The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Richard Kellermayer

Department of Medical Genetics and Child Development Medicine

University of Pécs

Szigeti ut 12

7623 Pécs



Name/email consistency: high



  • Department of Medical Genetics and Child Development Medicine, University of Pécs, Szigeti ut 12, 7623 Pécs, Hungary. 2004 - 2006
  • Department of Neurosurgery, Pécs University, H-7623 Pécs, Rét utca 2, Hungary. 2006
  • Department of Medical Genetics, University of Pécs, Hungary. 2005


  1. Electrically induced gel-to-gel phase-transition in neurons. Kellermayer, R., Zsombok, A., Auer, T., Gallyas, F. Cell Biol. Int. (2006) [Pubmed]
  2. A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency. Kellermayer, R., Hsu, A.P., Stankovics, J., Balogh, P., Hadzsiev, K., Vojcek, A., Maródi, L., Kajtár, P., Kosztolányi, G., Puck, J.M. J. Hum. Genet. (2006) [Pubmed]
  3. Translational readthrough induction of pathogenic nonsense mutations. Kellermayer, R. Eur. J. Med. Genet (2006) [Pubmed]
  4. Alpha-thalassemia/mental retardation syndrome in a 45,X male. Kellermayer, R., Czakó, M., Kiss-László, Z., Gyuris, P., Kozári, A., Melegh, B., Kosztolányi, G. Am. J. Med. Genet. A (2005) [Pubmed]
  5. Hailey-Hailey disease as an orthodisease of PMR1 deficiency in Saccharomyces cerevisiae. Kellermayer, R. FEBS Lett. (2005) [Pubmed]
  6. A patient with Rothmund-Thomson syndrome and all features of RAPADILINO. Kellermayer, R., Siitonen, H.A., Hadzsiev, K., Kestilä, M., Kosztolányi, G. Arch. Dermatol (2005) [Pubmed]
  7. A novel frame shift mutation in the HMG box of the SRY gene in a patient with complete 46,XY pure gonadal dysgenesis. Kellermayer, R., Halvax, L., Czakó, M., Shahid, M., Dhillon, V.S., Husain, S.A., Süle, N., Gömöri, E., Mammel, M., Kosztolányi, G. Diagn. Mol. Pathol. (2005) [Pubmed]
  8. The intracellular dissipation of cytosolic calcium following glucose re-addition to carbohydrate depleted Saccharomyces cerevisiae. Kellermayer, R., Szigeti, R., Kellermayer, M., Miseta, A. FEBS Lett. (2004) [Pubmed]
WikiGenes - Universities