O. Didierjean

发表

Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.

Y. Agid, B. Dubois, D. Campion, 1998, Archives of neurology.

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.

Y. Agid, G. Yvert, T. Klockgether, 1997, Human molecular genetics.

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

Y. Agid, B. Dubois, F. Pasquier, 1997, American journal of human genetics.

Clinical and molecular features of spinocerebellar ataxia type 6

Y. Agid, S. Rivaud, A. Dürr, 1997, Neurology.

Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon.

Y. Agid, A. Dürr, A. Brice, 1997, American journal of human genetics.

Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.

Y. Agid, A. Durr, A. Dürr, 1995, American journal of human genetics.

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

M Skalej, T Klockgether, M. Skalej, 1996, Brain : a journal of neurology.

Linkage disequilibrium at the SCA2 locus

T. Klockgether, A. Dürr, A. Brice, 1999, Journal of medical genetics.

No eVect of the á1-antichymotrypsin A allele in Alzheimer’s disease

Y. Agid, F. Pasquier, D. Campion, 1998 .

Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations

Y. Agid, A. Dürr, A. Brice, 1996 .

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.

B. Dubois, D. Campion, D. Hannequin, 1995, Human molecular genetics.

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Yves Agid, Jean-Louis Mandel, Gaël Yvert, 1996, Nature Genetics.

Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features

Alexandra Durr, Charles Duyckaerts, Yves Agid, 1996, Annals of neurology.

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.

H. Zoghbi, S. Tsuji, A. Durr, 1998, American journal of human genetics.

Apolipoprotein E ϵ4 Allele and Familial Aggregation of Alzheimer Disease

Y. Agid, B. Dubois, D. Campion, 1998 .

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

Miguel Ángel Martínez, Y Agid, Y. Agid, 1997, American journal of human genetics.

Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado‐Joseph disease

E. Hirsch, Y. Agid, A. Brice, 1998, Human mutation.

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.

Y. Agid, A. Durr, T. Klockgether, 1996, Human molecular genetics.

Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus

M. Skalej, J. Dichgans, T. Klockgether, 1997, Journal of Neurology.

No effect of the α1-antichymotrypsin A allele in Alzheimer’s disease

Y. Agid, B. Dubois, F. Pasquier, 1997 .

No e V ect of the á 1-antichymotrypsin A allele in Alzheimer ’ s disease

Y. Agid, B. Dubois, F. Pasquier, 1998 .

Apolipoprotein E (cid:101) 4 Allele and Familial Aggregation of Alzheimer Disease

Y. Agid, B. Dubois, D. Campion, 2000 .

Miguel Ángel Martínez, D. Campion, D. Hannequin, 2006 .