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Author
Samuel F. Berkovic
also known as BERKOVIC, SF, Berkovic, S, Berkovic, S.
The University of Melbourne · Austin Health · Université Claude Bernard Lyon 1 · Montreal Neurological Institute and Hospital
About this author
Works
1,146
Cited by
79,869
h-index
145
i10
644
ORCID ↗
Top papers
<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology
Ingrid E. Scheffer, Samuel F. Berkovic, Giuseppe Capovilla, et al.
·
2017
·
Epilepsia
↗ 4,812
OA
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
Anne T. Berg, Samuel F. Berkovic, Martin J. Brodie, et al.
·
2010
·
Epilepsia
↗ 4,346
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
Ortrud K. Steinlein, John C. Mulley, Peter Propping, et al.
·
1995
·
Nature Genetics
↗ 1,131
doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox, et al.
·
1998
·
Cell
↗ 1,083
OA
A Potassium Channel Mutation in Neonatal Human Epilepsy
Christian Biervert, Björn C. Schroeder, Christian Kubisch, et al.
·
1998
·
Science
↗ 1,077
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
Robyn H. Wallace, Dao Wen Wang, Rita Singh, et al.
·
1998
·
Nature Genetics
↗ 1,000
Prediction of seizure likelihood with a long-term, implanted seizure advisory system in patients with drug-resistant epilepsy: a first-in-man study
Mark Cook, Terence J. O’Brien, Samuel F. Berkovic, et al.
·
2013
·
The Lancet Neurology
↗ 881
Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia
Jeremy W. Fox, Edward D. Lamperti, Yaman Z. Ekşioğlu, et al.
·
1998
·
Neuron
↗ 870
OA
Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures
Robyn H. Wallace, Carla Marini, Steven Petrou, et al.
·
2001
·
Nature Genetics
↗ 782
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle, et al.
·
2013
·
Nature Genetics
↗ 690
OA
Epileptology of the first-seizure presentation: a clinical, electroencephalographic, and magnetic resonance imaging study of 300 consecutive patients
Mark A. King, Mark R. Newton, Graeme D. Jackson, et al.
·
1998
·
The Lancet
↗ 625
The spectrum of SCN1A-related infantile epileptic encephalopathies
Louise A. Harkin, Jacinta M. McMahon, Xenia Iona, et al.
·
2007
·
Brain
↗ 529
OA