Show items per page
Elements: 51
Page 1 on 3
 TitleAuthors / EditorsDate
add to browser selection
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1) Lalioti, M. D.; Mirotsou, M.; Buresi, C.; Peitsch, M. C.; ... Antonarakis, Stylianos 1997
add to browser selection
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy Lalioti, M. D.; Scott, Hamish Steele; Buresi, C.; Rossier, Colette; ... Antonarakis, Stylianos 1997
add to browser selection
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset Lalioti, M. D.; Scott, Hamish Steele; Genton, P.; Grid, D.; ... Antonarakis, Stylianos 1998
add to browser selection
No association between DUP25 and anxiety disorders Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie 2004
add to browser selection
Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
add to browser selection
Candidate genes for temporal lobe epilepsy: a replication study Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain 2008
add to browser selection
Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter gene Vincze, Ilona; Perroud, Nader; Buresi, Catherine; Baud, Patrick; ... Malafosse, Alain 2008
add to browser selection
The electroencephalographic fingerprint of sleep is genetically determined: a twin study De Gennaro, Luigi; Marzano, Cristina; Malafosse, Alain; Finelli, Luca A.; ... Sforza, Emilia 2008
add to browser selection
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt Perroud, N.; Courtet, P.; Vincze, Ilona; Jaussent, I.; ... Malafosse, Alain 2008
add to browser selection
Somatic markers and explicit knowledge are both involved in decision-making Guillaume, Sébastien; Jollant, Fabrice; Jaussent, Isabelle; Lawrence, Natalia; ... Courtet, Philippe 2009
add to browser selection
Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression Ritchie, Karen; Jaussent, Isabelle; Stewart, Robert; Dupuy, Anne-Marie; ... Malafosse, Alain 2009
add to browser selection
Modulation of anger control in suicide attempters by TPH-1 Baud, Patrick; Perroud, N.; Courtet, P.; Jaussent, I.; ... Malafosse, Alain 2009
add to browser selection
Childhood trauma as a correlative factor of suicidal behavior - via aggression traits. Similar results in an Italian and in a French sample Sarchiapone, M.; Jaussent, I.; Roy, A.; Carli, V.; ... Courtet, P. 2009
add to browser selection
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Sharp, Andrew James; Guipponi, Michel; Fuchs, Katrin; Malafosse, Alain 2009
add to browser selection
Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence Etter, Jean-François; Hoda-Jourdan, Jean-Charles; Perroud, Nader; Munafò, Marcus; ... Bertrand, Daniel 2009
add to browser selection
Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior Guipponi, Michel; Deutsch, Samuel; Kohler, Karine; Perroud, Nader; ... Malafosse, Alain 2009
add to browser selection
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits Perroud, Nader Ali; Jaussent, I.; Guillaume, Sébastien; Bellivier, F.; ... Courtet, P. 2010
add to browser selection
Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder Perroud, Nader Ali; Salzmann, Annick; Saiz, Pilar A.; Baca-Garcia, Enrique; ... Malafosse, Alain 2010
add to browser selection
Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies Layouni, S.; Chouchane, L.; Malafosse, Alain; Dogui, M. 2010
add to browser selection
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family Layouni, Samia; Salzmann, Annick; Guipponi, Michel; Mouthon, Dominique; ... Malafosse, Alain 2010
<< previous | 1 | 2 | 3 |