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Clinical Chemistry and Laboratory Medicine|July 13, 2002
Novel haptoglobin insertion/deletion polymorphism is associated with the lipid profile and C-reactive protein (CRP) concentrationBirgitte Wuyts, Gilles Hetet, Bernard Grandchamp, et al.
Blood|May 6, 2003
Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutationsGilles Hetet, Isabelle Devaux, Nadem Soufir, et al.
Blood|January 28, 2006
Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overloadCarole Beaumont, Jean Delaunay, Gilles Hetet, et al.
FEBS Letters|September 11, 2004
Transferrin receptor 1 mRNA is downregulated in placenta of hepcidin transgenic embryosMarie Elise Martin, Gaël Nicolas, Gilles Hetet, et al.
Experimental Cell Research|August 13, 2005
A physiological model to study iron recycling in macrophagesConstance Delaby, Nathalie Pilard, Gilles Hetet, et al.
The Biochemical Journal|February 7, 2006
Wild-type and mutant ferroportins do not form oligomers in transfected cellsAna Sofia Gonçalves, Françoise Muzeau, Rand Blaybel, et al.
Journal of Neurology|July 26, 2002
Association study between iron-related genes polymorphisms and Parkinson's diseaseClaire Borie, Francesca Gasparini, Patrice Verpillat, et al.
Genes, Chromosomes & Cancer|January 17, 2002
Molecular analysis of nonrandom 8q12 deletions in acute lymphoblastic leukemia: identification of two candidate genesValérie Bardet, Nathalie Couque, Laurence Cattolico, et al.
Blood|October 28, 2011
A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 geneBernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, et al.
Haematologica|January 30, 2009
A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overloadCaroline Kannengiesser, Anne-Marie Jouanolle, Gilles Hetet, et al.
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