• 2025
  Moreau CA, Ayrolles A, Ching CRK, Bonicel R, Mathieu A, Stordeur C, El Khantour C, Bergeret P, Traut N, Tran L, Germanaud D, Alison M, Elmaleh-Bergès M, Ehrlich S, Thompson PM, Bourgeron T, Delorme R, Neuroimaging insights into brain mechanisms of early-onset restrictive eating disorders., Nat Ment Health 2025 ; 3(7): 780-788.
• 2023
  Rolland T, Cliquet F, Anney RJL, Moreau C, Traut N, Mathieu A, Huguet G, Duan J, Warrier V, Portalier S, Dry L, Leblond CS, Douard E, Amsellem F, Malesys S, Maruani A, Toro R, Børglum AD, Grove J, Baron-Cohen S, Packer A, Chung WK, Jacquemont S, Delorme R, Bourgeron T, Phenotypic effects of genetic variants associated with autism., Nat Med 2023 Jun; (): .
• 2023
  Ferhat AT, Verpy E, Biton A, Forget B, De Chaumont F, Mueller F, Le Sourd AM, Coqueran S, Schmitt J, Rochefort C, Rondi-Reig L, Leboucher A, Boland A, Fin B, Deleuze JF, Boeckers TM, Ey E, Bourgeron T, , Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice., Front Mol Neurosci 2023 ; 16(): 1139118.
• 2022
  Moreau CA, Kumar K, Harvey A, Huguet G, Urchs S, Schultz LM, Sharmarke H, Jizi K, Martin CO, Younis N, Tamer P, Martineau JL, Orban P, Silva AI, Hall J, van den Bree MBM, Owen MJ, Linden DEJ, Lippé S, Bearden CE, Almasy L, Glahn DC, Thompson PM, Bourgeron T, Bellec P, Jacquemont S, , Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions., Brain 2022 Sep; (): .
• 2022
  Traut N, Heuer K, Lemaître G, Beggiato A, Germanaud D, Elmaleh M, Bethegnies A, Bonnasse-Gahot L, Cai W, Chambon S, Cliquet F, Ghriss A, Guigui N, de Pierrefeu A, Wang M, Zantedeschi V, Boucaud A, van den Bossche J, Kegl B, Delorme R, Bourgeron T, Toro R, Varoquaux G, , Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery., Neuroimage 2022 Jul; 255(): 119171.
• 2021
  Lefebvre A, Cohen A, Maruani A, Amsellem F, Beggiato A, Amestoy A, Moal ML, Umbricht D, Chatham C, Murtagh L, Bouvard M, Leboyer M, Bourgeron T, Delorme R, , Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probands., Autism Res 2021 Jul; (): .
• 2021
  Leblond CS, Le TL, Malesys S, Cliquet F, Tabet AC, Delorme R, Rolland T, Bourgeron T, , Operative list of genes associated with autism and neurodevelopmental disorders based on database review., Mol Cell Neurosci 2021 Jun; 113(): 103623.
• 2020
  Dumas G, Goubran-Botros H, Matondo M, Pagan C, Boulègue C, Chaze T, Chamot-Rooke J, Maronde E, Bourgeron T, , Mass-spectrometry analysis of the human pineal proteome during night and day and in autism., J Pineal Res 2020 Dec; (): e12713.
• 2020
  Moreau CA, Urchs SGW, Kuldeep K, Orban P, Schramm C, Dumas G, Labbe A, Huguet G, Douard E, Quirion PO, Lin A, Kushan L, Grot S, Luck D, Mendrek A, Potvin S, Stip E, Bourgeron T, Evans AC, Bearden CE, Bellec P, Jacquemont S, , Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia., Nat Commun 2020 Oct; 11(1): 5272.
• 2020
  Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, Demonet JF, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Kirsten H, Müller B, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G, , Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia., Mol Psychiatry 2020 Oct; (): .
• 2020
  Ayrolles A, Brun F, Chen P, Djalovski A, Beauxis Y, Delorme R, Bourgeron T, Dikker S, Dumas G, , HyPyP: a Hyperscanning Python Pipeline for inter-brain connectivity analysis., Soc Cogn Affect Neurosci 2020 Oct; (): .
• 2020
  Douard E, Zeribi A, Schramm C, Tamer P, Loum MA, Nowak S, Saci Z, Lord MP, Rodríguez-Herreros B, Jean-Louis M, Moreau C, Loth E, Schumann G, Pausova Z, Elsabbagh M, Almasy L, Glahn DC, Bourgeron T, Labbe A, Paus T, Mottron L, Greenwood CMT, Huguet G, Jacquemont S, , Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome., Am J Psychiatry 2020 Sep; (): appiajp202019080834.
• 2020
  Tillmann J, Uljarevic M, Crawley D, Dumas G, Loth E, Murphy D, Buitelaar J, Charman T, , , Dissecting the phenotypic heterogeneity in sensory features in autism spectrum disorder: a factor mixture modelling approach., Mol Autism 2020 Aug; 11(1): 67.
• 2020
  Floris DL, Wolfers T, Zabihi M, Holz NE, Zwiers MP, Charman T, Tillmann J, Ecker C, Dell'Acqua F, Banaschewski T, Moessnang C, Baron-Cohen S, Holt R, Durston S, Loth E, Murphy DGM, Marquand A, Buitelaar JK, Beckmann CF, , , Atypical Brain Asymmetry in Autism-A Candidate for Clinically Meaningful Stratification., Biol Psychiatry Cogn Neurosci Neuroimaging 2020 Aug; (): .
• 2020
  Vitrac A, Pons S, Balkota M, Lemière N, Raïs C, Bourgeois JP, Maskos U, Bourgeron T, Cloëz-Tayarani I, , A chimeric mouse model to study human iPSC-derived neurons: the case of a truncating SHANK3 mutation., Sci Rep 2020 08; 10(1): 13315.
• 2020
  Lin BD, Colas F, Nijman IJ, Medic J, Brands W, Parr JR, van Eijk KR, Klauck SM, Chiocchetti AG, Freitag CM, Maestrini E, Bacchelli E, Coon H, Vicente A, Oliveira G, Pagnamenta AT, Gallagher L, Ennis S, Anney R, Bourgeron T, Luykx JJ, Vorstman J, , The role of rare compound heterozygous events in autism spectrum disorder., Transl Psychiatry 2020 06; 10(1): 204.
• 2020
  Lutz AK, Pfaender S, Incearap B, Ioannidis V, Ottonelli I, Föhr KJ, Cammerer J, Zoller M, Higelin J, Giona F, Stetter M, Stoecker N, Alami NO, Schön M, Orth M, Liebau S, Barbi G, Grabrucker AM, Delorme R, Fauler M, Mayer B, Jesse S, Roselli F, Ludolph AC, Bourgeron T, Verpelli C, Demestre M, Boeckers TM, , Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles., Sci Transl Med 2020 Jun; 12(547): .
• 2020
  Myers SM, Challman TD, Bernier R, Bourgeron T, Chung WK, Constantino JN, Eichler EE, Jacquemont S, Miller DT, Mitchell KJ, Zoghbi HY, Martin CL, Ledbetter DH, , Insufficient Evidence for “Autism-Specific” Genes., Am J Hum Genet 2020 05; 106(5): 587-595.
• 2020
  Biton A, Traut N, Poline JB, Aribisala BS, Bastin ME, Bülow R, Cox SR, Deary IJ, Fukunaga M, Grabe HJ, Hagenaars S, Hashimoto R, Kikuchi M, Muñoz Maniega S, Nauck M, Royle NA, Teumer A, Valdés Hernández M, Völker U, Wardlaw JM, Wittfeld K, Yamamori H, , Bourgeron T, Toro R, , Polygenic Architecture of Human Neuroanatomical Diversity., Cereb Cortex 2020 04; 30(4): 2307-2320.
• 2020
  Ey E, Bourgeron T, Boeckers TM, Kim E, Han K, , Editorial: Shankopathies: Shank Protein Deficiency-Induced Synaptic Diseases., Front Mol Neurosci 2020 ; 13(): 11.
• 2019
  de Chaumont F, Ey E, Torquet N, Lagache T, Dallongeville S, Imbert A, Legou T, Le Sourd AM, Faure P, Bourgeron T, Olivo-Marin JC, Real-time analysis of the behaviour of groups of mice via a depth-sensing camera and machine learning., Nat Biomed Eng 2019 Nov; 3(11): 930-942.
• 2019
  Pinel P, Forgeot d'Arc B, Dehaene S, Bourgeron T, Thirion B, Le Bihan D, Poupon C, The functional database of the ARCHI project: Potential and perspectives, Neuroimage. 2019 May 4.
• 2019
  Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Theroux JF, Jefri M, Tanti A, Wu H, Kolobova I, Silviera H, Manzano-Vargas K, Ehresmann S, Hamdan FF, Hettige N, Zhang X, Antonyan L, Nassif C, Ghaloul-Gonzalez L, Sebastian J, Vockley J, Begtrup AG, Wentzensen IM, Crunk A, Nicholls RD, Herman KC, Deignan JL, Al-Hertani W, Efthymiou S, Salpietro V, Miyake N, Makita Y, Matsumoto N, Østern R, Houge G, Hafström M, Fassi E, Houlden H, Klein Wassink-Ruiter JS, Nelson D, Goldstein A, Dabir T, van Gils J, Bourgeron T, Delorme R, Cooper GM, Martinez JE, Finnila CR, Carmant L, Lortie A, Oegema R, van Gassen K, Mehta SG, Huhle D, Abou Jamra R, Martin S, Brunner HG, Lindhout D, Au M, Graham JM Jr, Coubes C, Turecki G, Gravel S, Mechawar N, Rossignol E, Michaud JL, Lessard J, Ernst C, Campeau PM, Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons, Am J Hum Genet. 2019 May 2;104(5):815-834.
• 2019
  Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G., Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia, Transl Psychiatry. 2019 Feb 11;9(1):77.
• 2019
  Leblond CS, Cliquet F, Carton C, Huguet G, Mathieu A, Kergrohen T, Buratti J, Lemière N, Cuisset L, Bienvenu T, Boland A, Deleuze JF, Stora T, Biskupstoe R, Halling J, Andorsdóttir G, Billstedt E, Gillberg C, Bourgeron T, , Both rare and common genetic variants contribute to autism in the Faroe Islands., NPJ Genom Med 2019 ; 4(): 1.
• 2019
  Bouvet L, Amsellem F, Maruani A, Tonus-Vic Dupont A, Mathieu A, Bourgeron T, Delorme R, Mottron L, Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor, Behav. Brain Res. 2019 Jan;.
• 2019
  Maruani A, Dumas G, Beggiato A, Traut N, Peyre H, Cohen-Freoua A, Amsellem F, Elmaleh M, Germanaud D, Launay JM, Bourgeron T, Toro R, Delorme R, , Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume., Front Psychiatry 2019 ; 10(): 11.
• 2018
  Lahbib S, Leblond CS, Hamza M, Regnault B, Lemée L, Mathieu A, Jaouadi H, Mkaouar R, Youssef-Turki IB, Belhadj A, Kraoua I, Bourgeron T, Abdelhak S, Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology, J. Appl. Genet. 2019 Feb;60(1):49-56.
• 2018
  Huguet G, Schramm C, Douard E, Jiang L, Labbe A, Tihy F, Mathonnet G, Nizard S, Lemyre E, Mathieu A, Poline JB, Loth E, Toro R, Schumann G, Conrod P, Pausova Z, Greenwood C, Paus T, Bourgeron T, Jacquemont S, , , Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples., JAMA Psychiatry 2018 05; 75(5): 447-457.
• 2018
  Traut N, Beggiato A, Bourgeron T, Delorme R, Rondi-Reig L, Paradis AL, Toro R, , Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort., Biol Psychiatry 2018 Apr; 83(7): 579-588.
• 2018
  Warrier V, Toro R, Chakrabarti B, , Børglum AD, Grove J, , Hinds DA, Bourgeron T, Baron-Cohen S, , Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa., Transl Psychiatry 2018 03; 8(1): 35.
• 2017
  Warrier V, Grasby KL, Uzefovsky F, Toro R, Smith P, Chakrabarti B, Khadake J, Mawbey-Adamson E, Litterman N, Hottenga JJ, Lubke G, Boomsma DI, Martin NG, Hatemi PK, Medland SE, Hinds DA, Bourgeron T, Baron-Cohen S., Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition, Mol Psychiatry. 2017 Jun 6..
• 2017
  Tabet AC, Rolland T, Ducloy M, Lévy J, Buratti J, Mathieu A, Haye D, Perrin L, Dupont C, Passemard S, Capri Y, Verloes A, Drunat S, Keren B, Mignot C, Marey I, Jacquette A, Whalen S, Pipiras E, Benzacken B, Chantot-Bastaraud S, Afenjar A, Héron D, Le Caignec C, Beneteau C, Pichon O, Isidor B, David A, El Khattabi L, Kemeny S, Gouas L, Vago P, Mosca-Boidron AL, Faivre L, Missirian C, Philip N, Sanlaville D, Edery P, Satre V, Coutton C, Devillard F, Dieterich K, Vuillaume ML, Rooryck C, Lacombe D, Pinson L, Gatinois V, Puechberty J, Chiesa J, Lespinasse J, Dubourg C, Quelin C, Fradin M, Journel H, Toutain A, Martin D, Benmansour A, Leblond CS, Toro R, Amsellem F, Delorme R, Bourgeron T, , A framework to identify contributing genes in patients with Phelan-McDermid syndrome., NPJ Genom Med 2017 ; 2(): 32.
• 2016
  Torquet N, de Chaumont F, Faure P, Bourgeron T, Ey E, mouseTube – a database to collaboratively unravel mouse ultrasonic communication, F1000Res 2016;5:2332.
• 2016
  Ferhat AT, Torquet N, Le Sourd AM, de Chaumont F, Olivo-Marin JC, Faure P, Bourgeron T, Ey E, Recording mouse ultrasonic vocalizations to evaluate social communication, J. Vis. Exp. 2016; 112, e53871.
• 2016
  Mercati O, Huguet G, Danckaert A, André-Leroux G, Maruani A, Bellinzoni M, Rolland T, Gouder L, Mathieu A, Buratti J, Amsellem F, Benabou M, Van-Gils J, Beggiato A, Konyukh M, Bourgeois JP, Gazzellone MJ, Yuen RK, Walker S, Delépine M, Boland A, Régnault B, Francois M, Van Den Abbeele T, Mosca-Boidron AL, Faivre L, Shimoda Y, Watanabe K, Bonneau D, Rastam M, Leboyer M, Scherer SW, Gillberg C, Delorme R, Cloëz-Tayarani I, Bourgeron T, CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders, Mol. Psychiatry 2017 04;22(4):625-633.
• 2015
  Loth E, Spooren W, Ham LM, Isaac MB, Auriche-Benichou C, Banaschewski T, Baron-Cohen S, Broich K, Bölte S, Bourgeron T, Charman T, Collier D, de Andres-Trelles F, Durston S, Ecker C, Elferink A, Haberkamp M, Hemmings R, Johnson MH, Jones EJ, Khwaja OS, Lenton S, Mason L, Mantua V, Meyer-Lindenberg A, Lombardo MV, O'Dwyer L, Okamoto K, Pandina GJ, Pani L, Persico AM, Simonoff E, Tauscher-Wisniewski S, Llinares-Garcia J, Vamvakas S, Williams S, Buitelaar JK, Murphy DG, Identification and validation of biomarkers for autism spectrum disorders, Nat Rev Drug Discov 2015 Dec;15(1):70-3.
• 2015
  Maruani A, Huguet G, Beggiato A, ElMaleh M, Toro R, Leblond CS, Mathieu A, Amsellem F, Lemière N, Verloes A, Leboyer M, Gillberg C, Bourgeron T, Delorme R, , 11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures., Am J Med Genet A 2015 Dec; 167A(12): 3019-30.
• 2015
  Mosca-Boidron AL, Gueneau L, Huguet G, Goldenberg A, Henry C, Gigot N, Pallesi-Pocachard E, Falace A, Duplomb L, Thevenon J, Duffourd Y, St-Onge J, Chambon P, Rivière JB, Thauvin-Robinet C, Callier P, Marle N, Payet M, Ragon C, Goubran Botros H, Buratti J, Calderari S, Dumas G, Delorme R, Lagarde N, Pinoit JM, Rosier A, Masurel-Paulet A, Cardoso C, Mugneret F, Saugier-Veber P, Campion D, Faivre L, Bourgeron T, A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability, Eur. J. Hum. Genet. 2016 Jun;24(6):838-43.
• 2015
  Bourgeron T, From the genetic architecture to synaptic plasticity in autism spectrum disorder, Nat. Rev. Neurosci. 2015 Aug;16(9):551-63.
• 2015
  Lefebvre A, Beggiato A, Bourgeron T, Toro R, , Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation., Biol Psychiatry 2015 Jul; 78(2): 126-34.
• 2015
  Bourgeron T, The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture, Nord J Psychiatry 2015 May;:1-9.
• 2015
  Ferhat AT, Le Sourd AM, de Chaumont F, Olivo-Marin JC, Bourgeron T, Ey E, Social communication in mice–are there optimal cage conditions?, PLoS ONE 2015;10(3):e0121802.
• 2014
  Frank E, Benabou M, Bentzley B, Bianchi M, Goldstein T, Konopka G, Maywood E, Pritchett D, Sheaves B, Thomas J, Influencing circadian and sleep-wake regulation for prevention and intervention in mood and anxiety disorders: what makes a good homeostat?, Ann. N. Y. Acad. Sci. 2014 Dec;1334:1-25.
• 2014
  Kočovská E, Andorsdóttir G, Weihe P, Halling J, Fernell E, Stóra T, Biskupstø R, Gillberg IC, Shea R, Billstedt E, Bourgeron T, Minnis H, Gillberg C, Vitamin d in the general population of young adults with autism in the faroe islands, J Autism Dev Disord 2014 Dec;44(12):2996-3005.
• 2014
  Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T, , Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments., PLoS Genet 2014 Sep; 10(9): e1004580.
• 2014
  Fernell E, Wilson P, Hadjikhani N, Bourgeron T, Neville B, Taylor D, Minnis H, Gillberg C, Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials, J Autism Dev Disord 2014 Aug;44(8):2074-6.
• 2014
  Karayannis T, Au E, Patel JC, Kruglikov I, Markx S, Delorme R, Héron D, Salomon D, Glessner J, Restituito S, Gordon A, Rodriguez-Murillo L, Roy NC, Gogos JA, Rudy B, Rice ME, Karayiorgou M, Hakonarson H, Keren B, Huguet G, Bourgeron T, Hoeffer C, Tsien RW, Peles E, Fishell G, Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission, Nature 2014 Jul;511(7508):236-40.
• 2014
  Pinel P, Lalanne C, Bourgeron T, Fauchereau F, Poupon C, Artiges E, Le Bihan D, Dehaene-Lambertz G, Dehaene S, Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas, Cereb. Cortex 2015 Sep;25(9):2478-93.
• 2014
  Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, Conceição IC, Chiocchetti AG, Casey JP, Cai G, Cabrol C, Bolshakova N, Bacchelli E, Anney R, Gallinger S, Cotterchio M, Casey G, Zwaigenbaum L, Wittemeyer K, Wing K, Wallace S, van Engeland H, Tryfon A, Thomson S, Soorya L, Rogé B, Roberts W, Poustka F, Mouga S, Minshew N, McInnes LA, McGrew SG, Lord C, Leboyer M, Le Couteur AS, Kolevzon A, Jiménez González P, Jacob S, Holt R, Guter S, Green J, Green A, Gillberg C, Fernandez BA, Duque F, Delorme R, Dawson G, Chaste P, Café C, Brennan S, Bourgeron T, Bolton PF, Bölte S, Bernier R, Baird G, Bailey AJ, Anagnostou E, Almeida J, Wijsman EM, Vieland VJ, Vicente AM, Schellenberg GD, Pericak-Vance M, Paterson AD, Parr JR, Oliveira G, Nurnberger JI, Monaco AP, Maestrini E, Klauck SM, Hakonarson H, Haines JL, Geschwind DH, Freitag CM, Folstein SE, Ennis S, Coon H, Battaglia A, Szatmari P, Sutcliffe JS, Hallmayer J, Gill M, Cook EH, Buxbaum JD, Devlin B, Gallagher L, Betancur C, Scherer SW, Convergence of genes and cellular pathways dysregulated in autism spectrum disorders, Am. J. Hum. Genet. 2014 May;94(5):677-94.
• 2014
  Huguet G, Nava C, Lemière N, Patin E, Laval G, Ey E, Brice A, Leboyer M, Szepetowski P, Gillberg C, Depienne C, Delorme R, Bourgeron T, Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders, PLoS ONE 2014;9(3):e88600.
• 2014
  Waltes R, Duketis E, Knapp M, Anney RJ, Huguet G, Schlitt S, Jarczok TA, Sachse M, Kämpfer LM, Kleinböck T, Poustka F, Bölte S, Schmötzer G, Voran A, Huy E, Meyer J, Bourgeron T, Klauck SM, Freitag CM, Chiocchetti AG, Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders, Hum. Genet. 2014 Jun;133(6):781-92.
• 2013
  Scheid I, Maruani A, Huguet G, Leblond CS, Nygren G, Anckarsäter H, Beggiato A, Rastam M, Amsellem F, Gillberg IC, Elmaleh M, Leboyer M, Gillberg C, Betancur C, Coleman M, Hama H, Cook EH, Bourgeron T, Delorme R, Heterozygous FA2H mutations in autism spectrum disorders, BMC Med. Genet. 2013;14:124.
• 2013
  Guilmatre A, Huguet G, Delorme R, Bourgeron T, The emerging role of SHANK genes in neuropsychiatric disorders, Dev Neurobiol 2014 Feb;74(2):113-22.
• 2013
  Ey E, Torquet N, Le Sourd AM, Leblond CS, Boeckers TM, Faure P, Bourgeron T, The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations, Behav. Brain Res. 2013 Nov;256:677-89.
• 2013
  Huguet G, Ey E, Bourgeron T, The genetic landscapes of autism spectrum disorders, Annu Rev Genomics Hum Genet 2013;14:191-213.
• 2013
  Delorme R, Ey E, Toro R, Leboyer M, Gillberg C, Bourgeron T, , Progress toward treatments for synaptic defects in autism., Nat Med 2013 Jun; 19(6): 685-94.
• 2012
  Botros HG, Legrand P, Pagan C, Bondet V, Weber P, Ben-Abdallah M, Lemière N, Huguet G, Bellalou J, Maronde E, Beguin P, Haouz A, Shepard W, Bourgeron T, Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway, J. Pineal Res. 2013 Jan;54(1):46-57.
• 2012
  Chaste P, Betancur C, Gérard-Blanluet M, Bargiacchi A, Kuzbari S, Drunat S, Leboyer M, Bourgeron T, Delorme R, High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters, Mol Autism 2012;3(1):5.
• 2012
  Schmeisser MJ, Ey E, Wegener S, Bockmann J, Stempel AV, Kuebler A, Janssen AL, Udvardi PT, Shiban E, Spilker C, Balschun D, Skryabin BV, Dieck St, Smalla KH, Montag D, Leblond CS, Faure P, Torquet N, Le Sourd AM, Toro R, Grabrucker AM, Shoichet SA, Schmitz D, Kreutz MR, Bourgeron T, Gundelfinger ED, Boeckers TM, , Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2., Nature 2012 Apr; 486(7402): 256-60.
• 2012
  Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, Klauck SM, Poustka F, Freitag CM, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira AF, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer SW, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren MC, Leboyer M, Gillberg C, Boeckers TM, Bourgeron T, , Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders., PLoS Genet 2012 Feb; 8(2): e1002521.
• 2012
  Chabout J, Serreau P, Ey E, Bellier L, Aubin T, Bourgeron T, Granon S, Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment, PLoS ONE 2012;7(1):e29401.
• 2011
  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, , Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders., J Pineal Res 2011 Nov; 51(4): 394-9.
• 2011
  Konyukh M, Delorme R, Chaste P, Leblond C, Lemière N, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Amsellem F, Gillberg IC, Mouren-Simeoni MC, Herbrecht E, Fauchereau F, Toro R, Gillberg C, Leboyer M, Bourgeron T, , Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations., PLoS One 2011 Mar; 6(3): e17289.
• 2011
  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, Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability, BMC Med. Genet. 2011;12:17.
• 2011
  Ey E, Leblond CS, Bourgeron T, Behavioral profiles of mouse models for autism spectrum disorders, Autism Res 2011 Feb;4(1):5-16.
• 2010
  Ben-Abdallah M, Bondet V, Fauchereau F, Béguin P, Goubran-Botros H, Pagan C, Bourgeron T, Bellalou J, Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae, Protein Expr. Purif. 2011 Jan;75(1):114-8.
• 2010
  Chaste P, Clement N, Mercati O, Guillaume JL, Delorme R, Botros HG, Pagan C, Périvier S, Scheid I, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Gillberg C, Serrano E, Lemière 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 population, PLoS ONE 2010;5(7):e11495.
• 2010
  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.
• 2010
  Delorme R, Betancur C, Scheid I, Anckarsäter H, Chaste P, Jamain S, Schuroff F, Nygren G, Herbrecht E, Dumaine A, Mouren MC, Råstam M, Leboyer M, Gillberg C, Bourgeron T, Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls, BMC Med. Genet. 2010;11:108.
• 2009
  Bourgeron T, A synaptic trek to autism, Curr. Opin. Neurobiol. 2009 Apr;19(2):231-4.
• 2009
  Bourgeron T, Leboyer M, Delorme R, [Autism: more evidence of a genetic cause], Bull. Acad. Natl. Med. 2009 Feb;193(2):299-304; discussion 304-5.
• 2009
  Gong X, Delorme R, Fauchereau F, Durand CM, Chaste P, Betancur C, Goubran-Botros H, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Kopp S, Mouren-Simeoni MC, Gillberg C, Leboyer M, Bourgeron T, An investigation of ribosomal protein L10 gene in autism spectrum disorders, BMC Med. Genet. 2009;10:7.
• 2008
  Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Gillberg C, Moreno-De-Luca D, Carone S, Nummela I, Rossi M, Battaglia A, , Jarvela I, Maestrini E, Bourgeron T, Analysis of X chromosome inactivation in autism spectrum disorders, Am. J. Med. Genet. B Neuropsychiatr. Genet. 2008 Sep;147B(6):830-5.
• 2008
  Durand CM, Chaste P, Fauchereau F, Betancur C, Leboyer M, Bourgeron T, [Alterations in synapsis formation and function in autism disorders], Med Sci (Paris) 2008 Jan;24(1):25-8.
• 2006
  Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsäter H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T, Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders, Nat. Genet. 2007 Jan;39(1):25-7.
• 2006
  Durand CM, Kappeler C, Betancur C, Delorme R, Quach H, Goubran-Botros H, Melke J, Nygren G, Chabane N, Bellivier F, Szoke A, Schurhoff F, Rastam M, Anckarsäter H, Gillberg C, Leboyer M, Bourgeron T, Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders, Am. J. Med. Genet. B Neuropsychiatr. Genet. 2006 Jan;141B(1):67-70.
• 2003
  Jamain S, Betancur C, Giros B, Leboyer M, Bourgeron T, [Genetics of autism: from genome scans to candidate genes], Med Sci (Paris) 2003 Nov;19(11):1081-90.
• 2003
  Bourgeron T, Giros B, Genetic markers in psychiatric genetics, Methods Mol. Med. 2003;77:63-98.