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HyPyP: a Hyperscanning Python Pipeline for inter-brain connectivity analysis.
Ayrolles A, Brun F, Chen P, Djalovski A, Beauxis Y, Delorme R, Bourgeron T, Dikker S, Dumas G. Ayrolles A, et al. Among authors: bourgeron t. Soc Cogn Affect Neurosci. 2021 Jan 18;16(1-2):72-83. doi: 10.1093/scan/nsaa141. Soc Cogn Affect Neurosci. 2021. PMID: 33031496 Free PMC article.
Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.
Delorme R, Betancur C, Chaste P, Kernéis S, Stopin A, Mouren MC, Collet C, Bourgeron T, Leboyer M, Launay JM. Delorme R, et al. Among authors: bourgeron t. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-548. doi: 10.1002/ajmg.b.31016. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19676096 Free PMC article.
[Autism: more evidence of a genetic cause].
Bourgeron T, Leboyer M, Delorme R. Bourgeron T, et al. Bull Acad Natl Med. 2009 Feb;193(2):299-304; discussion 304-5. Bull Acad Natl Med. 2009. PMID: 19718887 French.
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Toro R, Konyukh M, Delorme R, Leblond C, Chaste P, Fauchereau F, Coleman M, Leboyer M, Gillberg C, Bourgeron T. Toro R, et al. Among authors: bourgeron t. Trends Genet. 2010 Aug;26(8):363-72. doi: 10.1016/j.tig.2010.05.007. Epub 2010 Jul 6. Trends Genet. 2010. PMID: 20609491 Free article. Review.
Progress toward treatments for synaptic defects in autism.
Delorme R, Ey E, Toro R, Leboyer M, Gillberg C, Bourgeron T. Delorme R, et al. Among authors: bourgeron t. Nat Med. 2013 Jun;19(6):685-94. doi: 10.1038/nm.3193. Epub 2013 Jun 6. Nat Med. 2013. PMID: 23744158 Review.
The emerging role of SHANK genes in neuropsychiatric disorders.
Guilmatre A, Huguet G, Delorme R, Bourgeron T. Guilmatre A, et al. Among authors: bourgeron t. Dev Neurobiol. 2014 Feb;74(2):113-22. doi: 10.1002/dneu.22128. Epub 2013 Oct 7. Dev Neurobiol. 2014. PMID: 24124131 Review.
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
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. Maruani A, et al. Among authors: bourgeron t. Am J Med Genet A. 2015 Dec;167A(12):3019-30. doi: 10.1002/ajmg.a.37345. Epub 2015 Sep 3. Am J Med Genet A. 2015. PMID: 26334118 Free article.
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.
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. Mosca-Boidron AL, et al. Among authors: bourgeron t. Eur J Hum Genet. 2016 Jun;24(6):838-43. doi: 10.1038/ejhg.2015.211. Epub 2015 Sep 23. Eur J Hum Genet. 2016. PMID: 26395558 Free PMC article.
Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome.
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, Benchoua A. Darville H, et al. Among authors: bourgeron t. EBioMedicine. 2016 Jul;9:293-305. doi: 10.1016/j.ebiom.2016.05.032. Epub 2016 May 27. EBioMedicine. 2016. PMID: 27333044 Free PMC article.
247 results