G. Mercier

发表

Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson’s disease: no association found

G. Lucotte, J. Turpin, G. Mercier, 1999, Journal of Neurology.

Population Distribution of the Methionine Allele at the PRNP Codon 129 Polymorphism in Europe and the Middle East

G. Lucotte, F. Diéterlen, G. Mercier, 2008, Human biology.

The population distribution of the Met allele at the PRNP129 polymorphism (a high risk factor for Creutzfeldt-Jakob disease) in various regions of France and in West Europe.

G. Lucotte, G. Mercier, 2005, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians.

G. Lucotte, G. Mercier, 2003, Genetic testing.

Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects.

G. Lucotte, G. Mercier, N. Change, 2008, Genetic testing.

Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's disease.

B. Funalot, J. Pérez-Tur, W. Nichols, 2006, Genetic testing.

Haplotypes du chromosome Y en Corse

G. Lucotte, G. Mercier, A. Pinna, 2002 .

Elevated frequencies of the mutant allele delta32 at the CCR5 gene in Ashkenazic Jews.

G. Lucotte, G. Mercier, P. Smets, 1999, AIDS research and human retroviruses.

Distribution of the CCR5 gene 32-bp deletion in Europe.

G. Lucotte, G. Mercier, 1998, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.

A Decreasing Gradient of 374F Allele Frequencies in the Skin Pigmentation Gene SLC45A2, from the North of West Europe to North Africa

I. Yuasa, G. Lucotte, F. Diéterlen, 2010, Biochemical Genetics.

The vitamin D receptor FokI start codon polymorphism and bone mineral density in osteoporotic postmenopausal French women

G. Lucotte, G. Mercier, A. Burckel, 1999, Clinical genetics.

Population genetics of factor V Leiden in Europe.

G. Lucotte, G. Mercier, 2001, Blood cells, molecules & diseases.

Localization of the gene for fibrodysplasia ossificans progressiva (FOP) to chromosome 17q21-22.

G. Lenoir, K. Fontaine, G. Lucotte, 2000, Genetic counseling.

Celtic origin of the C282Y mutation of hemochromatosis.

G. Lucotte, G. Mercier, 1998, Genetic testing.

Association of a polymorphism in the collagen I alpha1 gene with osteoporosis in French women.

M. Dougados, C. Roux, G. Lucotte, 1998, Arthritis and rheumatism.

Detection of Borrelia burgdorferi DNA by polymerase chain reaction in urine specimens of patients with erythema migrans lesions.

G. Lucotte, G. Mercier, A. Burckel, 1997, Molecular and cellular probes.

Y-Chromosome DNA Haplotype XI in Eastern Europe

G. Lucotte, G. Mercier, Florent Diertelen, 2003, Human biology.

Brief communication: Y-chromosome haplotypes in Egypt.

G. Lucotte, G. Mercier, 2003, American journal of physical anthropology.

Y-Haplotype X in the Balkans

G. Lucotte, F. Diéterlen, G. Mercier, 2006 .

Characterization of the Y-Chromosome Sardinian–Corsican Haplotype

G. Lucotte, F. Diéterlen, G. Mercier, 2006 .

Frequency of the C282Y mutation of hemochromatosis in five French populations.

G. Lucotte, G. Mercier, C. Bathelier, 1998, Blood cells, molecules & diseases.

Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in families.

G. Lucotte, G. Mercier, E. Boillat, 1998, Genetic counseling.

A simplified semiquantitative determination of hepatitis C virus genome molecules by the end-point dilution method.

G. Lucotte, G. Mercier, C. Bathelier, 1996, Molecular and cellular probes.

TNF-α polymorphisms in multiple sclerosis: no association with −238 and −308 promoter alleles, but the microsatellite allele all is associated with the disease in French patients

G. Lucotte, G. Mercier, Gérard Lucotte, 2000, Multiple sclerosis.

Connexin 26 mutation 35delG: prevalence of carriers in various regions in France.

G. Lucotte, G. Mercier, C. Bathelier, 2005, International journal of pediatric otorhinolaryngology.

Fibrodysplasie ossifiante progressive: étude de 20 cas

G. Lucotte, G. Mercier, C. Bathelier, 2000 .

Meta-analysis of GJB2 mutation 35delG frequencies in Europe.

G. Lucotte, G. Mercier, 2001, Genetic testing.

Frequency of factor V Leiden (Arg506Gln) in France.

G. Lucotte, G. Mercier, 1997, British journal of haematology.

FokI polymorphism at the human vitamin D receptor gene locus in Europeans and Africans

G. Lucotte, G. Mercier, A. Burckel, 1999, Clinical genetics.

North African Genes in Iberia Studied by Y-Chromosome DNA Haplotype 5

G. Lucotte, N. Gérard, G. Mercier, 2001, Human biology.

TNF-α polymorphisms in multiple sclerosis: no association with −238 and −308 promoter alleles, but the microsatellite allele all is associated with the disease in French patients

G. Lucotte, G. Mercier, C. Bathelier, 2000, Multiple sclerosis.

The use of nested RT-PCR of prostate-specific membrane antigen in blood cells: implications for the detection of haematogenous neoplastic cells in patients with prostate adenocarcinoma.

G. Mercier, A. Burckel, Gérard Lucotte, 1998, Molecular and cellular probes.