A. Chaventré

发表

Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe.

Anne Cambon-Thomsen, Wolfgang Scheffrahn, Dragan Primorac, 2004, American journal of human genetics.

Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma.

H. Garchon, A. Chaventré, A. Brézin, 1997, Human molecular genetics.

The western and eastern roots of the Saami--the story of genetic "outliers" told by mitochondrial DNA and Y chromosomes.

P. Rudan, R. Villems, T. Kivisild, 2004, American journal of human genetics.

Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.

D. Labie, C. Junien, J. Kaplan, 1982, Human heredity.

Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France

V. Probst, A. Chaventré, J. Schott, 2006, Circulation.

A NEW FAST VARIANT (BF*F08) OF THE BF POLYMORPHISM

A. Chaventré, C. Rivat, M. Cazes, 1982, Journal of immunogenetics.

Distribution of HIV-1 disease modifying regulated on activation normal T cell expressed and secreted haplotypes in Asian, African and Caucasian individuals. French ALT and IMMUNOCO Study Group.

P. Debré, Y. Takebe, Y. Nagai, 1999, AIDS.

Nucleotide sequence evidence of the unicentric origin of the βC mutation in Africa

D. Labie, R. Nagel, J. Elion, 1991, Human Genetics.

A new polymorphism of thyroxin-binding globulin in three African groups (Mali) with endemic nodular goitre

A. Chaventré, J. Constans, C. Gouaillard, 1992, Human Genetics.

Hemoglobinopathies in the dogon country: Presence of βs, βc, and δa'genes

R. Nagel, A. Chaventré, G. Bellis, 1994 .

Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.

A. Chaventré, C. Le Caignec, J. Schott, 2002, American journal of human genetics.

Disuniting uniformity: a pied cladistic canvas of mtDNA haplogroup H in Eurasia.

P. Rudan, R. Villems, T. Kivisild, 2004, Molecular biology and evolution.

Origin and diffusion of mtDNA haplogroup X.

P. Rudan, R. Villems, T. Kivisild, 2003, American journal of human genetics.

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis

C. Férec, A. Chaventré, M. Audrézet, 2000, The Lancet.

Registers and follow-up methods of populations in a public health survey: the example of the village Glanlé in Ivory Coast.

A. Chaventré, G. Bellis, M. Gaimard, 1998, Collegium antropologicum.

The HL-A gene structure of Twareg populations. II. The Kel Dinig.

A. Chaventré, A. Jacquard, L. Degos, 2008, Tissue antigens.

Selective pressure on HL-A polymorphism

A. Chaventré, A. Jacquard, L. Degos, 1974, Nature.

An mtDNA perspective of French genetic variation

P. Rudan, R. Villems, T. Kivisild, 2007, Annals of human biology.

Neonatal Screening for Cystic Fibrosis in Brittany, France: Assessment of 10 Years’ Experience and Impact on Prenatal Diagnosis

C. Férec, A. Chaventré, M. Audrézet, 2001 .

Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany

G. Bertorelle, C. Férec, A. Chaventré, 1996, Human Genetics.

[Gene mutations of cystic fibrosis in Brittany population].

C. Férec, A. Chaventré, H. Guillermit, 1991, Pathologie-biologie.

[Linkage between juvenile glaucoma and chromosome 1q in 2 French families].

J. Rouland, C. Férec, H. Garchon, 1994, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Founder effect in GLC1A-linked familial open-angle glaucoma in Northern France.

J. Rouland, H. Garchon, A. Chaventré, 1998, American journal of medical genetics.

[Genetic aspects of valvulopathies].

J. Gueffet, V. Probst, A. Chaventré, 2007, Archives des maladies du coeur et des vaisseaux.

[Management strategies for endemic goiter in developing countries].

A. Chaventré, O. Aké, P. Kouame, 1999, Medecine tropicale : revue du Corps de sante colonial.

Origin of Hb A2′ (Hb B2) [δ16(A13)Gly→Arg (GGC→CGC)]

R. Nagel, A. Chaventré, R. Ducrocq, 2003 .

Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations.

E. Denamur, O. Clermont, J. Elion, 2001, Microbiology.

Haemoglobinopathies C and S in the Dogons.

A. Chaventré, G. Bellis, M. Baby, 1994, Nouvelle revue francaise d'hematologie.

Treatment by iodized oil (Lipiodol® UF) of a population in Mali suffering from endemic goiter

A. Chaventré, G. Bellis, F. Roux, 1996, Journal of endocrinological investigation.

Growth of Plasmodium falciparum inhibited by HbD-Ouled-Rabah

A. Chaventré, R. Krishnamoorthy, S. Schulman, 1991, The Lancet.