Grégory Raux
Affiliations: | University of Rouen |
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Parents
Sign in to add mentor| Dominique Campion | grad student | 2002 | University of Rouen | |
| (Bases moléculaires des pathologies mendéliennes et complexes : stratégies d'études moléculaires et avancées technologiques) | ||||
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| Bastard C, Raux G, Fruchart C, et al. (2007) Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients. Leukemia. 21: 1460-3 |
| Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, et al. (2007) Variations in the APP gene promoter region and risk of Alzheimer disease. Neurology. 68: 684-7 |
| Raux G, Bumsel E, Hecketsweiler B, et al. (2007) Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human Molecular Genetics. 16: 83-91 |
| Quenard A, Yilmaz S, Fontaine H, et al. (2006) Deleterious mutations in exon 1 of MECP2 in Rett syndrome. European Journal of Medical Genetics. 49: 313-22 |
| Lesca G, Burnichon N, Raux G, et al. (2006) Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients. Human Mutation. 27: 598 |
| Rovelet-Lecrux A, Hannequin D, Raux G, et al. (2006) APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38: 24-6 |
| Raux G, Guyant-Maréchal L, Martin C, et al. (2005) Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: An update Journal of Medical Genetics. 42: 793-795 |
| Jacquet H, Demily C, Houy E, et al. (2005) Hyperprolinemia is a risk factor for schizoaffective disorder. Molecular Psychiatry. 10: 479-85 |
| Le Ber I, Martinez M, Campion D, et al. (2004) A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. Brain : a Journal of Neurology. 127: 1979-92 |
| Houy E, Raux G, Thibaut F, et al. (2004) The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit. Molecular Psychiatry. 9: 320-2 |