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.

Бусад хувилбаруудыг харуулах (1)

Genetic studies indicate that chromosome 7q is likely to contain an autism susceptibility locus (AUTS1). We have followed a positional candidate gene approach to identify the relevant gene and report the analysis of four adjacent genes localised to a 800 kb region in 7q32 that contains an imprinted...

Бүрэн тодорхойлолт

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид:	Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E
Формат:	Journal article
Хэл сонгох:	English
Хэвлэсэн:	2002

Ижил төстэй зүйлс

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-н: Bonora, E, зэрэг
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-н: Lamb, J, зэрэг
Хэвлэсэн: (2004)

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-н: Blasi, F, зэрэг
Хэвлэсэн: (2006)

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-н: Sykes, N, зэрэг
Хэвлэсэн: (2006)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
-н: Bonora, E, зэрэг
Хэвлэсэн: (2003)

Molecular genetic investigations of autism.
-н: Maestrini, E, зэрэг
Хэвлэсэн: (1998)

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
-н: Lamb, J, зэрэг
Хэвлэсэн: (2005)

Linkage and candidate gene studies of autism spectrum disorders in European populations.
-н: Holt, R, зэрэг
Хэвлэсэн: (2010)

A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus
-н: Bacchelli, E, зэрэг
Хэвлэсэн: (2006)

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
-н: Toma, C, зэрэг
Хэвлэсэн: (2007)

Analysis of reelin as a candidate gene for autism.
-н: Bonora, E, зэрэг
Хэвлэсэн: (2003)

Identifying autism susceptibility genes.
-н: Maestrini, E, зэрэг
Хэвлэсэн: (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.
-н: Maestrini, E, зэрэг
Хэвлэсэн: (1999)

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
-н: Sykes, N, зэрэг
Хэвлэсэн: (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.
-н: Newbury, D, зэрэг
Хэвлэсэн: (2009)

Strategies for autism candidate gene analysis.
-н: Barnby, G, зэрэг
Хэвлэсэн: (2003)

Strategies for autism candidate gene analysis
-н: Barnby, G, зэрэг
Хэвлэсэн: (2003)

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

Analysis of Reelin in autism.
-н: Bonora, E, зэрэг
Хэвлэсэн: (2002)

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

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

A 15q13.3 microdeletion segregating with autism.
-н: Pagnamenta, A, зэрэг
Хэвлэсэн: (2009)

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

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-н: Marta Viggiano, зэрэг
Хэвлэсэн: (2024-03-01)

Genomic map of candidate human imprint control regions: the imprintome
-н: Dereje D. Jima, зэрэг
Хэвлэсэн: (2022-12-01)

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

Association and mutation analyses of 16p11.2 autism candidate genes.
-н: Ravinesh A Kumar, зэрэг
Хэвлэсэн: (2009-01-01)

Association of four imprinting disorders and ART
-н: Hiromitsu Hattori, зэрэг
Хэвлэсэн: (2019-02-01)

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

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

Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region
-н: Esra Tuğ, зэрэг
Хэвлэсэн: (2018-02-01)

MET and autism susceptibility: family and case-control studies.
-н: Sousa, I, зэрэг
Хэвлэсэн: (2009)

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
-н: Anney, RJL, зэрэг
Хэвлэсэн: (2017)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
-н: Casey, J, зэрэг
Хэвлэсэн: (2012)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
-н: Casey, J, зэрэг
Хэвлэсэн: (2012)

A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31
-н: Hale Onder Yilmaz, зэрэг
Хэвлэсэн: (2020-12-01)

DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome.
-н: Paul Haggarty, зэрэг
Хэвлэсэн: (2013-01-01)