Yves Agid

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Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

Y. Agid, A. Brice, R. Gouider, 1995, Neurology.

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Y. Agid, J. Melki, A. Dürr, 1994, Human molecular 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.

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

A Dürr, Y Agid, Y. Agid, 2004, The Lancet.

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Y. Agid, M. Vidailhet, A. Dürr, 2000, Archives of neurology.

DYT1 mutation in French families with idiopathic torsion dystonia.

Y. Agid, M. Vidailhet, A. Durr, 1999, Brain : a journal of 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.

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

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

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Y. Agid, P. Pollak, A. Dürr, 2004, Neurology.

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

Y. Agid, G. Stevanin, M. Hamida, 1994, Neurology.

Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Y. Agid, A. Brice, N. Birouk, 1996, American journal of human genetics.

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

Familial essential tremor and idiopathic torsion dystonia are different genetic entities

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

Are cognitive changes the first symptoms of Huntington’s disease? A study of gene carriers

Y. Agid, B. Dubois, B. Pillon, 1998, Journal of neurology, neurosurgery, and psychiatry.

The phenotype of “pure” autosomal dominant spastic paraplegia

Y. Agid, A. Dürr, A. Brice, 1994, Neurology.

Clinical and molecular features of spinocerebellar ataxia type 6

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

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.