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Intracellular iron uptake is favored in Hfe‐KO mouse primary chondrocytes mimicking an osteoarthritis‐related phenotype

BioFactors (Oxford), 2019-07, Vol.45 (4), p.583-597

2019

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Iron, HFE hemochromatosis, and infections

Blood, 2024-08, Vol.144 (7), p.796

2024

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Iron overload in a murine model of hereditary hemochromatosis is associated with accelerated progression of osteoarthritis under mechanical stress

Osteoarthritis and cartilage, 2016-03, Vol.24 (3), p.494-502

2016

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Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy

JAMA : the journal of the American Medical Association, 2020-11, Vol.324 (20), p.2048

2020

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HJV mutations causing hemochromatosis: variable phenotypic expression in a pair of twins

Haematologica (Roma), 2024-08, Vol.109 (8), p.2741

2024

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Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

BMJ (Online), 2019-01, Vol.364, p.k5222

2019

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Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort

Hepatology (Baltimore, Md.), 2022-12, Vol.76 (6), p.1735-1745

2022

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Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

Blood, 2018-07, Vol.132 (1), p.101-110

2018

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Liraglutide Impacts Iron Homeostasis in a Murine Model of Hereditary Hemochromatosis

Endocrinology (Philadelphia), 2024-07, Vol.165 (9)

2024

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Regression of Fibrosis Stage With Treatment Reduces Long-Term Risk of Liver Cancer in Patients With Hemochromatosis Caused by Mutation in HFE

Clinical gastroenterology and hepatology, 2020-07, Vol.18 (8), p.1851-1857

2020

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Pathophysiological consequences and benefits of HFE mutations: 20 years of research

Haematologica (Roma), 2017-05, Vol.102 (5), p.809-817

2017

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Clinical penetrance in hereditary hemochromatosis: estimates of the cumulative incidence of severe liver disease among HFE C282Y homozygotes

Genetics in medicine, 2018-04, Vol.20 (4), p.383-389

2018

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Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group

British journal of haematology, 2024-01, Vol.204 (1), p.306-314

2024

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EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)

European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.479-495

2016

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In vivo adenine base editing reverts C282Y and improves iron metabolism in hemochromatosis mice

Nature communications, 2022-09, Vol.13 (1), p.5215-10, Article 5215

2022

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A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population

Clinica chimica acta, 2023-01, Vol.538, p.211-215

2023

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IgG subclass levels in referred hemochromatosis probands with HFE p.C282Y/p.C282Y

PloS one, 2024-05, Vol.19 (5), p.e0302817-e0302817

2024

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Genetic Diagnosis in Hereditary Hemochromatosis: Discovering and Understanding the Biological Relevance of Variants

Clinical chemistry (Baltimore, Md.), 2021-10, Vol.67 (10), p.1324-1341

2021

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Left Ventricular Global Longitudinal Strain to Assess Left Ventricular Systolic Dysfunction in Chronically Treated Cardiac Asymptomatic Hereditary Hemochromatosis With HFE C282Y Homozygosity

Journal of the American Society of Echocardiography, 2024-05, Vol.37 (5), p.568-570

2024

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Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes

Digestive diseases and sciences, 2023, Vol.68 (1), p.312-322

2023

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Association of Genetic Variant Linked to Hemochromatosis With Brain Magnetic Resonance Imaging Measures of Iron and Movement Disorders

JAMA neurology, 2022-09, Vol.79 (9), p.919

2022

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Disruption of Hfe leads to skeletal muscle iron loading and reduction of hemoproteins involved in oxidative metabolism in a mouse model of hereditary hemochromatosis

Biochimica et biophysica acta. General subjects, 2022-03, Vol.1866 (3), p.130082, Article 130082

2022

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MRI‐Based Iron Phenotyping and Patient Selection for Next‐Generation Sequencing of Non–Homeostatic Iron Regulator Hemochromatosis Genes

Hepatology (Baltimore, Md.), 2021-11, Vol.74 (5), p.2424-2435

2021

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Juvenile Hemochromatosis With Non-transfused Hemolytic Anemia Caused by a De Novo PIEZO1 Gene Mutation

Journal of pediatric hematology/oncology, 2023-05, Vol.45 (4), p.e510-e513

2023

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Hereditary hemochromatosis with homozygous C282Y HFE mutation: possible clinical model to assess effects of elevated reactive oxygen species on the development of cardiovascular disease

Molecular and cellular biochemistry, 2024-03, Vol.479 (3), p.617-627

2024

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Intracellular iron uptake is favored in Hfe‐KO mouse primary chondrocytes mimicking an osteoarthritis‐related phenotype

Iron, HFE hemochromatosis, and infections

Iron overload in a murine model of hereditary hemochromatosis is associated with accelerated progression of osteoarthritis under mechanical stress

Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy

HJV mutations causing hemochromatosis: variable phenotypic expression in a pair of twins

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort

Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

Liraglutide Impacts Iron Homeostasis in a Murine Model of Hereditary Hemochromatosis

Regression of Fibrosis Stage With Treatment Reduces Long-Term Risk of Liver Cancer in Patients With Hemochromatosis Caused by Mutation in HFE

Pathophysiological consequences and benefits of HFE mutations: 20 years of research

Clinical penetrance in hereditary hemochromatosis: estimates of the cumulative incidence of severe liver disease among HFE C282Y homozygotes

Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group

EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)

In vivo adenine base editing reverts C282Y and improves iron metabolism in hemochromatosis mice

A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population

IgG subclass levels in referred hemochromatosis probands with HFE p.C282Y/p.C282Y

Genetic Diagnosis in Hereditary Hemochromatosis: Discovering and Understanding the Biological Relevance of Variants

Left Ventricular Global Longitudinal Strain to Assess Left Ventricular Systolic Dysfunction in Chronically Treated Cardiac Asymptomatic Hereditary Hemochromatosis With HFE C282Y Homozygosity

Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes

Association of Genetic Variant Linked to Hemochromatosis With Brain Magnetic Resonance Imaging Measures of Iron and Movement Disorders

Disruption of Hfe leads to skeletal muscle iron loading and reduction of hemoproteins involved in oxidative metabolism in a mouse model of hereditary hemochromatosis

MRI‐Based Iron Phenotyping and Patient Selection for Next‐Generation Sequencing of Non–Homeostatic Iron Regulator Hemochromatosis Genes

Juvenile Hemochromatosis With Non-transfused Hemolytic Anemia Caused by a De Novo PIEZO1 Gene Mutation

Hereditary hemochromatosis with homozygous C282Y HFE mutation: possible clinical model to assess effects of elevated reactive oxygen species on the development of cardiovascular disease

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