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Fabienne PICARD
Fabienne PICARD
Département des Neurosciences, University Hospital of Geneva
Verified email at hcuge.ch
Title
Cited by
Cited by
Year
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33
S Baulac, I Gourfinkel-An, F Picard, M Rosenberg-Bourgin, ...
The American Journal of Human Genetics 65 (4), 1078-1085, 1999
3061999
Definition and diagnostic criteria of sleep-related hypermotor epilepsy
P Tinuper, F Bisulli, JH Cross, D Hesdorffer, P Kahane, L Nobili, F Provini, ...
Neurology 86 (19), 1834-1842, 2016
2982016
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations
S Baulac, S Ishida, E Marsan, C Miquel, A Biraben, DK Nguyen, D Nordli, ...
Annals of neurology 77 (4), 675-683, 2015
2922015
Nocturnal hypermotor seizures, suggesting frontal lobe epilepsy, can originate in the insula
P Ryvlin, L Minotti, G Demarquay, E Hirsch, A Arzimanoglou, D Hoffman, ...
Epilepsia 47 (4), 755-765, 2006
2862006
Mutations of DEPDC5 cause autosomal dominant focal epilepsies
S Ishida, F Picard, G Rudolf, E Noé, G Achaz, P Thomas, P Genton, ...
Nature genetics 45 (5), 552-555, 2013
2652013
Electrical stimulation of a small brain area reversibly disrupts consciousness
MZ Koubeissi, F Bartolomei, A Beltagy, F Picard
Epilepsy & Behavior 37, 32-35, 2014
2482014
Bodyweight gain and anticonvulsants: a comparative review
P Jallon, F Picard
Drug safety 24, 969-978, 2001
2382001
Genome search for susceptibility loci of common idiopathic generalised epilepsies
T Sander, H Schulz, K Saar, E Gennaro, MC Riggio, A Bianchi, F Zara, ...
Human molecular genetics 9 (10), 1465-1472, 2000
2172000
How mutations in the nAChRs can cause ADNFLE epilepsy
D Bertrand, F Picard, S Le Hellard, S Weiland, I Favre, H Phillips, ...
Epilepsia 43, 112-122, 2002
2122002
Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study
F Picard, D Bruel, D Servent, W Saba, C Fruchart-Gaillard, ...
Brain 129 (8), 2047-2060, 2006
1942006
The landscape of epilepsy-related GATOR1 variants
S Baldassari, F Picard, NE Verbeek, M van Kempen, EH Brilstra, G Lesca, ...
Genetics in Medicine 21 (2), 398-408, 2019
1882019
Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine
F Picard, S Bertrand, OK Steinlein, D Bertrand
Epilepsia 40 (9), 1198-1209, 1999
1791999
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia
F Clot, D Grabli, C Cazeneuve, E Roze, P Castelnau, B Chabrol, ...
Brain 132 (7), 1753-1763, 2009
1742009
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
S Weckhuysen, E Marsan, V Lambrecq, C Marchal, M Morin‐Brureau, ...
Epilepsia 57 (6), 994-1003, 2016
1732016
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy
F Picard, P Makrythanasis, V Navarro, S Ishida, J de Bellescize, D Ville, ...
Neurology 82 (23), 2101-2106, 2014
1632014
Chorea-acanthocytosis: genetic linkage to chromosome 9q21
JP Rubio, A Danek, C Stone, R Chalmers, N Wood, C Verellen, X Ferrer, ...
The American Journal of Human Genetics 61 (4), 899-908, 1997
1291997
PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population
A Méneret, D Grabli, C Depienne, C Gaudebout, F Picard, A Dürr, ...
Neurology 79 (2), 170-174, 2012
1232012
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25‐q31
S Baulac, F Picard, A Herman, J Feingold, E Genin, E Hirsch, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
1212001
Dominant partial epilepsies: a clinical, electrophysiological and genetic study of 19 European families
F Picard, S Baulac, P Kahane, E Hirsch, R Sebastianelli, P Thomas, ...
Brain 123 (6), 1247-1262, 2000
1202000
Ecstatic epileptic seizures: a potential window on the neural basis for human self-awareness
F Picard, AD Craig
Epilepsy & Behavior 16 (3), 539-546, 2009
1122009
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