2025
Journal - Research Article
Hossain, S. M., Gimenez, G., Stockwell, P., Weeks, R., Almomani, S., Jones, G. T., Ratajska, M., Shuen, M., Bhat, B., … Rodger, E., Jackson, C., Chatterjee, A., & Eccles, M. R. (2025). Pre-treatment DNA methylome and transcriptome profiles correlate with melanoma response to anti-PD1 immunotherapy. Cancer Letters. Advance online publication. doi: 10.1016/j.canlet.2025.217638
2024
Conference Contribution - Verbal presentation and other Conference outputs
Sarkar, D., Gyanwali, G. C., Patel, J., Shevchuk, P., Woolley, A., Siddiqui, H., Ratajska, M., Sarwar, M., Drummond, C. J., McKinney, C., Antony, J., McCormick, S. P., Braithwaite, A., & Mehta, S. (2024, August-September). Role of H179 p53 mutation in driving aggressive tumours in patients. Verbal presentation at the Queenstown Research Week (QRW) Cancer Meeting, Queenstown, New Zealand.
2023
Journal - Research Article
Jasiak, A., Koczkowska, M., Stukan, M., Wydra, D., Biernat, W., Izycka-Swieszewska, E., … Eccles, M. R., Walker, L., … Ratajska, M. (2023). Analysis of BRCA1 and BRCA2 alternative splicing in predisposition to ovarian cancer. Experimental & Molecular Pathology, 130(104856). doi: 10.1016/j.yexmp.2023.104856
Journal - Research Other
Ratajska, M., Sette, C., & Cunliffe, H. E. (2023). 365 days of progress in cancer genetics. Frontiers in Oncology, 13. doi: 10.3389/fonc.2023.1270902
Conference Contribution - Poster Presentation (not in published proceedings)
Jasiak, A., Anderson, L., Neumann, S., Wasag, B., Weeks, R., Walker, L., Cunliffe, H., & Ratajska, M. (2023, September). Adaptive homeostasis as a possible non-genetic regulator of BRCA1/2 splicing in ovarian cancer. Poster session presented at the New Zealand Society for Oncology (NZSO) Conference, Napier, New Zealand.
Conference Contribution - Verbal presentation and other Conference outputs
Weeks, R., Almomani, S. N., Macaulay, E., Powell, R., Bhat, B., Zuk, M., … Eccles, M. R., & Ratajska, M. (2023, August). Early detection of lung cancer and identification of potential molecular targets for novel therapies via genetic and epigenetic screening. Verbal presentation at the Queenstown Molecular Biology (QMB) Genomics Satellite, Queenstown, New Zealand.
2022
Journal - Research Article
Suszynska, M., Ratajska, M., Galka-Marciniak, P., Ryszkowska, A., Wydra, D., Debniak, J., … Kozlowski, P. (2022). Variant identification in BARD1, PRDM9, RCC1, and RECQL in patients with ovarian cancer by targeted next-generation sequencing of DNA pools. Cancer Prevention Research, 15(3), 151-160. doi: 10.1158/1940-6207.CAPR-21-0295
Conference Contribution - Published proceedings: Abstract
Suszynska, M., Ratajska, M., Ryszkowska, A., Debniak, J., Wydra, D., Cybulski, C., … Kozlowski, P. (2022). Analysis of BARD1, PRDM9, RCC1, and RECQL in patients with ovarian cancer by targeted next-generation sequencing of DNA pools. European Journal of Human Genetics, 30(Suppl. 1), (pp. 418). doi: 10.1038/s41431-021-01026-1
2021
Journal - Research Article
Łukasiewicz, M., Pastuszak, K., Łapińska-Szumczyk, S., Różański, R., In 't Veld, S. G. J. G., Bieńkowski, M., … Ratajska, M., … Jassem, J. (2021). Diagnostic accuracy of liquid biopsy in endometrial cancer. Cancers, 13, 5731. doi: 10.3390/cancers13225731
Pilyugin, M., Ratajska, M., Stukan, M., Concin, N., Zeillinger, R., & Irminger-Finger, I. (2021). BARD1 autoantibody blood test for early detection of ovarian cancer. Genes, 12, 969. doi: 10.3390/genes12070969
Golden, E., Rashwan, R., Woodward, E. A., Sgro, A., Wang, E., Sorolla, A., … Ratajska, M., … Blancafort, P. (2021). The oncogene AAMDC links P13K-AKT-mTOR signaling with metabolic reprograming in estrogen receptor-positive breast cancer. Nature Communications, 12, 1920. doi: 10.1038/s41467-021-22101-7
McDougall, L. I., Powell, R. M., Ratajska, M., Lynch-Sutherland, C. F., Hossain, S. M., Wiggins, G. A. R., … Motwani, J., Macaulay, E. C., Reid, G., Walker, L. C., … Eccles, M. R. (2021). Differential expression of BARD1 isoforms in melanoma. Genes, 12(2), 320. doi: 10.3390/genes12020320
2020
Journal - Research Article
Suszynska, M., Ratajska, M., & Kozlowski, P. (2020). BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: Mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases. Journal of Ovarian Research, 13(1), 50. doi: 10.1186/s13048-020-00654-3
2019
Journal - Research Article
Wiczling, P., Daghir-Wojtkowiak, E., Kaliszan, R., Markuszewski, M. J., Limon, J., Koczkowska, M., … Ratajska, M. (2019). Bayesian multilevel model of micro RNA levels in ovarian-cancer and healthy subjects. PLoS ONE, 14(8), e0221764. doi: 10.1371/journal.pone.0221764
Suszynska, M., Kluzniak, W., Wokolorczyk, D., Jakubowska, A., Huzarski, T., Gronwald, J., … Ratajska, M., … Kozlowski, P. (2019). BARD1 is a low/moderate breast cancer risk gene: Evidence based on an association study of the Central European p.Q564x recurrent mutation. Cancers, 11(6), 740. doi: 10.3390/cancers11060740
2018
Journal - Research Article
Koczkowska, M., Krawczynska, N., Stukan, M., Kuzniacka, A., Brozek, I., Sniadecki, M., … Ratajska, M. (2018). Spectrum and prevalence of pathogenic variants in ovarian cancer susceptibility genes in a group of 333 patients. Cancers, 10(11), 442. doi: 10.3390/cancers10110442
2017
Journal - Research Article
Szutowicz-Kielińska, E., Konopa, K., Kowalczyk, A., Suszko-Każarnowicz, M., Duchnowska, R., Szczęsna, A., Ratajska, M., … Dziadziuszko, R. (2017). An open label phase II study evaluating first-line EGFR tyrosine kinase inhibitor erlotinib in non-small cell lung cancer patients with tumors showing high EGFR gene copy number. Oncotarget, 8(10), 17270-17278. doi: 10.18632/oncotarget.13793
Ratajska, M., Koczkowska, M., Żuk, M., Gorczyński, A., Kuźniacka, A., Stukan, M., … Wasąg, B. (2017). Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer. Oncotarget, 8(60), 101325-101332. doi: 10.18632/oncotarget.20722
Pilyugin, M., André, P.-A., Ratajska, M., Kuzniacka, A., Limon, J., Tournier, B. B., … Irminger-Finger, I. (2017). Antagonizing functions of BARD1 and its alternatively spliced variant BARD1δ in telomere stability. Oncotarget, 8(6), 9339-9353. doi: 10.18632/oncotarget.14068
Klonowska, K., Kluzniak, W., Rusak, B., Jakubowska, A., Ratajska, M., Krawczynska, N., … Kozlowski, P. (2017). The 30 kb deletion in the APOBEC3 cluster decreases APOBEC3A and APOBEC3B expression and creates a transcriptionally active hybrid gene but does not associate with breast cancer in the European population. Oncotarget, 8(44), 76357-76374. doi: 10.18632/oncotarget.19400
2016
Journal - Research Article
Koczkowska, M., Zuk, M., Gorczynski, A., Ratajska, M., Lewandowska, M., Biernat, W., … Wasag, B. (2016). Detection of somatic BRCA1/2 mutations in ovarian cancer: Next-generation sequencing analysis of 100 cases. Cancer Medicine, 5(7), 1640-1646. doi: 10.1002/cam4.748
Journal - Research Other
Irminger-Finger, I., Ratajska, M., & Pilyugin, M. (2016). New concepts on BARD1: Regulator of BRCA pathways and beyond. International Journal of Biochemistry & Cell Biology, 72, 1-17. doi: 10.1016/j.biocel.2015.12.008
2015
Journal - Research Article
Klonowska, K., Ratajska, M., Czubak, K., Kuzniacka, A., Brozek, I., Koczkowska, M., … Kozlowski, P. (2015). Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: The Polish population as an example. Scientific Reports, 5, 10424. doi: 10.1038/srep10424
Kreimann, E. L., Ratajska, M., Kuzniacka, A., Demacopulo, B., Stukan, M., & Limon, J. (2015). A novel splicing mutation in the SLC9A3R1 gene in tumors from ovarian cancer patients. Oncology Letters, 10(6), 3722-3726. doi: 10.3892/ol.2015.3796
Ratajska, M., Krygier, M., Stukan, M., Kuźniacka, A., Koczkowska, M., Dudziak, M., … Wasąg, B. (2015). Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing. Journal of Applied Genetics, 56(2), 193-198. doi: 10.1007/s13353-014-0254-5
Ronowicz, A., Janaszak-Jasiecka, A., Skokowski, J., Madanecki, P., Bartoszewski, R., Bałut, M., … Ratajska, M., … Piotrowski, A. (2015). Concurrent DNA copy-number alterations and mutations in genes related to maintenance of genome stability in uninvolved mammary glandular tissue from breast cancer patients. Human Mutation, 36(11), 1088-1099. doi: 10.1002/humu.22845
Ratajska, M., Matusiak, M., Kuzniacka, A., Wasag, B., Brozek, I., Biernat, W., … Irminger-Finger, I. (2015). Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms. Oncology Reports, 34(5), 2609-2617. doi: 10.3892/or.2015.4235
Journal - Research Other
Bogdanova, N., Togo, A. V., Ratajska, M., Kluźniak, W., Takhirova, Z., Tarp, T., … Dörk, T. (2015). Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe [Short communication]. Familial Cancer, 14(1), 145-149. doi: 10.1007/s10689-014-9748-x
2013
Journal - Research Article
Kuzniacka, A., Wierzba, J., Ratajska, M., Lipska, B. S., Koczkowska, M., Malinowska, M., & Limon, J. (2013). Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome. Journal of Applied Genetics, 54(1), 27-33. doi: 10.1007/s13353-012-0126-9
2012
Journal - Research Article
Brozek, I., Ratajska, M., Piatkowska, M., Kluska, A., Balabas, A., Dabrowska, M., … Limon, J. (2012). Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases. Familial Cancer, 11(3), 351-354. doi: 10.1007/s10689-012-9519-5
Ratajska, M., Antoszewska, E., Piskorz, A., Brozek, I., Borg, Å., Kusmierek, H., … Limon, J. (2012). Cancer predisposing BARD1 mutations in breast-ovarian cancer families. Breast Cancer Research & Treatment, 131(1), 89-97. doi: 10.1007/s10549-011-1403-8
2011
Journal - Research Article
Brozek, I., Cybulska, C., Ratajska, M., Piatkowska, M., Kluska, A., Balabas, A., … Limon, J. (2011). Prevalence of the most frequent BRCA1 mutations in Polish population. Journal of Applied Genetics, 52(3), 325-330. doi: 10.1007/s13353-011-0040-6
Journal - Research Other
Wierzba, J., Kuzniacka, A., Ratajska, M., Lipska, B. S., Kardas, I., Iliszko, M., & Limon, J. (2011). Cornelia de Lange syndrome associated with a de-novo novel NIPBL splice-site mutation and a coincidental inherited translocation t(3;5)(p13;q11). Clinical Dysmorphology, 20(4), 222-224. doi: 10.1097/MCD.0b013e3283455175
2010
Journal - Research Article
Ratajska, M., Wierzba, J., Pehlivan, D., Xia, Z., Brundage, E. K., Cheung, S. W., … Limon, J. (2010). Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL. European Journal of Medical Genetics, 53(6), 378-382. doi: 10.1016/j.ejmg.2010.08.002
Niedoszytko, M., Ratajska, M., Chelmińska, M., Makowiecki, M., Malek, E., Siemińska, A., … Jassem, E. (2010). The angiotensinogen AGT p.M235T gene polymorphism may be responsible for the development of severe anaphylactic reactions to insect venom allergens. International Archives of Allergy & Immunology, 153(2), 166-172. doi: 10.1159/000312634
2009
Journal - Research Article
Brożek, I., Ochman, K., Dębniak, J., Morzuch, L., Ratajska, M., Stepnowska, M., … Limon, J. (2009). Loss of heterozygosity at BRCA1/2 loci in hereditary and sporadic ovarian cancers. Journal of Applied Genetics, 50(4), 379-384. doi: 10.1007/BF03195697
2008
Journal - Research Article
Brozek, I., Ochman, K., Debnik, J., Morzuch, L., Ratajska, M., Stepnowska, M., … Limon, J. (2008). High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecologic Oncology, 108(2), 433-437. doi: 10.1016/j.ygyno.2007.09.035
Ratajska, M., Brozek, I., Senkus-Konefka, E., Jassem, J., Stepnowska, M., Palomba, G., … Limon, J. (2008). BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland. Oncology Reports, 19(1), 263-268. doi: 10.3892/or.19.1.263
2006
Journal - Research Article
Brożek, I., Kardaś, I., Ochman, K., Dębniak, J., Stukan, M., Ratajska, M., … Limon, J. (2006). HER2 amplification has no prognostic value in sporadic and hereditary ovarian tumours. Hereditary Cancer in Clinical Practice, 4(1), 39-42. doi: 10.1186/1897-4287-4-1-39
2005
Journal - Research Article
Majdak, E. J., De Bock, G. H., Brozek, I., Perkowska, M., Ochman, K., Debniak, J., … Devilee, P. (2005). Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases: Preliminary report. European Journal of Cancer, 41(1), 143-150. doi: 10.1016/j.ejca.2004.10.011
2003
Journal - Research Article
Menkiszak, J., Gronwald, J., Górski, B., Jakubowska, A., Huzarski, T., Byrski, T., … Perkowska, M., … Lubiński, J. (2003). Hereditary ovarian cancer in Poland. International Journal of Cancer, 106(6), 942-945. doi: 10.1002/ijc.11338
Journal - Research Other
Perkowska, M., Brozek, I., Wysocka, B., Haraldsson, K., Sandberg, T., Johansson, U., … Limon, J. (2003). BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland. Human Mutation, 21(5), 553-554. doi: 10.1002/humu.9139
2001
Journal - Research Article
Perkowska, M., Szczygieł, M., & Woźniak, A. (2001). Influence of diethylenetriamine (DETA) and sodium nitroprusside (NaNP) on sister chromatid exchange frequency and cell kinetics in cultured human lymphocytes. Journal of Applied Genetics, 42(2), 233-235.