| TESS3: fast inference of spatial population structure and genome scans for selection K Caye, TM Deist, H Martins, O Michel, O François Molecular Ecology Resources 16 (2), 540-548, 2016 | 262 | 2016 |
| Controlling false discoveries in genome scans for selection O François, H Martins, K Caye, SD Schoville Molecular ecology 25 (2), 454-469, 2016 | 237 | 2016 |
| Identifying outlier loci in admixed and in continuous populations using ancestral population differentiation statistics H Martins, K Caye, K Luu, MGB Blum, O François Molecular ecology 25 (20), 5029-5042, 2016 | 53 | 2016 |
| Climate change and epilepsy: Insights from clinical and basic science studies MI Gulcebi, E Bartolini, O Lee, CP Lisgaras, F Onat, J Mifsud, P Striano, ... Epilepsy & Behavior 116, 107791, 2021 | 44 | 2021 |
| RHOBTB2 Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of Childhood S Zagaglia, D Steel, S Krithika, L Hernandez-Hernandez, HM Custodio, ... Neurology 96 (11), e1539-e1550, 2021 | 17 | 2021 |
| The role of common genetic variation in presumed monogenic epilepsies C Campbell, C Leu, YCA Feng, S Wolking, C Moreau, C Ellis, S Ganesan, ... EBioMedicine 81, 2022 | 14 | 2022 |
| Postictal psychosis in epilepsy: A Clinicogenetic study V Braatz, H Martins Custodio, C Leu, L Agrò, B Wang, S Calafato, ... Annals of neurology 90 (3), 464-476, 2021 | 12 | 2021 |
| Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’condition H Martins Custodio, LM Clayton, R Bellampalli, S Pagni, K Silvennoinen, ... Brain 146 (9), 3885-3897, 2023 | 11 | 2023 |
| Late diagnoses of Dravet syndrome: How many individuals are we missing? K Silvennoinen, C Puvirajasinghe, K Hudgell, MK Sidhu, ... Epilepsia Open 6 (4), 770-776, 2021 | 9 | 2021 |
| Identifying outlier loci in admixed and in continuous populations using ancestral population differentiation statistics. bioRxiv: 054585 H Martins, K Caye, K Luu, MGB Blum, O Francois | 5 | 2016 |
| SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility K Silvennoinen, K Gawel, D Tsortouktzidis, J Pitsch, S Alhusaini, ... Acta neuropathologica 144 (1), 107-127, 2022 | 4 | 2022 |
| Polygenic risk score analysis reveals shared genetic burden between epilepsy and psychiatric comorbidities C Campbell, D Lewis-Smith, C Leu, H Martins, R Krause, T O'Brien, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 31-32, 2022 | 3 | 2022 |
| Complex epilepsy: it’s all in the history K Silvennoinen, HM Custodio, S Balestrini, F Rugg-Gunn, SM Sisodiya, ... Practical Neurology 21 (2), 153-156, 2021 | 3 | 2021 |
| Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing A Coppola, S Krithika, M Iacomino, D Bobbili, S Balestrini, I Bagnasco, ... Epilepsia 65 (3), 779-791, 2024 | 2 | 2024 |
| Risk-conferring HLA variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice A Vakrinou, R Bellampalli, MI Gulcebi, HM Custodio, S Balestrini, ... Journal of Neurology, Neurosurgery & Psychiatry 94 (11), 887-892, 2023 | 1 | 2023 |
| SCN1A: bioinformatically informed revised boundaries for promoter and enhancer regions S Pagni, HM Custodio, A Frankish, JM Mudge, JD Mills, SM Sisodiya Human Molecular Genetics 32 (10), 1753-1763, 2023 | 1 | 2023 |
| Beyond monogenic: widespread genomic influences on the phenotype in Dravet syndrome LM Clayton, H Custodio, H Martins, R Ravishankara, S Pagni, ... EPILEPSIA 63, 195-195, 2022 | | 2022 |
| Statistical Methods to Identify Local Adaptation in Continuous and Admixed Populations H Martins Université Grenoble Alpes, 2018 | | 2018 |
| Méthodes statistiques pour identifier l'adaptation locale dans les populations continues et mélangées H Martins Université Grenoble Alpes (ComUE), 2018 | | 2018 |
| SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. K Gawel, D Tsortouktzidis, J Pitsch, S Alhusaini, KMJ van Loo, R Picardo, ... | | |
