Unifying Views of Autism Spectrum Disorders: A Consideration of Autoregulatory Feedback Loops

Mullins, Caitlin, Fishell, Gord, Tsien, Richard W.·2016·Neuron
DOI 10.1016/j.neuron.2016.02.017

Cites (261)

Items 201–261 of 261

  1. Altered Hippocampal Synaptic Plasticity in the <i>Fmr1</i> Gene Family Knockout Mouse Models
    Zhang, Jing, Hou, Lingfei, Klann, Eric, Nelson, David L. · 2009 · Journal of Neurophysiology
  2. GKAP orchestrates activity-dependent postsynaptic protein remodeling and homeostatic scaling
    Shin, Seung Min, Zhang, Nanyan, Hansen, Jonathan, Gerges, Nashaat Z, Pak, Daniel T S, Sheng, Morgan, Lee, Sang H · 2012 · Nature Neuroscience
  3. Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
    Chahrour, Maria H., Yu, Timothy W., Lim, Elaine T., Ataman, Bulent, Coulter, Michael E., Hill, R. Sean, Stevens, Christine R., Schubert, Christian R., ARRA Autism Sequencing Collaboration, Greenberg, Michael E. et al. · 2012 · PLoS Genetics
  4. Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
    STAART Psychopharmacology Network, Alex S. Nord, Wendy Roeb, Diane E. Dickel, Tom Walsh, Mary Kusenda, Kristen Lewis O’Connor, Dheeraj Malhotra, Shane McCarthy, Sunday M. Stray et al. · 2011 · European Journal of Human Genetics
  5. Sequential ionic and conformational signaling by calcium channels drives neuronal gene expression
    Boxing Li, Michael R. Tadross, Richard W. Tsien · 2016 · Science
  6. From mTOR to cognition: molecular and cellular mechanisms of cognitive impairments in tuberous sclerosis
    Ehninger, D., De Vries, P. J., Silva, A. J. · 2009 · Journal of Intellectual Disability Research
  7. Mutations ofANK3identified by exome sequencing are associated with autism susceptibility
    Cheng Bi, Jinyu Wu, Tao Jiang, Qi Liu, Wanshi Cai, Ping Yu, Tao Cai, Mei Zhao, Yong‐hui Jiang, Zhong Sheng Sun · 2012 · Human Mutation
  8. Reciprocal signaling between translational control pathways and synaptic proteins in autism spectrum disorders
    Santini, Emanuela, Klann, Eric · 2014 · Science Signaling
  9. Is birth a critical period in the pathogenesis of autism spectrum disorders?
    Ben-Ari, Yehezkel · 2015 · Nature Reviews Neuroscience
  10. Altered neuronal network and rescue in a human MECP2 duplication model
    Nageshappa, S, Carromeu, C, Trujillo, C A, Mesci, P, Espuny-Camacho, I, Pasciuto, E, Vanderhaeghen, P, Verfaillie, C M, Raitano, S, Kumar, A et al. · 2016 · Molecular Psychiatry
  11. Increased Expression of the PI3K Enhancer PIKE Mediates Deficits in Synaptic Plasticity and Behavior in Fragile X Syndrome
    Gross, Christina, Chang, Chia-Wei, Kelly, Seth M., Bhattacharya, Aditi, McBride, Sean M.J., Danielson, Scott W., Jiang, Michael Q., Chan, Chi Bun, Ye, Keqiang, Gibson, Jay R. et al. · 2015 · Cell Reports
  12. Autism in Tuberous Sclerosis Complex
    Griselda Gutierrez, Susan L. Smalley, Peter E. Tanguay · 1998 · Journal of Autism and Developmental Disorders
  13. Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation
    Bing-Mei Li, Xiao‐Rong Liu, Yong‐Hong Yi, Yuhong Deng, Tao Su, Xin Zou, Wei‐Ping Liao · 2011 · Epilepsy & Behavior
  14. The Neuron Identity Problem: Form Meets Function
    Fishell, Gord, Heintz, Nathaniel · 2013 · Neuron
  15. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
    Alistair T. Pagnamenta, Hameed Khan, Susan Walker, Dianne Gerrelli, Kirsty Wing, María Clara Bonaglia, Roberto Giorda, Tom P. Berney, Elisa Mani, Massimo Molteni et al. · 2010 · Journal of Medical Genetics
  16. The FMRP regulon: from targets to disease convergence
    Esperanza Fernández, Nicholas Rajan, Claudia Bagni · 2013 · Frontiers in Neuroscience
  17. The molecular and gene regulatory signature of a neuron
    Hobert, Oliver, Carrera, Inés, Stefanakis, Nikolaos · 2010 · Trends in Neurosciences
  18. Wnt-7a Induces Presynaptic Colocalization of α7-Nicotinic Acetylcholine Receptors and Adenomatous Polyposis Coli in Hippocampal Neurons
    Farías, Ginny G., Vallés, Ana S., Colombres, Marcela, Godoy, Juan A., Toledo, Enrique M., Lukas, Ronald J., Barrantes, Francisco J., Inestrosa, Nibaldo C. · 2007 · The Journal of Neuroscience
  19. Pharmacological reversal of synaptic plasticity deficits in the mouse model of Fragile X syndrome by group II mGluR antagonist or lithium treatment
    Catherine H. Choi, Brian P. Schoenfeld, Aaron J. Bell, Paul Hinchey, Maria Kollaros, Michael J. Gertner, Newton H. Woo, Michael R. Tranfaglia, Mark F. Bear, Ruth Suzanne Zukin et al. · 2010 · Brain Research
  20. Association of common variants in the Joubert syndrome gene (AHI1) with autism
    Alvarez Retuerto, Ana I., Cantor, Rita M., Gleeson, Joseph G., Ustaszewska, Anna, Schackwitz, Wendy S., Pennacchio, Len A., Geschwind, Daniel H. · 2008 · Human Molecular Genetics
  21. Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome
    Tian, Yuan, Voineagu, Irina, Paşca, Sergiu P, Won, Hyejung, Chandran, Vijayendran, Horvath, Steve, Dolmetsch, Ricardo E, Geschwind, Daniel H · 2014 · Genome Medicine
  22. The GABAAreceptor is an FMRP target with therapeutic potential in fragile X syndrome
    Sien Braat, Charlotte D’Hulst, Inge Heulens, Silvia De Rubeis, Edwin Mientjes, David Lee Nelson, Rob Willemsen, Claudia Bagni, Debby Van Dam, Peter Paul De Deyn et al. · 2015 · Cell Cycle
  23. Activity-dependent current distributions in model neurons
    Siegel, M, Marder, E, Abbott, L F · 1994 · Proceedings of the National Academy of Sciences
  24. Two opposing plasticity mechanisms pulling a single synapse
    Ithai Rabinowitch, Idan Segev · 2008 · Trends in Neurosciences
  25. Mechanisms of asymmetric cell division during animal development
    Knoblich, Juergen A · 1997 · Current Opinion in Cell Biology
  26. Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology
    Steven A. McCarroll, Steven E. Hyman · 2013 · Neuron
  27. Autism genetics: searching for specificity and convergence
    Jamee M Berg, Daniel H. Geschwind · 2012 · Genome biology
  28. Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
    Robert A. Kozol, Holly N. Cukier, Bing Zou, Vera Mayo, Silvia De Rubeis, Guiqing Cai, Anthony J. Griswold, Patrice L. Whitehead, Jonathan L. Haines, John R. Gilbert et al. · 2015 · Human Molecular Genetics
  29. Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism
    Rebeca Mejı́as, Abby L. Adamczyk, Victor Anggono, Tejasvi Niranjan, Gareth M. Thomas, Kamal Sharma, Cindy D. Skinner, Charles E. Schwartz, Roger E. Stevenson, M. Daniele Fallin et al. · 2011 · Proceedings of the National Academy of Sciences
  30. Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex
    Chévere-Torres, Itzamarie, Kaphzan, Hanoch, Bhattacharya, Aditi, Kang, Areum, Maki, Jordan M., Gambello, Michael J., Arbiser, Jack L., Santini, Emanuela, Klann, Eric · 2012 · Neurobiology of Disease
  31. Nanoscale analysis of structural synaptic plasticity
    Bourne, Jennifer N, Harris, Kristen M · 2012 · Current Opinion in Neurobiology
  32. Recent Advances in the Genetics of Autism Spectrum Disorder
    Silvia De Rubeis, Joseph D. Buxbaum · 2015 · Current Neurology and Neuroscience Reports
  33. Calcium influx through L-type CaV1.2 Ca2+ channels regulates mandibular development
    Ramachandran, Kapil V., Hennessey, Jessica A., Barnett, Adam S., Yin, Xinhe, Stadt, Harriett A., Foster, Erika, Shah, Raj A., Yazawa, Masayuki, Dolmetsch, Ricardo E., Kirby, Margaret L. et al. · 2013 · Journal of Clinical Investigation
  34. Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
    Waltes, Regina, Duketis, Eftichia, Knapp, Michael, Anney, Richard J. L., Huguet, Guillaume, Schlitt, Sabine, Jarczok, Tomasz A., Sachse, Michael, Kämpfer, Laura M., Kleinböck, Tina et al. · 2014 · Human Genetics
  35. The Role of Ionotropic Glutamate Receptors in Childhood Neurodevelopmental Disorders: Autism Spectrum Disorders and Fragile X Syndrome
    Genoveva Uzunova, Eric Hollander, Jason D. Shepherd · 2014 · Current Neuropharmacology
  36. Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism
    Jun Li, Linnan Zhao, Yang You, Tianlan Lu, Meixiang Jia, Hao Yu, Yanyan Ruan, Weihua Yue, Jing Liu, Lin Lu et al. · 2015 · PLoS ONE
  37. Insights into pathophysiology and therapy from a mouse model of Dravet syndrome
    Oakley, John C., Kalume, Franck, Catterall, William A. · 2011 · Epilepsia
  38. Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral Problems
    Anneke T. Vulto‐van Silfhout, Shivakumar Rajamanickam, Philip J. Jensik, Sarah Vergult, Nina De Rocker, Kathryn J. Newhall, Ramya Raghavan, Sara Reardon, Kelsey E. Jarrett, Tara McIntyre et al. · 2014 · The American Journal of Human Genetics
  39. Inhibition of Group I Metabotropic Glutamate Receptors Reverses Autistic-Like Phenotypes Caused by Deficiency of the Translation Repressor eIF4E Binding Protein 2
    Argel Aguilar‐Valles, Edna Matta‐Camacho, Arkady Khoutorsky, Christos G. Gkogkas, Karim Nader, Jean‐Claude Lacaille, Nahum Sonenberg · 2015 · Journal of Neuroscience
  40. Dock4 regulates dendritic development in hippocampal neurons.
    Ueda, Shuhei, Fujimoto, Satoshi, Hiramoto, Kiyo, Negishi, Manabu, Katoh, Hironori · 2008 · Journal of Neuroscience Research
  41. The determination of the neuronal phenotype
    David J. Anderson, Yuh Nung Jan · 1998 · Oxford University Press eBooks
  42. De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies
    Darrell Lee Dinwiddie, Sarah Elizabeth Soden, Carol Saunders, Neil Miller, Emily Farrow, Laurie D. Smith, Stephen Francis Kingsmore · 2013 · BMC Medical Genomics
  43. G quadruplex RNA structures in PSD-95 mRNA: potential regulators of miR-125a seed binding site accessibility
    Snezana Stefanovic, Gary Jonathan Bassell, Mihaela‐Rita Mihailescu · 2014 · RNA
  44. Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function
    Breitenkamp, Alexandra F. S., Matthes, Jan, Nass, Robert Daniel, Sinzig, Judith, Lehmkuhl, Gerd, Nürnberg, Peter, Herzig, Stefan · 2014 · PLoS ONE
  45. A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation
    P-M Martin, Xiaoyong Yang, Nick C. Robin, Ernest T. Lam, Jeremy S. Rabinowitz, Carolyn A. Erdman, Jeffrey F. Quinn, Lauren A. Weiss, Steven P. Hamilton, P-Y Kwok et al. · 2013 · Translational Psychiatry
  46. Expanding the phenotype of Timothy syndrome type 2: An adolescent with ventricular fibrillation but normal development
    Anita Hiippala, Jonna Tallila, Samuel Myllykangas, Juha W. Koskenvuo, Tero‐Pekka Alastalo · 2015 · American Journal of Medical Genetics Part A
  47. A new synaptic player leading to autism risk: Met receptor tyrosine kinase
    Judson, Matthew C., Eagleson, Kathie L., Levitt, Pat · 2011 · Journal of Neurodevelopmental Disorders
  48. Fragile X disappointments upset autism ambitions
    Asher Mullard · 2015 · Nature Reviews Drug Discovery
  49. Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)
    Sebastian Fröhler, Moritz Kieslich, Claudia Langnick, Mirjam Feldkamp, Bernd Opgen‐Rhein, Felix F. Berger, Joachim C. Will, Wei Chen · 2014 · BMC Medical Genetics
  50. CRISPR/Cas9: Prospects and Challenges
    Feng Zhang · 2015 · Human Gene Therapy
  51. Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene
    Tetsuya Marui, Ikuko Funatogawa, Shinko Koishi, Kenji Yamamoto, Hideo Matsumoto, Ohiko Hashimoto, Seiichiro Jinde, Hisami Nishida, Toshiro Sugiyama, Kiyoto Kasai et al. · 2009 · The International Journal of Neuropsychopharmacology
  52. The SWI/SNF Chromatin Remodeling Complex Selectively Affects Multiple Aspects of Serotonergic Neuron Differentiation
    Peter Weinberg, Nuria Flames, Hitoshi Sawa, Gian Garriga, Oliver Hobert · 2013 · Genetics
  53. Low lead levels stunt neuronal growth in a reversible manner.
    Hollis T. Cline, S Witte, Kristin Jones · 1996 · Proceedings of the National Academy of Sciences
  54. State-dependent signaling by Ca<sub>v</sub>1.2 regulates hair follicle stem cell function
    Yucel, Gozde, Altindag, Banu, Gomez-Ospina, Natalia, Rana, Anshul, Panagiotakos, Georgia, Lara, Maria Fernanda, Dolmetsch, Ricardo, Oro, Anthony E. · 2013 · Genes &amp; Development
  55. Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism
    Kacie J. Meyer, Michael Axelsen, Val C. Sheffield, Shivanand R. Patil, Thomas H. Wassink · 2011 · Psychiatric Genetics
  56. Abnormal development of the sinuatrial venous valve and posterior hindbrain may contribute to late fetal resorption of vitamin A-deficient rat embryos
    Jeffrey C. White, Margaret A. Highland, Margaret Clagett‐Dame · 2000 · Teratology
  57. Erratum: Functional implications of a psychiatric risk variant within CACNA1C in induced human neurons
    Yoshimizu, T, Pan, J Q, Mungenast, A E, Madison, J M, Su, S, Ketterman, J, Ongur, D, McPhie, D, Cohen, B, Perlis, R et al. · 2015 · Molecular Psychiatry
  58. Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis
    Kong, Sek Won, Sahin, Mustafa, Collins, Christin D, Wertz, Mary H, Campbell, Malcolm G, Leech, Jarrett D, Krueger, Dilja, Bear, Mark F, Kunkel, Louis M, Kohane, Isaac S · 2014 · Molecular Autism
  59. Book forum
    James C. Harris · 2016 · Journal of the American Academy of Child & Adolescent Psychiatry
  60. <i>Retinal Waves Drive Calcium Transients in Undifferentiated Retinal Cells.</i> Focus on “Spontaneous Waves in the Ventricular Zone of Developing Mammalian Retina”
    Feller, Marla B. · 2004 · Journal of Neurophysiology
  61. Aristaless‐related homeobox mutations
    Eric D. Marsh, Jeffrey Alan Golden · 2010 · Epilepsia