Claudine M Kraan
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Explore the profile of Claudine M Kraan including associated specialties, affiliations and a list of published articles.
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17
Citations
260
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Recent Articles
1.
Xifaras R, Amor D, Turbitt E, Kraan C
J Dev Behav Pediatr
. 2025 Feb;
46(1):e4-e9.
PMID: 39960782
Objective: Wearable technology has potential benefits for clinical measurement with children who have neurodevelopmental disorders (NDDs). However, this cohort may experience sensory processing disorder, behavioral dysregulation, and cognitive challenges. For...
2.
Kraan C, Bui M, Archibald A, Davison S, Cvejic R, Metcalfe S, et al.
Genet Med Open
. 2024 Dec;
1(1):100829.
PMID: 39669254
Purpose: Clear understanding of mental health phenotypes and associated socioeconomic, physical health and well-being impacts in adult women with an premutation (PM) is needed for counseling and primary healthcare. Methods:...
3.
Tassone F, Protic D, Allen E, Archibald A, Baud A, Brown T, et al.
Cells
. 2023 Sep;
12(18).
PMID: 37759552
The premutation of the fragile X messenger ribonucleoprotein 1 () gene is characterized by an expansion of the CGG trinucleotide repeats (55 to 200 CGGs) in the 5' untranslated region...
4.
Baker E, Arpone M, Bui M, Kraan C, Ling L, Francis D, et al.
Am J Med Genet A
. 2022 Nov;
191(2):357-369.
PMID: 36349505
Fragile X syndrome (FXS) is caused by hypermethylation of the FMR1 promoter due to the full mutation expansion (full mutation [FM]: CGG ≥ 200 repeats) and silencing of FMR1. Assessment...
5.
Martin E, Zhu Y, Kraan C, Kumar K, Godler D, Field M
J Med Genet
. 2021 Jul;
59(7):706-709.
PMID: 34321326
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset condition characterised by cerebellar ataxia and intention tremor, usually found in individuals with FMR1 premutation alleles (PM-CGG expansion of 55-199 repeats). Population...
6.
Kraan C, Baker E, Arpone M, Bui M, Ling L, Gamage D, et al.
Int J Mol Sci
. 2020 Oct;
21(20).
PMID: 33086711
Fragile X syndrome (FXS) is a leading single-gene cause of intellectual disability (ID) with autism features. This study analysed diagnostic and prognostic utility of the Fragile X-Related Epigenetic Element 2...
7.
Baker E, Arpone M, Vera S, Bretherton L, Ure A, Kraan C, et al.
J Neurodev Disord
. 2019 Dec;
11(1):41.
PMID: 31878865
Background: Fragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM: CGG ≥ 200),...
8.
Baker E, Arpone M, Aliaga S, Bretherton L, Kraan C, Bui M, et al.
Mol Autism
. 2019 May;
10:21.
PMID: 31073396
Background: Fragile X syndrome (FXS) is a common monogenic cause of intellectual disability with autism features. While it is caused by loss of the 1 product (FMRP), mosaicism for active...
9.
Kraan C, Godler D, Amor D
Dev Med Child Neurol
. 2018 Aug;
61(2):121-127.
PMID: 30084485
The fragile X mental retardation 1 gene (FMR1)-related disorder fragile X syndrome (FXS) is the most common heritable form of cognitive impairment and the second most common cause of comorbid...
10.
Kraan C, Bui Q, Field M, Archibald A, Metcalfe S, Christie L, et al.
Genet Med
. 2018 Mar;
20(12):1627-1634.
PMID: 29595813
Purpose: Developmental delay phenotypes have been associated with FMR1 premutation (PM: 55-200 CGG repeats) and "gray zone" (GZ: 45-54 CGG repeats) alleles. However, these associations have not been confirmed by...