| Year |
Citation |
Score |
| 2007 |
Bastard C, Raux G, Fruchart C, Parmentier F, Vaur D, Penther D, Troussard X, Nagib D, Lepretre S, Tosi M, Frebourg T, Tilly H. Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients. Leukemia. 21: 1460-3. PMID 17495973 DOI: 10.1038/Sj.Leu.2404727 |
0.316 |
|
| 2007 |
Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D. Variations in the APP gene promoter region and risk of Alzheimer disease. Neurology. 68: 684-7. PMID 17325276 DOI: 10.1212/01.Wnl.0000255938.33739.46 |
0.709 |
|
| 2007 |
Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, et al. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human Molecular Genetics. 16: 83-91. PMID 17135275 DOI: 10.1093/Hmg/Ddl443 |
0.674 |
|
| 2006 |
Quenard A, Yilmaz S, Fontaine H, Bienvenu T, Moncla A, des Portes V, Rivier F, Mathieu M, Raux G, Jonveaux P, Philippe C. Deleterious mutations in exon 1 of MECP2 in Rett syndrome. European Journal of Medical Genetics. 49: 313-22. PMID 16829352 DOI: 10.1016/J.Ejmg.2005.11.002 |
0.409 |
|
| 2006 |
Lesca G, Burnichon N, Raux G, Tosi M, Pinson S, Marion MJ, Babin E, Gilbert-Dussardier B, Rivière S, Goizet C, Faivre L, Plauchu H, Frébourg T, Calender A, Giraud S, et al. Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients. Human Mutation. 27: 598. PMID 16705692 DOI: 10.1002/Humu.9421 |
0.41 |
|
| 2006 |
Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38: 24-6. PMID 16369530 DOI: 10.1038/Ng1718 |
0.645 |
|
| 2005 |
Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: An update Journal of Medical Genetics. 42: 793-795. PMID 16033913 DOI: 10.1136/Jmg.2005.033456 |
0.613 |
|
| 2005 |
Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, et al. Hyperprolinemia is a risk factor for schizoaffective disorder. Molecular Psychiatry. 10: 479-85. PMID 15494707 DOI: 10.1038/Sj.Mp.4001597 |
0.669 |
|
| 2004 |
Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, et al. 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. PMID 15215218 DOI: 10.1093/Brain/Awh216 |
0.583 |
|
| 2004 |
Houy E, Raux G, Thibaut F, Belmont A, Demily C, Allio G, Haouzir S, Fouldrin G, Petit M, Frebourg T, Campion D. 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. PMID 14569275 DOI: 10.1038/Sj.Mp.4001443 |
0.631 |
|
| 2003 |
Portet F, Dauvilliers Y, Campion D, Raux G, Hauw JJ, Lyon-Caen O, Camu W, Touchon J. Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu). Neurology. 61: 1136-7. PMID 14581682 DOI: 10.1212/01.Wnl.0000086811.39675.79 |
0.586 |
|
| 2003 |
Maréchal L, Raux G, Dumanchin C, Lefebvre G, Deslandre E, Girard C, Campion D, Parain D, Frebourg T, Hannequin D. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation American Journal of Medical Genetics - Neuropsychiatric Genetics. 119: 114-117. PMID 12707948 DOI: 10.1002/Ajmg.B.10062 |
0.608 |
|
| 2003 |
Bougeard G, Brugières L, Chompret A, Gesta P, Charbonnier F, Valent A, Martin C, Raux G, Feunteun J, Bressac-de Paillerets B, Frébourg T. Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene. Oncogene. 22: 840-6. PMID 12584563 DOI: 10.1038/Sj.Onc.1206155 |
0.402 |
|
| 2003 |
Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T. The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene Journal of Medical Genetics. 40: e7. PMID 12525555 DOI: 10.1136/Jmg.40.1.E7 |
0.554 |
|
| 2002 |
Raux G, Bonnet-Brilhault F, Louchart S, Houy E, Gantier R, Levillain D, Allio G, Haouzir S, Petit M, Martinez M, Frebourg T, Thibaut F, Campion D. The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit Molecular Psychiatry. 7: 1006-1011. PMID 12399955 DOI: 10.1038/Sj.Mp.4001140 |
0.573 |
|
| 2002 |
Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frébourg T. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients Human Molecular Genetics. 11: 2243-2249. PMID 12217952 DOI: 10.1093/Hmg/11.19.2243 |
0.601 |
|
| 2002 |
Zitouni M, Martel P, Ben Ayed M, Raux G, Gilbert D, Joly P, Mokhtar I, Ridha Kamoun M, Turki H, Zahaf A, Mokni M, Ben Osman A, Masmoudi H, Makni S, Tron F. Pemphigus is not associated with allotypic markers of immunoglobulin kappa. Genes and Immunity. 3: 50-2. PMID 11857063 DOI: 10.1038/Sj.Gene.6363817 |
0.339 |
|
| 2001 |
Raux G, Gilbert D, Joly P, Martel P, Roujeau JC, Prost C, Lefranc MP, Tron F. IGHV3-associated restriction fragment length polymorphisms confer susceptibility to bullous pemphigoid. Experimental and Clinical Immunogenetics. 18: 59-66. PMID 11340293 DOI: 10.1159/000049183 |
0.345 |
|
| 2001 |
Martel P, Gilbert D, Drouot L, Prost C, Raux G, Delaporte E, Joly P, Tron F. A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease. Genes and Immunity. 2: 41-3. PMID 11294567 DOI: 10.1038/Sj.Gene.6363718 |
0.408 |
|
| 2000 |
Raux G, Gantier R, Thomas-Anterion C, Boulliat J, Verpillat P, Hannequin D, Brice A, Frebourg T, Campion D. Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation Neurology. 55: 1577-1578. PMID 11094121 DOI: 10.1212/Wnl.55.10.1577 |
0.569 |
|
| 2000 |
Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T. APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population European Journal of Human Genetics. 8: 713-716. PMID 10980578 DOI: 10.1038/Sj.Ejhg.5200513 |
0.575 |
|
| 2000 |
Raux G, Gantier R, Martin C, Pothin Y, Brice A, Frebourg T, Campion D. A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease. Human Mutation. 16: 95. PMID 10874324 DOI: 10.1002/1098-1004(200007)16:1<95::Aid-Humu28>3.0.Co;2-H |
0.596 |
|
| 2000 |
Raux G, Gilbert D, Joly P, Daveau M, Martel P, Christ M, Tron F. Association of KM genotype with bullous pemphigoid. Journal of Autoimmunity. 14: 79-82. PMID 10648118 DOI: 10.1006/Jaut.1999.0345 |
0.303 |
|
| 2000 |
Camuzat A, Verpillat P, Dubois B, Penet C, Agid Y, Brice A, Moreaud O, Puel M, Clerget-Darpoux F, Kinter J, Kozlov S, Berger P, Sonderegger P, Raux G, Campion C, et al. Mutations in the neuroserpin gene are rare in familial dementia Annals of Neurology. 47: 688-688. DOI: 10.1002/1531-8249(200005)47:5<688::Aid-Ana31>3.0.Co;2-0 |
0.416 |
|
| 1999 |
Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, et al. Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum American Journal of Human Genetics. 65: 664-670. PMID 10441572 DOI: 10.1086/302553 |
0.611 |
|
| 1998 |
Raux G, Gilbert D, Joly P, Daveau M, Tron F, Lauret P. Determination of susceptibility factors in bullous pemphigoid: Genetic polymorphisms of immunoglobulin light-chain genes Journal of Dermatological Science. 16: S42. DOI: 10.1016/S0923-1811(98)83246-5 |
0.308 |
|
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