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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Lamb, J, Bonora, E, Barnby, G, Sykes, N, Maestrini, E, Blasi, F, Bacchelli, E, Beyer, K, Klauck, S, Poustka, A, Bailey, A, Monaco, A
التنسيق:	Conference item
منشور في:	2004

مواد مشابهة

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
حسب: Lamb, J, وآخرون
منشور في: (2005)

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
حسب: Blasi, F, وآخرون
منشور في: (2006)

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
حسب: Sykes, N, وآخرون
منشور في: (2009)

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

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.
حسب: Bacchelli, E, وآخرون
منشور في: (2003)

High-density SNP association study of the autism susceptibility loci on chromosome 7q
حسب: Sykes, N, وآخرون
منشور في: (2006)

Analysis of Reelin in autism.
حسب: Bonora, E, وآخرون
منشور في: (2002)

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus
حسب: Bacchelli, E, وآخرون
منشور في: (2006)

Linkage and candidate gene studies of autism spectrum disorders in European populations.
حسب: Holt, R, وآخرون
منشور في: (2010)

Identifying autism susceptibility genes.
حسب: Maestrini, E, وآخرون
منشور في: (2000)

Analysis of reelin as a candidate gene for autism.
حسب: Bonora, E, وآخرون
منشور في: (2003)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
حسب: Bonora, E, وآخرون
منشور في: (2002)

Analysis of nine candidate genes for autism on chromosome 2q.
حسب: Maestrini, E, وآخرون
منشور في: (2002)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
حسب: Bonora, E, وآخرون
منشور في: (2002)

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
حسب: Bonora, E, وآخرون
منشور في: (2005)

MET and autism susceptibility: family and case-control studies.
حسب: Sousa, I, وآخرون
منشور في: (2009)

Autism: in search of susceptibility genes.
حسب: Lamb, J, وآخرون
منشور في: (2002)

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
حسب: Toma, C, وآخرون
منشور في: (2007)

MET and autism susceptibility: family and case-control studies
حسب: Sousa, I, وآخرون
منشور في: (2009)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
حسب: Sousa, I, وآخرون
منشور في: (2010)

Autism. The search for susceptibility genes.
حسب: Monaco, A, وآخرون
منشور في: (2001)

A 15q13.3 microdeletion segregating with autism.
حسب: Pagnamenta, A, وآخرون
منشور في: (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.
حسب: Maestrini, E, وآخرون
منشور في: (1999)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
حسب: Barnby, G, وآخرون
منشور في: (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.
حسب: Newbury, D, وآخرون
منشور في: (2009)

Molecular genetic investigations of autism.
حسب: Maestrini, E, وآخرون
منشور في: (1998)

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

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
حسب: Newbury, D, وآخرون
منشور في: (2002)

Strategies for autism candidate gene analysis.
حسب: Barnby, G, وآخرون
منشور في: (2003)

Strategies for autism candidate gene analysis
حسب: Barnby, G, وآخرون
منشور في: (2003)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
حسب: Bonora, E, وآخرون
منشور في: (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.
حسب: Maestrini, E, وآخرون
منشور في: (2010)

Autism: recent molecular genetic advances.
حسب: Lamb, J, وآخرون
منشور في: (2000)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
حسب: Sousa Inês, وآخرون
منشور في: (2010-03-01)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
حسب: Elena Bonora, وآخرون
منشور في: (2014-04-01)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
حسب: Elena Bonora, وآخرون
منشور في: (2014-12-01)

Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.
حسب: Parr, JR, وآخرون
منشور في: (2006)

MICROBIAL CONSORTIUM AND OXYTOCINE IN THE SOCIAL BEHAVIOR OF CHILDREN WITH AUTISM SPECTRUM DISORDERS
حسب: A. L. Burmistova, وآخرون
منشور في: (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
حسب: Zachary J. Williams, وآخرون
منشور في: (2023-08-01)

Relevance of Neuroinflammation and Encephalitis in Autism
حسب: Janet eKern, وآخرون
منشور في: (2016-01-01)