Literature DB >> 17028369

The genetics of autism spectrum disorders.

Dorothy E Grice1, Joseph D Buxbaum.   

Abstract

Epidemiological twin studies demonstrate that autism spectrum disorders (ASDs) represent genetic disorders. Subsequent analyses indicate that the causes of ASDs include less common single-gene mutations and chromosomal abnormalities, as well as ASDs caused by multiple interacting genes of weak effect. Genome-wide linkage analysis has identified several susceptibility loci for the ASDs, and positional and functional candidate genes have been identified that appear to represent susceptibility genes for the ASDs. Analysis of additional larger samples and the use of genome-wide association and high-throughput variant detection will lead to the identification of further genes for ASDs.

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Year:  2006        PMID: 17028369     DOI: 10.1385/NMM:8:4:451

Source DB:  PubMed          Journal:  Neuromolecular Med        ISSN: 1535-1084            Impact factor:   3.843


  51 in total

1.  Increased rate of twins among affected sibling pairs with autism.

Authors:  Catalina Betancur; Marion Leboyer; Christopher Gillberg
Journal:  Am J Hum Genet       Date:  2002-05       Impact factor: 11.025

2.  Aetiology of autism: findings and questions.

Authors:  M Rutter
Journal:  J Intellect Disabil Res       Date:  2005-04

3.  Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Authors:  James S Sutcliffe; Ryan J Delahanty; Harish C Prasad; Jacob L McCauley; Qiao Han; Lan Jiang; Chun Li; Susan E Folstein; Randy D Blakely
Journal:  Am J Hum Genet       Date:  2005-07-01       Impact factor: 11.025

4.  An expanded evaluation of the relationship of four alleles to the level of response to alcohol and the alcoholism risk.

Authors:  Xianzhang Hu; Gabor Oroszi; Jeffrey Chun; Tom L Smith; David Goldman; Marc A Schuckit
Journal:  Alcohol Clin Exp Res       Date:  2005-01       Impact factor: 3.455

5.  The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Authors:  C Lord; S Risi; L Lambrecht; E H Cook; B L Leventhal; P C DiLavore; A Pickles; M Rutter
Journal:  J Autism Dev Disord       Date:  2000-06

Review 6.  The search for autism disease genes.

Authors:  Thomas H Wassink; Linda M Brzustowicz; Christopher W Bartlett; Peter Szatmari
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2004

7.  Association between a GABRB3 polymorphism and autism.

Authors:  J D Buxbaum; J M Silverman; C J Smith; D A Greenberg; M Kilifarski; J Reichert; E H Cook; Y Fang; C-Y Song; R Vitale
Journal:  Mol Psychiatry       Date:  2002       Impact factor: 15.992

Review 8.  Autism as a paradigmatic complex genetic disorder.

Authors:  Jeremy Veenstra-Vanderweele; Susan L Christian; Edwin H Cook
Journal:  Annu Rev Genomics Hum Genet       Date:  2004       Impact factor: 8.929

9.  Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.

Authors:  H L Wilson; A C C Wong; S R Shaw; W-Y Tse; G A Stapleton; M C Phelan; S Hu; J Marshall; H E McDermid
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

10.  Implications of the broader phenotype for concepts of autism.

Authors:  Anthony Bailey; Jeremy Parr
Journal:  Novartis Found Symp       Date:  2003
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  12 in total

Review 1.  Are Molecules Involved in Neuritogenesis and Axon Guidance Related to Autism Pathogenesis?

Authors:  Jan Bakos; Zuzana Bacova; Stephen G Grant; Ana M Castejon; Daniela Ostatnikova
Journal:  Neuromolecular Med       Date:  2015-05-20       Impact factor: 3.843

2.  [Autism and autistic disorders. Historical and current aspects].

Authors:  E Kumbier; G Domes; B Herpertz-Dahlmann; S C Herpertz
Journal:  Nervenarzt       Date:  2010-01       Impact factor: 1.214

3.  Disruption of neurexin 1 associated with autism spectrum disorder.

Authors:  Hyung-Goo Kim; Shotaro Kishikawa; Anne W Higgins; Ihn-Sik Seong; Diana J Donovan; Yiping Shen; Eric Lally; Lauren A Weiss; Juliane Najm; Kerstin Kutsche; Maria Descartes; Lynn Holt; Stephen Braddock; Robin Troxell; Lee Kaplan; Fred Volkmar; Ami Klin; Katherine Tsatsanis; David J Harris; Ilse Noens; David L Pauls; Mark J Daly; Marcy E MacDonald; Cynthia C Morton; Bradley J Quade; James F Gusella
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

4.  Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability.

Authors:  Mu Yang; Andrew M Clarke; Jacqueline N Crawley
Journal:  Eur J Neurosci       Date:  2009-04       Impact factor: 3.386

5.  High KEAP1, NRF2 and Low HO-1 Serum Levels in Children with Autism.

Authors:  Hamza Ayaydin; İsmail Akaltun; İsmail Koyuncu; Hakim Çelİk; Adnan Kİrmİt; Hatice Takatak
Journal:  Noro Psikiyatr Ars       Date:  2020-09-21       Impact factor: 1.339

6.  DNA methylation, the early-life social environment and behavioral disorders.

Authors:  Moshe Szyf
Journal:  J Neurodev Disord       Date:  2011-03-11       Impact factor: 4.025

7.  Dysregulated mTORC1-Dependent Translational Control: From Brain Disorders to Psychoactive Drugs.

Authors:  Emanuela Santini; Eric Klann
Journal:  Front Behav Neurosci       Date:  2011-11-08       Impact factor: 3.558

Review 8.  Delineating the Common Biological Pathways Perturbed by ASD's Genetic Etiology: Lessons from Network-Based Studies.

Authors:  Oded Oron; Evan Elliott
Journal:  Int J Mol Sci       Date:  2017-04-14       Impact factor: 5.923

9.  Role of SIRT1/PGC-1α in mitochondrial oxidative stress in autistic spectrum disorder.

Authors:  Xiaosong Bu; Xiaomei Lu; Li Yang; Xiaoyan Xu; Juan Wang; Jiulai Tang
Journal:  Neuropsychiatr Dis Treat       Date:  2017-06-23       Impact factor: 2.570

10.  Environmental risk factors for autism.

Authors:  Rodney R Dietert; Janice M Dietert; Jamie C Dewitt
Journal:  Emerg Health Threats J       Date:  2011-04-20
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