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M. Jennesson · SciRah

Researcher profile · Semantic Scholar

M. Jennesson

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M. Jennesson — researcher profile on SciRah

h-index: 11
Works: 18
Citations: 600

Most-cited papers

The landscape of epilepsy-related GATOR1 variants
S. Baldassari, F. Picard, N. Verbeek, M. van Kempen +84 more
2018Genetics in Medicine214 citations Open access
Semantic Scholar
Impact of pediatric epilepsy on sleep patterns and behaviors in children and parents
Anna M. Larson, R. Ryther, M. Jennesson, Alexandra L. Geffrey +5 more
2012Epilepsia128 citations Open access
Semantic Scholar
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature
C. Bar, G. Barcia, M. Jennesson, G. Le Guyader +39 more
2019Human Mutation58 citations Open access
Semantic Scholar
Epileptic spasms in tuberous sclerosis complex.
David T. Hsieh, M. Jennesson, E. Thiele
2013Epilepsy Research28 citations
Semantic Scholar
Cardiac Investigations in Sudden Unexpected Death in DEPDC5 ‐Related Epilepsy
A. Bacq, Delphine Roussel, Thomas Bonduelle, S. Zagaglia +84 more
2021Annals of Neurology27 citations Open access
Semantic Scholar
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome
C. Bar, M. Kuchenbuch, G. Barcia, Amy L. Schneider +57 more
2020Epilepsia25 citations Open access
Semantic Scholar
Clobazam therapy of refractory epilepsy in tuberous sclerosis complex.
M. Jennesson, A. V. van Eeghen, P. Caruso, Jan L. Paolini +1 more
2013Epilepsy Research25 citations
Semantic Scholar
Posterior glucose hypometabolism in Lafora disease: Early and late FDG‐PET assessment
M. Jennesson, M. Milh, N. Villeneuve, E. Guedj +6 more
2010Epilepsia22 citations Open access
Semantic Scholar
Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect
Fang Yang, A. Begemann, Nadine Reichhart, A. Haeckel +28 more
2024American Journal of Human Genetics13 citations Open access
Semantic Scholar
Electroencephalographic patterns during sleep in children with chromosome 15q11.2-13.1 duplications (Dup15q).
Dimitrios Arkilo, O. Devinsky, B. Mudigoudar, S. Boronat +7 more
2016Epilepsy & Behavior13 citations Open access
Semantic Scholar
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype–phenotype spectrum and functional impact on GPI‐anchored proteins
S. Salian, M. Scala, T. Nguyen, M. Severino +22 more
2021Clinical Genetics12 citations Open access
Semantic Scholar
Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy.
C. Bar, D. Breuillard, M. Kuchenbuch, M. Jennesson +23 more
2021Epilepsy & Behavior11 citations Open access
Semantic Scholar
Brain and spinal manifestations of Miller-Dieker syndrome.
David T. Hsieh, M. Jennesson, E. Thiele, P. Caruso +2 more
2013Neurology Clinical Practice10 citations Open access
Semantic Scholar
Correction: The landscape of epilepsy-related GATOR1 variants
S. Baldassari, F. Picard, N. Verbeek, M. van Kempen +84 more
2018Genetics in Medicine7 citations Open access
Semantic Scholar
Further characterisation of ARX-related disorders in females due to inherited or de novo variants
Mathilde Gras, S. Heide, B. Keren, S. Valence +18 more
2023Journal of Medical Genetics6 citations Open access
Semantic Scholar
Correction to: The landscape of epilepsy-related GATOR1 variants
S. Baldassari, F. Picard, N. Verbeek, M. van Kempen +84 more
2018Genetics in Medicine3 citations Open access
Semantic Scholar
Title Electroencephalographic patterns during sleep in children with chromosome 15 q 11
O. Devinsky, B. Mudigoudar, S. Boronat, M. Jennesson +6 more
20160 citations
Semantic Scholar
P26.17 Transitory expression of infantile spasms syndrome
J. Misson, C. Kaputu, M. Jennesson, J. Dubru +2 more
20110 citations
Semantic Scholar

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