Adrianna Szponar

Trisomy 7 and 17 mark papillary renal cell tumours irrespectively of variation of the phenotype

A. Jauch, G. Kovacs, A. Szponar, 2009, Journal of Clinical Pathology.

How useful is α‐methylacyl‐CoA racemase (AMACR) immunohistochemistry in the differential diagnosis of kidney cancers?

Tamas Beothe, G. Kovacs, A. Szponar, 2010, Histopathology.

Three genetic developmental stages of papillary renal cell tumors: Duplication of chromosome 1q marks fatal progression

A. Jauch, G. Kovacs, D. Zubakov, 2009, International journal of cancer.

High‐resolution array CGH of metanephric adenomas: lack of DNA copy number changes

G. Kovacs, M. Yusenko, A. Szponar, 2010, Histopathology.

Genomic profiling of papillary renal cell tumours identifies small regions of DNA alterations: a possible role of HNF1B in tumour development

A. V. van Kessel, R. Kuiper, G. Kovacs, 2011, Histopathology.

Inflammatory protein serum amyloid A1 marks a subset of conventional renal cell carcinomas with fatal outcome.

G. Kovacs, C. Paret, A. Szponar, 2010, European urology.