Literature DB >> 12230302

Autism: in search of susceptibility genes.

Janine A Lamb1, Jeremy R Parr, Anthony J Bailey, Anthony P Monaco.   

Abstract

Autism is a neurodevelopmental disorder of unknown etiology. There is convincing data for the involvement of genetic factors in the development of autism, and the absence of any consistent evidence for an environmental, neuroanatomical, or biochemical cause has led to an increasing number of genetic studies to determine the basis of this complex disorder. The results of recent genetic linkage and candidate gene studies are reviewed in relation to the challenge of clinical and genetic heterogeneity, and prospects for the future of genetic research in autism are considered.

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Year:  2002        PMID: 12230302     DOI: 10.1385/NMM:2:1:11

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


  157 in total

Review 1.  The epidemiology of autism: a review.

Authors:  E Fombonne
Journal:  Psychol Med       Date:  1999-07       Impact factor: 7.723

2.  How commonly are known medical conditions associated with autism?

Authors:  M Barton; F Volkmar
Journal:  J Autism Dev Disord       Date:  1998-08

3.  Obstetric complications in autism: consequences or causes of the condition?

Authors:  P F Bolton; M Murphy; H Macdonald; B Whitlock; A Pickles; M Rutter
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1997-02       Impact factor: 8.829

4.  Association between idiopathic infantile macrocephaly and autism spectrum disorders.

Authors:  P F Bolton; M Roobol; L Allsopp; A Pickles
Journal:  Lancet       Date:  2001-09-01       Impact factor: 79.321

5.  Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism.

Authors:  A Pickles; P Bolton; H Macdonald; A Bailey; A Le Couteur; C H Sim; M Rutter
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

6.  Incorporating language phenotypes strengthens evidence of linkage to autism.

Authors:  Y Bradford; J Haines; H Hutcheson; M Gardiner; T Braun; V Sheffield; T Cassavant; W Huang; K Wang; V Vieland; S Folstein; S Santangelo; J Piven
Journal:  Am J Med Genet       Date:  2001-08-08

7.  Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome.

Authors:  S L Donnelly; C M Wolpert; M M Menold; M P Bass; J R Gilbert; M L Cuccaro; G R Delong; M A Pericak-Vance
Journal:  Am J Med Genet       Date:  2000-06-12

8.  SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

Authors:  E R Martin; E H Lai; J R Gilbert; A R Rogala; A J Afshari; J Riley; K L Finch; J F Stevens; K J Livak; B D Slotterbeck; S H Slifer; L L Warren; P M Conneally; D E Schmechel; I Purvis; M A Pericak-Vance; A D Roses; J M Vance
Journal:  Am J Hum Genet       Date:  2000-06-21       Impact factor: 11.025

9.  Fluoxetine in treatment of adolescent patients with autism: a longitudinal open trial.

Authors:  S H Fatemi; G M Realmuto; L Khan; P Thuras
Journal:  J Autism Dev Disord       Date:  1998-08

10.  Seizure disorders in autism.

Authors:  F R Volkmar; D S Nelson
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1990-01       Impact factor: 8.829

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  14 in total

Review 1.  Autism.

Authors:  Jeremy Parr
Journal:  BMJ Clin Evid       Date:  2010-01-07

Review 2.  Autism research: lessons from the past and prospects for the future.

Authors:  Michael Rutter
Journal:  J Autism Dev Disord       Date:  2005-04

Review 3.  Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy.

Authors:  John A Tsiouris; W Ted Brown
Journal:  CNS Drugs       Date:  2004       Impact factor: 5.749

4.  Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.

Authors:  Mohammed A Junaid; Dagmar Kowal; Madhabi Barua; Premila S Pullarkat; Susan Sklower Brooks; Raju K Pullarkat
Journal:  Am J Med Genet A       Date:  2004-11-15       Impact factor: 2.802

Review 5.  Conducting genetic epidemiology studies of autism spectrum disorders: issues in matching.

Authors:  Peter Szatmari; Lonnie Zwaigenbaum; Susan Bryson
Journal:  J Autism Dev Disord       Date:  2004-02

Review 6.  Electrophysiological signatures: magnetoencephalographic studies of the neural correlates of language impairment in autism spectrum disorders.

Authors:  Timothy P L Roberts; Gwen L Schmidt; Marc Egeth; Lisa Blaskey; Michael M Rey; J Christopher Edgar; Susan E Levy
Journal:  Int J Psychophysiol       Date:  2008-02-12       Impact factor: 2.997

7.  Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.

Authors:  Gabrielle Barnby; Aaron Abbott; Nuala Sykes; Andrew Morris; Daniel E Weeks; Richard Mott; Janine Lamb; Anthony J Bailey; Anthony P Monaco
Journal:  Am J Hum Genet       Date:  2005-04-13       Impact factor: 11.025

8.  Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

Authors:  J A Lamb; G Barnby; E Bonora; N Sykes; E Bacchelli; F Blasi; E Maestrini; J Broxholme; J Tzenova; D Weeks; A J Bailey; A P Monaco
Journal:  J Med Genet       Date:  2005-02       Impact factor: 6.318

9.  Autism and metabolic cytopathy.

Authors:  Mehmet Emin Ceylan; Ayse Fulya Maner; Ahmet Turkcan; Agah Aydin
Journal:  Open Neuroimag J       Date:  2011-08-05

10.  De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.

Authors:  Nadia Bayou; Ridha M'rad; Ahlem Belhaj; Hussein Daoud; Lamia Ben Jemaa; Ramzi Zemni; Sylvain Briault; M Bechir Helayem; Habiba Chaabouni
Journal:  J Biomed Biotechnol       Date:  2008
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