A possible genetic predisposition to suspected hypoxic-ischaemic encephalopathy
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Date
Authors
Holborn, Megan A.
Mellet, Juanita
Joubert, Fourie
Ballot, D.
Pepper, Michael Sean
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Within the last decade, several studies have explored whether there might be a genetic component in hypoxic-ischaemic encephalopathy (HIE) that influences susceptibility to or outcomes following hypoxic-ischaemic injury. This review provides a comprehensive overview of the findings to date from published studies investigating the genetics of HIE. It also highlights some of the challenges faced by researchers, as well as recommendations for future research.
Description
DATA AVAILABILITY : No data was used for the research described in the article.
Keywords
Hypoxic-ischaemic encephalopathy (HIE), Genetics research, Genomics, Variants, SDG-03: Good health and well-being, SDG-15: Life on land
Sustainable Development Goals
SDG-03:Good heatlh and well-being
SDG-15:Life on land
SDG-15:Life on land
Citation
Holborn, M.A., Mellet, J., Joubert, F. et al. 2025, 'A possible genetic predisposition to suspected hypoxic-ischaemic encephalopathy', Biochimica et Biophysica Acta - Molecular Basis of Disease, vol. 1871, no. 4, art. 167732, pp. 1-13, doi : 10.1016/j.bbadis.2025.167732.