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Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study

Molecular psychiatry, 2009-08, Vol.14 (8), p.804-819

2009

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Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia

Molecular psychiatry, 2009-11, Vol.14 (11), p.1024-1031

2009

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Tasimelteon treatment entrains the circadian clock and demonstrates significant benefit on sleep and wake parameters in totally blind individuals with non-24 hour circadian rhythms

Sleep medicine, 2013-12, Vol.14, p.e178-e178

2013

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The synuclein family

Genome research, 1998-09, Vol.8 (9), p.871-880

Lavedan, C

1998

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Scénographies numériques du patrimoine: Expérimentations, recherches et médiations

2020

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Myotonic dystrophy : size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism

American journal of human genetics, 1993-05, Vol.52 (5), p.875-883

1993

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Absence of Mutation in the - and -Synuclein Genes in Familial Autosomal Dominant Parkinson's Disease

DNA research, 1998-01, Vol.5 (6), p.401-402

Lavedan, C.

1998

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The ubiquitin pathway in Parkinson's disease

Nature (London), 1998-10, Vol.395 (6701), p.451-452

1998

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Mutation in the α-synuclein gene identified in families with Parkinson's disease

Science (American Association for the Advancement of Science), 1997-06, Vol.276 (5321), p.2045-2047

1997

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Genes that co-cluster with estrogen receptor alpha in microarray analysis of breast biopsies

The pharmacogenomics journal, 2001, Vol.1 (2), p.135-141

2001

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Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy

American journal of human genetics, 1994-03, Vol.54 (3), p.414-423

1994

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Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

Neurology, 1996-01, Vol.46 (1), p.208-213

1996

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Trinucleotide repeats (CGG)22TGG(CGG)43TGG(CGG)21 from the fragile X gene remain stable in transgenic mice

Human genetics, 1997-09, Vol.100 (3-4), p.407-414

1997

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Identification, localization and characterization of the human γ-synuclein gene

Human genetics, 1998-07, Vol.103 (1), p.106-112

1998

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Deletions in the Parkin gene and genetic heterogeneity in a greek family with early onset Parkinson's disease

Human genetics, 1998-10, Vol.103 (4), p.424-427

1998

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Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy

The Lancet (British edition), 1993-01, Vol.341 (8839), p.237-237

1993

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Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease

DNA research, 1998-12, Vol.5 (6), p.401-402

1998

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A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration

Neuroscience letters, 2002-03, Vol.322 (1), p.57-61

2002

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Contig map of the Parkinson's disease region on 4q21-q23

DNA research, 1998-02, Vol.5 (1), p.19-23

1998

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French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion

Journal of medical genetics, 1994-01, Vol.31 (1), p.33-36

1994

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Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice

Genomics (San Diego, Calif.), 1998-06, Vol.50 (2), p.229-240

1998

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NcoI RFLP at 19q13 identified by the DNA sequence pW119B (D19S169)

Nucleic acids research, 1991-10, Vol.19 (20), p.5804-5804

1991

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Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): Application to myotonic dystrophy diagnosis

Genomics (San Diego, Calif.), 1990-12, Vol.8 (4), p.739-740

1990

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Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor

Genomics (San Diego, Calif.), 1990, Vol.7 (3), p.434-438

1990

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Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers

Journal of medical genetics, 1991-02, Vol.28 (2), p.89-91

1991

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Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study

Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia

Tasimelteon treatment entrains the circadian clock and demonstrates significant benefit on sleep and wake parameters in totally blind individuals with non-24 hour circadian rhythms

The synuclein family

Scénographies numériques du patrimoine: Expérimentations, recherches et médiations

Myotonic dystrophy : size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism

Absence of Mutation in the - and -Synuclein Genes in Familial Autosomal Dominant Parkinson's Disease

The ubiquitin pathway in Parkinson's disease

Mutation in the α-synuclein gene identified in families with Parkinson's disease

Genes that co-cluster with estrogen receptor alpha in microarray analysis of breast biopsies

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

Trinucleotide repeats (CGG)22TGG(CGG)43TGG(CGG)21 from the fragile X gene remain stable in transgenic mice

Identification, localization and characterization of the human γ-synuclein gene

Deletions in the Parkin gene and genetic heterogeneity in a greek family with early onset Parkinson's disease

Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy

Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease

A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration

Contig map of the Parkinson's disease region on 4q21-q23

French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion

Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice

NcoI RFLP at 19q13 identified by the DNA sequence pW119B (D19S169)

Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): Application to myotonic dystrophy diagnosis

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers

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