Literature DB >> 15666342

The search for autism disease genes.

Thomas H Wassink1, Linda M Brzustowicz, Christopher W Bartlett, Peter Szatmari.   

Abstract

Autism is a heritable disorder characterized by phenotypic and genetic complexity. This review begins by surveying current linkage, gene association, and cytogenetic studies performed with the goal of identifying autism disease susceptibility variants. Though numerous linkages and associations have been identified, they tend to diminish upon closer examination or attempted replication. The review therefore explores challenges to current methodologies presented by the complexities of autism that might underlie some of the current difficulties, and finishes by describing emerging phenotypic, statistical, and molecular investigational approaches that offer hope of overcoming those challenges. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15666342     DOI: 10.1002/mrdd.20041

Source DB:  PubMed          Journal:  Ment Retard Dev Disabil Res Rev        ISSN: 1080-4013


  26 in total

1.  Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains.

Authors:  Sheryl S Moy; Jessica J Nadler; Nancy B Young; Antonio Perez; L Paige Holloway; Ryan P Barbaro; Justin R Barbaro; Lindsay M Wilson; David W Threadgill; Jean M Lauder; Terry R Magnuson; Jacqueline N Crawley
Journal:  Behav Brain Res       Date:  2006-09-12       Impact factor: 3.332

Review 2.  The genetics of autism spectrum disorders.

Authors:  Dorothy E Grice; Joseph D Buxbaum
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

3.  ITGB3 shows genetic and expression interaction with SLC6A4.

Authors:  Lauren A Weiss; Carole Ober; Edwin H Cook
Journal:  Hum Genet       Date:  2006-05-24       Impact factor: 4.132

Review 4.  A generic research paradigm for identification and validation of early molecular diagnostics and new therapeutics in common disorders.

Authors:  Keith D Coon; Travis L Dunckley; Dietrich A Stephan
Journal:  Mol Diagn Ther       Date:  2007       Impact factor: 4.074

5.  Impaired social interactions and motor learning skills in tuberous sclerosis complex model mice expressing a dominant/negative form of tuberin.

Authors:  Itzamarie Chévere-Torres; Jordan M Maki; Emanuela Santini; Eric Klann
Journal:  Neurobiol Dis       Date:  2011-07-30       Impact factor: 5.996

6.  Slower cortisol response during ACTH stimulation test in autistic children.

Authors:  Jasna Marinović-Curin; Ivana Marinović-Terzić; Zorana Bujas-Petković; Ljubinka Zekan; Veselin Skrabić; Zoran Dogas; Janos Terzić
Journal:  Eur Child Adolesc Psychiatry       Date:  2007-09-14       Impact factor: 4.785

7.  Adolescent siblings of individuals with an autism spectrum disorder: testing a diathesis-stress model of sibling well-being.

Authors:  Gael I Orsmond; Marsha Mailick Seltzer
Journal:  J Autism Dev Disord       Date:  2009-03-17

8.  Predicting social impairment and ASD diagnosis in younger siblings of children with autism spectrum disorder.

Authors:  Paul Yoder; Wendy L Stone; Tedra Walden; Elizabeth Malesa
Journal:  J Autism Dev Disord       Date:  2009-05-16

9.  Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

Authors:  Thomas H Wassink; Veronica J Vieland; Val C Sheffield; Christopher W Bartlett; Rhinda Goedken; Deborah Childress; Joseph Piven
Journal:  Psychiatr Genet       Date:  2008-04       Impact factor: 2.458

10.  High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.

Authors:  S P Strom; J L Stone; J R Ten Bosch; B Merriman; R M Cantor; D H Geschwind; S F Nelson
Journal:  Mol Psychiatry       Date:  2009-05-19       Impact factor: 15.992

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