Finberg, Karin E.

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

Finberg, K. E., Heeney, M. M., Campagna, D. R., Aydınok, Y., Pearson, H. A., Hartman, K. R., Mayo, M. M., Samuel, S. M., Strouse, J. J., Markianos, K., et al. (2008) · Nature Genetics

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 675

Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice

Finberg, K. E., Whittlesey, R. L., & Andrews, N. C. (2011) · Blood

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 81

Regulation of systemic iron homeostasis

Finberg, K. E. (2013) · Current Opinion in Hematology

Iron Metabolism and DisordersIron and Steelmaking Processes

Cited by 72

Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency

Heeney, M. M., Guo, D., De Falco, L., Campagna, D. R., Olbina, G., Kao, P. P.-C., Schmitz-Abe, K., Rahimov, F., Gutschow, P., Westerman, K., et al. (2018) · Blood

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 25