Grégory Raux

Publications by Year

Research Areas

Alzheimer's disease research and treatments, Autoimmune Bullous Skin Diseases, Genetics and Neurodevelopmental Disorders, Coagulation, Bradykinin, Polyphosphates, and Angioedema, Urticaria and Related Conditions

Most-Cited Works

• → APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy(2005)1,241 cited
• → Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum(1999)786 cited
• → Molecular diagnosis of autosomal dominant early onset Alzheimer’s disease: an update: Table 1(2005)198 cited
• Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments.(2000)
• → Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome(2006)170 cited
• → Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation(2000)137 cited
• → Hyperprolinemia is a risk factor for schizoaffective disorder(2004)109 cited
• → 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(2002)94 cited
• → Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients(2006)83 cited
• → Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene(2003)75 cited