The fragile X continuum: new advances and perspectives (Q37150380)

18 August 2017

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title

The fragile X continuum: new advances and perspectives (English)

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18 August 2017

K Cornish

1

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author name string

J Turk

series ordinal

2

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PubMed ID

18444988

18 August 2017

R Hagerman

series ordinal

3

1 reference

18 August 2017

28 April 2008

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Journal of Intellectual Disability Research

18 August 2017

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18 August 2017

52

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18 August 2017

Pt 6

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18 August 2017

469-482

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A study of the distributional characteristics of FMR1 transcript levels in 238 individuals

18 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Prevalence of the fragile X anomaly amongst autistic twins and singletons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Does the autistic child have a "theory of mind"?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Conversational characteristics of children with fragile X syndrome: repetitive speech.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Psychopharmacology in fragile X syndrome--present and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Neuropathic features in fragile X premutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X premutation screening in women with premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Attention and language in fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Theory of mind deficits in children with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The emerging fragile X premutation phenotype: evidence from the domain of social cognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X Syndrome and Autism: Common Developmental Pathways?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Tracing syndrome-specific trajectories of attention across the lifespan

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Heterozygous fragile X female: historical, physical, cognitive, and cytogenetic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Premutation alleles associated with Parkinson disease and essential tremor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

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/10.1111%2FJ.1365-2788.2008.01056.X

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/10.1111%2FJ.1365-2788.2008.01056.X

Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X gene premutation in multiple system atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Executive function and theory of mind performance of boys with fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Here's looking at you, kid: neural systems underlying face and gaze processing in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Is theory of mind understanding impaired in males with fragile X syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Testicular and pituitary inclusion formation in fragile X associated tremor/ataxia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Cognitive impairment in a 65-year-old male with the fragile X-associated tremor-ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Lessons from fragile X regarding neurobiology, autism, and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The fragile-X premutation: a maturing perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Prevalence of FMR1 repeat expansions in movement disorders. A systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Problem behavior in boys with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Amygdala dysfunction in men with the fragile X premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Altered synaptic plasticity in a mouse model of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The use of clonidine for severe and intractable sleep problems in children with neurodevelopmental disorders--a case series

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Aging in individuals with the FMR1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Size bias of fragile X premutation alleles in late-onset movement disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

New insights into fragile X syndrome: from molecules to neurobehaviors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Visual fixation patterns during viewing of naturalistic social situations as predictors of social competence in individuals with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X syndrome at the turn of the century.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Phenotypic variation and FMRP levels in fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Implications of the FMR1 gene in menopause: study of 147 Spanish women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Association between idiopathic premature ovarian failure and fragile X premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Social functioning among girls with fragile X or Turner syndrome and their sisters

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

A neuropsychological investigation of male premutation carriers of fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

A neuropsychological profile of attention deficits in young males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Nature of the working memory deficit in fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Anxiolytic activity of progesterone in progesterone receptor knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

To look or not to look? Typical and atypical development of oculomotor control.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Delineation of early attentional control difficulties in fragile X syndrome: focus on neurocomputational changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Obstetrical and gynecological complications in fragile X carriers: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

FXTAS, SCA10, and SCA17 in American patients with movement disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Eye contact does not facilitate detection in children with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Premature ovarian failure among fragile X premutation carriers: parent-of-origin effect?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Premature ovarian failure in the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X syndrome: diagnostic and carrier testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Mapping nonverbal IQ in young boys with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Symptoms of schizotypal personality disorder in fragile X women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Molecular/clinical correlations in females with fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Association of FMR1 repeat size with ovarian dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

ADHD symptoms in children with FXS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Sustained attention and response inhibition in boys with fragile X syndrome: measures of continuous performance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Expanded FMR1 alleles are rare in idiopathic Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

FMRP expression as a potential prognostic indicator in fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Transcription of the FMR1 gene in individuals with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Melatonin supplementation for severe and intractable sleep disturbance in young people with genetically determined developmental disabilities: short review and commentary

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Screening with the FMR1 protein test among mentally retarded males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Evidence of early ovarian aging in fragile X premutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Further delineation of the executive deficit in males with fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

The fragile X syndrome: from molecular genetics to neurobiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2008.01056.X

10.1111/J.1365-2788.2008.01056.X

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18444988