Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

Show other versions (1)

Bibliographic Details
Main Authors:	Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E, Conso, I
Format:	Journal article
Published:	2002

Similar Items

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

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

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

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

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

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

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

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

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

Linkage and candidate gene studies of autism spectrum disorders in European populations.
by: Holt, R, et al.
Published: (2010)

Molecular genetic investigations of autism.
by: Maestrini, E, et al.
Published: (1998)

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

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

Analysis of reelin as a candidate gene for autism.
by: Bonora, E, et al.
Published: (2003)

Identifying autism susceptibility genes.
by: Maestrini, E, et al.
Published: (2000)

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.
by: Maestrini, E, et al.
Published: (1999)

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

Strategies for autism candidate gene analysis
by: Barnby, G, et al.
Published: (2003)

Strategies for autism candidate gene analysis.
by: Barnby, G, et al.
Published: (2003)

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

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

Analysis of Reelin in autism.
by: Bonora, E, et al.
Published: (2002)

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta 3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families
by: Maestrini, E, et al.
Published: (1999)

Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
by: Marta Viggiano, et al.
Published: (2024-03-01)

Discovering candidate imprinted genes and imprinting control regions in the human genome
by: Minou Bina
Published: (2020-05-01)

A 15q13.3 microdeletion segregating with autism.
by: Pagnamenta, A, et al.
Published: (2009)

Genomic map of candidate human imprint control regions: the imprintome
by: Dereje D. Jima, et al.
Published: (2022-12-01)

Association of four imprinting disorders and ART
by: Hiromitsu Hattori, et al.
Published: (2019-02-01)

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

A MicroRNA Cluster in the DLK1-DIO3 Imprinted Region on Chromosome 14q32.2 Is Dysregulated in Metastatic Hepatoblastomas
by: Shohei Honda, et al.
Published: (2020-11-01)

Association and mutation analyses of 16p11.2 autism candidate genes.
by: Ravinesh A Kumar, et al.
Published: (2009-01-01)

The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.
by: Masayo Kagami, et al.
Published: (2010-06-01)

A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31
by: Hale Onder Yilmaz, et al.
Published: (2020-12-01)

Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)
by: Detera-Wadleigh S, et al.
Published: (2002-10-01)

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
by: Anney, RJL, et al.
Published: (2017)

Defining Candidate Imprinted loci in <i>Bos taurus</i>
by: Minou Bina
Published: (2023-05-01)

DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome.
by: Paul Haggarty, et al.
Published: (2013-01-01)

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

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