| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
The serine protease TMPRSS6 is required to sense iron deficiency.
|
Science
|
2008
|
3.70
|
|
2
|
Bone morphogenetic proteins 2, 4, and 9 stimulate murine hepcidin 1 expression independently of Hfe, transferrin receptor 2 (Tfr2), and IL-6.
|
Proc Natl Acad Sci U S A
|
2006
|
3.13
|
|
3
|
EPO-mediated reduction in Hamp expression in vivo corrects iron deficiency anaemia in TMPRSS6 deficiency.
|
Br J Haematol
|
2010
|
2.20
|
|
4
|
Haptoglobin polymorphism and iron homeostasis.
|
Clin Chem
|
2002
|
1.63
|
|
5
|
Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6.
|
Br J Haematol
|
2009
|
1.36
|
|
6
|
Different regulatory elements are required for response of hepcidin to interleukin-6 and bone morphogenetic proteins 4 and 9.
|
Br J Haematol
|
2007
|
1.33
|
|
7
|
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features.
|
Blood Cells Mol Dis
|
2005
|
1.30
|
|
8
|
Pro-active call center treatment support (PACCTS) to improve glucose control in type 2 diabetes: a randomized controlled trial.
|
Diabetes Care
|
2005
|
1.20
|
|
9
|
Two BMP responsive elements, STAT, and bZIP/HNF4/COUP motifs of the hepcidin promoter are critical for BMP, SMAD1, and HJV responsiveness.
|
Blood
|
2008
|
1.09
|
|
10
|
In vivo imaging of hepcidin promoter stimulation by iron and inflammation.
|
Blood Cells Mol Dis
|
2007
|
1.07
|
|
11
|
The distal location of the iron responsive region of the hepcidin promoter.
|
Blood
|
2007
|
1.02
|
|
12
|
Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degeneration.
|
Arch Ophthalmol
|
2012
|
1.02
|
|
13
|
Brain iron metabolism and neurodegenerative disorders.
|
Dev Neurosci
|
2002
|
0.98
|
|
14
|
Erythropoietin, GDF15, IL6, hepcidin and testosterone levels in a large cohort of elderly individuals with anaemia of known and unknown cause.
|
Eur J Haematol
|
2011
|
0.95
|
|
15
|
Exome analysis identified a novel mutation in the RBP4 gene in a consanguineous pedigree with retinal dystrophy and developmental abnormalities.
|
PLoS One
|
2012
|
0.93
|
|
16
|
The role of STAT, AP-1, E-box and TIEG motifs in the regulation of hepcidin by IL-6 and BMP-9: lessons from human HAMP and murine Hamp1 and Hamp2 gene promoters.
|
Blood Cells Mol Dis
|
2007
|
0.93
|
|
17
|
Soluble transferrin receptor-1 levels in mice do not affect iron absorption.
|
Acta Haematol
|
2006
|
0.85
|
|
18
|
Iron overload secondary to cirrhosis: a mimic of hereditary haemochromatosis?
|
Histopathology
|
2014
|
0.83
|
|
19
|
Characteristics of HFE C282Y homozygotes younger than age 30 years.
|
Acta Haematol
|
2004
|
0.77
|
|
20
|
A late presentation of a fatal disease: juvenile hemochromatosis.
|
Case Rep Med
|
2013
|
0.75
|
|
21
|
Response to the letter by Nicolas et al, BJH-2010-01422.
|
Br J Haematol
|
2011
|
0.75
|
|
22
|
IOD in rhinos--epidemiology group report: report from the Epidemiology Working Group of the International Workshop on Iron Overload Disorder in Browsing Rhinoceros (February 2011).
|
J Zoo Wildl Med
|
2012
|
0.75
|