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Insulin resistance–associated hepatic iron overload

Gastroenterology (New York, N.Y. 1943), 1999-11, Vol.117 (5), p.1155-1163

1999

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Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

Gastroenterology (New York, N.Y. 1943), 1999-02, Vol.116 (2), p.372-377

1999

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Haemochromatosis and HLA-H

Nature genetics, 1996-11, Vol.14 (3), p.251-252

1996

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Diagnostic d’une surcharge hépatique en fer

La Revue de médecine interne (Paris), 2012-06, Vol.33, p.S10-S14

2012

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A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis

Haematologica (Roma), 2009-05, Vol.94 (5), p.720-724

2009

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A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Human genetics, 1997-10, Vol.100 (5-6), p.544-547

1997

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Métabolisme du fer et outils diagnostiques pour le clinicien

La Revue de médecine interne (Paris), 2012-06, Vol.33, p.S3-S9

2012

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Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications

Diabetes & metabolism, 2002-09, Vol.28 (4), p.297-304

2002

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A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

Journal of hepatology, 1999-04, Vol.30 (4), p.588-593

1999

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The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

Journal of medical genetics, 2004-01, Vol.41 (1), p.6-10

2004

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Haemochromatosis Cys282Tyr mutation in pyridoxine-responsive sideroblastic anaemia

The Lancet (British edition), 1997-05, Vol.349 (9063), p.1475-1476

1997

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Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis

Journal of medical genetics, 1998-11, Vol.35 (11), p.954-956

1998

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Localization of seven new genes around the HLA-A locus

Human molecular genetics, 1993-01, Vol.2 (1), p.55-60

1993

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Common Variants in the BMP2, BMP4, and HJV Genes of the Hepcidin Regulation Pathway Modulate HFE Hemochromatosis Penetrance

American journal of human genetics, 2007-10, Vol.81 (4), p.799-807

2007

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Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis

American journal of hematology, 2016-12, Vol.91 (12), p.1202-1205

2016

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A novel coding sequence belonging to a new multicopy gene family mapping within the human MHC class I region

Immunogenetics (New York), 1993-03, Vol.38 (1), p.47-53

1993

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Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

American journal of human genetics, 1994-02, Vol.54 (2), p.252-263

1994

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A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload

Haematologica (Roma), 2009-03, Vol.94 (3), p.335-339

2009

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Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region : implications for mapping the hemochromatosis gene (HFE)

Human genetics, 1996, Vol.97 (1), p.103-113

1996

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Dinucleotide repeat polymorphism at the D6S510 locus

Human molecular genetics, 1994-07, Vol.3 (7), p.1210-1210

1994

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Hereditary iron overload

Pathologie biologie (Paris), 2010-10, Vol.58 (5), p.316

2010

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Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families

Hepatology (Baltimore, Md.), 1997-10, Vol.26 (4), p.986-990

1997

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Geography of HFE C282Y and H63D mutations

Genetic testing, 2000, Vol.4 (2), p.183-198

2000

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A highly informative dinucleotide repeat polymorphism telomeric to HLA-F

Immunogenetics (New York), 1997, Vol.46 (4), p.355-356

1997

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A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

Immunogenetics (New York), 1992-02, Vol.35 (3), p.183-189

1992

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Insulin resistance–associated hepatic iron overload

Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

Haemochromatosis and HLA-H

Diagnostic d’une surcharge hépatique en fer

A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis

A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Métabolisme du fer et outils diagnostiques pour le clinicien

Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications

A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

Haemochromatosis Cys282Tyr mutation in pyridoxine-responsive sideroblastic anaemia

Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis

Localization of seven new genes around the HLA-A locus

Common Variants in the BMP2, BMP4, and HJV Genes of the Hepcidin Regulation Pathway Modulate HFE Hemochromatosis Penetrance

Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis

A novel coding sequence belonging to a new multicopy gene family mapping within the human MHC class I region

Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload

Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region : implications for mapping the hemochromatosis gene (HFE)

Dinucleotide repeat polymorphism at the D6S510 locus

Hereditary iron overload

Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families

Geography of HFE C282Y and H63D mutations

A highly informative dinucleotide repeat polymorphism telomeric to HLA-F

A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

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