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Alina Kuźniacka · SciRah

Researcher profile · Semantic Scholar

Alina Kuźniacka

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Alina Kuźniacka — researcher profile on SciRah

h-index: 12
Works: 24
Citations: 370

Most-cited papers

Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer
M. Ratajska, Magdalena Koczkowska, M. Żuk, A. Gorczyński +5 more
2017OncoTarget45 citations Open access
Semantic Scholar
Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients
Magdalena Koczkowska, Natalia Krawczyńska, M. Stukan, Alina Kuźniacka +9 more
2018Cancers34 citations Open access
Semantic Scholar
Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example
K. Klonowska, M. Ratajska, Karol Czubak, Alina Kuźniacka +12 more
2015Scientific Reports33 citations Open access
Semantic Scholar
Alterations in key signaling pathways in sinonasal tract melanoma. A molecular genetics and immunohistochemical study of 90 cases and comprehensive review of the literature
Małgorzata Chłopek, J. Lasota, Lester D. R. Thompson, M. Szczepaniak +24 more
2022Modern Pathology32 citations Open access
Semantic Scholar
COLORECTAL ADENOCARCINOMAS HARBORING ALK FUSION GENES: A CLINICOPATHOLOGIC AND MOLECULAR GENETIC STUDY OF 12 CASES AND REVIEW OF THE LITERATURE
J. Lasota, Małgorzata Chłopek, B. Wasąg, A. Kowalik +35 more
2020American Journal of Surgical Pathology31 citations Open access
Semantic Scholar
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma.
Alina Kuźniacka, F. Mertens, B. Strömbeck, J. Wiegant +1 more
2004Cancer Genetics and Cytogenetics28 citations
Semantic Scholar
MAML2 rearrangement as a useful diagnostic marker discriminating between Warthin tumour and Warthin-like mucoepidermoid carcinoma
M. Bienkowski, M. Kunc, M. Iliszko, Alina Kuźniacka +2 more
2020Virchows Archiv24 citations Open access
Semantic Scholar
Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms.
M. Ratajska, M. Matusiak, Alina Kuźniacka, B. Wasąg +12 more
2015Oncology Report23 citations Open access
Semantic Scholar
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
M. Ratajska, M. Krygier, M. Stukan, Alina Kuźniacka +10 more
2014Journal of Applied Genetics22 citations Open access
Semantic Scholar
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe
N. Bogdanova, A. Togo, M. Ratajska, W. Kluźniak +25 more
2014Familial Cancer18 citations
Semantic Scholar
Concurrent DNA Copy‐Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients
Anna Ronowicz, Anna Janaszak-Jasiecka, J. Skokowski, P. Madanecki +22 more
2015Human Mutation16 citations Open access
Semantic Scholar
Antagonizing functions of BARD1 and its alternatively spliced variant BARD1δ in telomere stability
Maxim Pilyugin, Pierre-Alain André, M. Ratajska, Alina Kuźniacka +5 more
2016OncoTarget12 citations Open access
Semantic Scholar
Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome
Alina Kuźniacka, J. Wierzba, M. Ratajska, B. Lipska +3 more
2012Journal of Applied Genetics11 citations Open access
Semantic Scholar
Bayesian multilevel model of micro RNA levels in ovarian-cancer and healthy subjects
P. Wiczling, Emilia Daghir-Wojtkowiak, R. Kaliszan, M. Markuszewski +5 more
2019PLoS ONE10 citations Open access
Semantic Scholar
Mosaic Intronic NIPBL Variant in a Family With Cornelia de Lange Syndrome
Natalia Krawczyńska, Alina Kuźniacka, J. Wierzba, I. Parenti +2 more
2018Frontiers in Genetics8 citations Open access
Semantic Scholar
A novel splicing mutation in the SLC9A3R1 gene in tumors from ovarian cancer patients.
E. Kreimann, M. Ratajska, Alina Kuźniacka, Brenda Demacopulo +2 more
2015Oncology Letters8 citations Open access
Semantic Scholar
Karyotypic characterization of 64 nonmalignant thyroid goiters.
M. Iliszko, Alina Kuźniacka, A. Łachiński, M. Babińska +2 more
2005Cancer Genetics and Cytogenetics6 citations
Semantic Scholar
Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome
Alina Kuźniacka, J. Wierzba, M. Ratajska, B. Lipska +3 more
2013Journal of Applied Genetics3 citations Open access
Semantic Scholar
Cornelia de Lange syndrome associated with a de-novo novel NIPBL splice-site mutation and a coincidental inherited translocation t(3;5)(p13;q11).
J. Wierzba, Alina Kuźniacka, M. Ratajska, B. Lipska +3 more
2011Clinical Dysmorphology3 citations
Semantic Scholar
Erratum to: Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome
Alina Kuźniacka, J. Wierzba, M. Ratajska, B. Lipska +3 more
2013Journal of Applied Genetics2 citations Open access
Semantic Scholar
Cancer predisposing BARD 1 mutations affect exon skipping and are associated with overexpression of specific BARD 1 isoforms
M. Ratajska, M. Matusiak, Alina Kuźniacka, B. Wasąg +12 more
20151 citations
Semantic Scholar
ovarian cancer in a family with coexistence of germline nf1 and brca1 mutations case report
I. Brożek, M. Ratajska, Magdalena Koczkowska, Alina Kuźniacka +4 more
20180 citations
Semantic Scholar
Abstract P2-06-01: Characterisation of C11orf67, an oncogenic driver in a new subtype of aggressive endocrine receptor positive breast cancer
A. Redfern, R. Rashwan, A. Sorolla, M. Ratajska +7 more
20160 citations
Semantic Scholar
Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome
Alina Kuźniacka, J. Wierzba, M. Ratajska, B. Lipska +3 more
2012Journal of Applied Genetics0 citations Open access
Semantic Scholar

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