Citation Impact
Citing Papers
Genomewide Pharmacogenetics of Bisphosphonate-Induced Osteonecrosis of the Jaw: The Role of RBMS3
2012
The Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency
2008 StandoutScienceNobel
The Hitchhiking Effect on Linkage Disequilibrium Between Linked Neutral Loci
2006
Uncommon Mutations and Polymorphisms in the Hemochromatosis Gene
2000
Geography of HFE C282Y and H63D Mutations
2000
Regulation of growth differentiation factor 15 expression by intracellular iron
2008 StandoutNobel
The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals
2022 StandoutNobel
Novel genetic and epigenetic factors of importance for inter-individual differences in drug disposition, response and toxicity
2019
Racial/ethnic variation and risk factors for allopurinol-associated severe cutaneous adverse reactions: a cohort study
2018
Targeted resequencing of a genomic region influencing tameness and aggression reveals multiple signals of positive selection
2011 StandoutNobel
Disrupted hepcidin regulation in HFE -associated haemochromatosis and the liver as a regulator of body iron homoeostasis
2003
Lack of the bone morphogenetic protein BMP6 induces massive iron overload
2009
Hereditary Hemochromatosis in Adults without Pathogenic Mutations in the Hemochromatosis Gene
1999
Novel interferon-γ enzyme-linked immunoSpot assay using activated cells for identifying hypersensitivity-inducing drug culprits
2017 StandoutNobel
Comparative analysis of mouse hepcidin 1 and 2 genes: evidence for different patterns of expression and co‐inducibility during iron overload 1
2003
Peaks of Linkage Are Localized by a BAC/PAC Contig of the 6p Reading Disability Locus
2001
Allopurinol hypersensitivity: investigating the cause and minimizing the risk
2015
Haemochromatosis in the new millenium
2000
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group
1998
High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
2000
Clinical Pharmacogenetics Implementation Consortium Guidelines for Human Leukocyte Antigen-B Genotype and Allopurinol Dosing
2012
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin
2004 Standout
Mapping autoimmunity genes
1999
Absence of the TAP2 Human Recombination Hotspot in Chimpanzees
2004 StandoutNobel
Decreased Liver Hepcidin Expression in the Hfe Knockout Mouse
2002
High-Resolution Mapping of Crossovers in Human Sperm Defines a Minisatellite-Associated Recombination Hotspot
1998
The hereditary hemochromatosis gene (HFE)
1999
Balancing Acts
2004 Standout
Porphyrias
2010 Standout
Toxic epidermal necrolysis: Review of pathogenesis and management
2011
TFOS DEWS II pathophysiology report
2017 Standout
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
Uric Acid Lowering to Prevent Kidney Function Loss in Diabetes: The Preventing Early Renal Function Loss (PERL) Allopurinol Study
2013
Stevens–Johnson syndrome with sulfasalazine treatment: Report of two cases
2011
Two to Tango: Regulation of Mammalian Iron Metabolism
2010 Standout
Hereditary haemochromatosis
2004
The ferroportin disease
2003
Specificity of autoantibodies to epitopes of myelin proteins in multiple sclerosis
2002
The genetics of hyperuricaemia and gout
2012
Antioxidant therapy for treatment of inflammatory bowel disease: Does it work?
2015 Standout
Gout
2016 Standout
Ecological immunology: costly parasite defences and trade-offs in evolutionary ecology
1996 Standout
The Importance of Race and Ethnic Background in Biomedical Research and Clinical Practice
2003 Standout
The genetical archaeology of the human genome
1996 StandoutNobel
Toxic epidermal necrolysis
2013
Starting dose is a risk factor for allopurinol hypersensitivity syndrome: A proposed safe starting dose of allopurinol
2012
The epidemiology of Parkinson's disease: risk factors and prevention
2016 Standout
Linkage disequilibrium, mutational analysis and natural selection in the repetitive region of the clock gene, period, in Drosophila melanogaster
1997
Fine-scale recombination patterns differ between chimpanzees and humans
2005 StandoutNobel
Probability of HIV-1 transmission per coital act in monogamous, heterosexual, HIV-1-discordant couples in Rakai, Uganda
2001 Standout
Multiple Sclerosis
2000 Standout
Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis
2003
TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology
2016 Standout
A Map of Recent Positive Selection in the Human Genome
2006 Standout
Evolutionary Behavioral Genetics in Drosophila
2002
Hepatocellular carcinoma pathogenesis: from genes to environment
2006 Standout
Disorders of Iron Metabolism
1999 Standout
Treating to target: a strategy to cure gout
2009
Allopurinol Hypersensitivity: A Systematic Review of All Published Cases, 1950–2012
2013
Ocular Features and Histopathologic Changes during Follow-up of Toxic Epidermal Necrolysis
2010
A Population-Based Study of the Clinical Expression of the Hemochromatosis Gene
1999
Anemia of Chronic Disease
2005 Standout
Genetics and molecular biology of rhythms in Drosophila and other insects
2003 StandoutNobel
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
PHYSIOLOGY AND MOLECULAR BIOLOGY OF DIETARY IRON ABSORPTION
2003
Establishment of NOD-Pdcd1-/-mice as an efficient animal model of type I diabetes
2005 StandoutNobel
Advanced Intercross Line Mapping of Eae5 Reveals Ncf-1 and CLDN4 as Candidate Genes for Experimental Autoimmune Encephalomyelitis
2006
Down-regulation of hepcidin in porphyria cutanea tarda
2008
Expression of Th-1 Chemokines and Chemokine Receptors on the Ocular Surface of C57BL/6 Mice: Effects of Desiccating Stress
2007
HFE Mutations Analysis in 711 Hemochromatosis Probands: Evidence for S65C Implication in Mild Form of Hemochromatosis
1999
Predicting allopurinol response in patients with gout
2015
Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum
1999
Normoxic Stabilization of Hypoxia-Inducible Factor-1α by Modulation of the Labile Iron Pool in Differentiating U937 Macrophages: Effect of Natural Resistance–Associated Macrophage Protein 1
2006 StandoutNobel
Cardiac hypertrophy and sudden death in mice with a genetically clamped renin transgene
2004 StandoutNobel
Molecular coevolution within a Drosophila clock gene
1998 StandoutNobel
The discovery of the new haemochromatosis gene
2003
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
1997
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin
2004 Standout
Evolutionary Genetics of the Major Histocompatibility Complex
1994
IMMUNOLOGY OF MULTIPLE SCLEROSIS
2005 Standout
Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation
2003 Standout
Sequence Variation and Haplotype Structure at the Human HFE Locus
2002
Diabetic Kidney Disease
2017 Standout
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
2001 Standout
Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae
1999 Standout
Gout
2021 Standout
Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis
2002
Allopurinol hypersensitivity is primarily mediated by dose-dependent oxypurinol-specific T cell response
2013
Juvenile and adult hemochromatosis are distinct genetic disorders.
1998
Iron Overload, Public Health, and Genetics: Evaluating the Evidence for Hemochromatosis Screening
1998
Hydronephrosis associated with antiurothelial and antinuclear autoantibodies in BALB/c-Fcgr2b −/− Pdcd1 −/− mice
2005 StandoutNobel
BMP/Smad signaling is not enhanced in Hfe-deficient mice despite increased Bmp6 expression
2009
Understanding iron homeostasis through genetic analysis of hemochromatosis and related disorders
2005
Review of Toxic Epidermal Necrolysis
2016
American Association of Oral and Maxillofacial Surgeons Position Paper on Medication-Related Osteonecrosis of the Jaw—2014 Update
2014 Standout
Mutation of the gastric hydrogen-potassium ATPase alpha subunit causes iron-deficiency anemia in mice
2011 StandoutNobel
HFE gene knockout produces mouse model of hereditary hemochromatosis
1998
Works of Nicolas Borot being referenced
Genetic hemochromatosis is a rare disease entity among French Basques: a center-based study from the General Hospital of Basque Country
2001
The Human Myelin Oligodendrocyte Glycoprotein (MOG) Gene: Complete Nucleotide Sequence and Structural Characterization
1995
Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data.
1991
A marker for Stevens-Johnson syndrome …: ethnicity matters
2006
Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex
1997
Hereditary hemochromatosis: aHpal polymorphism within the HLA-H gene
1997
HLA-DRB1 * 01 associated with cutaneous hypersensitivity induced by nevirapine and efavirenz
2008
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG
1995
Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients
1997
A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs
2008
Inactivation of the hemochromatosis gene differentially regulates duodenal expression of iron-related mRNAs between mouse strains
2002
Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis
1992
A Genome-Wide Search Identifies Two Susceptibility Loci for Experimental Autoimmune Encephalomyelitis on Rat Chromosomes 4 and 10
1999