G. Imbert

Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families

Alexandra Dürr, Olivier Didierjean, G. Imbert et al. · Human Molecular Genetics · 1997 · 256 citations · Full text

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.

Dominique Heitz, Didier Devys, G. Imbert et al. · Journal of Medical Genetics · 1992 · 169 citations · Full text

Genetics, Molecular Genetics, Mendelian Disorder +16

The Gene for the TATA Binding Protein (TBP) That Contains a Highly Polymorphic Protein Coding CAG Repeat Maps to 6q27

G. Imbert, Yvon Trottier, J. Beckmann et al. · Genomics · 1994 · 68 citations

Sequence Motif, Protein Expression, Natural Sciences +9

O2‐05‐05: Results of the first‐in‐man study with the active Aβ Immunotherapy CAD106 in Alzheimer patients

Bengt Winblad, Lennart Minthon, A. Floesser et al. · Alzheimer s & Dementia · 2009 · 32 citations

Immunodeficiencies, Immunology, Alzheimer Patients +29