Literature DB >> 16721407

Genetics of autism spectrum disorder.

Sabine M Klauck1.   

Abstract

Autism is a highly heritable complex neurodevelopmental disorder characterized by distinct impairments of cognitive function in the field of social interaction and speech development. Different approaches have been undertaken worldwide to identify susceptibility loci or genes for autism spectrum disorders. No clear conclusions can be made today about genetic loci involved in these disorders. The review will focus on relevant results from the last decade of research with emphasis on whole genome screens and association studies.

Entities:  

Mesh：

Year:  2006        PMID： 16721407     DOI： 10.1038/sj.ejhg.5201610

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN： 1018-4813            Impact factor:   4.246


  28 in total

Review 1.  Early pharmacological treatment of autism: a rationale for developmental treatment.

Authors:  Terrence C Bethea; Linmarie Sikich
Journal:  Biol Psychiatry       Date:  2007-02-15       Impact factor: 13.382

Review 2.  Prenatal risk factors for autism: comprehensive meta-analysis.

Authors:  Hannah Gardener; Donna Spiegelman; Stephen L Buka
Journal:  Br J Psychiatry       Date:  2009-07       Impact factor: 9.319

Review 3.  Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis.

Authors:  Hannah Gardener; Donna Spiegelman; Stephen L Buka
Journal:  Pediatrics       Date:  2011-07-11       Impact factor: 7.124

Review 4.  Clinical Features in Patients with Microdeletion at 6q14.1-q15.

Authors:  Qing Zhou; Xiao-Hui Wu; Yi-Can Yang; Chao-Chun Zou
Journal:  Indian J Pediatr       Date:  2017-05-29       Impact factor: 1.967

Review 5.  Building an RNA Sequencing Transcriptome of the Central Nervous System.

Authors:  Xiaomin Dong; Yanan You; Jia Qian Wu
Journal:  Neuroscientist       Date:  2015-10-13       Impact factor: 7.519

6.  Heterogeneous dysregulation of microRNAs across the autism spectrum.

Authors:  Kawther Abu-Elneel; Tsunglin Liu; Francesca S Gazzaniga; Yuhei Nishimura; Dennis P Wall; Daniel H Geschwind; Kaiqin Lao; Kenneth S Kosik
Journal:  Neurogenetics       Date:  2008-06-19       Impact factor: 2.660

7.  A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.

Authors:  Khaled K Abu-Amero; Ali M Hellani; Mustafa A Salih; Mohammad Z Seidahmed; Tageldin S Elmalik; Ghassan Zidan; Thomas M Bosley
Journal:  BMC Med Genet       Date:  2010-09-21       Impact factor: 2.103

8.  Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism.

Authors:  Koichi Takeuchi; Michael J Gertner; Jing Zhou; Luis F Parada; Michael V L Bennett; R Suzanne Zukin
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-04       Impact factor: 11.205

9.  Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Authors:  Jyoti Rajan Sharma; Zainunisha Arieff; Hajirah Gameeldien; Muneera Davids; Mandeep Kaur; Lize van der Merwe
Journal:  Genet Test Mol Biomarkers       Date:  2012-12-05

10.  Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.

Authors:  Ivon Cuscó; Andrés Medrano; Blanca Gener; Mireia Vilardell; Fátima Gallastegui; Olaya Villa; Eva González; Benjamín Rodríguez-Santiago; Elisabet Vilella; Miguel Del Campo; Luis A Pérez-Jurado
Journal:  Hum Mol Genet       Date:  2009-02-26       Impact factor: 6.150
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