• 2025
  F. de Chaumont*, R. Icick, P*. Gorwood, S. Granon, B. Forget, C. Bouarab, J. Mattioni , T. Bourgeron, U. Maskos N. Ramoz, M. Besson, The influence of CHRNA5 and D398N missense variation onsocial and emotional behaviors in rodents and humans, Translational Psychiatry (2025) 15:507.
• 2025
  de Chaumont F, Yvenou G, Perez-Villalba A, Hérault Y, Bourgeron T, Ey E, Female C57BL/6J mice perform distinctive urination behaviour accompanied by ultrasonic vocalisation sequences with a stereotyped temporal organisation., Behav Brain Res 2025 Oct; 495(): 115788.
• 2025
  Seelemeyer H, Gurr C, Leyhausen J, Berg LM, Pretzsch CM, Schäfer T, Hermila B, Freitag CM, Loth E, Oakley B, Mason L, Buitelaar JK, Beckmann CF, Floris DL, Charman T, Banaschewski T, Jones E, Bourgeron T, , Murphy D, Ecker C, Decomposing the Brain in Autism: Linking Behavioral Domains to Neuroanatomical Variation and Genomic Underpinnings., Biol Psychiatry Cogn Neurosci Neuroimaging 2025 Oct; 10(10): 1067-1077.
• 2025
  Nielsen TT, Bali P, Grove J, Mohr-Jensen C, Werge T, Dalsgaard S, Børglum AD, Sonuga-Barke E, Minnis H, Demontis D, , Corfield EC, Tbartz van Elst L, Mattheisen M, de Wit MM, Uddin MJ, Anney RJL, Scherer SW, Bourgeron T, Polderman TJC, Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses., JAMA Psychiatry 2025 Aug; 82(8): 790-800.
• 2025
  Ecker C, Pretzsch CM, Leyhausen J, Berg LM, Gurr C, Seelemeyer H, McAlonan G, Puts NA, Loth E, Dell'Aqua F, Mason L, Charman T, Oakley B, Bourgeron T, Beckmann C, Buitelaar JK, Arango C, Banaschewski T, Chiocchetti AG, Freitag CM, Hattingen E, Krueger-Burg D, Schmeisser MJ, Repple J, Reif A, Murphy DG, Transcriptomic decoding of surface-based imaging phenotypes and its application to pharmacotranscriptomics., Nat Commun 2025 Jul; 16(1): 6727.
• 2025
  Leyhausen J, Gurr C, Berg LM, Seelemeyer H, Hermila B, Schäfer T, Chiocchetti AG, Pretzsch CM, Loth E, Oakley B, Buitelaar JK, Beckmann CF, Charman T, Bourgeron T, Barthome E, Banaschewski T, Jones EJH, , Murphy D, Ecker C, Parsing Autism Heterogeneity: Transcriptomic Subgrouping of Imaging-Derived Phenotypes in Autism., Biol Psychiatry Cogn Neurosci Neuroimaging 2025 Jul; (): .
• 2025
  Goldshtein I, Sadaka Y, Amit G, Kasir N, Bourgeron T, Warrier V, Akiva P, Avgil Tsadok M, Zimmerman DR, Breastfeeding Duration and Child Development., JAMA Netw Open 2025 Mar; 8(3): e251540.
• 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.
• 2025
  Floris DL, Llera A, Zabihi M, Moessnang C, Jones EJH, Mason L, Haartsen R, Holz NE, Mei T, Elleaume C, Vieira BH, Pretzsch CM, Forde NJ, Baumeister S, Dell'Acqua F, Durston S, Banaschewski T, Ecker C, Holt RJ, Baron-Cohen S, Bourgeron T, Charman T, Loth E, Murphy DGM, Buitelaar JK, Beckmann CF, , Langer N, A multimodal neural signature of face processing in autism within the fusiform gyrus., Nat Ment Health 2025 ; 3(1): 31-45.
• 2025
  Black MH, Remnélius KL, Alehagen L, Bourgeron T, Bölte S, From Symptomatology to Functioning – Applying the ICF to Autism Measures to Facilitate Neurodiversity-Affirmative Data Harmonization., J Autism Dev Disord 2025 Jan; 55(1): 114-129.
• 2024
  Pretzsch CM, Arenella M, Lerch JP, Lombardo MV, Beckmann C, Schaefer T, Leyhausen J, Gurr C, Bletsch A, Berg LM, Seelemeyer H, Floris DL, Oakley B, Loth E, Bourgeron T, Charman T, Buitelaar J, McAlonan G, Murphy D, Ecker C, Patterns of Brain Maturation in Autism and Their Molecular Associations., JAMA Psychiatry 2024 Dec; 81(12): 1253-1264.
• 2024
  Black MH, Buitelaar J, Charman T, Ecker C, Gallagher L, Hens K, Jones E, Murphy D, Sadaka Y, Schaer M, St Pourcain B, Wolke D, Bonnot-Briey S, Bourgeron T, Bölte S, Conceptual framework for data harmonisation in mental health using the International Classification of Functioning, Disability and Health: an example with the R2D2-MH consortium., BMJ Ment Health 2024 Nov; 27(1): .
• 2024
  Tönis KJM, Drossaert CHC, Ten Klooster PM, Schaer M, Bourgeron T, Buitelaar JK, Sadaka Y, Freitag CM, Lapidus KM, Chiocchetti AG, Staal WG, Bohlmeijer ET, Effectiveness of a positive psychology and mindfulness-based app on mental health for parents of children with a neurodevelopmental disorder: study protocol of a pragmatic international randomized controlled trial., Trials 2024 Jun; 25(1): 412.
• 2024
  Bloomfield M, Lautarescu A, Heraty S, Douglas S, Violland P, Plas R, Ghosh A, Van den Bosch K, Eaton E, Absoud M, Battini R, Blázquez Hinojosa A, Bolshakova N, Bölte S, Bonanni P, Borg J, Calderoni S, Calvo Escalona R, Castelo-Branco M, Castro-Fornieles J, Caro P, Cliquet F, Danieli A, Delorme R, Elia M, Hempel M, Leblond CS, Madeira N, McAlonan G, Milone R, Molloy CJ, Mouga S, Montiel V, Pina Rodrigues A, Schaaf CP, Serrano M, Tammimies K, Tye C, Vigevano F, Oliveira G, Mazzone B, O'Neill C, Pender J, Romero V, Tillmann J, Oakley B, Murphy DGM, Gallagher L, Bourgeron T, Chatham C, Charman T, European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry., BMJ Open 2024 Jun; 14(6): e080746.
• 2024
  Leyhausen J, Schäfer T, Gurr C, Berg LM, Seelemeyer H, Pretzsch CM, Loth E, Oakley B, Buitelaar JK, Beckmann CF, Floris DL, Charman T, Bourgeron T, Banaschewski T, Jones EJH, Tillmann J, Chatham C, , Murphy DG, Ecker C, Differences in Intrinsic Gray Matter Connectivity and Their Genomic Underpinnings in Autism Spectrum Disorder., Biol Psychiatry 2024 Jan; 95(2): 175-186.
• 2023
  Lefebvre A, Traut N, Pedoux A, Maruani A, Beggiato A, Elmaleh M, Germanaud D, Amestoy A, Ly-Le Moal M, Chatham C, Murtagh L, Bouvard M, Alisson M, Leboyer M, Bourgeron T, Toro R, Dumas G, Moreau C, Delorme R, Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications., Mol Autism 2023 Nov; 14(1): 45.
• 2023
  Dejean C, Dupont T, Verpy E, Gonçalves N, Coqueran S, Michalski N, Pucheu S, Bourgeron T, Gourévitch B, Detecting Central Auditory Processing Disorders in Awake Mice., Brain Sci 2023 Oct; 13(11): .
• 2023
  Berg LM, Gurr C, Leyhausen J, Seelemeyer H, Bletsch A, Schaefer T, Pretzsch CM, Oakley B, Loth E, Floris DL, Buitelaar JK, Beckmann CF, Banaschewski T, Charman T, Jones EJH, Tillmann J, Chatham CH, Bourgeron T, , Murphy DG, Ecker C, The neuroanatomical substrates of autism and ADHD and their link to putative genomic underpinnings., Mol Autism 2023 Oct; 14(1): 36.
• 2023
  Heraty S, Lautarescu A, Belton D, Boyle A, Cirrincione P, Doherty M, Douglas S, Plas JRD, Van Den Bosch K, Violland P, Tercon J, Ruigrok A, Murphy DGM, Bourgeron T, Chatham C, Loth E, Oakley B, McAlonan GM, Charman T, Puts N, Gallagher L, Jones EJH, Bridge-building between communities: Imagining the future of biomedical autism research., Cell 2023 Aug; 186(18): 3747-3752.
• 2023
  Isakoglou C, Haak KV, Wolfers T, Floris DL, Llera A, Oldehinkel M, Forde NJ, Oakley BFM, Tillmann J, Holt RJ, Moessnang C, Loth E, Bourgeron T, Baron-Cohen S, Charman T, Banaschewski T, Murphy DGM, Buitelaar JK, Marquand AF, Beckmann CF, Fine-grained topographic organization within somatosensory cortex during resting-state and emotional face-matching task and its association with ASD traits., Transl Psychiatry 2023 Jul; 13(1): 270.
• 2023
  Schön M, Lapunzina P, Nevado J, Mattina T, Gunnarsson C, Hadzsiev K, Verpelli C, Bourgeron T, Jesse S, van Ravenswaaij-Arts CMA, , Hennekam RC, Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome., Eur J Med Genet 2023 Jul; 66(7): 104754.
• 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 Jul; 29(7): 1671-1680.
• 2023
  de Coo IFM, Jesse S, Le TL, Sala C, Consensus recommendations on Epilepsy in Phelan-McDermid syndrome., Eur J Med Genet 2023 Jun; 66(6): 104746.
• 2023
  Pretzsch CM, Floris DL, Schäfer T, Bletsch A, Gurr C, Lombardo MV, Chatham CH, Tillmann J, Charman T, Arenella M, Jones E, Ambrosino S, Bourgeron T, Dumas G, Cliquet F, Leblond CS, Loth E, Oakley B, Buitelaar JK, Baron-Cohen S, Beckmann CF, Persico AM, Banaschewski T, Durston S, Freitag CM, , Murphy DGM, Ecker C, Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism., Mol Psychiatry 2023 May; 28(5): 2158-2169.
• 2023
  Vitrac A, Leblond CS, Rolland T, Cliquet F, Mathieu A, Maruani A, Delorme R, Schön M, Grabrucker AM, van Ravenswaaij-Arts C, Phelan K, Tabet AC, Bourgeron T, Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome., Eur J Med Genet 2023 May; 66(5): 104732.
• 2023
  Moreau CA, Kumar K, Harvey A, Huguet G, Urchs SGW, 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 2023 Apr; 146(4): 1686-1696.
• 2023
  Baumeister S, Moessnang C, Bast N, Hohmann S, Aggensteiner P, Kaiser A, Tillmann J, Goyard D, Charman T, Ambrosino S, Baron-Cohen S, Beckmann C, Bölte S, Bourgeron T, Rausch A, Crawley D, Dell'Acqua F, Dumas G, Durston S, Ecker C, Floris DL, Frouin V, Hayward H, Holt R, Johnson MH, Jones EJH, Lai MC, Lombardo MV, Mason L, Oakley B, Oldehinkel M, Persico AM, San José Cáceres A, Wolfers T, Loth E, Murphy DGM, Buitelaar JK, Tost H, Meyer-Lindenberg A, Banaschewski T, Brandeis D, Processing of social and monetary rewards in autism spectrum disorders., Br J Psychiatry 2023 Mar; 222(3): 100-111.
• 2023
  Lefebvre A, Tillmann J, Cliquet F, Amsellem F, Maruani A, Leblond C, Beggiato A, Germanaud D, Amestoy A, Ly-Le Moal M, Umbricht D, Chatham C, Murtagh L, Bouvard M, Leboyer M, Charman T, Bourgeron T, Delorme R, Dumas G, Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways., Autism Res 2023 Feb; 16(2): 364-378.
• 2023
  Hollestein V, Poelmans G, Forde NJ, Beckmann CF, Ecker C, Mann C, Schäfer T, Moessnang C, Baumeister S, Banaschewski T, Bourgeron T, Loth E, Dell'Acqua F, Murphy DGM, Puts NA, Tillmann J, Charman T, Jones EJH, Mason L, Ambrosino S, Holt R, Bölte S, Buitelaar JK, Naaijen J, Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure., Transl Psychiatry 2023 Jan; 13(1): 18.
• 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.
• 2023
  Floris DL, Peng H, Warrier V, Lombardo MV, Pretzsch CM, Moreau C, Tsompanidis A, Gong W, Mennes M, Llera A, van Rooij D, Oldehinkel M, Forde NJ, Charman T, Tillmann J, Banaschewski T, Moessnang C, Durston S, Holt RJ, Ecker C, Dell'Acqua F, Loth E, Bourgeron T, Murphy DGM, Marquand AF, Lai MC, Buitelaar JK, Baron-Cohen S, Beckmann CF, The Link Between Autism and Sex-Related Neuroanatomy, and Associated Cognition and Gene Expression., Am J Psychiatry 2023 Jan; 180(1): 50-64.
• 2023
  Gaudfernau F, Lefebvre A, Engemann DA, Pedoux A, Bánki A, Baillin F, Landman B, Maruani A, Amsellem F, Bourgeron T, Delorme R, Dumas G, Cortico-Cerebellar neurodynamics during social interaction in Autism Spectrum Disorders., Neuroimage Clin 2023 ; 39(): 103465.
• 2022
  Warrier V, Zhang X, Reed P, Havdahl A, Moore TM, Cliquet F, Leblond CS, Rolland T, Rosengren A, , , , Rowitch DH, Hurles ME, Geschwind DH, Børglum AD, Robinson EB, Grove J, Martin HC, Bourgeron T, Baron-Cohen S, Genetic correlates of phenotypic heterogeneity in autism., Nat Genet 2022 Sep; 54(9): 1293-1304.
• 2022
  Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates TC, Bernard M, Blokland K, Bonte M, Børglum AD, Bourgeron T, Brandeis D, Ceroni F, Csépe V, Dale PS, de Jong PF, DeFries JC, Démonet JF, Demontis D, Feng Y, Gordon SD, Guger SL, Hayiou-Thomas ME, Hernández-Cabrera JA, Hottenga JJ, Hulme C, Kere J, Kerr EN, Koomar T, Landerl K, Leonard GT, Lovett MW, Lyytinen H, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT, Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus F, Richer L, Simpson NH, Smith SD, Snowling MJ, Stein J, Strug LJ, Talcott JB, Tiemeier H, van der Schroeff MP, Verhoef E, Watkins KE, Wilkinson M, Wright MJ, Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-Myhsok B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Reilly S, Schulte-Körne G, Tomblin JB, van Bergen E, Whitehouse AJO, Willcutt EG, St Pourcain B, Francks C, Fisher SE, Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people., Proc Natl Acad Sci U S A 2022 Aug; 119(35): e2202764119.
• 2022
  Mason L, Moessnang C, Chatham C, Ham L, Tillmann J, Dumas G, Ellis C, Leblond CS, Cliquet F, Bourgeron T, Beckmann C, Charman T, Oakley B, Banaschewski T, Meyer-Lindenberg A, Baron-Cohen S, Bölte S, Buitelaar JK, Durston S, Loth E, Oranje B, Persico A, Dell'Acqua F, Ecker C, Johnson MH, Murphy D, Jones EJH, Stratifying the autistic phenotype using electrophysiological indices of social perception., Sci Transl Med 2022 Aug; 14(658): eabf8987.
• 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.
• 2022
  Garcés P, Baumeister S, Mason L, Chatham CH, Holiga S, Dukart J, Jones EJH, Banaschewski T, Baron-Cohen S, Bölte S, Buitelaar JK, Durston S, Oranje B, Persico AM, Beckmann CF, Bougeron T, Dell'Acqua F, Ecker C, Moessnang C, Charman T, Tillmann J, Murphy DGM, Johnson M, Loth E, Brandeis D, Hipp JF, Resting state EEG power spectrum and functional connectivity in autism: a cross-sectional analysis., Mol Autism 2022 May; 13(1): 22.
• 2022
  Pretzsch CM, Schäfer T, Lombardo MV, Warrier V, Mann C, Bletsch A, Chatham CH, Floris DL, Tillmann J, Yousaf A, Jones E, Charman T, Ambrosino S, Bourgeron T, Dumas G, Loth E, Oakley B, Buitelaar JK, Cliquet F, Leblond CS, Baron-Cohen S, Beckmann CF, Banaschewski T, Durston S, Freitag CM, , Murphy DGM, Ecker C, Neurobiological Correlates of Change in Adaptive Behavior in Autism., Am J Psychiatry 2022 May; 179(5): 336-349.
• 2022
  Ecker C, Pretzsch CM, Bletsch A, Mann C, Schaefer T, Ambrosino S, Tillmann J, Yousaf A, Chiocchetti A, Lombardo MV, Warrier V, Bast N, Moessnang C, Baumeister S, Dell'Acqua F, Floris DL, Zabihi M, Marquand A, Cliquet F, Leblond C, Moreau C, Puts N, Banaschewski T, Jones EJH, Mason L, Bölte S, Meyer-Lindenberg A, Persico AM, Durston S, Baron-Cohen S, Spooren W, Loth E, Freitag CM, Charman T, Dumas G, Bourgeron T, Beckmann CF, Buitelaar JK, Murphy DGM, Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder., Am J Psychiatry 2022 Mar; 179(3): 242-254.
• 2022
  Phelan K, Boccuto L, Powell CM, Boeckers TM, van Ravenswaaij-Arts C, Rogers RC, Sala C, Verpelli C, Thurm A, Bennett WE, Winrow CJ, Garrison SR, Toro R, Bourgeron T, Phelan-McDermid syndrome: a classification system after 30 years of experience., Orphanet J Rare Dis 2022 Jan; 17(1): 27.
• 2022
  Cooke J, Molloy CJ, Cáceres ASJ, Dinneen T, Bourgeron T, Murphy D, Gallagher L, Loth E, The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions., Front Neurosci 2022 ; 16(): 806990.
• 2021
  Loureiro LO, Howe JL, Reuter MS, Iaboni A, Calli K, Roshandel D, Pritišanac I, Moses A, Forman-Kay JD, Trost B, Zarrei M, Rennie O, Lau LYS, Marshall CR, Srivastava S, Godlewski B, Buttermore ED, Sahin M, Hartley D, Frazier T, Vorstman J, Georgiades S, Lewis SME, Szatmari P, Bradley CAL, Tabet AC, Willems M, Lumbroso S, Piton A, Lespinasse J, Delorme R, Bourgeron T, Anagnostou E, Scherer SW, A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder., NPJ Genom Med 2021 Nov; 6(1): 91.
• 2021
  Loth E, Ahmad J, Chatham C, López B, Carter B, Crawley D, Oakley B, Hayward H, Cooke J, San José Cáceres A, Bzdok D, Jones E, Charman T, Beckmann C, Bourgeron T, Toro R, Buitelaar J, Murphy D, Dumas G, The meaning of significant mean group differences for biomarker discovery., PLoS Comput Biol 2021 Nov; 17(11): e1009477.
• 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 Nov; 14(11): 2373-2382.
• 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.
• 2021
  Huguet G, Schramm C, Douard E, Tamer P, Main A, Monin P, England J, Jizi K, Renne T, Poirier M, Nowak S, Martin CO, Younis N, Knoth IS, Jean-Louis M, Saci Z, Auger M, Tihy F, Mathonnet G, Maftei C, Léveillé F, Porteous D, Davies G, Redmond P, Harris SE, Hill WD, Lemyre E, Schumann G, Bourgeron T, Pausova Z, Paus T, Karama S, Lippe S, Deary IJ, Almasy L, Labbe A, Glahn D, Greenwood CMT, Jacquemont S, Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability., Mol Psychiatry 2021 Jun; 26(6): 2663-2676.
• 2021
  Bertelsen N, Landi I, Bethlehem RAI, Seidlitz J, Busuoli EM, Mandelli V, Satta E, Trakoshis S, Auyeung B, Kundu P, Loth E, Dumas G, Baumeister S, Beckmann CF, Bölte S, Bourgeron T, Charman T, Durston S, Ecker C, Holt RJ, Johnson MH, Jones EJH, Mason L, Meyer-Lindenberg A, Moessnang C, Oldehinkel M, Persico AM, Tillmann J, Williams SCR, Spooren W, Murphy DGM, Buitelaar JK, , Baron-Cohen S, Lai MC, Lombardo MV, Imbalanced social-communicative and restricted repetitive behavior subtypes of autism spectrum disorder exhibit different neural circuitry., Commun Biol 2021 May; 4(1): 574.
• 2021
  Dumas G, Malesys S, Bourgeron T, Systematic detection of brain protein-coding genes under positive selection during primate evolution and their roles in cognition., Genome Res 2021 Mar; 31(3): 484-496.
• 2021
  Pagan C, Benabou M, Leblond C, Cliquet F, Mathieu A, Lemière N, Goubran-Botros H, Delorme R, Leboyer M, Callebert J, Bourgeron T, Launay JM, Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders., Transl Psychiatry 2021 Jan; 11(1): 23.
• 2021
  Lutz AK, Pérez Arévalo A, Ioannidis V, Stirmlinger N, Demestre M, Delorme R, Bourgeron T, Boeckers TM, SHANK2 Mutations Result in Dysregulation of the ERK1/2 Pathway in Human Induced Pluripotent Stem Cells-Derived Neurons and Shank2(-/-) Mice., Front Mol Neurosci 2021 ; 14(): 773571.
• 2021
  de Chaumont F, Lemière N, Coqueran S, Bourgeron T, Ey E, LMT USV Toolbox, a Novel Methodological Approach to Place Mouse Ultrasonic Vocalizations in Their Behavioral Contexts-A Study in Female and Male C57BL/6J Mice and in Shank3 Mutant Females., Front Behav Neurosci 2021 ; 15(): 735920.
• 2021
  Kikusui T, Sonobe M, Yoshida Y, Nagasawa M, Ey E, de Chaumont F, Bourgeron T, Nomoto K, Mogi K, Testosterone Increases the Emission of Ultrasonic Vocalizations With Different Acoustic Characteristics in Mice., Front Psychol 2021 ; 12(): 680176.
• 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 2021 Apr; 70(3): e12713.
• 2020
  Zabihi M, Floris DL, Kia SM, Wolfers T, Tillmann J, Arenas AL, Moessnang C, Banaschewski T, Holt R, Baron-Cohen S, Loth E, Charman T, Bourgeron T, Murphy D, Ecker C, Buitelaar JK, Beckmann CF, Marquand A, Fractionating autism based on neuroanatomical normative modeling., Transl Psychiatry 2020 Nov; 10(1): 384.
• 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 2021 Jul; 26(7): 3004-3017.
• 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 2021 Jan; 16(1-2): 72-83.
• 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 2021 Jan; 178(1): 87-98.
• 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 Aug; 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 Jun; 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 May; 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 Apr; 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
  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
  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
  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.