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Page 1
GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses.
Ung DC, Pietrancosta N, Badillo EB, Raux B, Tapken D, Zlatanovic A, Doridant A, Pode-Shakked B, Raas-Rothschild A, Elpeleg O, Abu-Libdeh B, Hamed N, Papon MA, Marouillat S, Thépault RA, Stevanin G, Elegheert J, Letellier M, Hollmann M, Lambolez B, Tricoire L, Toutain A, Hepp R, Laumonnier F. Ung DC, et al. Among authors: marouillat s. Mol Psychiatry. 2024 Apr;29(4):1205-1215. doi: 10.1038/s41380-024-02469-w. Epub 2024 Feb 28. Mol Psychiatry. 2024. PMID: 38418578 Free PMC article.
Association study of the NF1 gene and autistic disorder.
Mbarek O, Marouillat S, Martineau J, Barthélémy C, Müh JP, Andres C. Mbarek O, et al. Among authors: marouillat s. Am J Med Genet. 1999 Dec 15;88(6):729-32. Am J Med Genet. 1999. PMID: 10581497
GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability.
Bonnet-Brilhault F, Alirol S, Blanc R, Bazaud S, Marouillat S, Thépault RA, Andres CR, Lemonnier É, Barthélémy C, Raynaud M, Toutain A, Gomot M, Laumonnier F. Bonnet-Brilhault F, et al. Among authors: marouillat s. Mol Psychiatry. 2016 Mar;21(3):411-8. doi: 10.1038/mp.2015.75. Epub 2015 Jun 9. Mol Psychiatry. 2016. PMID: 26055424
A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population.
Amy M, Staehlin O, René F, Blasco H, Marouillat S, Daoud H, Vourc'h P, Gordon PH, Camu W, Corcia P, Loeffler JP, Palkovits M, Sommer WH, Andres CR. Amy M, et al. Among authors: marouillat s. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(7-8):490-6. doi: 10.3109/21678421.2015.1051988. Epub 2015 Jun 17. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 26083872
Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism.
Tastet J, Decalonne L, Marouillat S, Malvy J, Thépault RA, Toutain A, Paubel A, Tabagh R, Bénédetti H, Laumonnier F, Barthélémy C, Bonnet-Brilhault F, Andres CR, Vourc'h P. Tastet J, et al. Among authors: marouillat s. Psychiatr Genet. 2015 Dec;25(6):263-7. doi: 10.1097/YPG.0000000000000100. Psychiatr Genet. 2015. PMID: 26368817
Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism.
Patin F, Baranek T, Vourc'h P, Nadal-Desbarats L, Goossens JF, Marouillat S, Dessein AF, Descat A, Hounoum BM, Bruno C, Watier H, Si-Tahar M, Leman S, Lecron JC, Andres CR, Corcia P, Blasco H. Patin F, et al. Among authors: marouillat s. Neurotherapeutics. 2016 Oct;13(4):905-917. doi: 10.1007/s13311-016-0461-3. Neurotherapeutics. 2016. PMID: 27444617 Free PMC article.
37 results