International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample

International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample

Podrobná bibliografie
Hlavní autoři:	Lamb, J, Bonora, E, Barnby, G, Sykes, N, Maestrini, E, Blasi, F, Bacchelli, E, Beyer, K, Klauck, S, Poustka, A, Bailey, A, Monaco, A
Médium:	Conference item
Vydáno:	2004

Podobné jednotky

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
Autor: Lamb, J, a další
Vydáno: (2005)

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
Autor: Blasi, F, a další
Vydáno: (2006)

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
Autor: Sykes, N, a další
Vydáno: (2009)

A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p: International molecular genetic study of autism consortium, (IMGSAC)
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Vydáno: (2001)

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.
Autor: Bacchelli, E, a další
Vydáno: (2003)

High-density SNP association study of the autism susceptibility loci on chromosome 7q
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Vydáno: (2006)

Analysis of Reelin in autism.
Autor: Bonora, E, a další
Vydáno: (2002)

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus
Autor: Bacchelli, E, a další
Vydáno: (2006)

Linkage and candidate gene studies of autism spectrum disorders in European populations.
Autor: Holt, R, a další
Vydáno: (2010)

Identifying autism susceptibility genes.
Autor: Maestrini, E, a další
Vydáno: (2000)

Analysis of reelin as a candidate gene for autism.
Autor: Bonora, E, a další
Vydáno: (2003)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
Autor: Bonora, E, a další
Vydáno: (2002)

Analysis of nine candidate genes for autism on chromosome 2q.
Autor: Maestrini, E, a další
Vydáno: (2002)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
Autor: Bonora, E, a další
Vydáno: (2002)

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
Autor: Bonora, E, a další
Vydáno: (2005)

MET and autism susceptibility: family and case-control studies.
Autor: Sousa, I, a další
Vydáno: (2009)

Autism: in search of susceptibility genes.
Autor: Lamb, J, a další
Vydáno: (2002)

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
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Vydáno: (2007)

MET and autism susceptibility: family and case-control studies
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Vydáno: (2009)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
Autor: Sousa, I, a další
Vydáno: (2010)

Autism. The search for susceptibility genes.
Autor: Monaco, A, a další
Vydáno: (2001)

A 15q13.3 microdeletion segregating with autism.
Autor: Pagnamenta, A, a další
Vydáno: (2009)

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.
Autor: Maestrini, E, a další
Vydáno: (1999)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
Autor: Barnby, G, a další
Vydáno: (2005)

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
Autor: Newbury, D, a další
Vydáno: (2009)

Molecular genetic investigations of autism.
Autor: Maestrini, E, a další
Vydáno: (1998)

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
Autor: Bailey, A, a další
Vydáno: (1998)

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
Autor: Newbury, D, a další
Vydáno: (2002)

Strategies for autism candidate gene analysis.
Autor: Barnby, G, a další
Vydáno: (2003)

Strategies for autism candidate gene analysis
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Vydáno: (2003)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
Autor: Bonora, E, a další
Vydáno: (2003)

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.
Autor: Maestrini, E, a další
Vydáno: (2010)

Autism: recent molecular genetic advances.
Autor: Lamb, J, a další
Vydáno: (2000)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
Autor: Elena Bonora, a další
Vydáno: (2014-04-01)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
Autor: Elena Bonora, a další
Vydáno: (2014-12-01)

Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.
Autor: Parr, JR, a další
Vydáno: (2006)

MICROBIAL CONSORTIUM AND OXYTOCINE IN THE SOCIAL BEHAVIOR OF CHILDREN WITH AUTISM SPECTRUM DISORDERS
Autor: A. L. Burmistova, a další
Vydáno: (2018-08-01)

Examining the latent structure and correlates of sensory reactivity in autism: a multi-site integrative data analysis by the autism sensory research consortium
Autor: Zachary J. Williams, a další
Vydáno: (2023-08-01)

Relevance of Neuroinflammation and Encephalitis in Autism
Autor: Janet eKern, a další
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Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Autor: Anney, R, a další
Vydáno: (2012)