Citation Impact
Citing Papers
HIFα Targeted for VHL-Mediated Destruction by Proline Hydroxylation: Implications for O 2 Sensing
2001 StandoutScienceNobel
Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization
2004 StandoutScience
Iron overload in urban Africans in the 1990s
1999
African-centric TP53 variant increases iron accumulation and bacterial pathogenesis but improves response to malaria toxin
2020
Antimicrobial therapy for patients with severe sepsis and septic shock: An evidence-based review
2004
Body Iron Stores and the Risk of Cancer
1988
Signatures of natural selection in the human genome
2003
Iron homeostasis: insights from genetics and animal models
2000
DNA polymorphisms amplified by arbitrary primers are useful as genetic markers
1990 Standout
Iron storage disease in parents and sibs of infants with neonatal hemochromatosis: 30‐ year follow‐up
1990
Hereditary Hemochromatosis in Adults without Pathogenic Mutations in the Hemochromatosis Gene
1999
The β-Thalassemias
1999 Standout
Hereditary Hemochromatosis — A New Look at an Old Disease
2004
Genetic Ablation and Restoration of the Olfactory Topographic Map
2000 StandoutNobel
Nonalcoholic Fatty Liver Disease
2002 Standout
Iron Overload Cardiomyopathy
2010
Liver injury due to iron overload in thalassemia: histopathologic and ultrastructural studies
1996
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
2000
Ferroptosis turns 10: Emerging mechanisms, physiological functions, and therapeutic applications
2022 Standout
A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote☆
1999
The hereditary hemochromatosis gene (HFE)
1999
Neuroprotection by tempol in a model of iron-induced oxidative stress in acute ischemic stroke
2004
Porphyrias
2010 Standout
The Utility of DNA Typing in Forensic Work
1991 StandoutScience
Severe Sepsis and Septic Shock
2013 Standout
Human nutrition, the gut microbiome and the immune system
2011 StandoutNature
Fetal liver disease may precede extrahepatic siderosis in neonatal hemochromatosis
1990
The Rise and Fall of the Chemoattractant Receptor GPR33
2005 StandoutNobel
The apolipoprotein(a) gene resides on human chromosome 6q26?27, in close proximity to the homologous gene for plasminogen
1988
A Comparison of Observational Studies and Randomized, Controlled Trials
2000 Standout
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
Polycystic Ovary Syndrome
1995 Standout
Ferritin for the clinician
2008
Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron
2004 StandoutNature
Impaired Spatial Representation in CA1 after Lesion of Direct Input from Entorhinal Cortex
2008 StandoutNobel
Hepatic iron and nonalcoholic fatty liver disease
1999
Hematopoietic Stem-Cell Transplantation
2006 Standout
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
2000 StandoutNature
Identification of the haemoglobin scavenger receptor
2001 StandoutNature
Role of controlled cardiac reoxygenation in reducing nitric oxide production and cardiac oxidant damage in cyanotic infantile hearts.
1994 StandoutNobel
Iron and microbial infection
2004
The mosaic that is our genome
2003 StandoutNatureNobel
Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans
1998
Genetic and Nongenetic Determinants of Regional Fat Distribution
1993
Body Iron Stores in Relation to Risk of Type 2 Diabetes in Apparently Healthy Women
2004
AFLP: a new technique for DNA fingerprinting
1995 Standout
5 Thalassaemia: clinical management
1998
The Pathogenesis of Coronary Artery Disease and the Acute Coronary Syndromes
1992 Standout
HLA-DQβ gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus
1987 StandoutNature
Atherosclerosis
2000 StandoutNature
Fluoro-Jade: a novel fluorochrome for the sensitive and reliable histochemical localization of neuronal degeneration
1997
Disorders of Iron Metabolism
1999 Standout
The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients
1998
Genomic mismatch scanning: a new approach to genetic linkage mapping
1993 StandoutNobel
Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands
1999
Iron Loading and Disease Surveillance
1999
The iron paradigm of ischemic heart disease
1989
Anemia of Chronic Disease
2005 Standout
Morphological study of the effects of intranasal zinc sulfate irrigation on the mouse olfactory epithelium and olfactory bulb
1993
Linkage Disequilibrium and the Search for Complex Disease Genes
2000
Neonatal Hemochromatosis
1992
Lipoprotein(a). A unique risk factor for atherothrombotic disease.
1990
Oxidants, antioxidants, and the degenerative diseases of aging.
1993 Standout
Evidence of genetic transmission in African iron overload.
1998
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
1980 Standout
Aceruloplasminemia: molecular characterization of this disorder of iron metabolism.
1995
Genetic Models of Human Vascular Disease
1995 StandoutNobel
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
1983 StandoutNature
Associations of iron overload in Africa with hepatocellular carcinoma and tuberculosis: Strachan's 1929 thesis revisited
1996
Clinical iron deficiency disturbs normal human responses to hypoxia
2016 StandoutNobel
Multicopper Oxidases and Oxygenases
1996 Standout
Impaired retention of spatial memory after transection of longitudinally oriented axons of hippocampal CA3 pyramidal cells
2002 StandoutNobel
Estimates of iron sufficiency in the US population
1986
Distribution of Transferrin Saturations in the African-American Population
1998
A mixed-model likelihood approximation on large pedigrees
1982
HFE Mutations Analysis in 711 Hemochromatosis Probands: Evidence for S65C Implication in Mild Form of Hemochromatosis
1999
Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum
1999
[1] Role of free radicals and catalytic metal ions in human disease: An overview
1990 Standout
Hereditary and nutritional iron overload
1992
Inflammation triggers hypoferremia and de novo synthesis of serum transferrin and ceruloplasmin in mice
1984
The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation
2005
Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes.
1984 StandoutNobel
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
1989 Standout
Assessing the role of HLA-linked and unlinked determinants of disease.
1987
Oxidative Stress, Caloric Restriction, and Aging
1996 StandoutScience
A highly polymorphic locus in human DNA.
1980
Hemochromatosis: How Much Iron Is Too Much?
1986
The Mysteries Of Lipoprotein(a)
1989 Science
Perspectives in Iron Metabolism
1982
Iron and infection
1978
Idiopathic neonatal iron storage involving the liver, pancreas, heart, and endocrine and exocrine glands
1981
The Future of Genetic Studies of Complex Human Diseases
1996 StandoutScience
Is there a link between African iron overload and the described mutations of the hereditary haemochromatosis gene?
1998
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.
1983 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Increased Risk of Acute Myocardial Infarction in Carriers of the Hemochromatosis Gene Cys282Tyr Mutation
1999
Hypervariable ‘minisatellite’ regions in human DNA
1985 StandoutNature
Iron Is Hot: An Update on the Pathophysiology of Hemochromatosis
1998
Iron Is Hot: An Update on the Pathophysiology of Hemochromatosis
1998
Copper and iron are mobilized following myocardial ischemia: possible predictive criteria for tissue injury.
1993
Juvenile and adult hemochromatosis are distinct genetic disorders.
1998
Value of Hepatic Iron Measurements in Early Hemochromatosis and Determination of the Critical Iron Level Associated With Fibrosis
1986
HLA and Disease 1982 ‐ A Survey
1983
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Optimal sampling for pedigree analysis: Parameter estimation and genotypic uncertainty
1983
Metal–Organic Frameworks in Biomedicine
2011 Standout
Hereditary iron overload and African Americans
1996
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
1998
Iron-Chelating Therapy and the Treatment of Thalassemia
1997
GENETICS OF HLA DISEASE ASSOCIATION
1981
The Structure of Haplotype Blocks in the Human Genome
2002 StandoutScience
Isolation of a cDNA clone for the human HLA-DR antigen alpha chain by using a synthetic oligonucleotide as a hybridization probe.
1982 StandoutNobel
A polymorphic DNA marker genetically linked to Huntington's disease
1983 StandoutNature
The Effect of Long-term Near Normal Glycemic Control on Mild Diabetic Retinopathy
1985
HFE gene knockout produces mouse model of hereditary hemochromatosis
1998
HFE Genotype in Patients with Hemochromatosis and Other Liver Diseases
1999
Works of Corwin Q. Edwards being referenced
Southern Blood Club Symposium: An Update On Selected Aspects of Hemochromatosis
1990
Screening for Hemochromatosis
1993
Haplotype Analysis of Hemochromatosis: Evaluation of Different Linkage-Disequilibrium Approaches and Evolution of Disease Chromosomes
1997
Hereditary hemochromatosis
1996
Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors
1988 Standout
Anemia and the liver
2002
HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tarda
1989
Primary Iron Overload in African Americans
1996
HFE gene: Structure, function, mutations, and associated iron abnormalities
2015
Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis
1996
Disorders of Excess Iron
1991
Iron Overload in Africa
1992
Twenty‐four hour variation of transferrin saturation in treated and untreated haemochromatosis homozygotes
1989
Iron overload in African Americans
1995
Disease-Related Conditions in Relatives of Patients with Hemochromatosis
2000
Homozygosity for Hemochromatosis: Clinical Manifestations
1980
Effect of Insulin Infusion Pump Use on Diabetic Retinopathy
1984
An experimental study of hyperchromic nerve cells in the cerebral cortex
1972
The genetics of quantitative plasma Lp(a): Analysis of a large pedigree
1983
Iron overload in hereditary spherocytosis: Association with hla‐linked hemochromatosis
1982
Controlled Comparison of Amikacin and Gentamicin
1977
Genetic linkage between hereditary hemochromatosis and HLA.
1979
Hereditary Haemochromatosis
1982
Management of Hemochromatosis
1998
Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda
2000
Familial effects on plasma sex-steroid content in man: Testosterone, estradiol and sex-hormone-binding globulin
1982
Hereditary Hemochromatosis: Analysis of Laboratory Expression of the Disease by Genotype in 18 Pedigrees
1982
Hereditary hypoceruloplasminemia
1979
Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.
1986
Hereditary Hemochromatosis
1977
Hematologic Changes in Chronic Arthritis of Mice Induced by Mycoplasma arthritidis
1975
Genetic mapping of the hemochromatosis locus on chromosome six
1980
Hereditary Hemochromatosis
1979
Heterozygosity for HLA-Linked Hemochromatosis as a Likely Cause of the Hepatic Siderosis Associated With Sporadic Porphyria Cutanea Tarda
1985