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Epilepsia|August 10, 2023
Prophecy or empiricism? Clinical value of predicting versus determining genetic variant functionsAndreas Brunklaus, Alfred L George, Dennis Lal, et al.
Nucleic Acids Research|May 7, 2022
DDGun: an untrained predictor of protein stability changes upon amino acid variantsLudovica Montanucci, Emidio Capriotti, Giovanni Birolo, et al.
World Neurosurgery|February 16, 2020
Vasospasm Following Hemispherectomy: A Case Report of a Novel ComplicationAmr Morsi, Andres Maldonado, Dennis Lal, et al.
Epilepsia|November 17, 2020
Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta-analysisArthur Stefanski, Yamile Calle-López, Costin Leu, et al.
Epilepsia|May 30, 2026
Gene burden meta-analysis of 748 879 individuals identifies LGI1-ADAM23 protein complex association with epilepsyJessica Castrillon Lal, Costin Leu, Christian M Boßelmann, et al.
Bioinformatics (Oxford, England)|May 26, 2021
SimText: a text mining framework for interactive analysis and visualization of similarities among biomedical entitiesMarie Macnee, Eduardo Pérez-Palma, Sarah Schumacher-Bass, et al.
Current Opinion in Neurology|January 22, 2019
Spectrum of GABAA receptor variants in epilepsySnezana Maljevic, Rikke S Møller, Christopher A Reid, et al.
Epilepsia|June 10, 2025
SCN9A should not be considered an epilepsy gene; Refuting a gene-disease associationIsmael Ghanty, Eduardo Perez-Palma, Camilo Villaman, et al.
Scientific Reports|April 3, 2025
Polygenic score analysis identifies distinct genetic risk profiles in Alzheimer's disease comorbiditiesCarlos F Hernández, Camilo Villaman, Costin Leu, et al.
JAMA Network Open|February 1, 2020
Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN MutationsLamis Yehia, Marilyn Seyfi, Lisa-Marie Niestroj, et al.
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