CoChat
Sign Up
Cited by 974Iron Metabolism and DisordersNeurological diseases and metabolismGenetic factors in colorectal cancer

The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

Papanikolaou, George, Samuels, Mark E, Ludwig, Erwin H, MacDonald, Marcia L E, Franchini, Patrick L, Dubé, Marie-Pierre, Andres, Lisa, MacFarlane, Julie, Sakellaropoulos, Nikos, Politou, Marianna, Nemeth, Elizabeta, Thompson, Jay, Risler, Jenni K, Zaborowska, Catherine, Babakaiff, Ryan, Radomski, Christopher C, Pape, Terry D, Davidas, Owen, Christakis, John, Brissot, Pierre, Lockitch, Gillian, Ganz, Tomas, Hayden, Michael R, Goldberg, Y Paul·2004·Nature Genetics
DOI 10.1038/ng1274
Open this paper in CoChat — free account

Abstract

Juvenile hemochromatosis is an early-onset autosomal recessive disorder of iron overload resulting in cardiomyopathy, diabetes and hypogonadism that presents in the teens and early 20s (refs. 1,2). Juvenile hemochromatosis has previously been linked to the centromeric region of chromosome 1q (refs. 3-6), a region that is incomplete in the human genome assembly. Here we report the positional cloning of the locus associated with juvenile hemochromatosis and the identification of a new gene crucial to iron metabolism. We finely mapped the recombinant interval in families of Greek descent and identified multiple deleterious mutations in a transcription unit of previously unknown function (LOC148738), now called HFE2, whose protein product we call hemojuvelin. Analysis of Greek, Canadian and French families indicated that one mutation, the amino acid substitution G320V, was observed in all three populations and accounted for two-thirds of the mutations found. HFE2 transcript expression was restricted to liver, heart and skeletal muscle, similar to that of hepcidin, a key protein implicated in iron metabolism. Urinary hepcidin levels were depressed in individuals with juvenile hemochromatosis, suggesting that hemojuvelin is probably not the hepcidin receptor. Rather, HFE2 seems to modulate hepcidin expression.

Overview

Integrity signals

Registry

Crossref · 10.1038/ng1274

Cites

29 of 29 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Citations

Cites

Flagged first, then by citations

Show all 29 references

Cited by

Sorted by citations

Items 601–700 of 970

Related

See all

Metadata

Authors
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., Nemeth, E., Thompson, J., Risler, J. K., Zaborowska, C., Babakaiff, R., Radomski, C. C., Pape, T. D., Davidas, O., Christakis, J., Brissot, P., Lockitch, G., Ganz, T., Hayden, M. R., & Goldberg, Y. P.
Affiliations
  • National and Kapodistrian University of Athens (GR)
  • University of California, Los Angeles (US)
  • Theageneio General Hospital (GR)
  • Inserm (FR)
  • University of British Columbia (CA)
Corresponding author
Hayden, Michael R
ORCID
Venue
Nature Genetics
Publisher
Springer Science and Business Media LLC
Published
2003-11-30
Volume
36
Issue
1
Pages
77-82
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
DOI
10.1038/ng1274
OpenAlex
W2116064842
Cited by
974
References
29
Citations by year
2026: 5 · 2025: 10 · 2024: 12 · 2023: 14 · 2022: 13 · 2021: 27 · 2020: 23 · 2019: 20 · 2018: 31 · 2017: 44 · 2016: 32 · 2015: 35 · 2014: 32 · 2013: 47 · 2012: 55
FWCI
35.51
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)
Locations
  • Nature Genetics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • BC Children's Hospital
  • National and Kapodistrian University of Athens
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
juvenile hemochromatosis, hemojuvelin, iron overload, chromosome 1q, positional cloning, iron metabolism, hepcidin, autosomal recessive disorder
MeSH terms
Hemochromatosis Protein, Adolescent, Adult, Amino Acid Sequence, Base Sequence, Child, Chromosomes, Human, Pair 1, Hemochromatosis, Humans, Membrane Proteins, Middle Aged, Molecular Sequence Data, Mutation, Iron Overload, GPI-Linked Proteins

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