Publications & abstracts

2013

2011

Cytogenetic and Genome Research. 2011;135(3-4):228-40.
Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia
Poot M, van der Smagt JJ, Brilstra EH, Bourgeron T

Current Opinion in Neurobiology, (2011) 21(6): 858-865
New views on antidepressant action
Baudry, A., S. Mouillet-Richard, et al.

Encephale, (2011) 37: S218-S223
Guidelines for the biological treatment of bipolar depression
Samalin, L., T. Charpeaud, et al.

Journal of Affective Disorders, (2011) 135(1-3): 377-379
MRI exploration of pineal volume in bipolar disorder
Sarrazin, S., B. Etain, et al.

Encephale, (2011) 37: S214-S217
Which psychosocial interventions in bipolar depression ?
Scott, J. and B. Etain

Encephale, (2011) 37: S173-S175
Consequences of delayed diagnosis of bipolar disorders
Scott, J. and M. Leboyer

European Neuropsychopharmacology (2011) 21: S629-S629. (Abstract de conférence)
Beyond acute mood episodes: long-term management and revised concepts in bipolar disorder
Leboyer, M.  

Progress in Neuro-Psychopharmacology & Biological Psychiatry (2011) 35(8): 1820-1826.
A meta-analysis of whole-brain diffusion tensor imaging studies in bipolar disorder
Vederine, F. E., M. Wessa, et al.

Encéphale (2011) 37 Suppl 3: S163-8.
Major depression: features indicative of bipolarity?
Azorin, J. M.   

Encéphale (2011) 37 Suppl 3: S196-202.
Antidepressants in bipolar disorder
Courtet, P., L. Samalin, et al.  

Encéphale (2011) 37 Suppl 3: S179-84.
Emotional reactivity: a tool for diagnosis?  
Daban, C. and C. Henry

Encéphale (2011) 37 Suppl 3: S176-8.
What is the burden associated with bipolar depression?  
Etain, B.

Encéphale (2011) 37 Suppl 3: S169-72.
Bipolar depression and suicidal behavior
Guillaume, S., P. Courtet, et al.

Encéphale (2011) 37 Suppl 3: S185-90.
Can we identify biomarkers in bipolar depression? From imaging to biology
Leboyer, M. and P. Fossati (2011).

Encéphale (2011) 37 Suppl 3: S209-13.
Second generation antipsychotics in bipolar depression: a new therapeutic option?
Llorca, P. M.  

Encéphale (2011) 37 Suppl 3: S191-5.
Cognitive disturbances and bipolar depression
Raust, A. and F. Bellivier

Encéphale (2011) 37 Suppl 3: S218-23.
Guidelines for the biological treatment of bipolar depression
Samalin, L., T. Charpeaud, et al.

Encéphale (2011) 37 Suppl 3: S203-8.
Lithium and anticonvulsants in bipolar depression
Samalin, L., A. Nourry, et al.

Ann N Y Acad Sci. 2011 Dec;1242(1):1-25. doi: 10.1111/j.1749-6632.2011.06336.x.
Advances in bipolar disorder: selected sessions from the 2011 International Conference on Bipolar Disorder
Kupfer DJ, Angst J, Berk M, Dickerson F, Frangou S, Frank E, Goldstein BI, Harvey A, Laghrissi-Thode F, Leboyer M, Ostacher MJ, Sibille E, Strakowski SM, Suppes T, Tohen M, Yolken RH, Young LT, Zarate CA.

Cognition. 2011 Oct;121(1):115-26.
Moral judgment in adults with autism spectrum disorders
Zalla T, Barlassina L, Buon M, Leboyer M.

J Affect Disord. 2011 Nov 2
Estrogen receptor alpha gene variants and major depressive episodes
Ryan J, Scali J, Carriere I, Peres K, Rouaud O, Scarabin PY, Ritchie K, Ancelin ML.  

Cytogenetic And Genome Research, (2011)  Volume: 135  Issue: 3-4  Pages: 228-240    
Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia
Poot, M (Poot, M.); van der Smagt, JJ (van der Smagt, J. J.); Brilstra, EH (Brilstra, E. H.); Bourgeron, T (Bourgeron, T.)

Nature Genetics. 2011 Oct;43(10):977-U162
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan WH, Mattingsdal M, McQuillin A, Kwan P, Wienker TF, Daly M, Dudbridge F, Holmans PA, Lin DY, Burmeister M, Greenwood TA, Hamshere ML, Muglia P, Smith EN, Zandi PP, Nievergelt CM, McKinney R, Shilling PD, Schork NJ, Bloss CS, Foroud T, Koller DL, Gershon ES, Liu CY, Badner JA, Scheftner WA, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon FJ, Schulze TG, Berrettini W, Lohoff FW, Potash JB, Mahon PB, McInnis MG, Zollner S, Zhang P, Craig DW, Szelinger S, Barrett TB, Breuer R, Meier S, Strohmaier J, Witt SH, Tozzi F, Farmer A, McGuffin P, Strauss J, Xu W, Kennedy JL, Vincent JB, Matthews K, Day R, Ferreira MA, O'Dushlaine C, Perlis R, Raychaudhuri S, Ruderfer D, Hyoun PL, Smoller JW, Li J, Absher D, Thompson RC, Meng FG, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Watson SJ, Myers RM, Akil H, Boehnke M, Chambert K, Moran J, Scolnick E, Djurovic S, Melle I, Morken G, Gill M, Morris D, Quinn E, Muhleisen TW, Degenhardt FA, Mattheisen M, Schumacher J, Maier W, Steffens M, Propping P, Nothen MM, Anjorin A, Bass N, Gurling H, Kandaswamy R, Lawrence J, McGhee K, McIntosh A, McLean AW, Muir WJ, Pickard BS, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Jones IR, Kirov G, Moskvina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Williamson R, Young AH, Ferrier IN, Stefansson K, Stefansson H, Porgeirsson P, Steinberg S, Gustafsson O, Bergen SE, Nimgaonkar V, Hultman C, Landen M, Lichtenstein P, Sullivan P, Schalling M, Osby U, Backlund L, Frisen L, Langstrom N, Jamain S, Leboyer M, Etain B, Bellivier F, Petursson H, Sigurosson E, Muller-Mysok B, Lucae S, Schwarz M, Schofield PR, Martin N, Montgomery GW, Lathrop M, Oskarsson H, Bauer M, Wright A, Mitchell PB, Hautzinger M, Reif A, Kelsoe JR, Purcell SM, Psychiat GCBD.   

European Journal of Human Genetics. 2011 Oct;19(10):1082-9
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
Anney RJL, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L, Autism Genome P.  

British Journal of Psychiatry. 2011 Aug;199(2):126-31
Oestrogen receptor polymorphisms and late-life depression
Ryan J, Scali J, Carriere I, Peres K, Rouaud O, Scarabin PY, Ritchie K, Ancelin ML.

J Clin Psychiatry, 2011 [in press]
Clinical expression of bipolar disorder type I as a function of polarity and age at onset: convergent findings in samples from France and the USA
Etain B., Lajnef M., Bellivier F., Mathieu F., Raust A., Cochet B., Gard S., M'Bailara K., Kahn JP., Elgrabli O., Cohen R., Jamain S., Vieta E., Leboyer M., Henry C.

Nature Genetics, published online 18 September 2011
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Psychiatric GWAS Consortium Bipolar Disorder Working Group

Schizophrenia Research, 2011, 130 (1-3): 114-122
Neural basis of semantic priming in schizophrenia during a lexical decision task: A magneto-encephalography study.
Vistoli, D; Passerieux, C; Houze, B; Hardy-Bayle, MC; Brunet-Gouet, E.

Bipolar Disorders, 2011, 13 (4): 377-386
Suicidal attempts in bipolar disorder: results from an observational study (EMBLEM).
Bellivier, F; Yon, L; Luquiens, A; Azorin, JM; Bertsch, J; Gerard, S; Reed, C; Lukasiewicz, M.

Journal of Neurodevelopmental disorders, 2011, 3 (2): 113-123
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.
Vieland, VJ; Hallmayer, J; Huang, YG; Pagnamenta, AT; Pinto, D; Khan, H; Monaco, AP; Paterson, AD; Scherer, SW; Sutcliffe, JS; Szatmari, P.

European Psychiatry (2011), doi:10.1016/j.eurpsy.2011.05.005 [Epub ahead of print]
Clinical and dimensional characteristics of euthymic bipolar patients with or without suicidal behavior
C. Parmentier, B. Etain, L. Yon, H. Misson, F. Mathieu, M. Lajnef, B. Cochet, A. Raust, J.-P. Kahn, O. Wajsbrot-Elgrabli, R. Cohen, C. Henry, M. Leboyer, F. Bellivier

L’Encéphale (2011) 37, 199-206
Âge paternel élevé et risque de schizophrénie
A. Hubert, A. Szöke, M. Leboyer, F. Schürhoff

J Affect Disord. 2011 Jun 21. [Epub ahead of print]
MRI exploration of pineal volume in bipolar disorder.
Sarrazin S, Etain B, Vederine FE, d'Albis MA, Hamdani N, Daban C, Delavest M, Lépine JP, Leboyer M, Mangin JF, Poupon C, Houenou J.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 May 23. [Epub ahead of print]
A meta-analysis of whole-brain diffusion tensor imaging studies in bipolar disorder.
Vederine FE, Wessa M, Leboyer M, Houenou J.

Cognition. 2011 Jul 9. [Epub ahead of print]
Moral Judgment in Adults with Autism Spectrum Disorders
Zalla T, Barlassina L, Buon M, Leboyer M.

BMC Medical Genetics 2011, 12:17
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability
Cécile Pagan, Hany Goubran Botros, Karine Poirier, Anne Dumaine, Stéphane Jamain, Sarah Moreno, Arjan de Brouwer, Hilde Van Esch, Richard Delorme, Jean-Marie Launay, Andreas Tzschach, Vera Kalscheuer, Didier Lacombe, Sylvain Briault, Frédéric Laumonnier, Martine Raynaud, Bregje W van Bon, Marjolein H Willemsen, Marion Leboyer, Jamel Chelly, Thomas Bourgeron

Journal of Neurodevelopmental Disorders. 2011. 3: 113-123
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
Veronica J. Vieland, Joachim Hallmayer, Yungui Huang, Alistair T. Pagnamenta, Dalila Pinto, Hameed Khan, Anthony P. Monaco, Andrew D. Paterson, Stephen W. Scherer and James S. Sutcliffe, et al.

J Pineal Res. 2011 Apr 27. doi: 10.1111/j.1600-079X.2011.00902.x. [Epub ahead of print]
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Chaste P, Clement N, Botros HG, Guillaume JL, Konyukh M, Pagan C, Scheid I, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Gillberg IC, Melke J, Delorme R, Leblond C, Toro R, Huguet G, Fauchereau F, Durand C, Boudarene L, Serrano E, Lemière N, Launay JM, Leboyer M, Jockers R, Gillberg C, Bourgeron T.

Psychoneuroendocrinology. 2011 May 11. [Epub ahead of print]
Estrogen receptor gene variants are associated with anxiety disorders in older women.
Ryan J, Scali J, Carrière I, Scarabin PY, Ritchie K, Ancelin ML.

J Affect Disord. 2011 Jun;131(1-3):358-63. Epub 2010 Dec 8.
A French network of bipolar expert centres: A model to close the gap between evidence-based medicine and routine practice.
Henry C, Etain B, Mathieu F, Raust A, Vibert JF, Scott J, Leboyer M.

J Affect Disord. 2011 Apr 4. [Epub ahead of print]
Neuroimaging-based markers of bipolar disorder: Evidence from two meta-analyses.
Houenou J, Frommberger J, Carde S, Glasbrenner M, Diener C, Leboyer M, Wessa M.

Encephale 2011 Apr;37(2):119-26.
Aggregation of social deficits and psychiatric disorders in parents of children with autism: Toward a temperamental link?
Gousse V, Galera C, Bouvard M, Michel G.

Psychiatr Genet. 2011 Mar 10. [Epub ahead of print]
Genetic and molecular exploration of UHMK1 in schizophrenic patients.
Dumaine A, Maucuer A, Barbet A, Manceau V, Deshommes J, Méary A, Szöke A,Schürhoff F, Llorca PM, Lancon C, Leboyer M, Jamain S.

American Journal of Human Genetics. 2011 Mar;88(3):372-81.
Bipolar Disorder Genome Study Bi GS. Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder.
Cichon S, Muhleisen TW, Degenhardt FA, Mattheisen M, Miro X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Aexander M, Vollmer J, Breuer R, Schmal C, Tessmann P, Moebus S, Wichmann HE, Schreiber S, Muller-Myhsok B, Lucae S, Jamain S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn JP, Heath S, Hamshere M, O'Donovan MC, Owen MJ, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell PB, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Mayoral F, Chuchalin A, Babadjanova G, Tiganov AS, Pantelejeva G, Abramova LI, Grigoroiu-Serbanescu M, Diaconu CC, Czerski PM, Hauser J, Zimmer A, Lathrop M, Schulze TG, Wienker TF, Schumacher J, Maier W, Propping P, Rietschel M, Nothen MM

Bmc Medical Genetics. 2011 Jan;12.
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability.
Pagan C, Botros HG, Poirier K, Dumaine A, Jamain S, Moreno S, de Brouwer A, Van Esch H, Delorme R, Launay JM, Tzschach A, Kalscheuer V, Lacombe D, Briault S, Laumonnier F, Raynaud M, van Bon BW, Willemsen MH, Leboyer M, Chelly J, Bourgeron T.

Neuroimage. 2011 Jan 15;54(2):1406-14.
Anatomical and temporal architecture of theory of mind: a MEG insight into the early stages.
Vistoli D, Brunet-Gouet E, Baup-Bobin E, Hardy-Bayle MC, Passerieux C

SocialNeuroscience. 2011 Jan 20:1-11.
Abnormal temporal and parietal magnetic activations during the early stages of theory of mind in schizophrenic patients.
Vistoli D, Brunet-Gouet E, Lemoalle A, Hardy-Bayle MC, Passerieux C.

2010  

Andari E, Duhamel J-R, Zalla T, Herbrecht E, Leboyer M, Sirigu A
Promoting Social Behaviour with Oxytocin in High-Functioning Autism Spectrum Disorders
Proc Natl Acad Sci U S A. 2010 Mar 2;107(9):4389-94.

Balance investigators and collaborators, Geddes JR, Goodwin GM, Rendell J, Azorin JM, Cipriani A, Ostacher MJ, Morriss R, Alder N, Juszczak E.
Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial.
Lancet. 2010 Jan 30;375(9712):385-95.

Delorme R, Betancur C, Chaste P, Kernéis S, Stopin A, Mouren MC, Collet C, Bourgeron T, Leboyer M, Launay JM.
Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.
Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-8.

Perroud N, Jaussent I, Guillaume S, Bellivier F, Baud P, Jollant F, Leboyer M, Lewis CM, Malafosse A, Courtet P.
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits.
Genes Brain Behav. 2010 Mar 1;9(2):193-202.

Sampaio AS, Fagerness J, Crane J, Leboyer M, Delorme R, Pauls DL, Stewart SE.
Association Between Polymorphisms in GRIK2 Gene and Obsessive-Compulsive Disorder: A Family-Based Study.
CNS Neurosci Ther. 2010 Mar 29

Etain B, Mathieu F, Henry C, Raust A, Roy I, Germain A, Leboyer M, Bellivier F.
Preferential association between childhood emotional abuse and bipolar disorder
J Trauma Stress. 2010 Jun;23(3):376-83

Pinto et al
Functional impact of global rare copy number variation in autism spectrum
Autism Genome Project,
Nature. 2010 Jul 15;466(7304):368-72

Delorme R, Moreno De Luca D, Gennetier A, Maier W, Chaste P, Mossner R, Grabe Hj, Ruhrmann S, Falaki P, Mouren Mc, Leboyer M, Wagner M, Betancur C
Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
BMC Med Genet. 2010 Jun 21;11:100

Delorme R, Sheid I, Ankarsater H, Chaste P, Jamain S, Schurhoff F, Nygren G, Herbrecht E, Dumaine A, Mouren Mc, Rastam M, Leboyer M, Gillberg C, Bourgeron T
Mutations screening of NOS1AP gene in a large sample of psychiatric patients and controls
BMC Med Genet. 2010 Jul 5;11(1):108

Karege F, Perroud N, Schurhoff F, Meary A, Marillier G, Burkhardt S, Ballmann E, Fernandez R, Jamain S, Leboyer M, La Harpe R, Malafosse A
Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder
Genes Brain Behav, 2010, Jul, 9 (5), 503-511

Chaste P, Clement N, Mercati O, Guilllame Jl, Delorme R, Botros Hg, Pagan C, Perivier S, Scheid I, Nygren G, Anckarsater H, Rastam M, Stahlberg O, Gillberg C, Serrano E, Lemiere N, Launay Jm, Mouren Simeoni Mc, Leboyer M, Gillberg C, Jockers R, Bourgeron T
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general populations
PLoS One. 2010 Jul 15;5(7):e11495

Toro R, Konyukh M, Delorme R, Leblond C, Chaste P, Fauchereau F, Coleman M, Leboyer M, Gillberg C, Bourgeron T.
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
Trends Genet. 2010 Aug;26(8):363-72

Brousse G, Meary A, Blanc O, Lançon C, Llorca Pm, Leboyer M.
Clinical predictors of response to olanzapine or risperidone during acute episode of schizophrenia
Psychiatry Res. 2010 Aug 30, 179 (1):12-8

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes Tr, Correia C, Abrahams Bs, Sykes N, Pagnamenta At, Almeida J, Bacchelli E, Bailey Aj, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S, Bolton Pf, Bourgeron T, Brennan S, Brian J, Carson Ar, Casallo G, Casey J, Chu Sh, Cochrane L, Corsello C, Crawford El, Crossett A, Dawson G, De Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez Ba, Folstein Se, Fombonne E, Freitag Cm, Gilbert J, Gillberg C, Glessner Jt, Goldberg J, Green J, Guter Sj, Hakonarson H, Heron Ea, Hill M, Holt R, Howe Jl, Hughes G, Hus V, Igliozzi R, Kim C, Klauck Sm, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere Cm, Lamb Ja, Laskawiec M, Leboyer M, Le Couteur A, Leventhal Bl, Lionel Ac, Liu Xq, Lord C, Lotspeich L, Lund Sc, Maestrini E, Mahoney W, Mantoulan C, Marshall Cr, Mcconachie H, Mcdougle Cj, Mcgrath J, Mcmahon Wm, Melhem Nm, Merikangas A, Migita O, Minshew Nj, Mirza Gk, Munson J, Nelson Sf, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr Jr, Parrini B, Paton T, Pickles A, Piven J, Osey Dj, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter Ml, Bierut Lj, Rice Jp, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield Vc, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson Ap, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent Jb, Volkmar F, Wallace S, Wang K, Wang Zz, Wassink Th, Wing K, Wittemeyer K, Wood S, Yaspan Bl, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum Jd, Cantor Rm, Cook Eh, Coon H, Cuccaro Ml, Gallagher L, Geschwind Dh, Gill M, Haines Jl, Miller J, Monaco Ap, Nurnberger Ji, Paterson Ad, Pericak-Vance Ma, Schellenberg Gd, Scherer Sw, Sutcliffe Js, Szatmari P, Vicente Am, Vieland Vj, Wijsman Em, Devlin B, Ennis S, Hallmayer J,.
A genome-wide scan for common alleles affecting risk for autism
Hum. Mol. Genet., 2010, Oct 15, 19, 4072-4082

Devillard F, Guinchat V, Moreno-De-Luca D, Tabet Ac, Gruchy N, Guillem P, Nguyen Morel Ma, Leporrier N, Leboyer M, Jouk Ps, Lespinasse J, Betancur C.
Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.
Am J Med Genet A. 2010 Sep;152A(9):2346-54

Ferchiou A, Schurhoff F, Bulzacka E, Leboyer M, Szoke A,.
Selective Attention Impairment in Schizophrenia Can it Explain Source   Monitoring Failure ?
J. Nerv. Ment. Dis., 2010 Oct 198, 779-781.

Zalla T, Daprati E, Sav Am, Chaste P, Nico D, Leboyer M.
Memory for self-performed actions in individuals with Asperger syndrome.
PLoS One. 2010 Oct 12;5, 10

Mathieu F, Dizier Mh, Etain B, Jamain S, Rietschel M, Maier W, Albus M, Mckeon P, Roche S, Blackwood D, Muir Wj, Henry C, Malafosse A, Preisig M, Ferrero F, Cichon S, Schumacher J, Ohlraun S, Propping P, Abou Jamra R, Schulze Tg, Zelenica D, Charon C, Marusic A, Dernovsek Mc, Gurling H, Nöthen M, Lathrop M, Leboyer M, Bellivier F.
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset.
Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1425-33

Henry C, Etain B, Mathieu F, Raust A, Vibert Jf, Scott J, Leboyer M.
A French network of bipolar expert centres: A model to close the gap between evidence-based medicine and routine practice.
J Affect Disord. 2010 Dec 6.

Henry C, M'Bailara K, Lépine Jp, Lajnef M, Leboyer M.
Defining bipolar mood states with quantitative measurement of inhibition/activation and emotional reactivity
J Affect Disord. 2010 Dec, 127 (1-3), 300-4

Leboyer M, Kupfer D.
Bipolar disorder: new perspectives in health care and prevention.
J Clin Psychiatry. 2010 Dec;71(12):1689-95

Eric Brunet-Gouet, Amélie M., Achim c, Damien Vistoli, Christine Passerieux,
Marie-Christine Hardy-Baylé, Philip L. Jackson
The study of social cognition with neuroimaging methods as a means to explore
future directions of deficit evaluation in schizophrenia?
Psychiatry Res. 2010 Dec 22

Etain B, Dumaine A, Mathieu F, Chevalier F, Henry C, Kahn JP, Deshommes J, Bellivier F, Leboyer M, Jamain S.
A SNAP25 promoter variant is associated with early-onset bipolar disorder and a high expression level in brain.
Molecular Psychiatry2010 Jul; 15(7):748-55.

Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BHY, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, Piven J, Ponting CP, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Sequeira AF, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stein O, Sykes N, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang ZZ, Wassink TH, Webber C, Weksberg R, Wing K, Wittemeyer K, Wood S, Wu J, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Devlin B, Ennis S, Gallagher L, Geschwind DH, Gill M, Haines JL, Hallmayer J, Miller J, Monaco AP, Nurnberger JI, Paterson AD, Pericak-Vance MA, Schellenberg GD, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Scherer SW, Sutcliffe JS, Betancur C.
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature2010 Jul; 466(7304):368-72.