Literature DB >> 11733747

Genetics of autism: complex aetiology for a heterogeneous disorder.

S E Folstein1, B Rosen-Sheidley.   

Abstract

Since autism was first recognized as a disorder in 1943, speculation about its aetiology has ranged from biological to psychological and back again. After twin studies during the 1970s and 1980s yielded unequivocal evidence for a genetic component, aetiological research in autism began to focus primarily on uncovering the genetic mechanisms involved. The identification of chromosomal abnormalities and Mendelian syndromes among individuals with autism, in conjunction with data from genome screens and candidate-gene studies, has helped to refine the view of the complex genetics that underlies autism spectrum conditions.

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Year:  2001        PMID: 11733747     DOI: 10.1038/35103559

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  217 in total

1.  Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

Authors:  Stéphane Jamain; Hélène Quach; Catalina Betancur; Maria Råstam; Catherine Colineaux; I Carina Gillberg; Henrik Soderstrom; Bruno Giros; Marion Leboyer; Christopher Gillberg; Thomas Bourgeron
Journal:  Nat Genet       Date:  2003-05       Impact factor: 38.330

2.  Increased rate of twins among affected sib pairs.

Authors:  Peter M Visscher
Journal:  Am J Hum Genet       Date:  2002-10       Impact factor: 11.025

Review 3.  Oxytocin receptor and Mecp2 308/Y knockout mice exhibit altered expression of autism-related social behaviors.

Authors:  Roger L H Pobbe; Brandon L Pearson; D Caroline Blanchard; Robert J Blanchard
Journal:  Physiol Behav       Date:  2012-03-03

4.  The causes of autism spectrum disorders.

Authors:  Peter Szatmari
Journal:  BMJ       Date:  2003-01-25

5.  Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.

Authors:  Christopher W Bartlett; Judy F Flax; Mark W Logue; Brett J Smith; Veronica J Vieland; Paula Tallal; Linda M Brzustowicz
Journal:  Hum Hered       Date:  2004       Impact factor: 0.444

6.  Evidence for sex-specific risk alleles in autism spectrum disorder.

Authors:  Jennifer L Stone; Barry Merriman; Rita M Cantor; Amanda L Yonan; T Conrad Gilliam; Daniel H Geschwind; Stanley F Nelson
Journal:  Am J Hum Genet       Date:  2004-10-05       Impact factor: 11.025

7.  Predicting white matter integrity from multiple common genetic variants.

Authors:  Omid Kohannim; Neda Jahanshad; Meredith N Braskie; Jason L Stein; Ming-Chang Chiang; April H Reese; Derrek P Hibar; Arthur W Toga; Katie L McMahon; Greig I de Zubicaray; Sarah E Medland; Grant W Montgomery; Nicholas G Martin; Margaret J Wright; Paul M Thompson
Journal:  Neuropsychopharmacology       Date:  2012-04-18       Impact factor: 7.853

Review 8.  CNVs: harbingers of a rare variant revolution in psychiatric genetics.

Authors:  Dheeraj Malhotra; Jonathan Sebat
Journal:  Cell       Date:  2012-03-16       Impact factor: 41.582

Review 9.  Developmentally regulated Ca2+-dependent activator protein for secretion 2 (CAPS2) is involved in BDNF secretion and is associated with autism susceptibility.

Authors:  Tetsushi Sadakata; Teiichi Furuichi
Journal:  Cerebellum       Date:  2009-02-24       Impact factor: 3.847

Review 10.  From loci to networks and back again: anomalies in the study of autism.

Authors:  Ralph-Axel Müller
Journal:  Ann N Y Acad Sci       Date:  2008-12       Impact factor: 5.691

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