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Helena Martins
Helena Martins
Other namesHelena Martins Custodio
Bioinformatician at University College London
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
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
2702016
Controlling false discoveries in genome scans for selection
O François, H Martins, K Caye, SD Schoville
Molecular ecology 25 (2), 454-469, 2016
2402016
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
552016
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
472021
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
172021
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
152022
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
142023
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
142021
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
92021
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
52022
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
52016
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
42021
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
32022
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
22024
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
12023
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
12023
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, ...
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