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Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.
Daoud H, Gruchy N, Constans JM, Moussaoui E, Saumureau S, Bayou N, Amy M, Védrine S, Vu PY, Rötig A, Laumonnier F, Vourc'h P, Andres CR, Leporrier N, Briault S. Daoud H, et al. Among authors: laumonnier f. Hum Genet. 2009 Jan;124(6):649-58. doi: 10.1007/s00439-008-0588-3. Epub 2008 Nov 16. Hum Genet. 2009. PMID: 19011903
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: laumonnier f. 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.
GC-MS-based urine metabolic profiling of autism spectrum disorders.
Emond P, Mavel S, Aïdoud N, Nadal-Desbarats L, Montigny F, Bonnet-Brilhault F, Barthélémy C, Merten M, Sarda P, Laumonnier F, Vourc'h P, Blasco H, Andres CR. Emond P, et al. Among authors: laumonnier f. Anal Bioanal Chem. 2013 Jun;405(15):5291-300. doi: 10.1007/s00216-013-6934-x. Epub 2013 Apr 10. Anal Bioanal Chem. 2013. PMID: 23571465 Free article.
1H-13C NMR-based urine metabolic profiling in autism spectrum disorders.
Mavel S, Nadal-Desbarats L, Blasco H, Bonnet-Brilhault F, Barthélémy C, Montigny F, Sarda P, Laumonnier F, Vourc'h P, Andres CR, Emond P. Mavel S, et al. Among authors: laumonnier f. Talanta. 2013 Sep 30;114:95-102. doi: 10.1016/j.talanta.2013.03.064. Epub 2013 Apr 9. Talanta. 2013. PMID: 23953447 Free article.
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: laumonnier f. Psychiatr Genet. 2015 Dec;25(6):263-7. doi: 10.1097/YPG.0000000000000100. Psychiatr Genet. 2015. PMID: 26368817
Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis.
Veyrat-Durebex C, Corcia P, Piver E, Devos D, Dangoumau A, Gouel F, Vourc'h P, Emond P, Laumonnier F, Nadal-Desbarats L, Gordon PH, Andres CR, Blasco H. Veyrat-Durebex C, et al. Among authors: laumonnier f. Mol Neurobiol. 2016 Dec;53(10):6910-6924. doi: 10.1007/s12035-015-9567-6. Epub 2015 Dec 14. Mol Neurobiol. 2016. PMID: 26666663
59 results