Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the <scp>DYRK1A</scp> and the <scp>Wiedemann–Steiner</scp> syndromes-Reference-Cited by-同舟云学术

Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the DYRK1A and the Wiedemann–Steiner syndromes

Published:2022-07-25 Issue:4 Volume:102 Page:296-304
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Durand Benjamin¹^ORCID,Schaefer Elise¹,Burger Pauline²,Baer Sarah³^ORCID,Schroder Carmen⁴,Mandel Jean‐Louis²⁵,Piton Amélie²⁶⁷,Coutelle Romain⁴⁸

Affiliation:

1. Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace Hôpitaux Universitaires de Strasbourg Strasbourg France

2. Institut de Génétique et de Biologie Moléculaire et Cellulaire Université de Strasbourg, Institut National de la Santé et de la Recherche Médicale U964 Centre National de la Recherche Scientifique UMR7104 Illkirch France

3. Service de Pédiatrie Spécialisée et Générale, Unité de Neurologie Pédiatrique, Hôpital de Hautepierre Hôpitaux Universitaires de Strasbourg Strasbourg France

4. Service de psychiatrie de l'enfant et de l'adolescent Hôpitaux Universitaires de Strasbourg Strasbourg France

5. University of Strasbourg's Institute for Advanced Studies (USIAS) Strasbourg France

6. Laboratoire de Diagnostic Génétique, IGMA Hôpitaux Universitaires de Strasbourg Strasbourg France

7. Institut Universitaire de France Paris France

8. INSERM U‐1114 Clinique Psychiatrique, Hôpitaux Universitaires de Strasbourg Strasbourg France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14190

Reference44 articles.

1. Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A

2. Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

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1. Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants;Autism Research;2024-07-30

2. Attention challenges in Kabuki syndrome;Journal of Intellectual Disability Research;2023-11-03

3. To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders;Neuroscience & Biobehavioral Reviews;2023-09

4. Associations Between Executive Functioning, Behavioral Functioning, and Adaptive Functioning Difficulties in Wiedemann–Steiner Syndrome;Archives of Clinical Neuropsychology;2023-08-10

5. Characterizing the autism spectrum phenotype in DYRK1A‐related syndrome;Autism Research;2023-07-27