Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study
Approved
Classifications
MinEdu publication type
A1 Journal article (peer-reviewed)
Definition
Article
Target group
Scientific
Peer reviewed
Peer-reviewed
Article type
Journal article
Host publication type
Journal
Publication channel information
Title of journal/series
Brain
ISSN (print)
0006-8950
ISSN (electronic)
1460-2156
ISSN (linking)
0006-8950
Publication forum ID
52614
Publication forum level
3
Internationality
Yes
Detailed publication information
Publication year
2022
Reporting year
2022
Journal/series volume number
145
Journal/series issue number
11
Page numbers
3859–3871
DOI
10.1093/brain/awac224
Language of publication
English
Co-publication information
International co-publication
Yes
Co-publication with a company
No
Availability
Link to online publication
Link to self-archived version
Classification and additional information
MinEdu field of science classification
3124 Neurology and psychiatry
Keywords
focal cortical dysplasia; epilepsy; structural MRI; machine learning
Funding information
Funding information in the publication
The MELD project is supported by the Rosetrees Trust (A2665). We are grateful to ENIGMA-Epilepsy for paving the way for collaborative neuroimaging cohorts in epilepsy and open protocols. This work is supported by the NIHR GOSH BRC. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health. KSW is supported by the Wellcome Trust (215901/Z/19/Z). N.T.C. is supported by the CNF/PERF Shields Award, and the CNRI Chief Research Officer Award. X.Y., N.T.C. and W.D.G. are supported by the Hess Foundation and [F.C. and C.Y. were supported by the Sao Paulo Research Foundation (FAPESP), Grant #2013/07559-3 (BRAINN Brazilian Institute of Neuroscience and Neurotechnology). J.O.M. is supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (Grant Number 206675/Z/17/Z) and received support from the Medical Research Council Centre for Neurodevelopmental Disorders, King's College London (grant MR/N026063/1). J.J.M. and K.Z. are funded by the National Natural Science Foundation of China (No. 82071457). PS acknowledges the DINOGMI Department of Excellence of MIUR 2018-2022 (legge 232 del 2016). G.P.W. is supported by the MRC (G0802012, MR/MR00841X/1). K.J.W. is supported by The Alan Turing Institute under the EPSRC grant EP/N510129/1. I.W. is supported by NIH R01 NS109439. R.G. and C.B. are supported by Tuscany Region Call for Health 2018 (grant DECODE-EE). J.D. is supported by NIHR and Wellcome Trust (218380). T.J.O., L.V., A.W. and B.S. were supported by an NHMRC Investigator Grant #APP1176426. A.C. is supported by a GOSH Children's Charity Surgeon-Scientist Fellowship. RK and YL have been funded by the Saastamoinen Foundation. K.H. and S.D. were supported as part of the BRAIN Unit Infrastructure Award (Grant no: UA05). The BRAIN Unit is funded by the Welsh Government through Health and Care Research Wales.
Source database ID
WoS ID
WOS:000839459500001
Scopus ID
2-s2.0-85146014296