Linkage and candidate gene studies of autism spectrum disorders in European populations.

Linkage and candidate gene studies of autism spectrum disorders in European populations.

Over the past decade, research on the genetic variants underlying susceptibility to autism and autism spectrum disorders (ASDs) has focused on linkage and candidate gene studies. This research has implicated various chromosomal loci and genes. Candidate gene studies have proven to be particularly in...

ver descrição completa

Detalhes bibliográficos
Main Authors:	Holt, R, Barnby, G, Maestrini, E, Bacchelli, E, Brocklebank, D, Sousa, I, Mulder, E, Kantojärvi, K, Järvelä, I, Klauck, S, Poustka, F, Bailey, A, Monaco, A
Formato:	Journal article
Idioma:	English
Publicado em:	2010

Registos relacionados

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
Por: Sousa, I, et al.
Publicado em: (2010)

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.
Por: Bacchelli, E, et al.
Publicado em: (2003)

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
Por: Toma, C, et al.
Publicado em: (2007)

International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample
Por: Lamb, J, et al.
Publicado em: (2004)

Analysis of nine candidate genes for autism on chromosome 2q.
Por: Maestrini, E, et al.
Publicado em: (2002)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
Por: Sousa Inês, et al.
Publicado em: (2010-03-01)

Analysis of reelin as a candidate gene for autism.
Por: Bonora, E, et al.
Publicado em: (2003)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
Por: Bonora, E, et al.
Publicado em: (2002)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
Por: Bonora, E, et al.
Publicado em: (2002)

Strategies for autism candidate gene analysis.
Por: Barnby, G, et al.
Publicado em: (2003)

Strategies for autism candidate gene analysis
Por: Barnby, G, et al.
Publicado em: (2003)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
Por: Bonora, E, et al.
Publicado em: (2003)

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
Por: Bonora, E, et al.
Publicado em: (2005)

High-density SNP association study of the autism susceptibility loci on chromosome 7q
Por: Sykes, N, et al.
Publicado em: (2006)

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
Por: Blasi, F, et al.
Publicado em: (2006)

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
Por: Lamb, J, et al.
Publicado em: (2005)

A 15q13.3 microdeletion segregating with autism.
Por: Pagnamenta, A, et al.
Publicado em: (2009)

Identifying autism susceptibility genes.
Por: Maestrini, E, et al.
Publicado em: (2000)

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
Por: Sykes, N, et al.
Publicado em: (2009)

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus
Por: Bacchelli, E, et al.
Publicado em: (2006)

Analysis of Reelin in autism.
Por: Bonora, E, et al.
Publicado em: (2002)

A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.
Por: Asher, J, et al.
Publicado em: (2009)

MET and autism susceptibility: family and case-control studies.
Por: Sousa, I, et al.
Publicado em: (2009)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Por: Casey, J, et al.
Publicado em: (2012)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Por: Casey, J, et al.
Publicado em: (2012)

Molecular genetic investigations of autism.
Por: Maestrini, E, et al.
Publicado em: (1998)

MET and autism susceptibility: family and case-control studies
Por: Sousa, I, et al.
Publicado em: (2009)

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
Por: Newbury, D, et al.
Publicado em: (2009)

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
Por: Maestrini, E, et al.
Publicado em: (2010)

Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.
Por: Parr, JR, et al.
Publicado em: (2006)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
Por: Barnby, G, et al.
Publicado em: (2005)

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Por: Claire S Leblond, et al.
Publicado em: (2012-02-01)

Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old
Por: Magali Jane Rochat, et al.
Publicado em: (2020-10-01)

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
Por: Bailey, A, et al.
Publicado em: (1998)

Candidate processes for autism spectrum disorders revealed by copy number variation analysis
Por: M. A. Zelenova, et al.
Publicado em: (2019-12-01)

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees
Por: Marc Woodbury-Smith, et al.
Publicado em: (2018-06-01)

CNVs leading to fusion transcripts in individuals with autism spectrum disorder
Por: Holt, R, et al.
Publicado em: (2012)

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.
Por: Maestrini, E, et al.
Publicado em: (1999)

Candidate gene study of <it>HOXB1 </it>in autism spectrum disorder
Por: Muscarella Lucia A, et al.
Publicado em: (2010-05-01)

CNVs leading to fusion transcripts in individuals with autism spectrum disorder.
Por: Holt, R, et al.
Publicado em: (2012)