Claudia Vingerhoets
Overview
Explore the profile of Claudia Vingerhoets including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
318
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Recent Articles
1.
Jaspers Faijer-Westerink H, von Scheibler E, van Rossum E, van Haelst M, Vingerhoets C, van Amelsvoort T, et al.
Int J Obes (Lond)
. 2024 Nov;
PMID: 39616274
Objective: Copy number variations (CNVs) may contribute to medical conditions. However, research on the impact of individual CNVs on endocrine disease is limited. This study aimed to provide new data...
2.
Serrarens C, Kashyap S, Otter M, Campforts B, Stumpel C, Linden D, et al.
Psychiatry Res Neuroimaging
. 2024 Nov;
345:111915.
PMID: 39546963
47,XXX (Triple X syndrome) is a sex chromosome aneuploidy characterized by the presence of a supernumerary X chromosome in affected females, and has been associated with a variable cognitive, behavioral,...
3.
Vingerhoets C, Ruiz-Fernandez J, von Scheibler E, Vergaelen E, Volbragt N, Soons N, et al.
BJPsych Open
. 2024 Nov;
10(6):e203.
PMID: 39523675
Background: 22q11.2 deletion syndrome (22q11.2DS) is associated with cognitive impairments and an increased risk of psychopathology. Most of the research has been conducted in children and adolescents, although the majority...
4.
Serrarens C, Ruiz-Fernandez J, Otter M, Campforts B, Stumpel C, Linden D, et al.
Cereb Cortex
. 2024 Aug;
34(8.
PMID: 39183364
47,XXX (Triple X syndrome) is a sex chromosome aneuploidy characterized by the presence of a supernumerary X chromosome in affected females and is associated with a variable cognitive, behavioral, and...
5.
Gur R, Bearden C, Jacquemont S, Swillen A, van Amelsvoort T, van den Bree M, et al.
Mol Psychiatry
. 2024 Jul;
30(2):379-387.
PMID: 39048645
Rare recurrent copy number variants (CNVs) at chromosomal loci 22q11.2 and 16p11.2 are genetic disorders with lifespan risk for neuropsychiatric disorders. Microdeletions and duplications are associated with neurocognitive deficits, yet...
6.
Gur R, Bearden C, Jacquemont S, Jizi K, Amelsvoort van T, van den Bree M, et al.
Res Sq
. 2024 Jan;
PMID: 38234766
Rare recurrent copy number variants (CNVs) at chromosomal loci 22q11.2 and 16p11.2 are among the most common rare genetic disorders associated with significant risk for neuropsychiatric disorders across the lifespan....
7.
Zhao Y, Wang Y, Shi L, McDonald-McGinn D, Crowley T, McGinn D, et al.
NPJ Genom Med
. 2023 Jul;
8(1):17.
PMID: 37463940
Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40-50% of patients with 22q11.2 deletion syndrome (22q11.2DS). This syndrome is a rare disorder with relative genetic...
8.
Oskarsdottir S, Boot E, Crowley T, Loo J, Arganbright J, Armando M, et al.
Genet Med
. 2023 Feb;
25(3):100338.
PMID: 36729053
This review aimed to update the clinical practice guidelines for managing children and adolescents with 22q11.2 deletion syndrome (22q11.2DS). The 22q11.2 Society, the international scientific organization studying chromosome 22q11.2 differences...
9.
Boot E, Oskarsdottir S, Loo J, Crowley T, Orchanian-Cheff A, Andrade D, et al.
Genet Med
. 2023 Feb;
25(3):100344.
PMID: 36729052
This review aimed to update the clinical practice guidelines for managing adults with 22q11.2 deletion syndrome (22q11.2DS). The 22q11.2 Society recruited expert clinicians worldwide to revise the original clinical practice...
10.
Serrarens C, Kashyap S, Riveiro-Lago L, Otter M, Campforts B, Stumpel C, et al.
Cereb Cortex
. 2022 Oct;
33(9):5210-5217.
PMID: 36255323
Triple X syndrome is a sex chromosomal aneuploidy characterized by the presence of a supernumerary X chromosome, resulting in a karyotype of 47,XXX in affected females. It has been associated...