Author

Linda S. de Vries

University Medical Center UtrechtORCID 0000-0002-7282-8304Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam M. CoombsiD· 1 shared Ana PopiD· 1 shared Ardem PatapoutianiD· 1 shared Cas SimonsiD· 1 shared Dongxiao LiiD· 1 shared Gajja Sophi SalomonsiD· 1 shared Guy HelmaniD· 1 shared Haoran JiiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Adam M. CoombsORCID

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2 papers

Recent·Most cited

Automated cot-side tracking of functional brain age in preterm infants

Nathan J. Stevenson, Lisa Oberdorfer, Maria Luisa Tataranno, Michael J Breakspear, Paul B. Colditz, Linda S. de Vries, Manon J.N.L. Benders, Katrin Klebermaß-Schrehof, Sampsa Vanhatalo, James A. Roberts

This paper develops a method to track functional brain age in preterm infants using EEG, showing it correlates strongly with postmenstrual age and predicts neurodevelopmental outcomes.

Annals of Clinical and Translational Neurology · May 5, 2020Peer-reviewedNeuroscience

Heterozygous variants in the mechanosensitive ion channel TMEM63A result in transient hypomyelination during infancy

Huifang Yan, Guy Helman, Swetha E. Murthy, Haoran Ji, Joanna Crawford, Thomas Kubisiak, Stephen J. Bent, Jiangxi Xiao, Ryan J. Taft, Adam M. Coombs, Ye Wu, Ana Pop, Dongxiao Li, Linda S. de Vries, Yuwu Jiang, , Nicole I. Wolf

This study identifies heterozygous TMEM63A variants causing transient hypomyelination in infancy, with clinical improvement over time.

The American Journal of Human Genetics · Oct 3, 2019Peer-reviewedGenomics