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  • Andras Bors, Hajnalka Andrikovics, +7 authors Attila Tordai
  • Biology, Medicine
  • International journal of molecular medicine
  • 2004 (First Publication: 1 December 2004)
  • The most common form of non-syndromic autosomal recessive deafness (NSRD) is caused by mutations in the gene GJB2, encoding the protein connexin 26 (Cx26). The mutation c.35delG is found in 30-70% ofContinue Reading
  • Peter L. Lakatos, Tamás Szamosi, +11 authors Hajnalka Andrikovics
  • Medicine
  • Digestive and liver disease : official journal of…
  • 2008 (First Publication: 1 November 2008)
  • BACKGROUND North American and European genome-wide association scans have identified ATG16L1 and IL23R as novel inflammatory bowel disease (IBD) susceptibility genes and subsequent reports confirmedContinue Reading
  • Katalin Balassa, Hajnalka Andrikovics, +12 authors Tamas Masszi
  • Medicine
  • Bone Marrow Transplantation
  • 2015 (First Publication: 1 October 2015)
  • Transplantation-associated thrombotic microangiopathy (TA-TMA) is a serious complication of allogeneic haematopoietic stem cell transplantation (allo-HSCT) with high mortality rate. WeContinue Reading
  • Ágnes F. Semsei, Dániel J. Erdélyi, +8 authors Csaba Szalai
  • Biology, Medicine
  • Leukemia research
  • 2008 (First Publication: 1 August 2008)
  • To investigate their possible roles in disease susceptibility and some disease characteristics we genotyped C3435T and G2677T/A polymorphisms in multidrug resistance-1 (MDR1) gene with a single baseContinue Reading
  • Gabriella Köblös, Hajnalka Andrikovics, Zoltán Prohászka, Attila Tordai, András Váradi, Tamás Arányi
  • Medicine
  • Genetic testing and molecular biomarkers
  • 2010 (First Publication: 1 February 2010)
  • Loss-of-function mutations of ABCC6 cause pseudoxanthoma elasticum (PXE). This Mendelian disorder is characterized by elastic calcification leading to dermal, ocular, and cardiovascular symptoms likeContinue Reading
  • Nóra Meggyesi, András Kozma, +13 authors Hajnalka Andrikovics
  • Medicine
  • Acta Haematologica
  • 2011
  • Background: Additional chromosome abnormalities (ACAs), mutations of the BCR-ABL tyrosine kinase domain (TKD) and BCR-ABL splice variants may cause resistance to first- and second-generation tyrosineContinue Reading