Literature DB >> 23744158

Progress toward treatments for synaptic defects in autism.

Richard Delorme1, Elodie Ey, Roberto Toro, Marion Leboyer, Christopher Gillberg, Thomas Bourgeron.   

Abstract

Autism spectrum disorder (ASD) encompasses a range of disorders that are characterized by social and communication deficits and repetitive behaviors. For the majority of affected individuals, the cause of ASD remains unknown, but in at least 20% of the cases, a genetic cause can be identified. There is currently no cure for ASD; however, results from mouse models indicate that some forms of the disorder could be alleviated even at the adult stage. Genes involved in ASD seem to converge on common pathways altering synaptic homeostasis. We propose, given the clinical heterogeneity of ASD, that specific 'synaptic clinical trials' should be designed and launched with the aim of establishing whether phenotype 'reversals' could also occur in humans.

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Year:  2013        PMID: 23744158     DOI: 10.1038/nm.3193

Source DB:  PubMed          Journal:  Nat Med        ISSN: 1078-8956            Impact factor:   53.440


  116 in total

1.  Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses.

Authors:  James P Clement; Massimiliano Aceti; Thomas K Creson; Emin D Ozkan; Yulin Shi; Nicholas J Reish; Antoine G Almonte; Brooke H Miller; Brian J Wiltgen; Courtney A Miller; Xiangmin Xu; Gavin Rumbaugh
Journal:  Cell       Date:  2012-11-09       Impact factor: 41.582

2.  The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

Authors:  Qiang Chang; Gargi Khare; Vardhan Dani; Sacha Nelson; Rudolf Jaenisch
Journal:  Neuron       Date:  2006-02-02       Impact factor: 17.173

3.  Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.

Authors:  Melanie Lacaria; Corinne Spencer; Wenli Gu; Richard Paylor; James R Lupski
Journal:  Hum Mol Genet       Date:  2012-04-05       Impact factor: 6.150

4.  Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Authors:  Joseph T Glessner; Kai Wang; Guiqing Cai; Olena Korvatska; Cecilia E Kim; Shawn Wood; Haitao Zhang; Annette Estes; Camille W Brune; Jonathan P Bradfield; Marcin Imielinski; Edward C Frackelton; Jennifer Reichert; Emily L Crawford; Jeffrey Munson; Patrick M A Sleiman; Rosetta Chiavacci; Kiran Annaiah; Kelly Thomas; Cuiping Hou; Wendy Glaberson; James Flory; Frederick Otieno; Maria Garris; Latha Soorya; Lambertus Klei; Joseph Piven; Kacie J Meyer; Evdokia Anagnostou; Takeshi Sakurai; Rachel M Game; Danielle S Rudd; Danielle Zurawiecki; Christopher J McDougle; Lea K Davis; Judith Miller; David J Posey; Shana Michaels; Alexander Kolevzon; Jeremy M Silverman; Raphael Bernier; Susan E Levy; Robert T Schultz; Geraldine Dawson; Thomas Owley; William M McMahon; Thomas H Wassink; John A Sweeney; John I Nurnberger; Hilary Coon; James S Sutcliffe; Nancy J Minshew; Struan F A Grant; Maja Bucan; Edwin H Cook; Joseph D Buxbaum; Bernie Devlin; Gerard D Schellenberg; Hakon Hakonarson
Journal:  Nature       Date:  2009-04-28       Impact factor: 49.962

5.  Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice.

Authors:  Daniela Tropea; Emanuela Giacometti; Nathan R Wilson; Caroline Beard; Cortina McCurry; Dong Dong Fu; Ruth Flannery; Rudolf Jaenisch; Mriganka Sur
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-10       Impact factor: 11.205

6.  Deregulation of EIF4E: a novel mechanism for autism.

Authors:  M Neves-Pereira; B Müller; D Massie; J H G Williams; P C M O'Brien; A Hughes; S-B Shen; David St Clair; Z Miedzybrodzka
Journal:  J Med Genet       Date:  2009-06-25       Impact factor: 6.318

7.  Spatio-temporal transcriptome of the human brain.

Authors:  Hyo Jung Kang; Yuka Imamura Kawasawa; Feng Cheng; Ying Zhu; Xuming Xu; Mingfeng Li; André M M Sousa; Mihovil Pletikos; Kyle A Meyer; Goran Sedmak; Tobias Guennel; Yurae Shin; Matthew B Johnson; Zeljka Krsnik; Simone Mayer; Sofia Fertuzinhos; Sheila Umlauf; Steven N Lisgo; Alexander Vortmeyer; Daniel R Weinberger; Shrikant Mane; Thomas M Hyde; Anita Huttner; Mark Reimers; Joel E Kleinman; Nenad Sestan
Journal:  Nature       Date:  2011-10-26       Impact factor: 49.962

8.  Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.

Authors:  João Peça; Cátia Feliciano; Jonathan T Ting; Wenting Wang; Michael F Wells; Talaignair N Venkatraman; Christopher D Lascola; Zhanyan Fu; Guoping Feng
Journal:  Nature       Date:  2011-03-20       Impact factor: 49.962

9.  Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Authors:  Brian J O'Roak; Pelagia Deriziotis; Choli Lee; Laura Vives; Jerrod J Schwartz; Santhosh Girirajan; Emre Karakoc; Alexandra P Mackenzie; Sarah B Ng; Carl Baker; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Simon E Fisher; Jay Shendure; Evan E Eichler
Journal:  Nat Genet       Date:  2011-05-15       Impact factor: 38.330

10.  Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype?

Authors:  Willem Ma Verhoeven; Jos Im Egger; Marjolein H Willemsen; Gert Jm de Leijer; Tjitske Kleefstra
Journal:  Neuropsychiatr Dis Treat       Date:  2012-04-19       Impact factor: 2.570

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  78 in total

Review 1.  From the genetic architecture to synaptic plasticity in autism spectrum disorder.

Authors:  Thomas Bourgeron
Journal:  Nat Rev Neurosci       Date:  2015-09       Impact factor: 34.870

Review 2.  Opportunities and challenges for using the zebrafish to study neuronal connectivity as an endpoint of developmental neurotoxicity.

Authors:  Galen W Miller; Vidya Chandrasekaran; Bianca Yaghoobi; Pamela J Lein
Journal:  Neurotoxicology       Date:  2018-04-25       Impact factor: 4.294

3.  Gene length matters in neurons.

Authors:  Mark J Zylka; Jeremy M Simon; Benjamin D Philpot
Journal:  Neuron       Date:  2015-04-22       Impact factor: 17.173

4.  Systematic reconstruction of autism biology from massive genetic mutation profiles.

Authors:  Weijun Luo; Chaolin Zhang; Yong-Hui Jiang; Cory R Brouwer
Journal:  Sci Adv       Date:  2018-04-11       Impact factor: 14.136

5.  Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2.

Authors:  Sofia Jurgensen; Pablo E Castillo
Journal:  J Neurosci       Date:  2015-10-28       Impact factor: 6.167

Review 6.  Etiology of autism spectrum disorder: a genomics perspective.

Authors:  John J Connolly; Hakon Hakonarson
Journal:  Curr Psychiatry Rep       Date:  2014-11       Impact factor: 5.285

Review 7.  Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.

Authors:  Anand K Srivastava; Charles E Schwartz
Journal:  Neurosci Biobehav Rev       Date:  2014-04-04       Impact factor: 8.989

8.  Genetic Suppression of mTOR Rescues Synaptic and Social Behavioral Abnormalities in a Mouse Model of Pten Haploinsufficiency.

Authors:  Wen-Chin Huang; Youjun Chen; Damon T Page
Journal:  Autism Res       Date:  2019-08-23       Impact factor: 5.216

Review 9.  Neurobiology of autism gene products: towards pathogenesis and drug targets.

Authors:  Kristel T E Kleijer; Michael J Schmeisser; Dilja D Krueger; Tobias M Boeckers; Peter Scheiffele; Thomas Bourgeron; Nils Brose; J Peter H Burbach
Journal:  Psychopharmacology (Berl)       Date:  2014-01-14       Impact factor: 4.530

10.  Social deficits in IRSp53 mutant mice improved by NMDAR and mGluR5 suppression.

Authors:  Woosuk Chung; Su Yeon Choi; Eunee Lee; Haram Park; Jaeseung Kang; Hanwool Park; Yeonsoo Choi; Dongsoo Lee; Sae-Geun Park; Ryunhee Kim; Yi Sul Cho; Jeonghoon Choi; Myoung-Hwan Kim; Jong Won Lee; Seungjoon Lee; Issac Rhim; Min Whan Jung; Daesoo Kim; Yong Chul Bae; Eunjoon Kim
Journal:  Nat Neurosci       Date:  2015-01-26       Impact factor: 24.884

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