Srour, Myriam
Montreal Children's Hospital · McGill University Health Centre
6 papers on CoChatORCID 0000-0003-1009-0508
Most cited papers
- Verified
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Hamdan, F. F., Myers, C. T., Cossette, P., Lemay, P., Spiegelman, D., Laporte, A. D., Nassif, C., Diallo, O., Monlong, J., Cadieux-Dion, M., et al. (2017) · The American Journal of Human Genetics
Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders
Cited by 445
- Verified
De Novo Mutations in Moderate or Severe Intellectual Disability
Hamdan, F. F., Srour, M., Capo-Chichi, J.-M., Daoud, H., Nassif, C., Patry, L., Massicotte, C., Ambalavanan, A., Spiegelman, D., Diallo, O., et al. (2014) · PLoS Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 419
- Verified
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
Hamdan, F. F., Gauthier, J., Araki, Y., Lin, D.-T., Yoshizawa, Y., Higashi, K., Park, A.-R., Spiegelman, D., Dobrzeniecka, S., Piton, A., et al. (2011) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 349
- Verified
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Marsh, A. P. L., Heron, D., Edwards, T. J., Quartier, A., Galea, C., Nava, C., Rastetter, A., Moutard, M.-L., Anderson, V., Bitoun, P., et al. (2017) · Nature Genetics
Fetal and Pediatric Neurological DisordersGenetics and Neurodevelopmental Disorders
Cited by 101
- Verified
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia
Muir, A. M., Gardner, J. F., van Jaarsveld, R. H., de Lange, I. M., van der Smagt, J. J., Wilson, G. N., Dubbs, H., Goldberg, E. M., Zitano, L., Bupp, C., et al. (2021) · Genetics in Medicine
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 35
- Verified
Mesocorticolimbic Connectivity and Volumetric Alterations in DCC Mutation Carriers
Vosberg, D. E., Zhang, Y., Menegaux, A., Chalupa, A., Manitt, C., Zehntner, S., Eng, C., DeDuck, K., Allard, D., Durand, F., et al. (2018) · The Journal of Neuroscience
Neurotransmitter Receptor Influence on BehaviorAxon Guidance and Neuronal Signaling
Cited by 25
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