| Year |
Citation |
Score |
| 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, et al. Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications. Molecular Autism. 14: 45. PMID 38012709 DOI: 10.1186/s13229-023-00576-z |
0.677 |
|
| 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. Clinical. 39: 103465. PMID 37454469 DOI: 10.1016/j.nicl.2023.103465 |
0.712 |
|
| 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, ... ... Bourgeron T, et al. Phenotypic effects of genetic variants associated with autism. Nature Medicine. PMID 37365347 DOI: 10.1038/s41591-023-02408-2 |
0.309 |
|
| 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, ... ... Bourgeron T, et al. Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of mutant mice. Frontiers in Molecular Neuroscience. 16: 1139118. PMID 37008785 DOI: 10.3389/fnmol.2023.1139118 |
0.718 |
|
| 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, et al. Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism. Molecular Psychiatry. PMID 36991132 DOI: 10.1038/s41380-023-02016-z |
0.685 |
|
| 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, et al. Processing of social and monetary rewards in autism spectrum disorders. The British Journal of Psychiatry : the Journal of Mental Science. 1-12. PMID 36700346 DOI: 10.1192/bjp.2022.157 |
0.702 |
|
| 2022 |
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, ... ... Bourgeron T, et al. Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways. Autism Research : Official Journal of the International Society For Autism Research. PMID 36464763 DOI: 10.1002/aur.2861 |
0.682 |
|
| 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, et al. Stratifying the autistic phenotype using electrophysiological indices of social perception. Science Translational Medicine. 14: eabf8987. PMID 35976994 DOI: 10.1126/scitranslmed.abf8987 |
0.702 |
|
| 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, ... ... Bourgeron T, et al. Genetic correlates of phenotypic heterogeneity in autism. Nature Genetics. PMID 35654973 DOI: 10.1038/s41588-022-01072-5 |
0.31 |
|
| 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, et al. Neurobiological Correlates of Change in Adaptive Behavior in Autism. The American Journal of Psychiatry. appiajp21070711. PMID 35331004 DOI: 10.1176/appi.ajp.21070711 |
0.693 |
|
| 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 Deletions. Frontiers in Neuroscience. 16: 806990. PMID 35250452 DOI: 10.3389/fnins.2022.806990 |
0.311 |
|
| 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, et al. The meaning of significant mean group differences for biomarker discovery. Plos Computational Biology. 17: e1009477. PMID 34793435 DOI: 10.1371/journal.pcbi.1009477 |
0.643 |
|
| 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, ... ... Bourgeron T, et al. A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder. Npj Genomic Medicine. 6: 91. PMID 34737294 DOI: 10.1038/s41525-021-00254-0 |
0.338 |
|
| 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 Mutant Females. Frontiers in Behavioral Neuroscience. 15: 735920. PMID 34720899 DOI: 10.3389/fnbeh.2021.735920 |
0.722 |
|
| 2021 |
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, ... ... Bourgeron T, et al. Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder. The American Journal of Psychiatry. appiajp202120050630. PMID 34503340 DOI: 10.1176/appi.ajp.2021.20050630 |
0.711 |
|
| 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 Research : Official Journal of the International Society For Autism Research. PMID 34278736 DOI: 10.1002/aur.2570 |
0.312 |
|
| 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. Frontiers in Psychology. 12: 680176. PMID 34248780 DOI: 10.3389/fpsyg.2021.680176 |
0.673 |
|
| 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, et al. Imbalanced social-communicative and restricted repetitive behavior subtypes of autism spectrum disorder exhibit different neural circuitry. Communications Biology. 4: 574. PMID 33990680 DOI: 10.1038/s42003-021-02015-2 |
0.706 |
|
| 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 Research. PMID 33441416 DOI: 10.1101/gr.262113.120 |
0.659 |
|
| 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. Translational Psychiatry. 11: 23. PMID 33414449 DOI: 10.1038/s41398-020-01125-5 |
0.314 |
|
| 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. Journal of Pineal Research. e12713. PMID 33368564 DOI: 10.1111/jpi.12713 |
0.647 |
|
| 2020 |
Baillin F, Lefebvre A, Pedoux A, Beauxis Y, Engemann DA, Maruani A, Amsellem F, Kelso JAS, Bourgeron T, Delorme R, Dumas G. Interactive Psychometrics for Autism With the Human Dynamic Clamp: Interpersonal Synchrony From Sensorimotor to Sociocognitive Domains. Frontiers in Psychiatry. 11: 510366. PMID 33324246 DOI: 10.3389/fpsyt.2020.510366 |
0.689 |
|
| 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, ... ... Bourgeron T, et al. Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia. Nature Communications. 11: 5272. PMID 33077750 DOI: 10.1038/s41467-020-18997-2 |
0.703 |
|
| 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. Social Cognitive and Affective Neuroscience. PMID 33031496 DOI: 10.1093/scan/nsaa141 |
0.662 |
|
| 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, ... ... Bourgeron T, et al. Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome. The American Journal of Psychiatry. appiajp202019080834. PMID 32911998 DOI: 10.1176/Appi.Ajp.2020.19080834 |
0.366 |
|
| 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. Scientific Reports. 10: 13315. PMID 32769989 DOI: 10.1038/S41598-020-70056-4 |
0.336 |
|
| 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, ... ... Bourgeron T, et al. The role of rare compound heterozygous events in autism spectrum disorder. Translational Psychiatry. 10: 204. PMID 32572023 DOI: 10.1038/S41398-020-00866-7 |
0.369 |
|
| 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, ... ... Bourgeron T, et al. Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles. Science Translational Medicine. 12. PMID 32522805 DOI: 10.1126/Scitranslmed.Aaz3267 |
0.337 |
|
| 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. American Journal of Human Genetics. PMID 32359473 DOI: 10.1016/J.Ajhg.2020.04.004 |
0.431 |
|
| 2020 |
Ey E, Bourgeron T, Boeckers TM, Kim E, Han K. Editorial: Shankopathies: Shank Protein Deficiency-Induced Synaptic Diseases. Frontiers in Molecular Neuroscience. 13: 11. PMID 32116544 DOI: 10.3389/Fnmol.2020.00011 |
0.686 |
|
| 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, ... ... Bourgeron T, et al. Polygenic Architecture of Human Neuroanatomical Diversity. Cerebral Cortex (New York, N.Y. : 1991). PMID 32109272 DOI: 10.1093/Cercor/Bhz241 |
0.307 |
|
| 2019 |
Florian RT, Kraft F, Leitão E, Kaya S, Klebe S, Magnin E, van Rootselaar AF, Buratti J, Kühnel T, Schröder C, Giesselmann S, Tschernoster N, Altmueller J, Lamiral A, Keren B, ... ... Bourgeron T, et al. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3. Nature Communications. 10: 4919. PMID 31664039 DOI: 10.1038/S41467-019-12763-9 |
0.303 |
|
| 2019 |
de Lombares C, Heude E, Alfama G, Fontaine A, Hassouna R, Vernochet C, de Chaumont F, Olivo-Marin C, Ey E, Parnaudeau S, Tronche F, Bourgeron T, Luquet S, Levi G, Narboux-Nême N. and expression in GABAergic neurons controls behavior, metabolism, healthy aging and lifespan. Aging. 11. PMID 31514171 DOI: 10.18632/aging.102141 |
0.694 |
|
| 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. Nature Biomedical Engineering. PMID 31110290 DOI: 10.1038/S41551-019-0396-1 |
0.741 |
|
| 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. 197: 527-543. PMID 31063817 DOI: 10.1016/J.Neuroimage.2019.04.056 |
0.33 |
|
| 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, ... ... Bourgeron T, et al. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. American Journal of Human Genetics. PMID 31031012 DOI: 10.1016/J.Ajhg.2019.03.022 |
0.365 |
|
| 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. Frontiers in Psychiatry. 10: 11. PMID 30787884 DOI: 10.3389/Fpsyt.2019.00011 |
0.682 |
|
| 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, ... ... Bourgeron T, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77. PMID 30741946 DOI: 10.1038/S41398-019-0402-0 |
0.346 |
|
| 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, ... ... Bourgeron T, et al. Both rare and common genetic variants contribute to autism in the Faroe Islands. Npj Genomic Medicine. 4: 1. PMID 30675382 DOI: 10.1038/S41525-018-0075-2 |
0.434 |
|
| 2019 |
Gouder L, Vitrac A, Goubran-Botros H, Danckaert A, Tinevez JY, André-Leroux G, Atanasova E, Lemière N, Biton A, Leblond CS, Poulet A, Boland A, Deleuze JF, Benchoua A, Delorme R, ... Bourgeron T, et al. Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations. Scientific Reports. 9: 94. PMID 30643170 DOI: 10.1038/S41598-018-36993-X |
0.387 |
|
| 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. Behavioural Brain Research. 362: 266-272. PMID 30639511 DOI: 10.1016/J.Bbr.2019.01.014 |
0.358 |
|
| 2019 |
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. Journal of Applied Genetics. 60: 49-56. PMID 30284680 DOI: 10.1007/S13353-018-0472-3 |
0.476 |
|
| 2019 |
Rolland T, Cliquet F, Anney R, Mathieu A, Huguet G, Leblond C, Douard E, Fartek S, Maruani A, Amsellem F, Packer A, Jacquemont S, Delorme R, Bourgeron T. 5 DIFFERENCES IN THE GENETIC BACKGROUND CONTRIBUTE TO RISK AND RESILIENCE TO AUTISM European Neuropsychopharmacology. 29: S61. DOI: 10.1016/J.Euroneuro.2019.07.146 |
0.325 |
|
| 2019 |
Warrier V, Toro R, Chakrabarti B, Won H, Børglum A, Grove J, Hinds DA, Bourgeron T, Baron-Cohen S. SA19SOCIAL AND NON-SOCIAL DOMAINS OF AUTISM ARE GENETICALLY DISSOCIABLE European Neuropsychopharmacology. 29: S1197-S1198. DOI: 10.1016/J.Euroneuro.2018.08.241 |
0.355 |
|
| 2019 |
Huguet G, Schramm C, Douard E, Jiang L, Labbe A, Poline J, Loth E, Toro R, Schumann G, Conrod P, Pausova Z, Greenwood C, Paus T, Bourgeron T, Jacquemont S. Quantifying The Effect Of Copy-Number Variants On General Intelligence In Unselected Populations European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.119 |
0.362 |
|
| 2018 |
Ey E, Torquet N, de Chaumont F, Lévi-Strauss J, Ferhat AT, Le Sourd AM, Boeckers TM, Bourgeron T. Mutant Mice Display Hyperactivity Insensitive to Methylphenidate and Reduced Flexibility in Social Motivation, but Normal Social Recognition. Frontiers in Molecular Neuroscience. 11: 365. PMID 30337855 DOI: 10.3389/Fnmol.2018.00365 |
0.753 |
|
| 2018 |
Lefebvre A, Delorme R, Delanoë C, Amsellem F, Beggiato A, Germanaud D, Bourgeron T, Toro R, Dumas G. Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity. Frontiers in Neuroscience. 12: 662. PMID 30327586 DOI: 10.3389/Fnins.2018.00662 |
0.683 |
|
| 2018 |
Septier M, Peyre H, Amsellem F, Beggiato A, Maruani A, Poumeyreau M, Amestoy A, Scheid I, Gaman A, Bolognani F, Honey G, Bouquet C, Ly-Le Moal M, Bouvard M, Leboyer M, ... Bourgeron T, et al. Increased risk of ADHD in families with ASD. European Child & Adolescent Psychiatry. PMID 30267210 DOI: 10.1007/S00787-018-1206-0 |
0.385 |
|
| 2018 |
Aubart M, Gazal S, Arnaud P, Benarroch L, Gross MS, Buratti J, Boland A, Meyer V, Zouali H, Hanna N, Milleron O, Stheneur C, Bourgeron T, Desguerre I, Jacob MP, et al. Association of modifiers and other genetic factors explain Marfan syndrome clinical variability. European Journal of Human Genetics : Ejhg. PMID 30087447 DOI: 10.1038/S41431-018-0164-9 |
0.352 |
|
| 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, ... ... Bourgeron T, et al. Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. Jama Psychiatry. PMID 29562078 DOI: 10.1001/Jamapsychiatry.2018.0039 |
0.337 |
|
| 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. Translational Psychiatry. 8: 35. PMID 29527006 DOI: 10.1038/S41398-017-0082-6 |
0.305 |
|
| 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, ... ... Bourgeron T, et al. A framework to identify contributing genes in patients with Phelan-McDermid syndrome. Npj Genomic Medicine. 2: 32. PMID 29263841 DOI: 10.1038/S41525-017-0035-2 |
0.394 |
|
| 2017 |
Benabou M, Rolland T, Leblond CS, Millot GA, Huguet G, Delorme R, Leboyer M, Pagan C, Callebert J, Maronde E, Bourgeron T. Heritability of the melatonin synthesis variability in autism spectrum disorders. Scientific Reports. 7: 17746. PMID 29255243 DOI: 10.1038/S41598-017-18016-3 |
0.398 |
|
| 2017 |
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. Biological Psychiatry. PMID 29146048 DOI: 10.1016/J.Biopsych.2017.09.029 |
0.4 |
|
| 2017 |
Charman T, Loth E, Tillmann J, Crawley D, Wooldridge C, Goyard D, Ahmad J, Auyeung B, Ambrosino S, Banaschewski T, Baron-Cohen S, Baumeister S, Beckmann C, Bölte S, Bourgeron T, et al. The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation. Molecular Autism. 8: 27. PMID 28649313 DOI: 10.1186/S13229-017-0145-9 |
0.707 |
|
| 2017 |
Loth E, Charman T, Mason L, Tillmann J, Jones EJH, Wooldridge C, Ahmad J, Auyeung B, Brogna C, Ambrosino S, Banaschewski T, Baron-Cohen S, Baumeister S, Beckmann C, Brammer M, ... ... Bourgeron T, et al. The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disorders. Molecular Autism. 8: 24. PMID 28649312 DOI: 10.1186/S13229-017-0146-8 |
0.714 |
|
| 2017 |
Ferhat AT, Halbedl S, Schmeisser MJ, Kas MJ, Bourgeron T, Ey E. Behavioural Phenotypes and Neural Circuit Dysfunctions in Mouse Models of Autism Spectrum Disorder. Advances in Anatomy, Embryology, and Cell Biology. 224: 85-101. PMID 28551752 DOI: 10.1007/978-3-319-52498-6_5 |
0.771 |
|
| 2017 |
Kleijer KTE, Huguet G, Tastet J, Bourgeron T, Burbach JPH. Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics. Advances in Anatomy, Embryology, and Cell Biology. 224: 1-25. PMID 28551748 DOI: 10.1007/978-3-319-52498-6_1 |
0.458 |
|
| 2017 |
Pagan C, Goubran-Botros H, Delorme R, Benabou M, Lemière N, Murray K, Amsellem F, Callebert J, Chaste P, Jamain S, Fauchereau F, Huguet G, Maronde E, Leboyer M, Launay JM, ... Bourgeron T, et al. Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders. Scientific Reports. 7: 2096. PMID 28522826 DOI: 10.1038/S41598-017-02152-X |
0.378 |
|
| 2017 |
Gillberg C, Fernell E, Kočovská E, Minnis H, Bourgeron T, Thompson L, Allely CS. The role of cholesterol metabolism and various steroid abnormalities in autism spectrum disorders: A hypothesis paper. Autism Research : Official Journal of the International Society For Autism Research. PMID 28401679 DOI: 10.1002/Aur.1777 |
0.361 |
|
| 2017 |
Kishimoto K, Nomura J, Ellegood J, Fukumoto K, Lerch JP, Moreno-De-Luca D, Bourgeron T, Tamada K, Takumi T. Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. PMID 28370817 DOI: 10.1111/Gtc.12487 |
0.358 |
|
| 2017 |
Pfaender S, Sauer AK, Hagmeyer S, Mangus K, Linta L, Liebau S, Bockmann J, Huguet G, Bourgeron T, Boeckers TM, Grabrucker AM. Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3. Scientific Reports. 7: 45190. PMID 28345660 DOI: 10.1038/Srep45190 |
0.348 |
|
| 2017 |
Lefebvre A, Delanoé C, Bourgeron T, Delorme R, Dumas G. Le rythme Alpha comme biomarqueur dans les troubles du spectre autistique : challenge de sa reproductibilité et son hétérogénéité Neurophysiologie Clinique/Clinical Neurophysiology. 47: 207-208. DOI: 10.1016/J.Neucli.2017.05.057 |
0.633 |
|
| 2017 |
Warrier V, Grasby K, Uzefovsky F, Toro R, Smith P, Chakrabarti B, Khadake J, Mawbey-Adamson E, Litterman N, Hottenga J, Lubke G, Boomsma D, Martin NG, Hatemi PK, Medland S, ... ... Bourgeron T, et al. A Meta-Analysis of Cognitive Empathy: Heritability and Correlates of the ‘Reading the Mind in the Eyes’ Test with Psychiatric Conditions, Psychological Traits and Subcortical Volumes European Neuropsychopharmacology. 27: S503-S504. DOI: 10.1016/J.Euroneuro.2016.09.608 |
0.307 |
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| 2016 |
Torquet N, de Chaumont F, Faure P, Bourgeron T, Ey E. mouseTube - a database to collaboratively unravel mouse ultrasonic communication. F1000research. 5: 2332. PMID 27830061 DOI: 10.12688/F1000Research.9439.1 |
0.722 |
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| 2016 |
Beggiato A, Peyre H, Maruani A, Scheid I, Rastam M, Amsellem F, Gillberg CI, Leboyer M, Bourgeron T, Gillberg C, Delorme R. Gender differences in autism spectrum disorders: Divergence among specific core symptoms. Autism Research : Official Journal of the International Society For Autism Research. PMID 27809408 DOI: 10.1002/Aur.1715 |
0.376 |
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| 2016 |
Torrico B, Chiocchetti AG, Bacchelli E, Trabetti E, Hervás A, Franke B, Buitelaar JK, Rommelse N, Yousaf A, Duketis E, Freitag CM, Caballero-Andaluz R, Martinez-Mir A, Scholl FG, Ribasés M, ... ... Bourgeron T, et al. Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Autism Research : Official Journal of the International Society For Autism Research. PMID 27417655 DOI: 10.1002/Aur.1662 |
0.345 |
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| 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. Journal of Visualized Experiments : Jove. PMID 27341321 DOI: 10.3791/53871 |
0.76 |
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| 2016 |
Darville H, Poulet A, Rodet-Amsellem F, Chatrousse L, Pernelle J, Boissart C, Héron D, Nava C, Perrier A, Jarrige M, Cogé F, Millan MJ, Bourgeron T, Peschanski M, Delorme R, et al. Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome. Ebiomedicine. PMID 27333044 DOI: 10.1016/J.Ebiom.2016.05.032 |
0.3 |
|
| 2016 |
Bourgeron T. Current knowledge on the genetics of autism and propositions for future research. Comptes Rendus Biologies. 339: 300-7. PMID 27289453 DOI: 10.1016/J.Crvi.2016.05.004 |
0.458 |
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| 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, ... ... Bourgeron T, et al. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. Molecular Psychiatry. PMID 27166760 DOI: 10.1038/Mp.2016.61 |
0.459 |
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| 2016 |
Bourgeron T. The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture. Nordic Journal of Psychiatry. 70: 1-9. PMID 25971862 DOI: 10.3109/08039488.2015.1042519 |
0.43 |
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| 2015 |
Ducloy M, Tabet AC, Bouvard M, Bourgeron T, Delorme R. Autism spectrum disorders: heterogeneous genetic etiologies La Revue Du Praticien. 65: 1179-1182. PMID 30512507 |
0.317 |
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| 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, et al. Identification and validation of biomarkers for autism spectrum disorders. Nature Reviews. Drug Discovery. 15: 70-3. PMID 26718285 DOI: 10.1038/Nrd.2015.7 |
0.394 |
|
| 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, ... ... Bourgeron T, et al. A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. European Journal of Human Genetics : Ejhg. PMID 26395558 DOI: 10.1038/Ejhg.2015.211 |
0.737 |
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| 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. American Journal of Medical Genetics. Part A. PMID 26334118 DOI: 10.1002/Ajmg.A.37345 |
0.414 |
|
| 2015 |
Bourgeron T. From the genetic architecture to synaptic plasticity in autism spectrum disorder. Nature Reviews. Neuroscience. 16: 551-63. PMID 26289574 DOI: 10.1038/Nrn3992 |
0.413 |
|
| 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. Biological Psychiatry. 78: 126-34. PMID 25850620 DOI: 10.1016/J.Biopsych.2015.02.010 |
0.322 |
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| 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. 10: e0121802. PMID 25806942 DOI: 10.1371/Journal.Pone.0121802 |
0.745 |
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| 2015 |
Boisgontier J, Beggiato A, Toro R, Duchesnay E, Poupon C, Amsellem F, Katz J, Petit J, D'albis M, Duclap D, Scimia N, Lettelier L, Leboyer M, Bourgeron T, Elmaheh M, et al. Fronto-occipital Structural Disconnectivity as an Endophenotype of ASD European Psychiatry. 30: 780. DOI: 10.1016/S0924-9338(15)30611-8 |
0.419 |
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| 2014 |
Pagan C, Delorme R, Callebert J, Goubran-Botros H, Amsellem F, Drouot X, Boudebesse C, Le Dudal K, Ngo-Nguyen N, Laouamri H, Gillberg C, Leboyer M, Bourgeron T, Launay JM. The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders. Translational Psychiatry. 4: e479. PMID 25386956 DOI: 10.1038/Tp.2014.120 |
0.377 |
|
| 2014 |
Toro R, Poline JB, Huguet G, Loth E, Frouin V, Banaschewski T, Barker GJ, Bokde A, Büchel C, Carvalho FM, Conrod P, Fauth-Bühler M, Flor H, Gallinat J, Garavan H, ... ... Bourgeron T, et al. Genomic architecture of human neuroanatomical diversity. Molecular Psychiatry. PMID 25224261 DOI: 10.7490/F1000Research.1096294.1 |
0.317 |
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| 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, ... ... Bourgeron T, et al. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments. Plos Genetics. 10: e1004580. PMID 25188300 DOI: 10.1371/Journal.Pgen.1004580 |
0.751 |
|
| 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. Journal of Autism and Developmental Disorders. 44: 2996-3005. PMID 24927807 DOI: 10.1007/S10803-014-2155-1 |
0.32 |
|
| 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, ... ... Bourgeron T, et al. Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. Nature. 511: 236-40. PMID 24870235 DOI: 10.1038/Nature13248 |
0.393 |
|
| 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, ... ... Bourgeron T, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.436 |
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| 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. 9: e88600. PMID 24594579 DOI: 10.1371/Journal.Pone.0088600 |
0.755 |
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| 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. Journal of Autism and Developmental Disorders. 44: 2074-6. PMID 24554162 DOI: 10.1007/S10803-014-2070-5 |
0.371 |
|
| 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, ... ... Bourgeron T, et al. Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics. 133: 781-92. PMID 24442360 DOI: 10.1007/S00439-013-1416-Y |
0.405 |
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| 2014 |
Kleijer KT, Schmeisser MJ, Krueger DD, Boeckers TM, Scheiffele P, Bourgeron T, Brose N, Burbach JP. Neurobiology of autism gene products: towards pathogenesis and drug targets. Psychopharmacology. 231: 1037-62. PMID 24419271 DOI: 10.1007/S00213-013-3403-3 |
0.4 |
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| 2014 |
Guilmatre A, Huguet G, Delorme R, Bourgeron T. The emerging role of SHANK genes in neuropsychiatric disorders. Developmental Neurobiology. 74: 113-22. PMID 24124131 DOI: 10.1002/Dneu.22128 |
0.458 |
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| 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, ... ... Bourgeron T, et al. Heterozygous FA2H mutations in autism spectrum disorders. Bmc Medical Genetics. 14: 124. PMID 24299421 DOI: 10.1186/1471-2350-14-124 |
0.409 |
|
| 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. Behavioural Brain Research. 256: 677-89. PMID 23994547 DOI: 10.1016/J.Bbr.2013.08.031 |
0.735 |
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| 2013 |
Huguet G, Ey E, Bourgeron T. The genetic landscapes of autism spectrum disorders. Annual Review of Genomics and Human Genetics. 14: 191-213. PMID 23875794 DOI: 10.1146/Annurev-Genom-091212-153431 |
0.779 |
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| 2013 |
Delorme R, Ey E, Toro R, Leboyer M, Gillberg C, Bourgeron T. Progress toward treatments for synaptic defects in autism. Nature Medicine. 19: 685-94. PMID 23744158 DOI: 10.1038/Nm.3193 |
0.778 |
|
| 2013 |
Mercati O, Danckaert A, André-Leroux G, Bellinzoni M, Gouder L, Watanabe K, Shimoda Y, Grailhe R, De Chaumont F, Bourgeron T, Cloëz-Tayarani I. Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites. Biology Open. 2: 324-34. PMID 23519440 DOI: 10.1242/Bio.20133343 |
0.317 |
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| 2013 |
Wang L, Li J, Ruan Y, Lu T, Liu C, Jia M, Yue W, Liu J, Bourgeron T, Zhang D. Sequencing ASMT identifies rare mutations in Chinese Han patients with autism. Plos One. 8: e53727. PMID 23349736 DOI: 10.1371/Journal.Pone.0053727 |
0.404 |
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| 2013 |
El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. Behavioural Brain Research. 251: 41-9. PMID 23183221 DOI: 10.1016/J.Bbr.2012.11.016 |
0.498 |
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| 2013 |
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. Journal of Pineal Research. 54: 46-57. PMID 22775292 DOI: 10.1111/J.1600-079X.2012.01020.X |
0.32 |
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| 2012 |
Nava C, Lamari F, Héron D, Mignot C, Rastetter A, Keren B, Cohen D, Faudet A, Bouteiller D, Gilleron M, Jacquette A, Whalen S, Afenjar A, Périsse D, Laurent C, ... ... Bourgeron T, et al. Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. Translational Psychiatry. 2: e179. PMID 23092983 DOI: 10.1038/Tp.2012.102 |
0.427 |
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| 2012 |
Ey E, Yang M, Katz AM, Woldeyohannes L, Silverman JL, Leblond CS, Faure P, Torquet N, Le Sourd AM, Bourgeron T, Crawley JN. Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4. Genes, Brain, and Behavior. 11: 928-41. PMID 22989184 DOI: 10.1111/J.1601-183X.2012.00849.X |
0.758 |
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| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.363 |
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| 2012 |
Le Floch E, Guillemot V, Frouin V, Pinel P, Lalanne C, Trinchera L, Tenenhaus A, Moreno A, Zilbovicius M, Bourgeron T, Dehaene S, Thirion B, Poline JB, Duchesnay E. Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares. Neuroimage. 63: 11-24. PMID 22781162 DOI: 10.1016/J.Neuroimage.2012.06.061 |
0.313 |
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| 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. Molecular Autism. 3: 5. PMID 22738402 DOI: 10.1186/2040-2392-3-5 |
0.41 |
|
| 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, ... ... Bourgeron T, et al. Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2. Nature. 486: 256-60. PMID 22699619 DOI: 10.1038/Nature11015 |
0.768 |
|
| 2012 |
Etain B, Dumaine A, Bellivier F, Pagan C, Francelle L, Goubran-Botros H, Moreno S, Deshommes J, Moustafa K, Le Dudal K, Mathieu F, Henry C, Kahn JP, Launay JM, Mühleisen TW, ... ... Bourgeron T, et al. Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Human Molecular Genetics. 21: 4030-7. PMID 22694957 DOI: 10.1093/Hmg/Dds227 |
0.374 |
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| 2012 |
Sato D, Lionel AC, Leblond CS, Prasad A, Pinto D, Walker S, O'Connor I, Russell C, Drmic IE, Hamdan FF, Michaud JL, Endris V, Roeth R, Delorme R, Huguet G, ... ... Bourgeron T, et al. SHANK1 Deletions in Males with Autism Spectrum Disorder. American Journal of Human Genetics. 90: 879-87. PMID 22503632 DOI: 10.1016/J.Ajhg.2012.03.017 |
0.433 |
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| 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, ... ... Bourgeron T, et al. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. Plos Genetics. 8: e1002521. PMID 22346768 DOI: 10.1371/Journal.Pgen.1002521 |
0.768 |
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| 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. 7: e29401. PMID 22238608 DOI: 10.1371/Journal.Pone.0029401 |
0.736 |
|
| 2012 |
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Bourgeron T, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6 |
0.478 |
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| 2012 |
Durand CM, Perroy J, Loll F, Perrais D, Fagni L, Bourgeron T, Montcouquiol M, Sans N. SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism. Molecular Psychiatry. 17: 71-84. PMID 21606927 DOI: 10.1038/Mp.2011.57 |
0.381 |
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| 2011 |
Poot M, Smagt JJvd, Brilstra EH, Bourgeron T. Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia Cytogenetic and Genome Research. 135: 228-240. PMID 22085975 DOI: 10.1159/000334064 |
0.376 |
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| 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, ... ... Bourgeron T, et al. Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. Journal of Pineal Research. 51: 394-9. PMID 21615493 DOI: 10.1111/J.1600-079X.2011.00902.X |
0.355 |
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| 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, ... ... Bourgeron T, et al. Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations. Plos One. 6: e17289. PMID 21394203 DOI: 10.1371/Journal.Pone.0017289 |
0.444 |
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| 2011 |
Ey E, Leblond CS, Bourgeron T. Behavioral profiles of mouse models for autism spectrum disorders. Autism Research : Official Journal of the International Society For Autism Research. 4: 5-16. PMID 21328568 DOI: 10.1002/Aur.175 |
0.778 |
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| 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, ... ... Bourgeron T, et al. Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. Bmc Medical Genetics. 12: 17. PMID 21251267 DOI: 10.1186/1471-2350-12-17 |
0.369 |
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| 2011 |
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 Expression and Purification. 75: 114-8. PMID 20688166 DOI: 10.1016/J.Pep.2010.07.011 |
0.333 |
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| 2010 |
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, ... ... Bourgeron T, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.353 |
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| 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, ... ... Bourgeron T, et al. Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population. Plos One. 5: e11495. PMID 20657642 DOI: 10.1371/Journal.Pone.0011495 |
0.399 |
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| 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 in Genetics : Tig. 26: 363-72. PMID 20609491 DOI: 10.1016/J.Tig.2010.05.007 |
0.492 |
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| 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 Medical Genetics. 11: 108. PMID 20602773 DOI: 10.1186/1471-2350-11-108 |
0.413 |
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| 2010 |
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, ... ... Bourgeron T, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.477 |
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| 2010 |
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. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 542-548. PMID 19676096 DOI: 10.1002/Ajmg.B.31016 |
0.31 |
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| 2009 |
Bourgeron T, Leboyer M, Delorme R. [Autism: more evidence of a genetic cause]. Bulletin De L'Academie Nationale De Medecine. 193: 299-304; discussion . PMID 19718887 |
0.319 |
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| 2009 |
Bourgeron T. A synaptic trek to autism. Current Opinion in Neurobiology. 19: 231-4. PMID 19545994 DOI: 10.1016/J.Conb.2009.06.003 |
0.441 |
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| 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, et al. An investigation of ribosomal protein L10 gene in autism spectrum disorders. Bmc Medical Genetics. 10: 7. PMID 19166581 DOI: 10.1186/1471-2350-10-7 |
0.429 |
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| 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, ... ... Bourgeron T, et al. Analysis of X chromosome inactivation in autism spectrum disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 830-5. PMID 18361425 DOI: 10.1002/Ajmg.B.30688 |
0.393 |
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| 2008 |
Jamain S, Radyushkin K, Hammerschmidt K, Granon S, Boretius S, Varoqueaux F, Ramanantsoa N, Gallego J, Ronnenberg A, Winter D, Frahm J, Fischer J, Bourgeron T, Ehrenreich H, Brose N. Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism. Proceedings of the National Academy of Sciences of the United States of America. 105: 1710-5. PMID 18227507 DOI: 10.1073/Pnas.0711555105 |
0.474 |
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| 2008 |
Melke J, Goubran Botros H, Chaste P, Betancur C, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Gillberg IC, Delorme R, Chabane N, Mouren-Simeoni MC, Fauchereau F, Durand CM, Chevalier F, ... ... Bourgeron T, et al. Abnormal melatonin synthesis in autism spectrum disorders Molecular Psychiatry. 13: 90-98. PMID 17505466 DOI: 10.1038/Sj.Mp.4002016 |
0.429 |
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| 2007 |
Bourgeron T. The Possible Interplay of Synaptic and Clock Genes in Autism Spectrum Disorders Cold Spring Harbor Symposia On Quantitative Biology. 72: 645-654. PMID 18419324 DOI: 10.1101/Sqb.2007.72.020 |
0.457 |
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| 2007 |
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Bourgeron T, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.401 |
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| 2007 |
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, ... ... Bourgeron T, et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nature Genetics. 39: 25-7. PMID 17173049 DOI: 10.1038/Ng1933 |
0.446 |
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| 2006 |
Belmonte MK, Bourgeron T. Fragile X syndrome and autism at the intersection of genetic and neural networks. Nature Neuroscience. 9: 1221-5. PMID 17001341 DOI: 10.1038/Nn1765 |
0.394 |
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| 2006 |
Persico AM, Bourgeron T. Searching for ways out of the autism maze: genetic, epigenetic and environmental clues. Trends in Neurosciences. 29: 349-358. PMID 16808981 DOI: 10.1016/J.Tins.2006.05.010 |
0.438 |
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| 2006 |
Delorme R, Durand CM, Betancur C, Wagner M, Ruhrmann S, Grabe HJ, Nygren G, Gillberg C, Leboyer M, Bourgeron T, Courtet P, Jollant F, Buresi C, Aubry JM, Baud P, et al. No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects. Biological Psychiatry. 60: 202-3. PMID 16581035 DOI: 10.1016/J.Biopsych.2005.12.014 |
0.302 |
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| 2006 |
Etain B, Mathieu F, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Kealey C, Blackwood D, Muir W, Bellivier F, Henry C, Dina C, Gallina S, Gurling H, ... ... Bourgeron T, et al. Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14. Molecular Psychiatry. 11: 685-94. PMID 16534504 DOI: 10.1038/Sj.Mp.4001815 |
0.308 |
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| 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, ... ... Bourgeron T, et al. Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders American Journal of Medical Genetics - Neuropsychiatric Genetics. 141: 67-70. PMID 16331680 DOI: 10.1002/Ajmg.B.30229 |
0.424 |
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| 2005 |
Delorme R, Betancur C, Wagner M, Krebs MO, Gorwood P, Pearl P, Nygren G, Durand CM, Buhtz F, Pickering P, Melke J, Ruhrmann S, Anckarsäter H, Chabane N, Kipman A, ... ... Bourgeron T, et al. Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder. Molecular Psychiatry. 10: 1059-61. PMID 16088327 DOI: 10.1038/Sj.Mp.4001728 |
0.382 |
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| 2004 |
Delorme R, Krebs MO, Chabane N, Roy I, Millet B, Mouren-Simeoni MC, Maier W, Bourgeron T, Leboyer M. Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder. Neuroreport. 15: 699-702. PMID 15094479 DOI: 10.1097/00001756-200403220-00025 |
0.346 |
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| 2003 |
Jamain S, Betancur C, Giros B, Leboyer M, Bourgeron T. [Genetics of autism: from genome scans to candidate genes]. Mã©Decine Sciences : M/S. 19: 1081-90. PMID 14648479 DOI: 10.1051/Medsci/200319111081 |
0.437 |
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| 2003 |
Jamain S, Quach H, Betancur C, RÃ¥stam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nature Genetics. 34: 27-9. PMID 12669065 DOI: 10.1038/Ng1136 |
0.412 |
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| 2002 |
Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T. Linkage and association of the glutamate receptor 6 gene with autism. Molecular Psychiatry. 7: 302-10. PMID 11920157 DOI: 10.1038/Sj.Mp.4000979 |
0.364 |
|
| 2002 |
Jamain S, Quach H, Quintana-Murci L, Betancur C, Philippe A, Gillberg C, Sponheim E, Skjeldal OH, Fellous M, Leboyer M, Bourgeron T. Y chromosome haplogroups in autistic subjects. Molecular Psychiatry. 7: 217-9. PMID 11840316 DOI: 10.1038/Sj.Mp.4000968 |
0.302 |
|
| 2001 |
Jamain S, Quach H, Fellous M, Bourgeron T. Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia. Genomics. 74: 36-44. PMID 11374900 DOI: 10.1006/Geno.2001.6535 |
0.307 |
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| 1998 |
Agulnik AI, Zharkikh A, Boettger-Tong H, Bourgeron T, McElreavey K, Bishop CE. Evolution of the DAZ gene family suggests that Y-linked DAZ plays little, or a limited, role in spermatogenesis but underlines a recent African origin for human populations. Human Molecular Genetics. 7: 1371-7. PMID 9700189 DOI: 10.1093/Hmg/7.9.1371 |
0.306 |
|
| 1997 |
Rustin P, Bourgeron T, Parfait B, Chretien D, Munnich A, Rötig A. Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human Biochimica Et Biophysica Acta. 1361: 185-197. PMID 9300800 DOI: 10.1016/S0925-4439(97)00035-5 |
0.313 |
|
| 1997 |
Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M, Algonik A. Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene. Genomics. 41: 227-35. PMID 9143498 DOI: 10.1006/Geno.1997.4635 |
0.309 |
|
| 1996 |
Bourgeron T, Barbaux S, Mcelreavey K, Fellous M. La génétique de la stérilité masculine M S-Medecine Sciences. 12. DOI: 10.4267/10608/672 |
0.369 |
|
| 1995 |
Bourgeron T, Rustin P, Chretien D, Birch-Machin M, Bourgeois M, Viegas-Péquignot E, Munnich A, Rötig A. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency Nature Genetics. 11: 144-149. PMID 7550341 DOI: 10.1038/Ng1095-144 |
0.311 |
|
| 1994 |
Rustin P, Chretien D, Bourgeron T, Gérard B, Rötig A, Saudubray JM, Munnich A. Biochemical and molecular investigations in respiratory chain deficiencies Clinica Chimica Acta. 228: 35-51. PMID 7955428 DOI: 10.1016/0009-8981(94)90055-8 |
0.315 |
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