Malafosse, Alain

 
 
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2011

Scientific Articles

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A novel exon 3 mutation in a Tunisian patient with Lafora's diseaseKhiari, H Mrabet; Lesca, G; Malafosse, Alain; Mrabet, A;
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Age at onset in bipolar I affective disorder in the USA and EuropeBellivier, Frank; Etain, Bruno; Malafosse, Alain; Henry, Chantal; ... Leboyer, Marion
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Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient samplePerroud, Nader Ali; Bondolfi, Guido; Uher, Rudolf; Gex-Fabry, Marianne; ... Kosel, Markus Mathaus
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Distinguishing the relevant features of frequent suicide attemptersLopez-Castroman, Jorge; Perez-Rodriguez, Maria de las Mercedes; Jaussent, Isabelle; Alegria, Analucia A; ... Courtet, Philippe
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Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphismCarrard, Anthony; Trachsler-Salzmann, Annick; Perroud, Nader Ali; Gafner, Jeremie Yves; ... Karege, Félicien
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Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of traumaPerroud, Nader Ali; Giacobino, Ariane; Prada, Paco Boris; Olié, E; ... Malafosse, Alain
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Le projet «SYNAPSY» : un point de rencontre entre clinique et neurosciencesConus, Philippe; Preisig, Martin; Aubry, Jean-Michel; Marquet, Pierre; ... Baumann, Philipp

Professional Articles

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Adverse childhood environment and late-life cognitive functioningRitchie, Karen; Jaussent, Isabelle; Stewart, Robert; Dupuy, Anne-Marie; ... Ancelin, Marie-Laure
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Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victimsKarege, Félicien; Perroud, Nader Ali; Burkhardt, Sandra Esther; Fernandez, Rafael; ... Malafosse, Alain
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Impulsivity, aggression and suicidal behavior in unipolar and bipolar disordersPerroud, Nader Ali; Baud, Patrick; Mouthon, Dominique; Courtet, Philippe; Malafosse, Alain
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Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorderCarrard, Anthony; Trachsler-Salzmann, Annick; Malafosse, Alain; Karege, Félicien;
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Replication of association between a SCN1A splice variant and febrile seizuresLe Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain;
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Suicidal behavior is associated with reduced corpus callosum areaCyprien, Fabienne; Courtet, Philippe; Malafosse, Alain; Maller, Jerome; ... Artero, Sylvaine
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War exposure, 5-HTTLPR genotype and lifetime risk of depressionArtero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen

Master's thesis supervisions

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Exploration de la matière grise et blanche chez des patients présentant un premier épisode psychotiqueRuef, Anne Dominique;

2010

Scientific Articles

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A case of SUDEP in a patient with Dravet syndrome with SCN1A mutationLe Gal, Francois; Korff, Christian; Monso-Hinard, Christine; Mund, Michael T.; ... Schmitt-Mechelke, Thomas
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Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorderKarege, Félicien; Perroud, Nader Ali; Schurhoff, F.; Meary, A.; ... Malafosse, Alain
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BRD2 and TAP-1 genes and juvenile myoclonic epilepsyLayouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed
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COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traitsPerroud, Nader Ali; Jaussent, I.; Guillaume, Sébastien; Bellivier, F.; ... Courtet, P.
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Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behaviorJollant, Fabrice; Lawrence, Natalia S.; Olie, Emilie; O'Daly, Owen; ... Phillips, Mary L.
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Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsiesLayouni, S.; Chouchane, L.; Malafosse, Alain; Dogui, M.;
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European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onsetMathieu, Flavie; Dizier, Marie-Helene; Etain, Bruno; Jamain, Stephane; ... Bellivier, Frank
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Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresJamali, Sarah; Salzmann, Annick; Perroud, Nader Ali; Ponsole-Lenfant, Magali; ... Szepetowski, Pierre
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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
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Genes, suicide and decisionsCourtet, P.; Guillaume, Sébastien; Malafosse, Alain; Jollant, F.;
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Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian familyLayouni, Samia; Salzmann, Annick; Guipponi, Michel; Mouthon, Dominique; ... Malafosse, Alain
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Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesMefford, Heather C.; Muhle, Hiltrud; Ostertag, Philipp; von Spiczak, S.; ... Eichler, E. E.
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Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorderPerroud, Nader Ali; Salzmann, Annick; Saiz, Pilar A.; Baca-Garcia, Enrique; ... Malafosse, Alain
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Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victimsPerroud, Nader Ali; Neidhart, Elizabeth; Petit, Brice; Vessaz, Monique; ... Guipponi, Michel
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Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depressionGuillaume, Sébastien; Jaussent, Isabelle; Jollant, Fabrice; Rihmer, Zoltan; ... Courtet, Philippe

Master's thesis supervisions

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Le trouble de la personnalité borderline et ses facteurs environnementaux, génétiques et épigénétiques: possible effet des abus sexuels sur la méthylation du brain-derived neurotrophic factor dans une population borderlineHoeppli, Marie-Eve;
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