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

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Lamb, J, Bonora, E, Barnby, G, Sykes, N, Maestrini, E, Blasi, F, Bacchelli, E, Beyer, K, Klauck, S, Poustka, A, Bailey, A, Monaco, A
Μορφή:	Conference item
Έκδοση:	2004

Παρόμοια τεκμήρια

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
ανά: Lamb, J, κ.ά.
Έκδοση: (2005)

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
ανά: Blasi, F, κ.ά.
Έκδοση: (2006)

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
ανά: Sykes, N, κ.ά.
Έκδοση: (2009)

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

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.
ανά: Bacchelli, E, κ.ά.
Έκδοση: (2003)

High-density SNP association study of the autism susceptibility loci on chromosome 7q
ανά: Sykes, N, κ.ά.
Έκδοση: (2006)

Analysis of Reelin in autism.
ανά: Bonora, E, κ.ά.
Έκδοση: (2002)

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus
ανά: Bacchelli, E, κ.ά.
Έκδοση: (2006)

Linkage and candidate gene studies of autism spectrum disorders in European populations.
ανά: Holt, R, κ.ά.
Έκδοση: (2010)

Identifying autism susceptibility genes.
ανά: Maestrini, E, κ.ά.
Έκδοση: (2000)

Analysis of reelin as a candidate gene for autism.
ανά: Bonora, E, κ.ά.
Έκδοση: (2003)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
ανά: Bonora, E, κ.ά.
Έκδοση: (2002)

Analysis of nine candidate genes for autism on chromosome 2q.
ανά: Maestrini, E, κ.ά.
Έκδοση: (2002)

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
ανά: Bonora, E, κ.ά.
Έκδοση: (2002)

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
ανά: Bonora, E, κ.ά.
Έκδοση: (2005)

MET and autism susceptibility: family and case-control studies.
ανά: Sousa, I, κ.ά.
Έκδοση: (2009)

Autism: in search of susceptibility genes.
ανά: Lamb, J, κ.ά.
Έκδοση: (2002)

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
ανά: Toma, C, κ.ά.
Έκδοση: (2007)

MET and autism susceptibility: family and case-control studies
ανά: Sousa, I, κ.ά.
Έκδοση: (2009)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
ανά: Sousa, I, κ.ά.
Έκδοση: (2010)

Autism. The search for susceptibility genes.
ανά: Monaco, A, κ.ά.
Έκδοση: (2001)

A 15q13.3 microdeletion segregating with autism.
ανά: Pagnamenta, A, κ.ά.
Έκδοση: (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.
ανά: Maestrini, E, κ.ά.
Έκδοση: (1999)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
ανά: Barnby, G, κ.ά.
Έκδοση: (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.
ανά: Newbury, D, κ.ά.
Έκδοση: (2009)

Molecular genetic investigations of autism.
ανά: Maestrini, E, κ.ά.
Έκδοση: (1998)

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

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
ανά: Newbury, D, κ.ά.
Έκδοση: (2002)

Strategies for autism candidate gene analysis.
ανά: Barnby, G, κ.ά.
Έκδοση: (2003)

Strategies for autism candidate gene analysis
ανά: Barnby, G, κ.ά.
Έκδοση: (2003)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
ανά: Bonora, E, κ.ά.
Έκδοση: (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.
ανά: Maestrini, E, κ.ά.
Έκδοση: (2010)

Autism: recent molecular genetic advances.
ανά: Lamb, J, κ.ά.
Έκδοση: (2000)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
ανά: Sousa Inês, κ.ά.
Έκδοση: (2010-03-01)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
ανά: Elena Bonora, κ.ά.
Έκδοση: (2014-04-01)

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
ανά: Elena Bonora, κ.ά.
Έκδοση: (2014-12-01)

Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.
ανά: Parr, JR, κ.ά.
Έκδοση: (2006)

MICROBIAL CONSORTIUM AND OXYTOCINE IN THE SOCIAL BEHAVIOR OF CHILDREN WITH AUTISM SPECTRUM DISORDERS
ανά: A. L. Burmistova, κ.ά.
Έκδοση: (2018-08-01)

Correction: Defining the Contribution of to Autism Susceptibility.
ανά: Srirangan Sampath, κ.ά.
Έκδοση: (2013-01-01)

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