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Epilepsia|May 18, 2021
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillationsRemi Stevelink, Jurjen J Luykx, Bochao D Lin, et al.
Molecular Biology of the Cell|July 18, 2024
The LCLAT1/LYCAT acyltransferase is required for EGF-mediated phosphatidylinositol-3,4,5-trisphosphate generation and Akt signalingVictoria Chan, Cristina Camardi, Kai Zhang, et al.
Annals of Neurology|July 13, 2019
SSBP1 mutations in dominant optic atrophy with variable retinal degenerationNeringa Jurkute, Costin Leu, Hans-Martin Pogoda, et al.
Small (Weinheim an Der Bergstrasse, Germany)|October 7, 2025
Exploring Sustainable Hydrogen Production from Alkaline Fresh and Seawater Using Natural Ore Derived 2D Bi<sub>2</sub>S<sub>3</sub>Shreyasi Chattopadhyay, Caique Campos de Oliveira, Rajarshi Bhar, et al.
Insights Into Imaging|December 12, 2025
AI medical device post-market surveillance regulations: consensus recommendations by the European Society of RadiologyRenato Cuocolo, Diana Bernardini, Daniel Pinto Dos Santos, et al.
International Journal of Integrated Care|October 30, 2013
Integrated care pilot in north-west London: a mixed methods evaluationNatasha Curry, Matthew Harris, Laura H Gunn, et al.
The Annals of Thoracic Surgery|October 28, 2017
Patients With Type A Acute Aortic Dissection Presenting With an Abnormal ElectrocardiogramNathaniel I Costin, Amit Korach, Gabriel Loor, et al.
Proceedings of Spie--The International Society for Optical Engineering|October 28, 2022
Multimodal neuroimaging in pediatric type 1 diabetes: a pilot multisite feasibility study of acquisition quality, motion, and variabilityLeon Y Cai, Costin Tanase, Adam W Anderson, et al.
Biological Psychiatry Global Open Science|November 14, 2025
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 PatientsSlavina B Goleva, Costin Leu, Yen-Chen Anne Feng, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
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