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The Endogenous Retroviral Locus ERVWE1 Is a Bona Fide Gene Involved in Hominoid Placental Physiology

Proceedings of the National Academy of Sciences - PNAS, 2004-02, Vol.101 (6), p.1731-1736

2004

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Brief communication: Y-chromosome haplotypes in Egypt

American journal of physical anthropology, 2003-05, Vol.121 (1), p.63-66

2003

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Celtic Origin of the C282Y Mutation of Hemochromatosis

Blood cells, molecules, & diseases, 1998-12, Vol.24 (4), p.433-438

Lucotte, Gérard

1998

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Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis

Annals of human genetics, 2006-11, Vol.70 (6), p.802-811

2006

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Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

American journal of human genetics, 1999, Vol.64 (1), p.89-98

1999

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Distribution of Two Asian-Related Coding SNPs in the MC1R and OCA2 Genes

Biochemical genetics, 2007-08, Vol.45 (7-8), p.535-542

2007

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Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients

Genetic counseling, 2010-01, Vol.21 (4), p.461

2010

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Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients

Genetic counseling, 2009, Vol.20 (1), p.53

2009

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Frequencies of the CC chemokine receptor 5 Δ32 allele in various populations of defined racial background

Biomedicine & pharmacotherapy, 1997, Vol.51 (10), p.469-473

Lucotte, G

1997

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Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent

Human molecular genetics, 1993-10, Vol.2 (10), p.1535-1540

1993

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Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease

European journal of neurology, 2004-04, Vol.11 (4), p.247-251

2004

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Duplex PCR-RFLP for simultaneous detection of factor V Leiden and prothrombin G20210A

Molecular and cellular probes, 2003-10, Vol.17 (5), p.267-269

2003

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Molecular basis of the TaqI p49a,f polymorphism in the DYS1 locus containing DAZ genes

Molecular human reproduction, 2003-09, Vol.9 (9), p.509-516

2003

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PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in France

Molecular and cellular probes, 2001-02, Vol.15 (1), p.57-59

2001

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Y-chromosome DNA haplotypes in Basques

Journal of molecular evolution, 1996-04, Vol.42 (4), p.472-475

1996

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Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)

Genetic counseling, 2007-01, Vol.18 (3), p.349

2007

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Bilan de dix années du diagnostic moléculaire de la maladie de Huntington en France

Immuno-analyse & biologie spécialisée, 2001-03, Vol.16 (2), p.92-95

Lucotte, G.

2001

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A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient

Clinical genetics, 1999-12, Vol.56 (6), p.469-470

1999

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Frequencies of 32 base pair deletion of the ( Δ32) allele of the CCR5 HIV-1 co-receptor gene in Caucasians: a comparative analysis

Infection, genetics and evolution, 2002-05, Vol.1 (3), p.201-205

Lucotte, Gérard

2002

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Distribution of the CCR5 gene 32-basepair deletion in West Europe. A hypothesis about the possible dispersion of the mutation by the Vikings in historical times

Human immunology, 2001-09, Vol.62 (9), p.933-936

Lucotte, G

2001

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

Human biology, 2001-10, Vol.73 (5), p.763-769

2001

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

Journal of neurology, 1999-01, Vol.246 (1), p.45-47

1999

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A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?

Blood cells, molecules, & diseases, 2003-09, Vol.31 (2), p.262-267

2003

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Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay

Molecular and cellular probes, 1999-10, Vol.13 (5), p.389-391

1999

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The Endogenous Retroviral Locus ERVWE1 Is a Bona Fide Gene Involved in Hominoid Placental Physiology

Brief communication: Y-chromosome haplotypes in Egypt

Celtic Origin of the C282Y Mutation of Hemochromatosis

Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis

BRCAness, SLFN11, and RB1 loss predict response to topoisomerase I inhibitors in triple-negative breast cancers

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

Distribution of Two Asian-Related Coding SNPs in the MC1R and OCA2 Genes

Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients

Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients

Frequencies of the CC chemokine receptor 5 Δ32 allele in various populations of defined racial background

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent

Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease

Duplex PCR-RFLP for simultaneous detection of factor V Leiden and prothrombin G20210A

Molecular basis of the TaqI p49a,f polymorphism in the DYS1 locus containing DAZ genes

PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in France

Y-chromosome DNA haplotypes in Basques

Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)

Bilan de dix années du diagnostic moléculaire de la maladie de Huntington en France

A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient

Frequencies of 32 base pair deletion of the ( Δ32) allele of the CCR5 HIV-1 co-receptor gene in Caucasians: a comparative analysis

Distribution of the CCR5 gene 32-basepair deletion in West Europe. A hypothesis about the possible dispersion of the mutation by the Vikings in historical times

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

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

A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?

Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay

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