Dewi Schrader
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Clinical Assistant Professor, Paediatric Neurologist
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Recent Grants
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LARGE SCALE GE3LS PROJECT: GenCOUNSEL: OPTIMIZATION OF GENETIC COUNSELLING FOR CLINICAL IMPLEMENTATION OF GENOME-WIDE SEQUENCING
Open Date: 2017-11-01
Close Date: 2022-10-31
Grant: Close
Improving whole genome sequencing as a clinical test for genetic causes of intellectual disability
Open Date: 2017-04-01
Close Date: 2018-03-31
Grant: Close
GenCOUNSEL: Optimization of genetic counselling for clinical implementation of genome-wide sequencing
Open Date: 2017-04-01
Close Date: 2018-03-31
Articles (12)
Focal cortical dysplasia (FCD) type II is a highly epileptogenic developmental malformation and a common cause of surgically treated drug-resistant epilepsy. While clinical observations suggest frequent occurrence in the frontal lobe, mechanisms for such propensity remain unexplored. Here, we hypothesized that cortex-wide spatial associations of FCD distribution with cortical cytoarchitecture, gene expression and organizational axes may offer complementary insights into processes that predispose given cortical regions to harbour FCD. We mapped the cortex-wide MRI distribution of FCDs in 337 patients collected from 13 sites worldwide. We then determined its associations with (i) cytoarchitectural features using histological atlases by Von Economo and Koskinas and BigBrain; (ii) whole-brain gene expression and spatiotemporal dynamics from prenatal to adulthood stages using the Allen Human Brain Atlas and PsychENCODE BrainSpan; and (iii) macroscale developmental axes of cortical organization. FCD lesions were preferentially located in the prefrontal and fronto-limbic cortices typified by low neuron density, large soma and thick grey matter. Transcriptomic associations with FCD distribution uncovered a prenatal component related to neuroglial proliferation and differentiation, likely accounting for the dysplastic makeup, and a postnatal component related to synaptogenesis and circuit organization, possibly contributing to circuit-level hyperexcitability. FCD distribution showed a strong association with the anterior region of the antero-posterior axis derived from heritability analysis of interregional structural covariance of cortical thickness, but not with structural and functional hierarchical axes. Reliability of all results was confirmed through resampling techniques. Multimodal associations with cytoarchitecture, gene expression and axes of cortical organization indicate that prenatal neurogenesis and postnatal synaptogenesis may be key points of developmental vulnerability of the frontal lobe to FCD. Concordant with a causal role of atypical neuroglial proliferation and growth, our results indicate that FCD-vulnerable cortices display properties indicative of earlier termination of neurogenesis and initiation of cell growth. They also suggest a potential contribution of aberrant postnatal synaptogenesis and circuit development to FCD epileptogenicity.
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2023
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2022
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2022
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2022
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2022
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2021
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2021
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2021
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2021
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2020
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2020
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2020
Collaborators (6)
Jonathan Rayment
Clinical Assistant Professor
The University of British Columbia
Andrea Bernasconi
McGill University
Cyril Goizet
Professeur PU-PH
University of Bordeaux
Niranjan Kissoon
Professor
The University of British Columbia
David M. Goldfarb
The University of British Columbia
Kevin Harris
Associate Professor
The University of British Columbia
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