Literature DB >> 31491383

Getting to the Cores of Autism.

Lilia M Iakoucheva1, Alysson R Muotri2, Jonathan Sebat3.   

Abstract

The genetic architecture of autism spectrum disorder (ASD) is itself a diverse allelic spectrum that consists of rare de novo or inherited variants in hundreds of genes and common polygenic risk at thousands of loci. ASD susceptibility genes are interconnected at the level of transcriptional and protein networks, and many function as genetic regulators of neurodevelopment or synaptic proteins that regulate neural activity. So that the core underlying neuropathologies can be further elucidated, we emphasize the importance of first defining subtypes of ASD on the basis of the phenotypic signatures of genes in model systems and humans.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31491383      PMCID: PMC7039308          DOI: 10.1016/j.cell.2019.07.037

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  118 in total

1.  Genetic heterogeneity in human disease.

Authors:  Jon McClellan; Mary-Claire King
Journal:  Cell       Date:  2010-04-16       Impact factor: 41.582

2.  Mapping 22q11.2 Gene Dosage Effects on Brain Morphometry.

Authors:  Amy Lin; Christopher R K Ching; Ariana Vajdi; Daqiang Sun; Rachel K Jonas; Maria Jalbrzikowski; Leila Kushan-Wells; Laura Pacheco Hansen; Emma Krikorian; Boris Gutman; Deepika Dokoru; Gerhard Helleman; Paul M Thompson; Carrie E Bearden
Journal:  J Neurosci       Date:  2017-05-23       Impact factor: 6.167

3.  Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development.

Authors:  Cleber A Trujillo; Richard Gao; Priscilla D Negraes; Jing Gu; Justin Buchanan; Sebastian Preissl; Allen Wang; Wei Wu; Gabriel G Haddad; Isaac A Chaim; Alain Domissy; Matthieu Vandenberghe; Anna Devor; Gene W Yeo; Bradley Voytek; Alysson R Muotri
Journal:  Cell Stem Cell       Date:  2019-08-29       Impact factor: 24.633

4.  Paternally inherited cis-regulatory structural variants are associated with autism.

Authors:  William M Brandler; Danny Antaki; Madhusudan Gujral; Morgan L Kleiber; Joe Whitney; Michelle S Maile; Oanh Hong; Timothy R Chapman; Shirley Tan; Prateek Tandon; Timothy Pang; Shih C Tang; Keith K Vaux; Yan Yang; Eoghan Harrington; Sissel Juul; Daniel J Turner; Bhooma Thiruvahindrapuram; Gaganjot Kaur; Zhuozhi Wang; Stephen F Kingsmore; Joseph G Gleeson; Denis Bisson; Boyko Kakaradov; Amalio Telenti; J Craig Venter; Roser Corominas; Claudio Toma; Bru Cormand; Isabel Rueda; Silvina Guijarro; Karen S Messer; Caroline M Nievergelt; Maria J Arranz; Eric Courchesne; Karen Pierce; Alysson R Muotri; Lilia M Iakoucheva; Amaia Hervas; Stephen W Scherer; Christina Corsello; Jonathan Sebat
Journal:  Science       Date:  2018-04-20       Impact factor: 47.728

5.  Protein interactome reveals converging molecular pathways among autism disorders.

Authors:  Yasunari Sakai; Chad A Shaw; Brian C Dawson; Diana V Dugas; Zaina Al-Mohtaseb; David E Hill; Huda Y Zoghbi
Journal:  Sci Transl Med       Date:  2011-06-08       Impact factor: 17.956

6.  Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.

Authors:  Dorien Lugtenberg; Tjitske Kleefstra; Astrid R Oudakker; Willy M Nillesen; Helger G Yntema; Andreas Tzschach; Martine Raynaud; Dietz Rating; Hubert Journel; Jamel Chelly; Cyril Goizet; Didier Lacombe; Jean-Michel Pedespan; Bernard Echenne; Gholamali Tariverdian; Declan O'Rourke; Mary D King; Andrew Green; Margriet van Kogelenberg; Hilde Van Esch; Jozef Gecz; Ben C J Hamel; Hans van Bokhoven; Arjan P M de Brouwer
Journal:  Eur J Hum Genet       Date:  2008-11-05       Impact factor: 4.246

7.  Investigating phenotypic heterogeneity in children with autism spectrum disorder: a factor mixture modeling approach.

Authors:  Stelios Georgiades; Peter Szatmari; Michael Boyle; Steven Hanna; Eric Duku; Lonnie Zwaigenbaum; Susan Bryson; Eric Fombonne; Joanne Volden; Pat Mirenda; Isabel Smith; Wendy Roberts; Tracy Vaillancourt; Charlotte Waddell; Teresa Bennett; Ann Thompson
Journal:  J Child Psychol Psychiatry       Date:  2012-08-01       Impact factor: 8.982

8.  Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

Authors:  Brian J O'Roak; Laura Vives; Santhosh Girirajan; Emre Karakoc; Niklas Krumm; Bradley P Coe; Roie Levy; Arthur Ko; Choli Lee; Joshua D Smith; Emily H Turner; Ian B Stanaway; Benjamin Vernot; Maika Malig; Carl Baker; Beau Reilly; Joshua M Akey; Elhanan Borenstein; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Jay Shendure; Evan E Eichler
Journal:  Nature       Date:  2012-04-04       Impact factor: 49.962

9.  Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.

Authors:  Yuqi Qiu; Thomas Arbogast; Sandra Martin Lorenzo; Hongying Li; Shih C Tang; Ellen Richardson; Oanh Hong; Shawn Cho; Omar Shanta; Timothy Pang; Christina Corsello; Curtis K Deutsch; Claire Chevalier; Erica E Davis; Lilia M Iakoucheva; Yann Herault; Nicholas Katsanis; Karen Messer; Jonathan Sebat
Journal:  Cell Rep       Date:  2019-09-24       Impact factor: 9.423

10.  CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function.

Authors:  Jacy L Wagnon; Michael Briese; Wenzhi Sun; Connie L Mahaffey; Tomaž Curk; Gregor Rot; Jernej Ule; Wayne N Frankel
Journal:  PLoS Genet       Date:  2012-11-29       Impact factor: 5.917

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  70 in total

1.  The Genetic Control of Stoichiometry Underlying Autism.

Authors:  Robert B Darnell
Journal:  Annu Rev Neurosci       Date:  2020-07-08       Impact factor: 12.449

2.  Towards the Framework of Understanding Autism Spectrum Disorders.

Authors:  Zilong Qiu; Bo Yuan
Journal:  Neurosci Bull       Date:  2019-11-09       Impact factor: 5.203

3.  Comprehensive Genetic Analysis of Non-syndromic Autism Spectrum Disorder in Clinical Settings.

Authors:  Kei Ohashi; Satomi Fukuhara; Taishi Miyachi; Tomoko Asai; Masayuki Imaeda; Masahide Goto; Yoshie Kurokawa; Tatsuya Anzai; Yoshinori Tsurusaki; Noriko Miyake; Naomichi Matsumoto; Takanori Yamagata; Shinji Saitoh
Journal:  J Autism Dev Disord       Date:  2021-02-15

4.  Deficiency of Autism-Related Gene Dock4 Leads to Impaired Spatial Memory and Hippocampal Function in Mice at Late Middle Age.

Authors:  Daji Guo; Xiaoman Yang; Ming Gao; Xiaoqing Chen; Yanping Tang; Lingling Shen; Keshen Li; Lei Shi
Journal:  Cell Mol Neurobiol       Date:  2022-05-30       Impact factor: 5.046

Review 5.  Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.

Authors:  Helen Rankin Willsey; A Jeremy Willsey; Belinda Wang; Matthew W State
Journal:  Nat Rev Neurosci       Date:  2022-04-19       Impact factor: 34.870

6.  Dysfunction of Trio GEF1 involves in excitatory/inhibitory imbalance and autism-like behaviors through regulation of interneuron migration.

Authors:  Xiaoxuan Sun; Lifang Wang; Chengwen Wei; Mengwen Sun; Qiongwei Li; Hu Meng; Weihua Yue; Dai Zhang; Jun Li
Journal:  Mol Psychiatry       Date:  2021-05-07       Impact factor: 15.992

7.  Plasma and Fecal Metabolite Profiles in Autism Spectrum Disorder.

Authors:  Brittany D Needham; Mark D Adame; Gloria Serena; Destanie R Rose; Gregory M Preston; Mary C Conrad; A Stewart Campbell; David H Donabedian; Alessio Fasano; Paul Ashwood; Sarkis K Mazmanian
Journal:  Biol Psychiatry       Date:  2020-10-10       Impact factor: 13.382

8.  The broader autism phenotype constellations-disability matrix paradigm: Theoretical model for autism and the broader autism phenotype.

Authors:  T A Meridian McDonald
Journal:  Med Hypotheses       Date:  2020-12-18       Impact factor: 1.538

9.  A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain.

Authors:  Shabeesh Balan; Yoshimi Iwayama; Tetsuo Ohnishi; Mikiko Fukuda; Atsuko Shirai; Ayumi Yamada; Sara Weirich; Maren Kirstin Schuhmacher; Kalarickal Vijayan Dileep; Toshihiro Endo; Yasuko Hisano; Kaoru Kotoshiba; Tomoko Toyota; Takeshi Otowa; Hitoshi Kuwabara; Mamoru Tochigi; Akiko Watanabe; Hisako Ohba; Motoko Maekawa; Manabu Toyoshima; Tsukasa Sasaki; Kazuhiko Nakamura; Masatsugu Tsujii; Hideo Matsuzaki; Kam Y J Zhang; Albert Jeltsch; Yoichi Shinkai; Takeo Yoshikawa
Journal:  Mol Psychiatry       Date:  2021-07-15       Impact factor: 15.992

Review 10.  Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.

Authors:  Joy Yoon; Yingwei Mao
Journal:  Int J Mol Sci       Date:  2021-05-28       Impact factor: 5.923

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