Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort-Reference-Cited by-同舟云学术

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Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort

Published:2022-03-24 Issue:2 Volume:23 Page:137-149
ISSN:1364-6753
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Nassir Nasna,Sati Isra,Al Shaibani Shaiban,Ahmed Awab,Almidani Omar,Akter Hosneara,Woodbury-Smith Marc,Tayoun Ahmad Abou,Uddin Mohammed,Albanna Ammar

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s10048-022-00689-2.pdf

Reference34 articles.

1. Hansen BH, Oerbeck B, Skirbekk B, Petrovski BE, Kristensen H (2018) Neurodevelopmental disorders: prevalence and comorbidity in children referred to mental health services. Nord J Psychiatry 72(4):285–291. https://doi.org/10.1080/08039488.2018.1444087

2. Parenti I, Rabaneda LG, Schoen H, Novarino G (2020) Neurodevelopmental disorders: from genetics to functional pathways. Trends Neurosci 43(8):608–621. https://doi.org/10.1016/j.tins.2020.05.004

3. Gilissen C et al (2014) Genome sequencing identifies major causes of severe intellectual disability. Nature 511(7509):344–347. https://doi.org/10.1038/nature13394

4. First MB (2013) Diagnostic and statistical manual of mental disorders, 5th edition, and clinical utility. J Nerv Ment Dis 201(9):727–9. https://doi.org/10.1097/NMD.0b013e3182a2168a

5. M. Woodbury-Smith et al. (2017) Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes. NPJ Genom Med. 2. https://doi.org/10.1038/s41525-017-0020-9

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