| unige:21080 | A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation | Le Gal, Francois; Korff, Christian; Monso-Hinard, Christine; Mund, Michael T.; ... Schmitt-Mechelke, Thomas |
| unige:21036 | Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder | Karege, Félicien; Perroud, Nader Ali; Schurhoff, F.; Meary, A.; ... Malafosse, Alain |
| unige:21077 | BRD2 and TAP-1 genes and juvenile myoclonic epilepsy | Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed |
| unige:21208 | 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. |
| unige:21028 | Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behavior | Jollant, Fabrice; Lawrence, Natalia S.; Olie, Emilie; O'Daly, Owen; ... Phillips, Mary L. |
| unige:21078 | 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.; |
| unige:21124 | European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset | Mathieu, Flavie; Dizier, Marie-Helene; Etain, Bruno; Jamain, Stephane; ... Bellivier, Frank |
| unige:20637 | Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures | Jamali, Sarah; Salzmann, Annick; Perroud, Nader Ali; Ponsole-Lenfant, Magali; ... Szepetowski, Pierre |
| unige:20736 | Gender and genotype modulation of the association between lipid levels and depressive symptomatology in community-dwelling elderly (the ESPRIT study) | Ancelin, Marie-Laure; Carriere, Isabelle; Boulenger, Jean-Philippe; Malafosse, Alain; ... Dupuy, Anne-Marie |
| unige:20859 | Genes, suicide and decisions | Courtet, P.; Guillaume, Sébastien; Malafosse, Alain; Jollant, F.; |
| unige:21079 | 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 |
| unige:20651 | Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies | Mefford, Heather C.; Muhle, Hiltrud; Ostertag, Philipp; von Spiczak, S.; ... Eichler, E. E. |
| unige:21209 | 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 |
| unige:21210 | Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims | Perroud, Nader Ali; Neidhart, Elizabeth; Petit, Brice; Vessaz, Monique; ... Guipponi, Michel |
| unige:20982 | Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depression | Guillaume, Sébastien; Jaussent, Isabelle; Jollant, Fabrice; Rihmer, Zoltan; ... Courtet, Philippe |
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