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Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.
Huc-Chabrolle M, Charon C, Guilmatre A, Vourc'h P, Tripi G, Barthez MA, Sizaret E, Thepault RA, Le Gallic S, Hager J, Toutain A, Raynaud M, Andres C, Campion D, Laumonnier F, Bonnet-Brilhault F. Huc-Chabrolle M, et al. Among authors: andres c. Behav Genet. 2013 Mar;43(2):132-40. doi: 10.1007/s10519-012-9575-5. Epub 2013 Jan 11. Behav Genet. 2013. PMID: 23307483 Free article.
MECP2 is highly mutated in X-linked mental retardation.
Couvert P, Bienvenu T, Aquaviva C, Poirier K, Moraine C, Gendrot C, Verloes A, Andrès C, Le Fevre AC, Souville I, Steffann J, des Portes V, Ropers HH, Yntema HG, Fryns JP, Briault S, Chelly J, Cherif B. Couvert P, et al. Among authors: andres c. Hum Mol Genet. 2001 Apr 15;10(9):941-6. doi: 10.1093/hmg/10.9.941. Hum Mol Genet. 2001. PMID: 11309367
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: andres cr. Mol Psychiatry. 2016 Mar;21(3):411-8. doi: 10.1038/mp.2015.75. Epub 2015 Jun 9. Mol Psychiatry. 2016. PMID: 26055424
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: andres c. Am J Med Genet. 1999 Dec 15;88(6):729-32. Am J Med Genet. 1999. PMID: 10581497
Typical bulbar ALS can be linked to GARS mutation.
Corcia P, Brulard C, Beltran S, Marouillat S, Bakkouche SE, Andres CR, Blasco H, Vourc'h P. Corcia P, et al. Among authors: andres cr. Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):275-277. doi: 10.1080/21678421.2018.1556699. Epub 2019 Jan 20. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30661401
669 results