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bourgeron t
(237 results)?
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
Nat Genet. 2022 Nov;54(11):1630-1639. doi: 10.1038/s41588-022-01203-y. Epub 2022 Oct 24.
Nat Genet. 2022.
PMID: 36280734
Free PMC article.
Resting state EEG power spectrum and functional connectivity in autism: a cross-sectional analysis.
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; EU-AIMS LEAP group authorship.
Garcés P, et al. Among authors: bougeron t.
Mol Autism. 2022 May 18;13(1):22. doi: 10.1186/s13229-022-00500-x.
Mol Autism. 2022.
PMID: 35585637
Free PMC article.
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Preference for biological motion is reduced in ASD: implications for clinical trials and the search for biomarkers.
Mason L, Shic F, Falck-Ytter T, Chakrabarti B, Charman T, Loth E, Tillmann J, Banaschewski T, Baron-Cohen S, Bölte S, Buitelaar J, Durston S, Oranje B, Persico AM, Beckmann C, Bougeron T, Dell'Acqua F, Ecker C, Moessnang C, Murphy D, Johnson MH, Jones EJH; LEAP Team*.
Mason L, et al. Among authors: bougeron t.
Mol Autism. 2021 Dec 15;12(1):74. doi: 10.1186/s13229-021-00476-0.
Mol Autism. 2021.
PMID: 34911565
Free PMC article.
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Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome.
Poulton J, Sewry C, Potter CG, Bougeron T, Chretien D, Wijburg FA, Morten KJ, Brown G.
Poulton J, et al. Among authors: bougeron t.
J Inherit Metab Dis. 1995;18(1):4-20. doi: 10.1007/BF00711367.
J Inherit Metab Dis. 1995.
PMID: 7623440
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