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Editorial
. 2023 May 25;14(6):1148.
doi: 10.3390/genes14061148.

Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023

David E Godler  1   2 , William T Brown  3   4
Affiliations
Editorial

Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023

David E Godler et al. Genes (Basel). .

Abstract

Fragile X syndrome (FXS) is the leading single-gene cause of inherited intellectual disability and autism [...].

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Conflict of interest statement

DEG is inventor on a number of patents including international application PCT/AU2010/000169, priority application AU2010903595 and international application PCT/AU2011/001024. He is also an Executive Director of E.D.G. Innovations & Consulting, which receives funds from this intellectual property related to these patents. He has also acted as a paid consultant for Bellberry, Ltd. and Actinogen Medical, Pty, Ltd. WTB has no conflicts or competing interests to declare.

References

    1. Cregenzán-Royo O., Brun-Gasca C., Fornieles-Deu A. Behavior Problems and Social Competence in Fragile X Syndrome: A Systematic Review. Genes. 2022;13:280. doi: 10.3390/genes13020280. - DOI - PMC - PubMed
    1. Lozano R., Thompson T., Dixon-Weber J., Erickson C.A., Berry-Kravis E., Williams S., Smith E., Frazier J.A., Rosselot H., Farmer C., et al. Observable Symptoms of Anxiety in Individuals with Fragile X Syndrome: Parent and Caregiver Perspectives. Genes. 2022;13:1660. doi: 10.3390/genes13091660. - DOI - PMC - PubMed
    1. Shuleski K., Zalles L., Lozano R. Exploring Parents’ Concerns Regarding Long-Term Support and Living Arrangements for Their Children with Fragile X Syndrome. Genes. 2022;13:1654. doi: 10.3390/genes13091654. - DOI - PMC - PubMed
    1. Lewis S., DePass A., Hagerman R.J., Lozano R. Case Reports of Aortic Aneurism in Fragile X Syndrome. Genes. 2022;13:1560. doi: 10.3390/genes13091560. - DOI - PMC - PubMed
    1. Hayward B.E., Usdin K. Mechanisms of Genome Instability in the Fragile X-Related Disorders. Genes. 2021;12:1633. doi: 10.3390/genes12101633. - DOI - PMC - PubMed

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