Editorial for the Molecular Mechanisms in Neurodevelopmental Disorders Special Issue-Reference-Cited by-同舟云学术

Editorial for the Molecular Mechanisms in Neurodevelopmental Disorders Special Issue

Published:2023-09-04 Issue:9 Volume:14 Page:1762
ISSN:2073-4425
Container-title:Genes
language:en
Short-container-title:Genes

Author:

Madrigal Irene¹^ORCID

Affiliation:

1. Hospital Clinic of Barcelona, Biochemistry and Molecular Genetics and Fundació de Recerca Clínic Barcelona—Institut d’Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS), 08036 Barcelona, Spain

Abstract

Neurodevelopmental disorders are a group of neurological disorders that may give rise to delayed or impaired cognition, communication, adaptive behavior, and psychomotor skills [...]

Funder

Fundación Mutua Madrileña

Instituto de Salud Carlos III

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Link

https://www.mdpi.com/2073-4425/14/9/1762/pdf

Reference11 articles.

1. Spataro, N., Trujillo-Quintero, J.P., Manso, C., Gabau, E., Capdevila, N., Martinez-Glez, V., Berenguer-Llergo, A., Reyes, S., Brunet, A., and Baena, N. (2023). High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Genes, 14.

2. Alvarez-Mora, M.I., Rodríguez-Revenga, L., Jodar, M., Potrony, M., Sanchez, A., Badenas, C., Oriola, J., Villanueva-Cañas, J.L., Muñoz, E., and Valldeoriola, F. (2023). Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders. Genes, 14.

3. Di Stazio, M., Zanus, C., Faletra, F., Pesaresi, A., Ziccardi, I., Morgan, A., Girotto, G., Costa, P., Carrozzi, M., and d’Adamo, A.P. (2023). Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders. Genes, 14.

4. Birkhoff, J.C., Korporaal, A.L., Brouwer, R.W.W., Nowosad, K., Milazzo, C., Mouratidou, L., van den Hout, M.C.G.N., van IJcken, W.F.J., Huylebroeck, D., and Conidi, A. (2023). Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome. Genes, 14.

5. Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex;Verstappen;Hum. Mol. Genet.,2008