Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder. (Q33926696)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22001913 AND SRC:MED&resulttype=core&format=json

14 January 2020

title

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder (English)

1 reference

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14 January 2020

main subject

autism spectrum disorder

0 references

1 reference

2

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14 January 2020

Andrea Schneider

3

1 reference

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14 January 2020

10

Randi J Hagerman

1 reference

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14 January 2020

8

Flora Tassone

1 reference

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14 January 2020

4

David Hessl

1 reference

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14 January 2020

author name string

Weerasak Chonchaiya

1

1 reference

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14 January 2020

Susan W Harris

5

1 reference

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14 January 2020

Meredith Laird

6

1 reference

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14 January 2020

Yi Mu

7

1 reference

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14 January 2020

Danh V Nguyen

9

1 reference

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14 January 2020

publication date

15 October 2011

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14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22001913 AND SRC:MED&resulttype=core&format=json

14 January 2020

volume

131

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14 January 2020

issue

4

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14 January 2020

page(s)

581-589

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A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis

14 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

The role of fragile X mental retardation protein in major mental disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Seizures in Fragile X Syndrome: Characteristics and Comorbid Diagnoses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Fragile X and autism: Intertwined at the molecular level leading to targeted treatments

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Autism spectrum disorders and epilepsy: moving towards a comprehensive approach to treatment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Progressive spatial processing deficits in a mouse model of the fragile X premutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Broad clinical involvement in a family affected by the fragile X premutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Fragile X: a family of disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

A quantitative ELISA assay for the fragile x mental retardation 1 protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Seizure visits in US emergency departments: epidemiology and potential disparities in care

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Autism profiles of males with fragile X syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Advances in the treatment of fragile X syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Epilepsy in North America: a report prepared under the auspices of the global campaign against epilepsy, the International Bureau for Epilepsy, the International League Against Epilepsy, and the World Health Organization.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Fragile X syndrome and autism at the intersection of genetic and neural networks

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

An open trial of divalproex sodium in autism spectrum disorders.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Prevalence and clinical features of epilepsy in a biracial United States population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Autism diagnostic interview: a standardized investigator-based instrument

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Prevalence of the epilepsies in children and adolescents.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Prevalence of epilepsy in Rochester, Minnesota: 1940-1980.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Clinical features of boys with fragile X premutations and intermediate alleles

5 July 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Epilepsy and autism spectrum disorders: are there common developmental mechanisms?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Origins of epilepsy in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Frequent association of autism spectrum disorder in patients with childhood onset epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Prevalence of epilepsy and epileptic seizures in 10-year-old children: results from the Metropolitan Atlanta Developmental Disabilities Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Epilepsy and EEG findings in males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00439-011-1106-6

Epilepsy surveillance among adults--19 States, Behavioral Risk Factor Surveillance System, 2005.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

Epilepsy in fragile X syndrome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105134

10.1007/S00439-011-1106-6

29 October 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22001913 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

14 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22001913 AND SRC:MED&resulttype=core&format=json

14 January 2020

PubMed publication ID

22001913

1 reference