The DOI matches its Crossref record; 99 of the 99 references it cites were found in a registry or an index.
Hereditary Hemochromatosis — A New Look at an Old Disease
Abstract
For many years, hereditary hemochromatosis was regarded as a clinically and genetically unique entity marked by a classic presentation consisting of diabetes, bronze skin pigmentation, and cirrhosis. In 1996, identification of “the hemochromatosis gene,” HFE, was reported; since then, several other iron-metabolism genes have also been identified. This article reviews the current understanding and management of hereditary iron-overload disorders.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The HFE mutation leads to an impaired formation of hepcidin and thus to an iron deficiency phenotype of MΦs, whereas excessively absorbed iron is stored in parenchymal organs such as the liver, heart, or pancreas.”
From Macrophage defense mechanisms against intracellular bacteria (2015) · cites this paper as [201]
In the citing paper
“Conversely, individuals with insufficient hepcidin production, suffer from iron-overload in the blood, and hepatitis (Pietrangelo, 2004).”
From The Role of Iron Regulation in Immunometabolism and Immune-Related Disease (2019) · cites this paper as Pietrangelo, 2004
In the citing paper
“HFE mutations, especially the homozygous C282Y substitution, result in type I (AKA classical) hereditary hemochromatosis (HH) (Camaschella et al., 2002; Pietrangelo, 2004; Weiss, 2010)”
From Genetic and Dietary Iron Overload Differentially Affect the Course of Salmonella Typhimurium Infection (2017) · cites this paper as Pietrangelo, 2004
In the citing paper
“HH is characterized by reduced serum levels of the antimicrobial peptide Hamp (hepcidin) and increased duodenal absorption of iron via divalent metal transporter 1 (Dmt1) and ferroportin 1 (Fpn1) despite progressive iron overload in parenchymal organs including the liver, pancreas, and heart (Zoller et al., 1999, 2001; Bridle et al., 2003; Pietrangelo, 2004; Bardou-Jacquet et al., 2013).”
From Genetic and Dietary Iron Overload Differentially Affect the Course of Salmonella Typhimurium Infection (2017) · cites this paper as Pietrangelo, 2004
In the citing paper
“Hfe deficiency results in reduced Hamp production and increased serum iron levels (Pietrangelo, 2004).”
From Genetic and Dietary Iron Overload Differentially Affect the Course of Salmonella Typhimurium Infection (2017) · cites this paper as Pietrangelo, 2004
In the citing paper
“The proximal region of the human ferritin H gene was activated by NF-Y and p300 during hemin-induced FLC differentiation, and this proximal region was also responsible for cAMP (80, 194, 248).”
From Intracellular iron transport and storage: from molecular mechanisms to health implications (2008) · cites this paper as [248]
Citations
Cites
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
Feder, J. N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D. A., Basava, A., Dormishian, F., Domingo, R., Ellis, M. C., Fullan, A., et al. (1996) · Nature Genetics · doi:10.1038/ng0896-399 · Cited by 3,664
Hepcidin, a urinary antimicrobial peptide synthesized in the liver
Park, C. H., Valore, E. V., Waring, A. J., & Ganz, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m008922200 · Cited by 2,168
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
den Dunnen, J. T., & Antonarakis, S. E. (2000) · Human Mutation · doi:10.1002/(sici)1098-1004(200001)15:1 · Cited by 1,757
Pigeon, C., Ilyin, G., Courselaud, B., Leroyer, P., Turlin, B., Brissot, P., & Loréal, O. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m008923200 · Cited by 1,697
Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation
Ganz, T. (2003) · Blood · doi:10.1182/blood-2003-03-0672 · Cited by 1,544
Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein
Nemeth, E., Valore, E. V., Territo, M., Schiller, G., Lichtenstein, A., & Ganz, T. (2003) · Blood · doi:10.1182/blood-2002-10-3235 · Cited by 1,417
LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity
Krause, A., Neitz, S., Mägert, H.-J., Schulz, A., Forssmann, W.-G., Schulz-Knappe, P., & Adermann, K. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01920-7 · Cited by 1,324
Survival and Causes of Death in Cirrhotic and in Noncirrhotic Patients with Primary Hemochromatosis
Niederau, C., Fischer, R., Sonnenberg, A., Stremmel, W., Trampisch, H. J., & Strohmeyer, G. W. (1985) · New England Journal of Medicine · doi:10.1056/nejm198511143132004 · Cited by 1,063
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
Papanikolaou, G., Samuels, M. E., Ludwig, E. H., MacDonald, M. L. E., Franchini, P. L., Dubé, M.-P., Andres, L., MacFarlane, J., Sakellaropoulos, N., Politou, M., et al. (2004) · Nature Genetics · doi:10.1038/ng1274 · Cited by 974
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
Roetto, A., Papanikolaou, G., Politou, M., Alberti, F., Girelli, D., Christakis, J., Loukopoulos, D., & Camaschella, C. (2003) · Nature Genetics · doi:10.1038/ng1053 · Cited by 860
Research works printed but not linked: 10
- Troisier M, 1871, Bull Soc Anat Paris, 44, 231
- von Recklinghausen FD, 1889, Tageblatt Versammlung Dtsche Naturforscher Arzte Heidelberg, 62, 324
- Sheldon JH. Haemochromatosis. London: Oxford University Press, 1935.
- Simon M, 1975, Nouv Presse Med, 4, 1432
- Simon M, 1987, Am J Hum Genet, 41, 89
- Cook JD, 1973, Am J Pathol, 72, 337
- Smith PM, 1969, Clin Sci, 37, 519
- McLaren GD, 1991, J Lab Clin Med, 117, 390
- Powell LW, 2002, Semin Gastrointest Dis, 13, 80
- Hayashi A, 1993, Am J Hum Genet, 53, 201
Cited by
Sorted by citations
Items 501–600 of 991
Chronic Fatigue Syndrome in Patients with Deteriorated Iron Metabolism
Świątczak, M., Młodziński, K., Sikorska, K., Raczak, A., Lipiński, P., & Daniłowicz‐Szymanowicz, L. (2022) · Diagnostics · doi:10.3390/diagnostics12092057 · Cited by 19
A compartmental model of iron regulation in the mouse
Lao, B. J., & Kamei, D. T. (2006) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2006.06.033 · Cited by 13
Branski, D. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4377-0755-7.00330-4 · Cited by 12
Krayenbuehl, P., Hersberger, M., Truninger, K., Müllhaupt, B., Maly, F. E., Bargetzi, M. J., & Schulthess, G. (2010) · European Journal of Gastroenterology & Hepatology · doi:10.1097/meg.0b013e3283322067 · Cited by 12
Sheraton, T. E., Gildersleve, C. D., & Hall, J. E. (2006) · Anaesthesia · doi:10.1111/j.1365-2044.2006.04857.x · Cited by 13
Bhagavan, N. V., & Ha, C. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-416687-5.00027-0 · Cited by 12
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China
Wu, L., Zhang, W., Li, Y., Zhou, D., Zhang, B., Xu, A., Wu, Z., Wu, L., Li, S., Wang, X., et al. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-02020-y · Cited by 12
Johnstone, D. M., Graham, R. M., Trinder, D., Riveros, C., Olynyk, J. K., Scott, R. J., Moscato, P., & Milward, E. A. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-112183 · Cited by 12
On-chip HA/SSCP for the detection of hereditary haemochromatosis
Manage, D. P., Zheng, Y., Somerville, M. J., & Backhouse, C. (2005) · Microfluidics and Nanofluidics · doi:10.1007/s10404-005-0045-8 · Cited by 12
Molecular basis of hereditary iron homeostasis defects
Horváthová, M., Ponka, P., & Divoký, V. (2010) · Hematology · doi:10.1179/102453310x12583347009810 · Cited by 12
Non-HFE hemochromatosis: Genetics, pathogenesis, and clinical management
Nelson, J. E., & Kowdley, K. V. (2005) · Current Gastroenterology Reports · doi:10.1007/s11894-005-0069-y · Cited by 12
Neri, S., Pulvirenti, D., Signorelli, S. S., Ignaccolo, L., Tsami, A., Mauceri, B., Misseri, M., Interlandi, D., Cutuli, N., & Castellino, P. (2007) · Internal Medicine Journal · doi:10.1111/j.1445-5994.2007.01474.x · Cited by 12
Total Iron-Overload Measurement in the Human Liver Region by the Magnetic Iron Detector
Marinelli, M., Gianesin, B., Balocco, M., Beruto, P., Bruzzone, C., Carrara, P., Gallusi, P., Macco, A., Musso, M., Oliveri, E., et al. (2010) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2010.2053204 · Cited by 12
Glucose-induced regulation of novel iron transporters in vascular endothelial cell dysfunction
Khan, Z. A., Farhangkhoee, H., Barbin, Y. P., Adams, P. C., & Chakrabarti, S. (2005) · Free Radical Research · doi:10.1080/10715760500143254 · Cited by 12
Sebastiani, G., & Pantopoulos, K. (2010) · CRC Press eBooks · doi:10.1201/9781420059984-c13 · Cited by 12
Cusick, S. E., Looker, A. C., Cogswell, M. E., Pfeiffer, C. M., & Grummer‐Strawn, L. M. (2008) · PEDIATRICS · doi:10.1542/peds.2007-2996 · Cited by 12
Haemochromatosis gene frequency in a control and diabetic Irish population
Kirk, L., Bird, J., Ramadan, S., Samad, A., Adebayo, G. I., Lourens, W., & Williams, J. (2008) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-008-0248-6 · Cited by 11
Tissue iron distribution in patients with anemia of inflammation: Results of a pilot study
Lanser, L., Plaikner, M., Schroll, A., Burkert, F. R., Seiwald, S., Fauser, J., Petzer, V., Bellmann‐Weiler, R., Fritsche, G., Tancevski, I., et al. (2023) · American Journal of Hematology · doi:10.1002/ajh.26909 · Cited by 11
A Late Presentation of a Fatal Disease: Juvenile Hemochromatosis
Cherfane, C. E., Lee, P. L., Guerin, L., & Brown, K. E. (2013) · Case Reports in Medicine · doi:10.1155/2013/875093 · Cited by 11
Perceptions of dentists, dentistry undergraduate students, and the lay public about dental sedation
Costa, L. R., Dias, A. D., Pinheiro, L. S., Chaves, M. E. P. D. S., Ferreira, R. D. A. R., de Almeida, R. B., & Lima, A. R. D. A. (2004) · Journal of Applied Oral Science · doi:10.1590/s1678-77572004000300004 · Cited by 11
Torbenson, M. S. (2011) · Advances in Anatomic Pathology · doi:10.1097/pap.0b013e318220fba0 · Cited by 11
Fan, Y., Dhaliwal, H. K., Menon, A. V., Chang, J., Choi, J. E., Amiji, M. M., & Kim, J. (2019) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2019.102091 · Cited by 11
Levy, H. P., LoPresti, L., & Seibert, D. C. (2008) · Genetics in Medicine · doi:10.1097/gim.0b013e318180639d · Cited by 11
Ganz, T. (2004) · Blood · doi:10.1182/blood-2004-09-3664 · Cited by 11
Iron overload in kidney transplants: Prospective analysis of biochemical and genetic markers
Lorenz, M., Kletzmayr, J., Huber, A., Hörl, W. H., Sunder–Plassmann, G., & Födinger, M. (2005) · Kidney International · doi:10.1111/j.1523-1755.2005.67129.x · Cited by 11
Wortmann, A. C., Fröehlich, P. E., Pinto, R. B., Magalhães, R. B., Álvares‐da‐Silva, M. R., Ferreira, J. J., & da Silveira, T. R. (2007) · Journal of Spectroscopy · doi:10.1155/2007/761029 · Cited by 11
HFE gene mutations increase the risk of coronary heart disease in women
Silva, M. C. P., Njajou, O. T., Alizadeh, B. Z., Albert Hofman, D., Witteman, J. C. M., van Duijn, C. M., & Janssens, A. C. J. W. (2010) · European Journal of Epidemiology · doi:10.1007/s10654-010-9489-6 · Cited by 12
Iron deficiency anemia, anemia of chronic disorders and iron overload
Pippard, M. J. (2011) · Elsevier eBooks · doi:10.1016/b978-0-7020-3147-2.00011-0 · Cited by 13
Heart and heart-liver transplantation in patients with hemochromatosis
Robinson, M. R., Al-Kindi, S. G., & Oliveira, G. H. (2017) · International Journal of Cardiology · doi:10.1016/j.ijcard.2017.06.075 · Cited by 11
Moysés, C. B., Moreira, E. S., Asprino, P. F., Guimarães, G. S., & Alberto, F. (2008) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2008001000001 · Cited by 11
Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis.
Jacobs, E. M. G., Meulendijks, C. F. M., Elving, L. D., van der Wilt, G. J., & Swinkels, D. W. (2005) · PubMed · Cited by 11
Yoo, K. Y., Jeong, S. T., Ha, I. H., & Lee, A. J. (2003) · Anesthesia & Analgesia · doi:10.1213/01.ane.0000058842.05373.e3 · Cited by 82
Ultrastructural cardiac pathology: the wide (yet so very small) world of cardiac electron microscopy
Fishbein, G. A., Bois, M. C., d’Amati, G., Glass, C., Masuelli, L., Rodriguez, E. R., & Seidman, M. A. (2024) · Cardiovascular Pathology · doi:10.1016/j.carpath.2024.107670 · Cited by 13
Blood transfusion in older surgical patients: the only option or is there a better approach?
Cozza, M., Boccardi, V., Duka, R., Vashist, Y. K., & Marano, L. (2025) · Aging Clinical and Experimental Research · doi:10.1007/s40520-025-03033-4 · Cited by 10
Hereditary hemochromatosis types 1, 2, and 3
Crawford, D. H. (2014) · Clinical Liver Disease · doi:10.1002/cld.339 · Cited by 10
A Case of Secondary Hemochromatosis With High Uptake of Liver in F-18 FDG PET/CT Imaging
Ito, K., Minamimoto, R., Morooka, M., & Kubota, K. (2011) · Clinical Nuclear Medicine · doi:10.1097/rlu.0b013e318217ae7c · Cited by 10
High Prevalence of Fibromyalgia in Patients with HFE-related Hereditary Hemochromatosis
Mohammad, A. F., CAREY, J. J., Storan, E. R., Scarry, M., Coughlan, R. J., & Lee, J. M. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31826f7ad7 · Cited by 10
High‐Definition X‐Ray Fluorescence: Applications
Gibson, W. M., Chen, Z. W., & Li, D. (2008) · X-Ray Optics and Instrumentation · doi:10.1155/2008/709692 · Cited by 10
MRI quantification of splenic iron concentration in mouse
Hitti, E., Eliat, P., Abgueguen, E., Ropert, M., Leroyer, P., Brissot, P., Gandon, Y., Saint‐Jalmes, H., & Loréal, O. (2010) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.22290 · Cited by 10
Remacha, A. F., Sardà, M. P., Barceló, M. J., Bach, V., Altés, A., Baiget, M., Guarner, C., & Blesa, I. (2006) · Annals of Hematology · doi:10.1007/s00277-006-0092-6 · Cited by 10
Factors affecting the body mass index, haemoglobin and serum ferritin level in students.
Jamali, N. H., Jamali, A. H., Khand, A. A., Mahesar, H., & Arain, M. I. (2017) · Europe PMC (PubMed Central) · Cited by 10
Nairz, M., Metzendorf, C., Spasić, M. V., Mitterstiller, A., Schroll, A., Haschka, D., Hoffmann, A., von Raffay, L., Sparla, R., Huck, C. W., et al. (2020) · Haematologica · doi:10.3324/haematol.2019.241745 · Cited by 11
Examining the Clinical Use of Hemochromatosis Genetic Testing
Lanktree, M. B., Lanktree, B. B., Paré, G., Waye, J. S., Sadiković, B., & Crowther, M. A. (2015) · Canadian Journal of Gastroenterology and Hepatology · doi:10.1155/2015/941406 · Cited by 10
Novembrino, C., Porcella, A., Conte, D., Vecchi, A. F. D., Buccianti, G., Lonati, S., Duca, L., Ciani, A., & Bamonti-Catena, F. (2005) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2005.079 · Cited by 10
Genetic background of Japanese patients with adult‐onset storage diseases in the liver
Hayashi, H., Wakusawa, S., Yano, M., & Okada, T. (2007) · Hepatology Research · doi:10.1111/j.1872-034x.2007.00114.x · Cited by 10
A Review of New Concepts in Iron Overload.
Sohal, A., & Kowdley, K. V. (2024) · PubMed Central · Cited by 8
Liraglutide Impacts Iron Homeostasis in a Murine Model of Hereditary Hemochromatosis
Bozadjieva-Kramer, N., Shin, J. H., Blok, N. B., Jain, C., Das, N. K., Polex-Wolf, J., Knudsen, L. B., Shah, Y. M., & Seeley, R. J. (2024) · Endocrinology · doi:10.1210/endocr/bqae090 · Cited by 10
[Progress on epigenetic regulation of iron homeostasis].
Duan, L., Yin, X., Meng, H., Fang, X., Min, J., & Wang, F. (2020) · PubMed · doi:10.3785/j.issn.1008-9292.2020.02.25 · Cited by 9
Niederau, C. (2009) · Medizinische Klinik - Intensivmedizin und Notfallmedizin · doi:10.1007/s00063-009-1192-6 · Cited by 9
Is the iron donor lipocalin 2 implicated in the pathophysiology of hereditary hemochromatosis?†
Huang, H., Akira, S., & Santos, M. M. (2008) · Hepatology · doi:10.1002/hep.22699 · Cited by 9
Iron Overload in anHFEHeterozygous Carrier: A Case Report and Literature Review
Turbiville, D., Du, X., Yo, J., Jana, B., & Dong, J. (2018) · Laboratory Medicine · doi:10.1093/labmed/lmy065 · Cited by 9
Aggett, P. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-66162-1.00022-6 · Cited by 9
Diagnosis of Hepatic Iron Overload
Schranz, M., Talasz, H., Graziadei, I. W., Winder, T. L., Sergi, C. M., Bogner, K., Vogel, W., & Zoller, H. (2009) · Diagnostic Molecular Pathology · doi:10.1097/pdm.0b013e31817cfd4b · Cited by 9
Wheeler, C. J., & Kowdley, K. V. (2006) · Comprehensive Therapy · doi:10.1385/comp:32:1:10 · Cited by 9
Diagnosis and current treatments for primary iron overload
Brissot, P. (2007) · American Journal of Hematology · doi:10.1002/ajh.21071 · Cited by 9
Castiella, A., Zapata, E., Otazua, P., Fernández, J., Alústiza, J. M., Ugarte, M., Legasa, L., Galardi, A., Ugalde, A., Barredo, I., et al. (2008) · Revista Española de Enfermedades Digestivas · doi:10.4321/s1130-01082008001000002 · Cited by 9
Crosstalk between Erythropoiesis and Iron Metabolism
Rivella, S., Nemeth, E., & Miller, J. L. (2010) · Advances in Hematology · doi:10.1155/2010/317095 · Cited by 9
Carneiro, M. V., Souza, F. F., Teixeira, A. C., Figueiredo, J. F. C., Villanova, M. G., Secaf, M., Passos, A. D. C., Ramalho, L. N. Z., Carneiro, F. P., Zucoloto, S., et al. (2010) · European Journal of Gastroenterology & Hepatology · doi:10.1097/meg.0b013e32833bec1e · Cited by 8
Juvenile Hereditary Hemochromatosis
Goldberg, Y. P. (2011) · Cited by 8
Alcohol consumption as a cofactor for other liver diseases
Altamirano, J., & Michelena, J. (2013) · Clinical Liver Disease · doi:10.1002/cld.197 · Cited by 8
Hemocromatosis hereditaria. Problemas en el diagnóstico y tratamiento
Altés, A., Sanz, C., & Bruguera, M. (2015) · Medicina Clínica · doi:10.1016/j.medcli.2014.10.019 · Cited by 8
Henninger, B., Rauch, S., Zoller, H., Plaikner, M., Jaschke, W. R., & Kremser, C. (2017) · European Journal of Radiology · doi:10.1016/j.ejrad.2017.02.006 · Cited by 8
Koelmel, S., Nowak, A., & Krayenbuehl, P. (2020) · Swiss Medical Weekly · doi:10.4414/smw.2020.20294 · Cited by 8
Albalat, E., Cavey, T., Leroyer, P., Ropert, M., Balter, V., & Loréal, O. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.711822 · Cited by 8
Acquired hemochromatosis with pronounced pigment deposition of the upper eyelids.
Chacon, A. H., Morrison, B. W., & Hu, S. (2013) · Europe PMC (PubMed Central) · Cited by 8
Proton Pump Inhibitors and Pain
Smith, H. S. (2009) · Pain Physician · doi:10.36076/ppj.2009/12/1013 · Cited by 8
Frequency of the S65C mutation in the hemochromatosis gene in Brazil
Oliveira, V. C., Caxito, F. A., Gomes, K. B., de Castro, A. M., Pardini, V. C., & Ferreira, A. C. D. S. (2009) · Genetics and Molecular Research · doi:10.4238/vol8-3gmr562 · Cited by 8
Prise en charge de l'hémochromatose liée au gène HFE
Brissot, P., & BELS, F. D. (2007) · La Presse Médicale · doi:10.1016/j.lpm.2006.12.035 · Cited by 8
Severyn, C. J., & Rotwein, P. S. (2010) · Genomics · doi:10.1016/j.ygeno.2010.09.001 · Cited by 8
Short term protective effects of iron in a murine model of ischemia/reperfusion
Metzler, B., Jehle, J., Theurl, I., Ludwiczek, S., Obrist, P., Pachinger, O. M., & Weiß, G. (2006) · BioMetals · doi:10.1007/s10534-006-9034-y · Cited by 8
Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and cons
Bach, V., Barceló, M. J., Altés, A., Remacha, A. F., Félez, J., & Baiget, M. (2006) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2005.12.030 · Cited by 8
Paterson, A. C., & Pietrangelo, A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-7020-3398-8.00005-2 · Cited by 9
Self-citationPoggio, P. D. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i33.5272 · Cited by 8
Freeman, R., & Carson, P. (2003) · International Journal of Paediatric Dentistry · doi:10.1046/j.1365-263x.2003.00480.x · Cited by 8
Clinical expression of hemochromatosis gene ( HFE ) variants
Ayonrinde, O. T., & Olynyk, J. K. (2007) · Hepatology · doi:10.1002/hep.21957 · Cited by 8
Ferroportin (SLC40A1) gene in thalassemic patients of Indian descent
Agarwal, S., Sankar, V., Tewari, D., & Pradhan, M. (2006) · Clinical Genetics · doi:10.1111/j.1399-0004.2006.00644.x · Cited by 8
The Penetrance of Hemochromatosis: Mice to the Rescue
Pietrangelo, A. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.01.011 · Cited by 8
Self-citationNeed for Reclassification of Diabetes Secondary to Iron Overload in the ADA and WHO Classifications
Ellervik, C., Birgens, H., & Mandrup-Poulsen, T. R. (2014) · Diabetes Care · doi:10.2337/dc14-0119 · Cited by 8
Hereditary hemochromatosis: The same old song
Zanella, I., Rossini, A., Lorenzo, D. D., & Biasiotto, G. (2015) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2015.06.015 · Cited by 7
Moris, W., Verhaegh, P. L. M., Verbeek, J., Swinkels, D. W., Laarakkers, C. M., Masclee, A., Koek, G. H., & van Deursen, C. T. B. M. (2021) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00371.2020 · Cited by 7
Association between inherited monogenic liver disorders and chronic hepatitis C
Piekuse, L., Kreile, M., Zariņa, A., Steinberga, Z., Sondore, V., Keišs, J., Lāce, B., & Krūmiņa, A. (2014) · World Journal of Hepatology · doi:10.4254/wjh.v6.i2.92 · Cited by 7
Wolff, C., Armas, R., Frank, J., & Poblete‐Gutiérrez, P. (2006) · PubMed · Cited by 7
Enhancing the selectivity of an iron binding hydrogel
Mohammadi, Z., Xie, S., Peltier, E. F., Veisi, M., & Berkland, C. J. (2011) · European Polymer Journal · doi:10.1016/j.eurpolymj.2011.04.007 · Cited by 7
Freixenet, N., Moreno‐Rosel, M. S., Barceló, M. J., Serrano, A., Payà, M., Crespo, L., Pérez-Lucena, M. J., Altés, A., Baiget, M., & Félez, J. (2010) · American Journal of Hematology · doi:10.1002/ajh.21634 · Cited by 7
Alkhateeb, A. M., Uzrail, A., & Bodoor, K. (2009) · Disease Markers · doi:10.1155/2009/329603 · Cited by 8
Mixture models of serum iron measures in population screening for hemochromatosis and iron overload
McLaren, C. E., Li, K.-T., McLaren, G. D., Gordeuk, V. R., Snively, B. M., Reboussin, D. M., Barton, J. C., Acton, R. T., Dawkins, F. W., Harris, E. L., et al. (2006) · Translational research · doi:10.1016/j.trsl.2006.05.006 · Cited by 7
Hemokromatose – fra underdiagnostisert kuriositet til folkesykdom
Hagve, T., Åsberg, A., Ulvik, R. J., Borch‐Iohnsen, B., & Thorstensen, K. (2009) · Tidsskrift for Den norske legeforening · doi:10.4045/tidsskr.08.0084 · Cited by 7
Transferrin receptor 2 is emerging as a major player in the control of iron metabolism
Calzolari, A., Oliviero, I., & Testa, U. (2007) · Open Life Sciences · doi:10.2478/s11535-007-0007-0 · Cited by 7
New hope for treatment of neonatal haemochromatosis
Gissen, P., & Kelly, D. A. (2004) · The Lancet · doi:10.1016/s0140-6736(04)17367-4 · Cited by 7
A New Approach for Potential Combined Chelation Therapy Using Mono- and Bis-Hydroxypyridinones
Santos, M. A., Gama, S., Gil, M., & Gano, L. (2008) · Hemoglobin · doi:10.1080/03630260701726939 · Cited by 7
Inherited metabolic liver disease
Schilsky, M. L., & Oikonomou, I. K. (2005) · Current Opinion in Gastroenterology · doi:10.1097/01.mog.0000159821.78532.21 · Cited by 7
Do Genetic Variations in Antioxidant Enzymes Influence the Course of Hereditary Hemochromatosis?
Nahon, P., Sutton, A., Pessayre, D., Rufat, P., Charnaux, N., Trinchet, J., Beaugrand, M., & Deugnier, Y. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3529 · Cited by 7
Garrido, L. L., Muñante, J. H., Caballero, V. V., Miranda, Z. L., & Nago, A. N. (2004) · New England Journal of Medicine · doi:10.1056/nejm200409163511223 · Cited by 7
Iron-Based Nanoparticles as Delivery Tools
Parang, K., Vadlapatla, R., Koomer, A., Moran, V., Jackson, L., & Shirazi, A. N. (2026) · Pharmaceuticals · doi:10.3390/ph19050654 · Cited by 6
The modified iron avidity index: a promising phenotypic predictor in HFE ‐related haemochromatosis
Verhaegh, P. L. M., Moris, W., Koek, G. H., & van Deursen, C. T. B. M. (2016) · Liver International · doi:10.1111/liv.13121 · Cited by 6
Koukoulas, K., Lygoura, V., Kartalidis, P., Gatselis, N., Petinaki, E. A., Dalekos, G. Ν., & Simos, G. (2022) · Diagnostics · doi:10.3390/diagnostics12061404 · Cited by 6
Do All Hemochromatosis Patients Have the Same Origin? A Pilot Study of Mitochondrial DNA and Y-DNA
Symonette, C. J., & Adams, P. C. (2011) · Canadian Journal of Gastroenterology · doi:10.1155/2011/463810 · Cited by 6
Surcharges en fer d’origine génétique et hépatosidérose dysmétabolique
Ruivard, M. (2008) · La Revue de Médecine Interne · doi:10.1016/j.revmed.2008.05.004 · Cited by 6
Brown, P. J., Whitbread, T., Burden, F. A., Bailey, M., Carley, K., Daniell, L., Jones, C., & Bell, N. J. (2010) · Research in Veterinary Science · doi:10.1016/j.rvsc.2010.06.016 · Cited by 6
MRI assessment of changes in liver iron deposition post-venesection
Beddy, P., McCann, J., Ahern, M., Norris, S., & Keogan, M. T. (2010) · European Journal of Radiology · doi:10.1016/j.ejrad.2010.05.010 · Cited by 6
Metadata
- Authors
- Pietrangelo, A.
- Affiliations
- University of Modena and Reggio Emilia (IT)
- Corresponding author
- Pietrangelo, Antonello
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2004-06-03
- Volume
- 350
- Issue
- 23
- Pages
- 2383-2397
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2168051647
- Cited by
- 992
- References
- 97
- Citations by year
- 2026: 12 · 2025: 11 · 2024: 16 · 2023: 17 · 2022: 22 · 2021: 18 · 2020: 21 · 2019: 21 · 2018: 38 · 2017: 38 · 2016: 37 · 2015: 42 · 2014: 34 · 2013: 42 · 2012: 41
- FWCI
- 11.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- IRIS UNIMORE (University of Modena and Reggio Emilia) (submittedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- hereditary hemochromatosis, HFE gene, iron overload, iron metabolism genes, disease management, diabetes mellitus, liver cirrhosis
- MeSH terms
- Hemochromatosis Protein, Genotype, Hemochromatosis, Homeostasis, Humans, Iron, Membrane Proteins, Mutation, Phenotype, Receptors, Transferrin, Histocompatibility Antigens Class I, Iron Overload, Antimicrobial Cationic Peptides, Hepcidins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review