(Q35113859)

English

Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

object named as

Ling M Wong

2

0 references

author name string

Naomi J Goodrich-Hunsaker

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Yingratana McLennan

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Flora Tassone

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Danielle Harvey

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Susan M Rivera

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Tony J Simon

7

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

publication date

14 July 2011

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Frontiers in Human Neuroscience

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

63

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Enhanced manual and oral motor reaction time in young adult female fragile X premutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Advances in understanding the molecular basis of FXTAS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Co-occurring diagnoses among FMR1 premutation allele carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Fragile X syndrome -- from genes to cognition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

A review of fragile X premutation disorders: expanding the psychiatric perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Lifespan changes in working memory in fragile X premutation males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

The fragile X prevalence paradox

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Linking visual attention and number processing in the brain: the role of the temporo-parietal junction in small and large symbolic and nonsymbolic number comparison

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Interactions between number and space in parietal cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Fragile X-associated tremor/ataxia syndrome (FXTAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Are subitizing and counting implemented as separate or functionally overlapping processes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Neurobehavioral effects of the fragile X premutation in adult women: a controlled study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Why are small and large numbers enumerated differently? A limited-capacity preattentive stage in vision

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Regression analyses of repeated measures data in cognitive research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Girls with fragile X syndrome: physical and neurocognitive status and outcome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Neuropsychological dysfunction among affected heterozygous fragile X females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Span and rate of apprehension in children and adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

9 July 2018

Age-dependent cognitive changes in carriers of the fragile X syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Arithmetic difficulties in females with the fragile X premutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Math learning disability and math LD subtypes: evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Profile of cognitive functioning in women with the fragile X mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Clinical involvement and protein expression in individuals with the FMR1 premutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Neural evidence linking visual object enumeration and attention.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

What enumeration studies can show us about spatial attention: evidence for limited capacity preattentive processing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Apparently enhanced visual information processing in female fragile X carriers: preliminary findings.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Cognitive profile in adult, normal intelligent female fragile X carriers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139190

27 September 2018

Cognitive profiles of the carrier fragile X woman

1 reference

https://pubmed.ncbi.nlm.nih.gov/21808616

12 December 2020

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10.3389/FNHUM.2011.00063

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

release_zpf5tdraurakdmziiu35ynnm4u

1 reference

https://api.fatcat.wiki/v0/release/zpf5tdraurakdmziiu35ynnm4u

24 November 2022

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Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

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6 August 2017

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