C. Penet

发表

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

B. Dubois, D. Campion, D. Hannequin, 1999, American journal of human genetics.

Latencies of visually guided saccades in unilateral hemispheric cerebral lesions

C. Pierrot-Deseilligny, S. Rivaud, C. Penet, 1987, Annals of neurology.

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

C. Gillberg, M. Leboyer, A. Brice, 1999, Human molecular genetics.

Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians

A. Durr, A. Brice, G. Stevanin, 2004, Neurology.

Variations in the APP gene promoter region and risk of Alzheimer disease

J. Lambert, P. Amouyel, D. Campion, 2007, Neurology.

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

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

SCA2 is not a major locus for ADCA type I in French families.

Y. Agid, A. Dürr, A. Brice, 1995, American journal of medical genetics.

A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.

Y. Agid, M. Ruberg, A. Durr, 1994, American journal of human genetics.

Clinical and genetic abnormalities in patients with Friedreich's ataxia.

A Dürr, Y Agid, Y. Agid, 1996, The New England journal of medicine.

Molecular diagnosis of autosomal dominant early onset Alzheimer’s disease: an update

D. Campion, D. Hannequin, A. Brice, 2005, Journal of Medical Genetics.

Genetic heterogeneity of autosomal dominant cerebellar ataxia type I: evidence for the existence of a third locus.

Y. Agid, A. Durr, A. Dürr, 1993, Human molecular genetics.

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.

A. Destée, Y. Agid, A. Bonnet, 2007, Archives of neurology.

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

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

Mutations in the neuroserpin gene are rare in familial dementia

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

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

Y. Agid, B. Dubois, D. Campion, 1998, Human molecular genetics.

Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.

B. Dubois, J. Mallet, D. Campion, 1995, American journal of medical genetics.

Genome-Wide Scan for Autism Susceptibility Genes

Christopher Gillberg, Maria Råstam, Marion Leboyer, 1999 .

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

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

Analysis of ten candidate genes in autism by association and linkage.

C. Gillberg, M. Leboyer, A. Brice, 2002, American journal of medical genetics.

Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.

Y. Agid, A. Brice, G. Stevanin, 1992, Journal of medical genetics.

Duplication within chromosome 17 p 11 . 2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type la

Y. Agid, A. Brice, G. Stevanin, 2022 .

Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations

Y. Agid, A. Durr, A. Dürr, 1995, Annals of neurology.

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

J. Weissenbach, Y. Agid, C. Broeckhoven, 1995, Nature Genetics.

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.

Familial essential tremor and idiopathic torsion dystonia are different genetic entities

A. Dürr, A. Brice, G. Stevanin, 1993, Neurology.

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.

H. Cann, Y. Agid, C. Duyckaerts, 1995, American journal of human genetics.

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Miguel Ángel Martínez, Y. Agid, B. Dubois, 1996, Journal of medical genetics.

A large pedigree with early-onset Alzheimer's disease

Y. Agid, B. Dubois, J. Mallet, 1995, Neurology.

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

J. Weissenbach, J. Burgunder, J. Prud'homme, 1996, Brain : a journal of neurology.

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.

Y. Agid, M. Baulac, C. Duyckaerts, 1996, Neuroreport.

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

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

Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene

J. Weissenbach, Y. Agid, A. Vignal, 1994, Neuromuscular Disorders.

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

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

Increased wave P 300 latency in progressive supranuclear palsy.

Y. Agid, B. Pillon, F. Chain, 1989, Journal of neurology, neurosurgery, and psychiatry.

APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population

D. Campion, D. Hannequin, A. Brice, 2000, European Journal of Human Genetics.

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

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

Age and Sex

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

A study of visual processes in a case of interhemispheric disconnexion

F. Chain, F. Chédru, F. Lhermitte, 1976, Journal of the Neurological Sciences.

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia

J. Weissenbach, Y. Agid, N. Baumann, 1995, Neuromuscular Disorders.