Randall C. Schatzman

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Histocompatibility, Immunogenetics, Autoimmune Disease +11

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

John N. Feder, David M. Penny, Alivelu Irrinki et al. · Proceedings of the National Academy of Sciences · 1998 · 837 citations · Full text

Histocompatibility, Gene Product, Signal Transduction +15

HFE gene knockout produces mouse model of hereditary hemochromatosis

Xiao Zhou, Shunji Tomatsu, Robert E. Fleming et al. · Proceedings of the National Academy of Sciences · 1998 · 527 citations · Full text

The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression

John N. Feder, Zenta Tsuchihashi, Alivelu Irrinki et al. · Journal of Biological Chemistry · 1997 · 479 citations · Full text

Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β ₂ -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells

Abdül Waheed, Seppo Parkkila, Xiao Zhou et al. · Proceedings of the National Academy of Sciences · 1997 · 387 citations