Frédérick Andermann

Montreal Neurological Institute and Hospital — Canada

Medicine · Health Sciences

101h-index32.3kcitations524works0.02yr avg
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Research Topics

Epilepsy research and treatment(245), Neuroscience and Neuropharmacology Research(90), Pharmacological Effects and Toxicity Studies(65), Fetal and Pediatric Neurological Disorders(60), Neurological disorders and treatments(57)

Publications519 total

Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing
European Journal of Human Genetics·2020· 16 citedOpen Access
Duplication 2p16 is associated with perisylvian polymicrogyria
American Journal of Medical Genetics Part A·2019· 4 cited
Kufs disease due to mutation of<i>CLN6</i>: clinical, pathological and molecular genetic features
Brain·2018· 35 citedOpen Access
Reply to Chang
2018
Factitious Disorders
Cambridge University Press eBooks·2018
Myoclonus epilepsy and ataxia due to <scp><i>KCNC</i></scp><i>1</i> mutation: Analysis of 20 cases and <scp>K</scp><sup>+</sup> channel properties
Annals of Neurology·2017· 86 citedOpen Access
Research conference summary from the 2014 International Task Force on <i>ATP1A3</i> -Related Disorders
Neurology Genetics·2017· 65 citedOpen Access
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
The Lancet Neurology·2017· 233 citedOpen Access
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children
2017
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
The American Journal of Human Genetics·2017· 47 citedOpen Access
Research conference summary from the 2014 International Task Force on
Neurology Genetics·2017Open Access
Table 1. [Summary of Molecular Genetic Testing Used in Action Myoclonus – Renal Failure Syndrome].
2015
Table 2. [Clinical Manifestations of AMRF].
2015
Table 3. [SCARB2 Pathogenic Variants Discussed in This GeneReview].
2015
Brivaracetam in Unverricht‐Lundborg disease (<scp>EPM</scp>1): Results from two randomized, double‐blind, placebo‐controlled studies
Epilepsia·2015· 52 citedOpen Access
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
PLoS ONE·2015· 12 citedOpen Access
The histopathology of polymicrogyria: a series of 71 brain autopsy studies
Developmental Medicine & Child Neurology·2015· 82 citedOpen Access
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
PLoS ONE·2015· 74 citedOpen Access
Phenotypic, molecular, functional, and structural aspects of novel DCX and LIS1 mutations causing the subcortical band heterotopia/lissencephaly (SBH/LIS) spectrum (P2.227)
Neurology·2015
Familial focal epilepsy with focal cortical dysplasia due to <scp><i>DEPDC</i></scp><i>5</i> mutations
Annals of Neurology·2015· 279 citedOpen Access
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Frequent Co-authors

Samuel F. Berkovic(18), Eva Andermann(17), André Olivier(14), François Dubeau(12), P. Gloor(10), Fernando Cendes(10), Ingrid E. Scheffer(9), Alan C. Evans(6), Denis Melanson(6), Íscia Lopes‐Cendes(6), E. Andermann(6), Stirling Carpenter(6), Douglas L. Arnold(6), L. F. Quesney(5), Marilyn Jones‐Gotman(5), Ruben Kuzniecky(5), William Feindel(5), André Palmini(4), Antonio Gambardella(4), Craig Watson(4)