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The human VGLUT3-pT8I mutation elicits uneven striatal DA signaling, food or drug maladaptive consumption in male mice
Author / Creator:Favier, Mathieu ; Martin Garcia, Elena ; Icick, Romain ; de Almeida, Camille ; Jehl, Joachim ; Desplanque, Mazarine ; Zimmermann, Johannes ; Henrion, Annabelle ; Mansouri-Guilani, Nina ; Mounier, Coline ; Ribeiro, Svethna ; Henderson, Fiona ; Geoffroy, Andrea ; Mella, Sebastien ; Poirel, Odile ; Bernard, Véronique ; Fabre, Véronique ; Li, Yulong ; Rosenmund, Christian ; Jamain, Stéphane ; Vorspan, Florence ; Mourot, Alexandre ; Duriez, Philibert ; Pinhas, Leora ; Maldonado, Rafael ; Pietrancosta, Nicolas ; Daumas, Stéphanie ; El Mestikawy, Salah
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2024-07, Vol.15 (1), p.5691-19, Article 5691
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Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes
Author / Creator:Guipponi, Michel ; Santoni, Federico A. ; Setola, Vincent ; Gehrig, Corinne ; Rotharmel, Maud ; Cuenca, Macarena ; Guillin, Olivier ; Dikeos, Dimitris ; Georgantopoulos, Georgios ; Papadimitriou, George ; Curtis, Logos ; Méary, Alexandre ; Schürhoff, Franck ; Jamain, Stéphane ; Avramopoulos, Dimitri ; Leboyer, Marion ; Rujescu, Dan ; Pulver, Ann ; Campion, Dominique ; Siderovski, David P. ; Antonarakis, Stylianos E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-11, Vol.9 (11), p.e112745-e112745
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Stratification and prediction of remission in first-episode psychosis patients: the OPTiMiSE cohort study
Author / Creator:Martinuzzi, Emanuela ; Barbosa, Susana ; Daoudlarian, Douglas ; Bel Haj Ali, Wafa ; Gilet, Cyprien ; Fillatre, Lionel ; Khalfallah, Olfa ; Troudet, Réjane ; Jamain, Stéphane ; Fond, Guillaume ; Sommer, Iris ; Leucht, Stefan ; Dazzan, Paola ; McGuire, Philip ; Arango, Celso ; Diaz-Caneja, Covadonga M. ; Fleischhacker, Wolfgang ; Rujescu, Dan ; Glenthøj, Birte ; Winter, Inge ; Kahn, René Sylvain ; Yolken, Robert ; Lewis, Shon ; Drake, Richard ; Davidovic, Laetitia ; Leboyer, Marion ; Glaichenhaus, Nicolas
Publisher:London: Nature Publishing Group UK
Journal title:Translational psychiatry, 2019-01, Vol.9 (1), p.20-20, Article 20
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Genetic association study of circadian genes with seasonal pattern in bipolar disorders
Author / Creator:Geoffroy, Pierre Alexis ; Lajnef, Mohamed ; Bellivier, Frank ; Jamain, Stéphane ; Gard, Sébastien ; Kahn, Jean-Pierre ; Henry, Chantal ; Leboyer, Marion ; Etain, Bruno
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2015-05, Vol.5 (1), p.10232-10232, Article 10232
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Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case–Control Study
Author / Creator:Tripoli, Giada ; Quattrone, Diego ; Ferraro, Laura ; Gayer-Anderson, Charlotte ; La Cascia, Caterina ; La Barbera, Daniele ; Sartorio, Crocettarachele ; Seminerio, Fabio ; Rodriguez, Victoria ; Tarricone, Ilaria ; Berardi, Domenico ; Jamain, Stéphane ; Arango, Celso ; Tortelli, Andrea ; Llorca, Pierre-Michel ; de Haan, Lieuwe ; Velthorst, Eva ; Bobes, Julio ; Bernardo, Miquel ; Sanjuán, Julio ; Luis Santos, Jose ; Arrojo, Manuel ; Marta Del-Ben, Cristina ; Rossi Menezes, Paulo ; van der Ven, Els ; Jones, Peter B ; Jongsma, Hannah E ; Kirkbride, James B ; Tosato, Sarah ; Lasalvia, Antonio ; Richards, Alex ; O’Donovan, Michael ; Rutten, Bart P F ; van Os, Jim ; Morgan, Craig ; Sham, Pak C ; Di Forti, Marta ; Murray, Robin M ; Murray, Graham K
Publisher:US: Oxford University Press
Journal title:Schizophrenia bulletin, 2022-09, Vol.48 (5), p.1104-1114
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Early onset bipolar disorder: validation from admixture analyses and biomarkers
Author / Creator:Geoffroy, Pierre Alexis ; Etain, Bruno ; Jamain, Stéphane ; Bellivier, Frank ; Leboyer, Marion
Publisher:United States
Journal title:Canadian journal of psychiatry, 2013-04, Vol.58 (4), p.240-248
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
Author / Creator:Jamain, Stéphane ; Quach, Hélène ; Betancur, Catalina ; Råstam, Maria ; Colineaux, Catherine ; Gillberg, I. Carina ; Soderstrom, Henrik ; Giros, Bruno ; Leboyer, Marion ; Gillberg, Christopher ; Bourgeron, Thomas
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2003-05, Vol.34 (1), p.27-29
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Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability
Author / Creator:Jamain, Stéphane ; Cichon, Sven ; Etain, Bruno ; Mühleisen, Thomas W. ; Georgi, Alexander ; Zidane, Nora ; Chevallier, Lucie ; Deshommes, Jasmine ; Nicolas, Aude ; Henrion, Annabelle ; Degenhardt, Franziska ; Mattheisen, Manuel ; Priebe, Lutz ; Mathieu, Flavie ; Kahn, Jean-Pierre ; Henry, Chantal ; Boland, Anne ; Zelenika, Diana ; Gut, Ivo ; Heath, Simon ; Lathrop, Mark ; Maier, Wolfgang ; Albus, Margot ; Rietschel, Marcella ; Schulze, Thomas G. ; McMahon, Francis J. ; Kelsoe, John R. ; Hamshere, Marian ; Craddock, Nicholas ; Nöthen, Markus M. ; Bellivier, Frank ; Leboyer, Marion
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-08, Vol.9 (8), p.e104326-e104326
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Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
Author / Creator:Delorme, Richard ; Betancur, Catalina ; Scheid, Isabelle ; Anckarsäter, Henrik ; Chaste, Pauline ; Jamain, Stéphane ; Schuroff, Franck ; Nygren, Gudrun ; Herbrecht, Evelyn ; Dumaine, Anne ; Mouren, Marie Christine ; Råstam, Maria ; Leboyer, Marion ; Gillberg, Christopher ; Bourgeron, Thomas
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2010-07, Vol.11 (1), p.108-108, Article 108
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Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1
Author / Creator:Chang, Hong ; Li, Lingyi ; Peng, Tao ; Grigoroiu-Serbanescu, Maria ; Bergen, Sarah E. ; Landén, Mikael ; Hultman, Christina M. ; Forstner, Andreas J. ; Strohmaier, Jana ; Hecker, Julian ; Schulze, Thomas G. ; Müller-Myhsok, Bertram ; Reif, Andreas ; Mitchell, Philip B. ; Martin, Nicholas G. ; Cichon, Sven ; Nöthen, Markus M. ; Jamain, Stéphane ; Leboyer, Marion ; Bellivier, Frank ; Etain, Bruno ; Kahn, Jean-Pierre ; Henry, Chantal ; Rietschel, Marcella ; Xiao, Xiao ; Li, Ming
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2017-09, Vol.54 (7), p.5166-5176
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Correction: Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes
Author / Creator:Guipponi, Michel ; Santoni, Federico A. ; Setola, Vincent ; Gehrig, Corinne ; Rotharmel, Maud ; Cuenca, Macarena ; Guillin, Olivier ; Dikeos, Dimitris ; Georgantopoulos, Georgios ; Papadimitriou, George ; Curtis, Logos ; Méary, Alexandre ; Schürhoff, Franck ; Jamain, Stéphane ; Avramopoulos, Dimitri ; Leboyer, Marion ; Rujescu, Dan ; Pulver, Ann ; Campion, Dominique ; Siderovski, David P. ; Antonarakis, Stylianos E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-10, Vol.10 (10), p.e0141630-e0141630
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Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability
Author / Creator:Pagan, Cecile ; Botros, Hany Goubran ; Poirier, Karine ; Dumaine, Anne ; Jamain, Stéphane ; Moreno, Sarah ; de Brouwer, Arjan ; Van Esch, Hilde ; Delorme, Richard ; Launay, Jean-Marie ; Tzschach, Andreas ; Kalscheuer, Vera ; Lacombe, Didier ; Briault, Sylvain ; Laumonnier, Frédéric ; Raynaud, Martine ; van Bon, Bregje W ; Willemsen, Marjolein H ; Leboyer, Marion ; Chelly, Jamel ; Bourgeron, Thomas
Publisher:England: BioMed Central Ltd
Journal title:BMC genetics, 2011-01, Vol.12 (1), p.17-17, Article 17
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Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders
Author / Creator:Pagan, Cécile ; Goubran-Botros, Hany ; Delorme, Richard ; Benabou, Marion ; Lemière, Nathalie ; Murray, Kerren ; Amsellem, Frédérique ; Callebert, Jacques ; Chaste, Pauline ; Jamain, Stéphane ; Fauchereau, Fabien ; Huguet, Guillaume ; Maronde, Erik ; Leboyer, Marion ; Launay, Jean-Marie ; Bourgeron, Thomas
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-05, Vol.7 (1), p.2096-11, Article 2096
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Desloratadine, an FDA-approved cationic amphiphilic drug, inhibits SARS-CoV-2 infection in cell culture and primary human nasal epithelial cells by blocking viral entry
Author / Creator:Morin-Dewaele, Margot ; Bartier, Sophie ; Berry, François ; Brillet, Rozenn ; López-Molina, Dennis Salomón ; Nguyễn, Công Trung ; Maille, Pascale ; Sereno, Kevin ; Nevers, Quentin ; Softic, Laurent ; Vaugeois, Jean-Marie ; Louis, Bruno ; Bequignon, Emilie ; Bruscella, Patrice ; Coste, André ; Pawlotsky, Jean-Michel ; Jamain, Stéphane ; Ahmed-Belkacem, Abdelhakim
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2022-12, Vol.12 (1), p.21053-21053, Article 21053
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A Conserved BDNF, Glutamate- and GABA-Enriched Gene Module Related to Human Depression Identified by Coexpression Meta-Analysis and DNA Variant Genome-Wide Association Studies
Author / Creator:Chang, Lun-Ching ; Jamain, Stephane ; Lin, Chien-Wei ; Rujescu, Dan ; Tseng, George C. ; Sibille, Etienne
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-03, Vol.9 (3), p.e90980-e90980
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Gene expression and response prediction to amisulpride in the OPTiMiSE first episode psychoses
Author / Creator:Troudet, Réjane ; Ali, Wafa Bel Haj ; Bacq-Daian, Delphine ; Rossum, Inge Winter van ; Boland-Auge, Anne ; Battail, Christophe ; Barau, Caroline ; van Rossum, Inge Winter ; Rujescu, Dan ; McGuire, Philip ; Kahn, René S. ; Leboyer, Marion ; Jamain, Stéphane ; Deleuze, Jean-François ; Jamain, Stéphane
Publisher:England: Nature Publishing Group
Journal title:Neuropsychopharmacology, 2020-09, Vol.45 (10), p.1637-1644
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Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
Author / Creator:Jamain, Stephane ; Radyushkin, Konstantin ; Hammerschmidt, Kurt ; Granon, Sylvie ; Boretius, Susann ; Varoqueaux, Frederique ; Ramanantsoa, Nelina ; Gallego, Jorge ; Ronnenberg, Anja ; Winter, Dorina ; Frahm, Jens ; Fischer, Julia ; Bourgeron, Thomas ; Ehrenreich, Hannelore ; Brose, Nils
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (5), p.1710-1715
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Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
Author / Creator:de Oliveira, Ana Sofia Lima Estevao ; Bloise, Giovanna ; Moltrasio, Chiara ; Coelho, Antonio ; Agrelli, Almerinda ; Moura, Ronald ; Tricarico, Paola Maura ; Jamain, Stéphane ; Marzano, Angelo Valerio ; Crovella, Sergio ; Cavalcanti Brandão, Lucas André
Publisher:Switzerland: MDPI AG
Journal title:Biomolecules (Basel, Switzerland), 2022-09, Vol.12 (10), p.1371
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CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress
Author / Creator:Sitbon, Jérémy ; Nestvogel, Dennis ; Kappeler, Caroline ; Nicolas, Aude ; Maciuba, Stephanie ; Henrion, Annabelle ; Troudet, Réjane ; Courtois, Elisa ; Grannec, Gaël ; Latapie, Violaine ; Barau, Caroline ; Le Corvoisier, Philippe ; Pietrancosta, Nicolas ; Henry, Chantal ; Leboyer, Marion ; Etain, Bruno ; Nosten-Bertrand, Marika ; Martin, Thomas F. J. ; Rhee, JeongSeop ; Jamain, Stéphane
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2022-02, Vol.27 (2), p.1145-1157
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Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome
Author / Creator:Courtois, Elisa ; Schmid, Mark ; Wajsbrot, Orly ; Barau, Caroline ; Le Corvoisier, Philippe ; Aouizerate, Bruno ; Bellivier, Frank ; Belzeaux, Raoul ; Dubertret, Caroline ; Kahn, Jean-Pierre ; Leboyer, Marion ; Olie, Emilie ; Passerieux, Christine ; Polosan, Mircea ; Etain, Bruno ; Jamain, Stéphane
Publisher:London: Nature Publishing Group UK
Journal title:Translational psychiatry, 2020-04, Vol.10 (1), p.124, Article 124
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Showing 1 to 20 of 57 results

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The human VGLUT3-pT8I mutation elicits uneven striatal DA signaling, food or drug maladaptive consumption in male mice

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Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes

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Stratification and prediction of remission in first-episode psychosis patients: the OPTiMiSE cohort study

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Genetic association study of circadian genes with seasonal pattern in bipolar disorders

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Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case–Control Study

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Early onset bipolar disorder: validation from admixture analyses and biomarkers

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability

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Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls

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Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1

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Correction: Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes

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Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability

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Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

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Desloratadine, an FDA-approved cationic amphiphilic drug, inhibits SARS-CoV-2 infection in cell culture and primary human nasal epithelial cells by blocking viral entry

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A Conserved BDNF, Glutamate- and GABA-Enriched Gene Module Related to Human Depression Identified by Coexpression Meta-Analysis and DNA Variant Genome-Wide Association Studies

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Gene expression and response prediction to amisulpride in the OPTiMiSE first episode psychoses

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Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

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Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling

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CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress

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Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome

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