C. Lavedan

M. Pericak-Vance, M. Polymeropoulos, R. Nussbaum, 1998, DNA research : an international journal for rapid publication of reports on genes and genomes.

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

C. Junien, C. Lavedan, Johnson, 1993, American journal of human genetics.

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

S E Ide, A. Dehejia, M. Polymeropoulos, 1997, Science.

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

M. Polymeropoulos, S. Volpi, L. Licamele, 2009, Molecular Psychiatry.

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

A. Dehejia, M. Polymeropoulos, R. Nussbaum, 1998, Human Genetics.

Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.

R. Nussbaum, C. Lavedan, K. Usdin, 1998, Genomics.

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

R. Nussbaum, C. Lavedan, L. Garrett, 1997, Human Genetics.

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.

C. Junien, C. Lavedan, P. Shelbourne, 1991, Journal of medical genetics.

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

C. Junien, B. Wieringa, C. Lavedan, 1991, Nucleic acids research.

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.

C. Junien, C. Lavedan, J. Rabès, 1993, Human molecular genetics.

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

C. Junien, J. Roume, C. Lavedan, 1993, The Lancet.

Mutations in American families with spinocerebellar ataxia (SCA) type 3

M. Polymeropoulos, J. Higgins, S. Ide, 1996, Neurology.

Translating the Genome into individualized therapeutics

M. Polymeropoulos, C. Wolfgang, C. Lavedan, 2004 .

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

C. Junien, R. Korneluk, C. Lavedan, 1990, Genomics.

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

C. Bonaïti‐pellié, C. Boileau, C. Lavedan, 1994, Journal of medical genetics.

Absence of weight gain association with the HTR2C −759C/T polymorphism in patients with schizophrenia treated with iloperidone

S. Volpi, A. Thompson, C. Lavedan, 2010, Psychiatry Research.

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

M. Polymeropoulos, M. Ellis, C. Lavedan, 2001, The Pharmacogenomics Journal.

Genomic organization and expression of the human beta-synuclein gene (SNCB).

A. Dehejia, M. Polymeropoulos, R. Nussbaum, 1998, Genomics.

Tasimelteon for non-24-hour sleep–wake disorder in totally blind people (SET and RESET): two multicentre, randomised, double-masked, placebo-controlled phase 3 trials

M. Polymeropoulos, L. Licamele, S. Lockley, 2015, The Lancet.

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

A. Dehejia, M. Polymeropoulos, R. Nussbaum, 1998, DNA Research.

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

M. Polymeropoulos, D. Anastasopoulos, C. Lavedan, 1998, Human Genetics.

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

C. Junien, H. Brunner, T. Ashizawa, 1994, American journal of human genetics.