neuron
  81. Chromatin crosstalk in development and disease: lessons from REST
    Lezanne Ooi, Ian C. Wood · 2007 · Nature Reviews Genetics
  82. Prions are a common mechanism for phenotypic inheritance in wild yeasts
    Randal Halfmann, Daniel F. Jarosz, Sandra K. Jones, Amelia Chang, Alex K. Lancaster, Susan Lee Lindquist · 2012 · Nature
  83. ADAPTIVE ROLES OF PROGRAMMED CELL DEATH DURING NERVOUS SYSTEM DEVELOPMENT
    Robert R. Buss, Woong Sun, Ronald W. Oppenheim · 2006 · Annual Review of Neuroscience
  84. MicroRNAs in neuronal function and dysfunction
    Im, Heh-In, Kenny, Paul J. · 2012 · Trends in Neurosciences
  85. Long noncoding RNAs in neuronal-glial fate specification and oligodendrocyte lineage maturation
    Tim R. Mercer, Irfan Qureshi, Şölen Gökhan, Marcel E. Dinger, Guangyu Li, John S. Mattick, Mark F. Mehler · 2010 · BMC Neuroscience
  86. Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome
    Tjitske Kleefstra, Han G. Brunner, Jeanne Amiel, Astrid R. Oudakker, Willy M. Nillesen, Alex C. Magee, David Geneviève, Valérie Cormier‐Daire, Hilde Van Esch, Jean‐Pierre Fryns et al. · 2006 · The American Journal of Human Genetics
  87. Post‐natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration
    Giovanna R. Mallucci, Stéphanie Ratté, Emmanuel A. Asante, Jacqueline M. Linehan, Ian Gowland, John G. R. Jefferys, John Collinge · 2002 · The EMBO Journal
  88. Regulation and function of the RSK family of protein kinases
    Yves Roméo, Xiaocui Zhang, Philippe P. Roux · 2011 · Biochemical Journal
  89. Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
    Huang, Hsien-Sung, Allen, John A., Mabb, Angela M., King, Ian F., Miriyala, Jayalakshmi, Taylor-Blake, Bonnie, Sciaky, Noah, Dutton, J. Walter, Lee, Hyeong-Min, Chen, Xin et al. · 2012 · Nature
  90. MeCP2 controls BDNF expression and cocaine intake through homeostatic interactions with microRNA-212
    Im, Heh-In, Hollander, Jonathan A, Bali, Purva, Kenny, Paul J · 2010 · Nature Neuroscience
  91. Hypersensitivity to mGluR5 and ERK1/2 Leads to Excessive Protein Synthesis in the Hippocampus of a Mouse Model of Fragile X Syndrome
    Osterweil, Emily K., Krueger, Dilja D., Reinhold, Kimberly, Bear, Mark F. · 2010 · The Journal of Neuroscience
  92. Epigenetics, DNA Methylation, and Chromatin Modifying Drugs
    Moshe Szyf · 2008 · The Annual Review of Pharmacology and Toxicology
  93. Epidemiology-driven neurodevelopmental animal models of schizophrenia
    Urs Meyer, Joram Feldon · 2009 · Progress in Neurobiology
  94. Genomic imprinting effects on brain development and function
    Lawrence S. Wilkinson, William Davies, Anthony R Isles · 2007 · Nature reviews. Neuroscience
  95. Genomic mapping of 5-hydroxymethylcytosine in the human brain
    Jin, Seung-Gi, Wu, Xiwei, Li, Arthur X., Pfeifer, Gerd P. · 2011 · Nucleic Acids Research
  96. Molecular mechanisms controlling cortical gliogenesis.
    C. Sauvageot, C. Stiles · 2002 · Current Opinion in Neurobiology
  97. Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
    Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre et al. · 2005 · The American Journal of Human Genetics
  98. A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
    Francesca Zalfa, Boris Eleuteri, Kirsten S. Dickson, Valentina Mercaldo, Silvia De Rubeis, Alessandra di Penta, Elisabetta Tabolacci, Pietro Chiurazzi, Giovanni Neri, Seth G. N. Grant et al. · 2007 · Nature Neuroscience
  99. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
    Gauthier, Julie, Champagne, Nathalie, Lafrenière, Ronald G., Xiong, Lan, Spiegelman, Dan, Brustein, Edna, Lapointe, Mathieu, Peng, Huashan, Côté, Mélanie, Noreau, Anne et al. · 2010 · Proceedings of the National Academy of Sciences
  100. Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice
    Yang, Mu, Bozdagi, Ozlem, Scattoni, Maria Luisa, Wöhr, Markus, Roullet, Florence I., Katz, Adam M., Abrams, Danielle N., Kalikhman, David, Simon, Harrison, Woldeyohannes, Leuk et al. · 2012 · The Journal of Neuroscience
  101. PTEN hamartoma tumor syndrome: an overview
    Hobert, Judith A., Eng, Charis · 2009 · Genetics in Medicine
  102. Targeting the correct HDAC(s) to treat cognitive disorders
    André Fischer, Farahnaz Sananbenesi, Alison E. Mungenast, Li‐Huei Tsai · 2010 · Trends in Pharmacological Sciences
  103. Multiple modes of RNA recognition by zinc finger proteins
    Traci M. Tanaka Hall · 2005 · Current Opinion in Structural Biology
  104. Reversible Inhibition of PSD-95 mRNA Translation by miR-125a, FMRP Phosphorylation, and mGluR Signaling
    Muddashetty, Ravi S., Nalavadi, Vijayalaxmi C., Gross, Christina, Yao, Xiaodi, Xing, Lei, Laur, Oskar, Warren, Stephen T., Bassell, Gary J. · 2011 · Molecular Cell
  105. Which Neurodevelopmental Disorders Get Researched and Why?
    Dorothy Bishop · 2010 · PLoS ONE
  106. Rett Syndrome Microglia Damage Dendrites and Synapses by the Elevated Release of Glutamate
    Izumi Maezawa, Lee‐Way Jin · 2010 · Journal of Neuroscience
  107. The neonatal ventral hippocampal lesion as a heuristic neurodevelopmental model of schizophrenia
    Kuei Yuan Tseng, Robert Andrew Chambers, Barbara K. Lipska · 2008 · Behavioural Brain Research
  108. Prefrontal Dysfunction in Schizophrenia Involves Mixed-Lineage Leukemia 1-Regulated Histone Methylation at GABAergic Gene Promoters
    Huang, Hsien-Sung, Matevossian, Anouch, Whittle, Catheryne, Kim, Se Young, Schumacher, Armin, Baker, Stephen P., Akbarian, Schahram · 2007 · The Journal of Neuroscience
  109. Histone Ubiquitination and Deubiquitination in Transcription, DNA Damage Response, and Cancer
    Jian Ping Cao, Qin Yan · 2012 · Frontiers in Oncology
  110. Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA , whose protein product is reduced in autistic brain
    Nguyen, Anhthu, Rauch, Tibor A., Pfeifer, Gerd P., Hu, Valerie W. · 2010 · The FASEB Journal
  111. Making synaptic plasticity and memory last: mechanisms of translational regulation
    Joel D. Richter, Eric Klann · 2009 · Genes & Development
  112. Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition
    Lerer, E, Levi, S, Salomon, S, Darvasi, A, Yirmiya, N, Ebstein, R P · 2008 · Molecular Psychiatry
  113. Sex-Specific Parent-of-Origin Allelic Expression in the Mouse Brain
    Christopher J. Gregg, Jiangwen Zhang, James E. Butler, David Haig, Catherine G. Dulac · 2010 · Science
  114. Genome-Wide Views of Chromatin Structure
    Oliver J. Rando, Howard Y. Chang · 2009 · Annual Review of Biochemistry
  115. Reduced meCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation
    Nagarajan, Raman, Hogart, Amber, Gwye, Ynnez, Martin, Michelle R, LaSalle, Janine M. · 2006 · Epigenetics
  116. Early Prenatal Stress Epigenetically Programs Dysmasculinization in Second-Generation Offspring via the Paternal Lineage
    Morgan, Christopher P., Bale, Tracy L. · 2011 · The Journal of Neuroscience
  117. Paternal Transmission of Stress-Induced Pathologies
    Dietz, David M., LaPlant, Quincey, Watts, Emily L., Hodes, Georgia E., Russo, Scott J., Feng, Jian, Oosting, Ronald S., Vialou, Vincent, Nestler, Eric J. · 2011 · Biological Psychiatry
  118. Epigenetic choreographers of neurogenesis in the adult mammalian brain
    Dengke K. Ma, Maria Carolina Marchetto, Junjie U. Guo, Guo‐li Ming, Fred H. Gage, Hongjun Song · 2010 · Nature Neuroscience
  119. NSD1 is essential for early post‐implantation development and has a catalytically active SET domain
    Geetha Vani Rayasam, Olivia Wendling, Pierre‐Olivier Angrand, Manuel P. Mark, Karen Niederreither, Luyan Song, Thierry Lerouge, Gordon L. Hager, Pierre Chambon, Régine Losson · 2003 · The EMBO Journal
  120. Epigenetics of autism spectrum disorders
    Schanen, N. Carolyn · 2006 · Human Molecular Genetics
  121. ERK/MAPK regulates hippocampal histone phosphorylation following contextual fear conditioning
    Chwang, Wilson B., O’Riordan, Kenneth J., Levenson, Jonathan M., Sweatt, J. David · 2006 · Learning & Memory
  122. Autism-like behaviours with transient histone hyperacetylation in mice treated prenatally with valproic acid
    Kataoka, Shunsuke, Takuma, Kazuhiro, Hara, Yuta, Maeda, Yuko, Ago, Yukio, Matsuda, Toshio · 2013 · International Journal of Neuropsychopharmacology
  123. Alterations of GABAergic Signaling in Autism Spectrum Disorders
    Rocco Pizzarelli, Enrico Cherubini · 2011 · Neural Plasticity
  124. The chromatoid body of male germ cells: Similarity with processing bodies and presence of Dicer and microRNA pathway components
    Noora Kotaja, Suvendra N. Bhattacharyya, Łukasz Jaśkiewicz, Sarah Kimmins, Martti Parvinen, Witold Filipowicz, Paolo Sassone‐Corsi · 2006 · Proceedings of the National Academy of Sciences
  125. Dysregulation of miRNA 181b in the temporal cortex in schizophrenia
    Natalie Jane Beveridge, Paul A. Tooney, Adam P. Carroll, Erin J. Gardiner, Nikola A. Bowden, Rodney J. Scott, Nham Tran, Irina V. Dedova, Murray J. Cairns · 2008 · Human Molecular Genetics
  126. Epigenetic Inheritance and the Missing Heritability Problem
    Slatkin, Montgomery · 2009 · Genetics
  127. Prader–Willi syndrome and Angelman syndrome
    Buiting, Karin · 2010 · American Journal of Medical Genetics Part C: Seminars in Medical Genetics
  128. A Histone H2A Deubiquitinase Complex Coordinating Histone Acetylation and H1 Dissociation in Transcriptional Regulation
    Ping Zhu, Wenlai Zhou, Jianxun Wang, Janusz Puc, Kenneth A. Ohgi, Hediye Erdjument‐Bromage, Paul Tempst, Christopher K. Glass, Michael G. Rosenfeld · 2007 · Molecular Cell
  129. On the use of the word ‘epigenetic’
    Mark Ptashne · 2007 · Current Biology
  130. Immune signalling in neural development, synaptic plasticity and disease
    Boulanger, Lisa M., Shatz, Carla J. · 2004 · Nature Reviews Neuroscience
  131. DNA methylation: TET proteins—guardians of CpG islands?
    Kristine Williams, Jesper Frank Christensen, Kristian Helin · 2011 · EMBO Reports
  132. Targeting DNA methylation for epigenetic therapy
    Xiaojing Yang, Fides D. Lay, Han Han, Peter A. Jones · 2010 · Trends in Pharmacological Sciences
  133. Adolescent brain maturation, the endogenous cannabinoid system and the neurobiology of cannabis-induced schizophrenia
    Bossong, Matthijs G., Niesink, Raymond J.M. · 2010 · Progress in Neurobiology
  134. CHARGE syndrome: an update
    Sanlaville, Damien, Verloes, Alain · 2007 · European Journal of Human Genetics
  135. Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
    Toro, Roberto, Konyukh, Marina, Delorme, Richard, Leblond, Claire, Chaste, Pauline, Fauchereau, Fabien, Coleman, Mary, Leboyer, Marion, Gillberg, Christopher, Bourgeron, Thomas · 2010 · Trends in Genetics
  136. Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
    Françoise Muscatelli · 2000 · Human Molecular Genetics
  137. Ube3a is required for experience-dependent maturation of the neocortex
    Yashiro, Koji, Riday, Thorfinn T, Condon, Kathryn H, Roberts, Adam C, Bernardo, Danilo R, Prakash, Rohit, Weinberg, Richard J, Ehlers, Michael D, Philpot, Benjamin D · 2009 · Nature Neuroscience
  138. AID/APOBEC deaminases disfavor modified cytosines implicated in DNA demethylation
    Christopher S. Nabel, Huijue Jia, Yu Ye, Li Shen, Hana L. Goldschmidt, James T. Stivers, Yi Zhang, Rahul M. Kohli · 2012 · Nature Chemical Biology
  139. CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
    Francesca Mari, Sara Azimonti, Ilaria Bertani, Fabrizio Bolognese, Elena Virginia Colombo, Rossella Caselli, Elisa Scala, Ilaria Longo, Salvatore Grosso, Chiara Pescucci et al. · 2005 · Human Molecular Genetics
  140. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome
    Angela L. Duker, Blake C. Ballif, Erawati V. Bawle, Richard Person, Sangeetha K. Mahadevan, Sarah Alliman, Regina Thompson, Ryan N. Traylor, Bassem A. Bejjani, Lisa G. Shaffer et al. · 2010 · European Journal of Human Genetics
  141. Bidirectional crosstalk between endoplasmic reticulum stress and mTOR signaling
    Christian Appenzeller‐Herzog, Michael N. Hall · 2012 · Trends in Cell Biology
  142. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn et al. · 2010 · The American Journal of Human Genetics
  143. Signaling at G-protein-coupled serotonin receptors: recent advances and future research directions
    Mark John Millan, Philippe Marin, Joël Bockaert, Clotilde Mannoury la Cour · 2008 · Trends in Pharmacological Sciences
  144. Mechanisms of imprinting of the Prader-Willi/Angelman region
    Horsthemke, Bernhard, Wagstaff, Joseph · 2008 · American Journal of Medical Genetics Part A
  145. CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype
    Jorieke E. H. Bergman, N Janssen, Lies H. Hoefsloot, Marjolijn C.J. Jongmans, Robert M.W. Hofstra, Conny M.A. van Ravenswaaij‐Arts · 2011 · Journal of Medical Genetics
  146. A mouse model of Rubinstein-Taybi syndrome: Defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4
    Rusiko Bourtchouladze, Regina Lidge, Ray Catapano, Jennifer Stanley, Scott Gossweiler, Darlene Romashko, Rod Scott, Tim Tully · 2003 · Proceedings of the National Academy of Sciences
  147. miR-137 forms a regulatory loop with nuclear receptor TLX and LSD1 in neural stem cells
    Guoqiang Sun, Peng Ye, Kiyohito Murai, Ming‐Fei Lang, Shengxiu Li, Heying Zhang, Wendong Li, Chelsea Fu, Jason Yin, Allen Wang et al. · 2011 · Nature Communications
  148. Structural basis for G9a-like protein lysine methyltransferase inhibition by BIX-01294
    Yanqi Chang, Xing Zhang, John R. Horton, Anup K. Upadhyay, Astrid Spannhoff, Jin Liu, James P. Snyder, Mark T. Bedford, Xiaodong Cheng · 2009 · Nature Structural & Molecular Biology
  149. Control of Cognition and Adaptive Behavior by the GLP/G9a Epigenetic Suppressor Complex
    Schaefer, Anne, Sampath, Srihari C., Intrator, Adam, Min, Alice, Gertler, Tracy S., Surmeier, D. James, Tarakhovsky, Alexander, Greengard, Paul · 2009 · Neuron
  150. SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism
    Durand, C M, Perroy, J, Loll, F, Perrais, D, Fagni, L, Bourgeron, T, Montcouquiol, M, Sans, N · 2012 · Molecular Psychiatry
  151. Maternal transfer of antibodies in vertebrates: trans-generational effects on offspring immunity
    Dennis Hasselquist, Jan‐Åke Nilsson · 2008 · Philosophical Transactions of the Royal Society B Biological Sciences
  152. Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice
    de Vrij, Femke M.S., Levenga, Josien, van der Linde, Herma C., Koekkoek, Sebastiaan K., De Zeeuw, Chris I., Nelson, David L., Oostra, Ben A., Willemsen, Rob · 2008 · Neurobiology of Disease
  153. Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome
    Steven D. Sheridan, Kraig M. Theriault, Surya A. Reis, Fen Zhou, Jon M. Madison, Laurence M. Daheron, Jeanne F. Loring, Stephen J. Haggarty · 2011 · PLoS ONE
  154. MicroRNA-132 dysregulation in schizophrenia has implications for both neurodevelopment and adult brain function
    Miller, Brooke H., Zeier, Zane, Xi, Li, Lanz, Thomas A., Deng, Shibing, Strathmann, Julia, Willoughby, David, Kenny, Paul J., Elsworth, John D., Lawrence, Matthew S. et al. · 2012 · Proceedings of the National Academy of Sciences
  155. Defective GABAergic Neurotransmission and Pharmacological Rescue of Neuronal Hyperexcitability in the Amygdala in a Mouse Model of Fragile X Syndrome
    Olmos-Serrano, J. L., Paluszkiewicz, S. M., Martin, B. S., Kaufmann, W. E., Corbin, J. G., Huntsman, M. M. · 2010 · Journal of Neuroscience
  156. The MECP2 duplication syndrome
    Melissa B. Ramocki, Y. Jane Tavyev, Sarika U. Peters · 2010 · American Journal of Medical Genetics Part A
  157. Proteomic Analysis Reveals Hyperactivation of the Mammalian Target of Rapamycin Pathway in Neurofibromatosis 1–Associated Human and Mouse Brain Tumors
    Biplab Dasgupta, Yijun Yi, David Y. Chen, Jason D. Weber, David H. Gutmann · 2005 · Cancer Research
  158. Is evolution Darwinian or/and Lamarckian?
    Eugene V. Koonin, Yuri I. Wolf · 2009 · Biology Direct
  159. Parsing Molecular and Behavioral Effects of Cocaine in Mitogen- and Stress-Activated Protein Kinase-1-Deficient Mice
    Karen Brami‐Cherrier, Emmanuel Valjent, Denis Hervé, Joanne Darragh, Jean‐Christophe Corvol, Christiane Pagès, Arthur J. Simon, Jean‐Antoine Girault, Jocelyne Caboche · 2005 · Journal of Neuroscience
  160. The conundrums of understanding genetic risks for autism spectrum disorders
    State, Matthew W, Levitt, Pat · 2011 · Nature Neuroscience
  161. Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development
    Hank Heng Qi, Madathia Sarkissian, Gangqing Hu, Zhibin Wang, Arindam Bhattacharjee, D. Benjamin Gordon, Michelle Gonzales, Fei Lan, Pat P. Ongusaha, Maite Huarte et al. · 2010 · Nature
  162. DNA-methyltransferase 1 mRNA is selectively overexpressed in telencephalic GABAergic interneurons of schizophrenia brains
    Marin Veldić, Héctor J. Caruncho, W. S. Liu, John M. Davis, Rosalba Satta, Dennis R. Grayson, Alessandro Guidotti, E. Costa · 2003 · Proceedings of the National Academy of Sciences
  163. Dietary histone deacetylase inhibitors: From cells to mice to man
    Roderick H. Dashwood, E HO · 2007 · Seminars in Cancer Biology
  164. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy
    Harm Boer, Anthony John Holland, Joyce E. Whittington, Jill Butler, Tessa P. Webb, David Clarke · 2002 · The Lancet
  165. Remote control of gene transcription
    West, Adam G., Fraser, Peter · 2005 · Human Molecular Genetics
  166. NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes
    Jenny B. Douglas, Sandra Hanks, I. Karen Temple, Sally J Davies, Alexandra Murray, Meena Upadhyaya, Susan E. Tomkins, Helen E. Hughes, R.P. Trevor Cole, Nazneen Rahman · 2003 · The American Journal of Human Genetics
  167. Epigenetic principles and mechanisms underlying nervous system functions in health and disease
    Mark F. Mehler · 2008 · Progress in Neurobiology
  168. MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunction
    Jannet Kocerha, Mohammad Ali Faghihi, Miguel Angel López-Toledano, Jia Huang, Amy J. Ramsey, Marc G. Caron, Nicole Salès, David Willoughby, Joacim Elmén, Henrik Frydenlund Hansen et al. · 2009 · Proceedings of the National Academy of Sciences
  169. Genome-Wide Activity-Dependent MeCP2 Phosphorylation Regulates Nervous System Development and Function
    Cohen, Sonia, Gabel, Harrison W., Hemberg, Martin, Hutchinson, Ashley N., Sadacca, L. Amanda, Ebert, Daniel H., Harmin, David A., Greenberg, Rachel S., Verdine, Vanessa K., Zhou, Zhaolan et al. · 2011 · Neuron
  170. Serotonin 5-HT2C Receptors as a Target for the Treatment of Depressive and Anxious States: Focus on Novel Therapeutic Strategies
    Mark John Millan · 2005 · Therapies
  171. Enhancers as information integration hubs in development: lessons from genomics
    Christa Buecker, Joanna Wysocka · 2012 · Trends in Genetics
  172. Pre‐, peri‐ and neonatal risk factors for autism
    GUINCHAT, VINCENT, THORSEN, POUL, LAURENT, CLAUDINE, CANS, CHRISTINE, BODEAU, NICOLAS, COHEN, DAVID · 2012 · Acta Obstetricia et Gynecologica Scandinavica
  173. Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*
    Victoria Leggett, Patricia A. Jacobs, Kate Nation, Gaia Scerif, Dorothy Bishop · 2010 · Developmental Medicine & Child Neurology
  174. SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
    Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M. Solomon, Sally Ann Camper, Pinchas Cohen, Uta Francke · 2008 · PLoS ONE
  175. Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1
    Faizaan Mohammad, Tanmoy Mondal, Natalia Guseva, Gaurav Kumar Pandey, Chandrasekhar Kanduri · 2010 · Development
  176. Biochemical, Structural, and Biological Evaluation of Tranylcypromine Derivatives as Inhibitors of Histone Demethylases LSD1 and LSD2
    Claudia Binda, Sérgio Valente, Mauro Romanenghi, Simona Pilotto, Roberto Cirilli, Aristotele Karytinos, Giuseppe Ciossani, Oronza Antonietta Botrugno, Federico Forneris, Maria Tardugno et al. · 2010 · Journal of the American Chemical Society
  177. Rett Syndrome Astrocytes Are Abnormal and Spread MeCP2 Deficiency through Gap Junctions
    Izumi Maezawa, Susan E. Swanberg, Danielle Jenine Harvey, Janine M. LaSalle, Lee‐Way Jin · 2009 · Journal of Neuroscience
  178. A Role for Repressive Histone Methylation in Cocaine-Induced Vulnerability to Stress
    Covington, Herbert E., Maze, Ian, Sun, HaoSheng, Bomze, Howard M., DeMaio, Kristine D., Wu, Emma Y., Dietz, David M., Lobo, Mary Kay, Ghose, Subroto, Mouzon, Ezekiel et al. · 2011 · Neuron
  179. Identification of piRNAs in the central nervous system
    Lee, Eun Joo, Banerjee, Sourav, Zhou, Hongjun, Jammalamadaka, Aruna, Arcila, Mary, Manjunath, B.S., Kosik, Kenneth S. · 2011 · RNA
  180. Down syndrome: the brain in trisomic mode
    Mara Dierssen · 2012 · Nature reviews. Neuroscience
  181. ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome
    Shigeki Iwase, Bin Xiang, Sharmistha Ghosh, Ting Ren, Peter W. Lewis, Jesse C. Cochrane, C. David Allis, David J. Picketts, Dinshaw J. Patel, Haitao Li et al. · 2011 · Nature Structural & Molecular Biology
  182. Mitochondrial DNA transmission, replication and inheritance: a journey from the gamete through the embryo and into offspring and embryonic stem cells
    Justin C. St. John, João Facucho-Oliveira, Yan Jiang, Richard D. Kelly, R. Salah · 2010 · Human Reproduction Update
  183. Combinatorial complexity in chromatin structure and function: revisiting the histone code
    Oliver J. Rando · 2012 · Current Opinion in Genetics & Development
  184. Decision by division: making cortical maps
    PASKO T. RAKIC, Albert E. Ayoub, Joshua J. Breunig, Martin H. Dominguez · 2009 · Trends in Neurosciences
  185. Prenatal stress: Role in psychotic and depressive diseases
    Julie A. Markham, James I. Koenig · 2010 · Psychopharmacology
  186. HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity
    Mitsumasa Kurita, Terrell D. Holloway, Aintzane García‐Bea, Alexey Kozlenkov, Allyson K. Friedman, José L. Moreno, Mitra Heshmati, Sam A. Golden, Pamela Kennedy, Nagahide Takahashi et al. · 2012 · Nature Neuroscience
  187. Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice
    Hayashi, Mansuo L., Rao, B. S. Shankaranarayana, Seo, Jin-Soo, Choi, Han-Saem, Dolan, Bridget M., Choi, Se-Young, Chattarji, Sumantra, Tonegawa, Susumu · 2007 · Proceedings of the National Academy of Sciences
  188. Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of αCaMKII inhibitory phosphorylation
    van Woerden, Geeske M, Harris, Karen D, Hojjati, Mohammad Reza, Gustin, Richard M, Qiu, Shenfeng, de Avila Freire, Rogerio, Jiang, Yong-hui, Elgersma, Ype, Weeber, Edwin J · 2007 · Nature Neuroscience
  189. The Dynamics of DNA Methylation in Schizophrenia and Related Psychiatric Disorders
    Dennis R. Grayson, Alessandro Guidotti · 2012 · Neuropsychopharmacology
  190. The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95
    Todd, Peter K., Mack, Kenneth J., Malter, James S. · 2003 · Proceedings of the National Academy of Sciences
  191. The piRNA pathway: a fly's perspective on the guardian of the genome
    Kirsten-André Senti, Julius Brennecke · 2010 · Trends in Genetics
  192. Paramutation: From Maize to Mice
    Vicki Lynn Chandler · 2007 · Cell
  193. Molecular genetic analysis of Down syndrome
    David Patterson · 2009 · Human Genetics
  194. A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution?
    Ulrich Zechner, Monika Wilda, Hildegard Kehrer‐Sawatzki, Walther Vogel, Rainald Fundele, Horst Hameister · 2001 · Trends in Genetics
  195. The discovery of zinc fingers and their development for practical applications in gene regulation and genome manipulation
    Aaron Klug · 2010 · Quarterly Reviews of Biophysics
  196. Drug discovery with engineered zinc-finger proteins
    Andrew C. Jamieson, Jeffrey C. Miller, Carl O. Pabo · 2003 · Nature Reviews Drug Discovery
  197. Epigenetic modifications of GABAergic interneurons are associated with the schizophrenia-like phenotype induced by prenatal stress in mice
    Matrisciano, Francesco, Tueting, Patricia, Dalal, Ishani, Kadriu, Bashkim, Grayson, Dennis R., Davis, John M., Nicoletti, Ferdinando, Guidotti, Alessandro · 2013 · Neuropharmacology
  198. The major form of MeCP2 has a novel N-terminus generated by alternative splicing
    Skirmantas Kriaučionis · 2004 · Nucleic Acids Research
  199. Maternal Care and DNA Methylation of a Glutamic Acid Decarboxylase 1 Promoter in Rat Hippocampus
    Tieyuan Zhang, Ian C. Hellstrom, Rosemary C. Bagot, Xianglan Wen, Josie C. Diorio, Michael Joseph Meaney · 2010 · Journal of Neuroscience
  200. Heterogeneous dysregulation of microRNAs across the autism spectrum
    Abu-Elneel, Kawther, Liu, Tsunglin, Gazzaniga, Francesca S., Nishimura, Yuhei, Wall, Dennis P., Geschwind, Daniel H., Lao, Kaiqin, Kosik, Kenneth S. · 2008 · neurogenetics