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Select record 41
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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy
Author / Creator:Layouni, Samia ; Buresi, Catherine ; Thomas, Pierre ; Malafosse, Alain ; Dogui, Mohamed
Publisher:Milan: Springer Milan
Journal title:Neurological sciences, 2010-02, Vol.31 (1), p.53-56
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Genetic association of the Phosphoinositide‐3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism
Author / Creator:Carrard, Anthony ; Salzmann, Annick ; Perroud, Nader ; Gafner, Jérémie ; Malafosse, Alain ; Karege, Félicien
Publisher:Hoboken, NJ, USA: Blackwell Publishing Inc
Journal title:Brain and behavior, 2011-11, Vol.1 (2), p.119-124
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War exposure, 5-HTTLPR genotype and lifetime risk of depression
Author / Creator:ARTERO, Sylvaine ; TOUCHON, Jacques ; DUPUY, Anne-Marie ; MALAFOSSE, Alain ; RITCHIE, Karen
Publisher:Leeds: Maney
Journal title:British journal of psychiatry, 2011, Vol.199 (JUL), p.43-48
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Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis: e1001326
Author / Creator:Tansey, Katherine E ; Guipponi, Michel ; Perroud, Nader ; Bondolfi, Guido ; Domenici, Enrico ; Evans, David ; Hall, Stephanie K ; Hauser, Joanna ; Henigsberg, Neven ; Hu, Xiaolan ; Jerman, Borut ; Maier, Wolfgang ; Mors, Ole ; Peters, Tim J ; Placentino, Anna ; Rietschel, Marcella ; Souery, Daniel ; Aitchison, Katherine J ; Craig, Ian ; Farmer, Anne ; Wendland, Jens R ; Malafosse, Alain ; Holmans, Peter ; Lewis, Glyn ; Lewis, Cathryn M ; Stensbøl, Tine Bryan ; Kapur, Shitij ; McGuffin, Peter ; Uher, Rudolf
Publisher:San Francisco: Public Library of Science
Journal title:PLoS medicine, 2012-10, Vol.9 (10)
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Select record 45
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Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14
Author / Creator:Etain, B ; Mathieu, F ; Rietschel, M ; Maier, W ; Albus, M ; McKeon, P ; Roche, S ; Kealey, C ; Blackwood, D ; Muir, W ; Bellivier, F ; Henry, C ; Dina, C ; Gallina, S ; Gurling, H ; Malafosse, A ; Preisig, M ; Ferrero, F ; Cichon, S ; Schumacher, J ; Ohlraun, S ; Borrmann-Hassenbach, M ; Propping, P ; Abou Jamra, R ; Schulze, T G ; Marusic, A ; Dernovsek, Z M ; Giros, B ; Bourgeron, T ; Lemainque, A ; Bacq, D ; Betard, C ; Charon, C ; Nöthen, M M ; Lathrop, M ; Leboyer, M
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2006-07, Vol.11 (7), p.685-694
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Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics
Author / Creator:Manchia, Mirko ; Adli, Mazda ; Akula, Nirmala ; Ardau, Raffaella ; Aubry, Jean-Michel ; Backlund, Lena ; Banzato, Claudio EM ; Baune, Bernhard T ; Bellivier, Frank ; Bengesser, Susanne ; Biernacka, Joanna M ; Brichant-Petitjean, Clara ; Bui, Elise ; Calkin, Cynthia V ; Cheng, Andrew Tai Ann ; Chillotti, Caterina ; Cichon, Sven ; Clark, Scott ; Czerski, Piotr M ; Dantas, Clarissa ; Zompo, Maria Del ; DePaulo, J. Raymond ; Detera-Wadleigh, Sevilla D ; Etain, Bruno ; Falkai, Peter ; Frisén, Louise ; Frye, Mark A ; Fullerton, Jan ; Gard, Sébastien ; Garnham, Julie ; Goes, Fernando S ; Grof, Paul ; Gruber, Oliver ; Hashimoto, Ryota ; Hauser, Joanna ; Heilbronner, Urs ; Hoban, Rebecca ; Hou, Liping ; Jamain, Stéphane ; Kahn, Jean-Pierre ; Kassem, Layla ; Kato, Tadafumi ; Kelsoe, John R ; Kittel-Schneider, Sarah ; Kliwicki, Sebastian ; Kuo, Po-Hsiu ; Kusumi, Ichiro ; Laje, Gonzalo ; Lavebratt, Catharina ; Leboyer, Marion ; Leckband, Susan G ; López Jaramillo, Carlos A ; Maj, Mario ; Malafosse, Alain ; Martinsson, Lina ; Masui, Takuya ; Mitchell, Philip B ; Mondimore, Frank ; Monteleone, Palmiero ; Nallet, Audrey ; Neuner, Maria ; Novák, Tomás ; O'Donovan, Claire ; Ösby, Urban ; Ozaki, Norio ; Perlis, Roy H ; Pfennig, Andrea ; Potash, James B ; Reich-Erkelenz, Daniela ; Reif, Andreas ; Reininghaus, Eva ; Richardson, Sara ; Rouleau, Guy A ; Rybakowski, Janusz K ; Schalling, Martin ; Schofield, Peter R ; Schubert, Oliver K ; Schweizer, Barbara ; Seemüller, Florian ; Grigoroiu-Serbanescu, Maria ; Severino, Giovanni ; Seymour, Lisa R ; Slaney, Claire ; Smoller, Jordan W ; Squassina, Alessio ; Stamm, Thomas ; Steele, Jo ; Stopkova, Pavla ; Tighe, Sarah K ; Tortorella, Alfonso ; Turecki, Gustavo ; Wray, Naomi R ; Wright, Adam ; Zandi, Peter P ; Zilles, David ; Bauer, Michael ; Rietschel, Marcella ; McMahon, Francis J ; Schulze, Thomas G ; Alda, Martin
Publisher:Public Library of Science
Journal title:PloS one, 2013-06, Vol.8 (6), p.e65636
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Association of genes coding for the a-4, a-5, b-2 and b-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence
Author / Creator:Etter, Jean-Francois ; Hoda, Jean-Charles ; Perroud, Nader ; Munafo, Marcus ; Buresi, Catherine ; Duret, Claudette ; Neidhart, Elisabeth ; Malafosse, Alain ; Bertrand, Daniel
Journal title:Addictive Behaviors, 2009-09, Vol.34 (9), p.772-775
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Collecting Saliva by Mail for Genetic and Cotinine Analyses in Participants Recruited through the Internet
Author / Creator:Etter, Jean-François ; Neidhart, Elisabeth ; Bertrand, Sonia ; Malafosse, Alain ; Bertrand, Daniel
Publisher:Dordrecht: Springer
Journal title:European journal of epidemiology, 2005-10, Vol.20 (10), p.833-838
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Select record 49
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Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies: e1000962
Author / Creator:Mefford, Heather C ; Muhle, Hiltrud ; Ostertag, Philipp ; Spiczak, Sarah von ; Buysse, Karen ; Baker, Carl ; Franke, Andre ; Malafosse, Alain ; Genton, Pierre ; Thomas, Pierre ; Gurnett, Christina A ; Schreiber, Stefan ; Bassuk, Alexander G ; Guipponi, Michel ; Stephani, Ulrich ; Helbig, Ingo ; Eichler, Evan E
Publisher:San Francisco: Public Library of Science
Journal title:PLoS genetics, 2010-05, Vol.6 (5)
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Study of the voltage-gated sodium channel β1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)
Author / Creator:Moulard, Bruno ; Buresi, Catherine ; Malafosse, Alain
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2000-08, Vol.16 (2), p.139-142
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Combined analysis of data from two granddaughter designs: A simple strategy for QTL confirmation and increasing experimental power in dairy cattle
Author / Creator:Bennewitz, J ; Reinsch, N ; Grohs, C ; Leveziel, H ; Malafosse, A ; Thomsen, H ; Xu, N ; Looft, C ; Kuehn, C ; Brockmann, G A ; Schwerin, M ; Weimann, C ; Hiendleder, S ; Erhardt, G
Publisher:BioMed Central
Journal title:Genetics selection evolution (Paris), 2003, Vol.35 (3), p.319-338
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Study of the voltage-gated sodium channel ²1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)
Author / Creator:Moulard, Bruno ; Buresi, Catherine ; Malafosse, Alain
Publisher:Hoboken: John Wiley & Sons, Inc
Journal title:Human mutation, 2000-08, Vol.16 (2), p.139
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Study of the voltage-gated sodium channel ?1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)
Author / Creator:Moulard, Bruno ; Buresi, Catherine ; Malafosse, Alain
Journal title:Human mutation, 2000-08, Vol.16 (2), p.139-142
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Implication des genes du syteme serotoninergique dans la vulnerabilite aux conduites suicidaires
Author / Creator:Jollant, Fabrice ; Astruc, Bernard ; Courtet, Philippe ; Castelnau, Didier ; Malafosse, Alain ; Buresi, Catherine
Publisher:CMA Impact Inc
Journal title:Journal of psychiatry & neuroscience, 2004-09, Vol.29 (5), p.350
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Implication of genes of the serotonergic system on vulnerability to suicidal behavior
Author / Creator:Courtet, Philippe ; Jollant, Fabrice ; Castelnau, Didier ; Astruc, Bernard ; Buresi, Catherine ; Malafosse, Alain
Publisher:Canada
Journal title:Journal of psychiatry & neuroscience, 2004-09, Vol.29 (5), p.350
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Expression of FMR1, FXR1, and FXR2 Genes in Human Prenatal Tissues
Author / Creator:Agulhon, Cendra ; Blanchet, Patricia ; Kobetz, Alexandra ; Marchant, Dominique ; Faucon, Nicole ; Sarda, Pierre ; Moraine, Claude ; Sittler, Annie ; Biancalana, Valérie ; Malafosse, Alain ; Abitbol, Marc
Publisher:England: American Association of Neuropathologists, Inc
Journal title:Journal of neuropathology and experimental neurology, 1999-08, Vol.58 (8), p.867-880
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Implication des gènes du système sérotoninergique dans la vulnérabilité aux conduites suicidaires
Author / Creator:COURTET, Philippe ; JOLLANT, Fabrice ; CASTELNAU, Didier ; ASTRUC, Bernard ; BURESI, Catherine ; MALAFOSSE, Alain
Publisher:Ottawa, ON: Canadian Medical Association
Journal title:Journal of psychiatry & neuroscience, 2004-09, Vol.29 (5), p.350-359
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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations
Author / Creator:Moulard, Bruno ; Genton, Pierre ; Grid, Djamel ; Jeanpierre, Marc ; Ouazzani, Réda ; Mrabet, Amel ; Morris, Mike ; LeGuern, Eric ; Dravet, Charlotte ; Mauguière, François ; Utermann, Barbara ; Baldy-Moulinier, Michel ; Belaidi, Halima ; Bertran, Françoise ; Biraben, Arnaud ; Ali Chérif, André ; Chkili, Taieb ; Crespel, Arielle ; Darcel, Françoise ; Dulac, Olivier ; Geny, Christian ; Humbert-Claude, Véronique ; Kassiotis, Philippe ; Buresi, Catherine ; Malafosse, Alain
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2002-09, Vol.111 (3), p.255-262
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A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family
Author / Creator:Belhedi, Nejla ; Bena, Frédérique ; Mrabet, Amel ; Guipponi, Michel ; Souissi, Chiraz ; Mrabet, Hela ; Elgaaied, Amel ; Malafosse, Alain ; Salzmann, Annick
Publisher:England: BioMed Central Ltd
Journal title:BMC genetics, 2013-09, Vol.14 (1), p.93-93
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Magnesium Involvement in Sleep: Genetic and Nutritional Models
Author / Creator:Chollet, Didier ; Franken, Paul ; Raffin, Yvette ; Henrotte, Jean-Georges ; Widmer, Jean ; Malafosse, Alain ; Tafti, Mehdi
Publisher:United States: Springer Nature B.V
Journal title:Behavior genetics, 2001-09, Vol.31 (5), p.413-425
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Showing 41 to 60 of 44 results

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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy

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Genetic association of the Phosphoinositide‐3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism

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War exposure, 5-HTTLPR genotype and lifetime risk of depression

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Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis: e1001326

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Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

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Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics

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Association of genes coding for the a-4, a-5, b-2 and b-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence

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Collecting Saliva by Mail for Genetic and Cotinine Analyses in Participants Recruited through the Internet

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Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies: e1000962

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Study of the voltage-gated sodium channel β1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

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Combined analysis of data from two granddaughter designs: A simple strategy for QTL confirmation and increasing experimental power in dairy cattle

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Study of the voltage-gated sodium channel ²1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

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Study of the voltage-gated sodium channel ?1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

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Implication des genes du syteme serotoninergique dans la vulnerabilite aux conduites suicidaires

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Implication of genes of the serotonergic system on vulnerability to suicidal behavior

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Expression of FMR1, FXR1, and FXR2 Genes in Human Prenatal Tissues

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Implication des gènes du système sérotoninergique dans la vulnérabilité aux conduites suicidaires

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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations

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A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family

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Magnesium Involvement in Sleep: Genetic and Nutritional Models

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