gpapanik[a]staff.hua.gr
+30 210 9549 352
Staff Offices, Part 2

Papanikolaou George

Assistant Professor - Pathophysiology and Human Genetics

Expert

George Papanikolaou is Assistant Professor of Pathophysiology and Human Genetics at the Department of Nutrition and Dietetics (Harokopio University of Athens). He teaches Pathophysiology and Genetics in undergraduated students and in the Postgraduate Program in Applied Nutrition and Dietetics. He graduated from the Medical School, specialized in Internal Medicine in the Departments of Pathophysiology and the First Department of Medicine in the National and Kapodistrian University of Athens. His research work contributed in the discovery of important mechanisms underlying iron homeostasis in humans, such as the role of hepcidin and haemojuvelin in systemic iron homeostasis. His research interests include inherited diseases of iron homeostasis, hereditary anemias, chemical senses and open educational resources.

Education

  • 2003 PhD Thesis “The genetic basis of hereditary haemochromatosis in Greece”, First Department of Medicine, School of Medicine, National and Kapodistrian University of Athens
  • 2001 Specialist in Internal Medicine
  • 1991 School of Medicine, Democritus University of Thrace

Reasearch Interests

  • Iron homeostasis
  • Genetic diseases of iron homeostasis and hereditary anaemias
  • Chemical senses

Publications

  • Papanikolaou G, Pantopoulos K. Systemic iron homeostasis and erythropoiesis. IUBMB Life. 2017 Jun;69(6):399-413. doi: 10.1002/iub.1629. Epub 2017 Apr 6. PMID: 28387022.
  • Heilmann-Heimbach S, Herold C, Hochfeld LM, Hillmer AM, Nyholt DR, Hecker J, Javed A, Chew EG, Pechlivanis S, Drichel D, Heng XT, Del Rosario RC, Fier HL, Paus R, Rueedi R, Galesloot TE, Moebus S, Anhalt T, Prabhakar S, Li R, Kanoni S, Papanikolaou G, Kutalik Z, Deloukas P, Philpott MP, Waeber G, Spector TD, Vollenweider P, Kiemeney LA, Dedoussis G, Richards JB, Nothnagel M, Martin NG, Becker T, Hinds DA, Nöthen MM. Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Nat Commun. 2017 Mar 8;8:14694. doi: 10.1038/ncomms14694. PMID: 28272467.
  • Papanikolaou G, Tzilianos M, Christakis JI, Bogdanos D, Tsimirika K, MacFarlane J, Goldberg YP, Sakellaropoulos N, Ganz T, Nemeth E. Hepcidin in iron overload disorders. Blood. 2005 May 15;105(10):4103-5. doi: 10.1182/blood-2004-12-4844. Epub 2005 Jan 25. PMID: 15671438; PMID: 15671438
  • Papanikolaou G, Samuels ME, Ludwig EH, MacDonald ML, Franchini PL, Dube MP, Andres L, MacFarlane J, Sakellaropoulos N, Politou M, Nemeth E, Thompson J, Risler JK, Zaborowska C, Babakaiff R, Radomski CC, Pape TD, Davidas O, Christakis J, Brissot P, Lockitch G, Ganz T, Hayden MR, Goldberg YP. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis. Nat Genet. 2004 Jan;36(1):77-82. Epub 2003 Nov 30. PMID: 14647275
  • Roetto A, Papanikolaou G, Politou M, Alberti F, Girelli D, Christakis J, Loukopoulos D, Camaschella C. Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis. Nat Genet. 2003 Jan;33(1):21-2. Epub 2002 Dec 9. PMID: 12469120