Katarzyna Borg

443 total citations
24 papers, 171 citations indexed

About

Katarzyna Borg is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Katarzyna Borg has authored 24 papers receiving a total of 171 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 8 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Katarzyna Borg's work include Acute Myeloid Leukemia Research (9 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Katarzyna Borg is often cited by papers focused on Acute Myeloid Leukemia Research (9 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Katarzyna Borg collaborates with scholars based in Poland, United States and United Kingdom. Katarzyna Borg's co-authors include Tadeusz Mazurczak, Paweł Stankiewicz, Ewa Bocian, Ewa Obersztyn, Magdalena Nawara, Marta Jurek, Jamel Chelly, Sarah Moreno, James R. Lupski and Przemysław Juszczyński and has published in prestigious journals such as Blood, Cancer Research and Human Genetics.

In The Last Decade

Katarzyna Borg

19 papers receiving 167 citations

Peers

Katarzyna Borg

GENET

HEMAT

GENET

Cinthya Zepeda‐Mendoza United States

Fred Petrij Netherlands

Federica Mottadelli Italy

Carmelo Laganà Italy

M. Alkan Switzerland

K. Kubzdela

Meera Patel United States

Abdul Wali Pakistan

Asif H. Chowdhury United States

Ahlem Amouri Tunisia

Cinthya Zepeda‐Mendoza United States

Katarzyna Borg

122 ×1.3

92 ×1.2

GENET

32 ×0.8

HEMAT

20 ×0.8

GENET

35 ×1.4

Citations per year, relative to Katarzyna Borg Katarzyna Borg (= 1×) peers Cinthya Zepeda‐Mendoza

Countries citing papers authored by Katarzyna Borg

Since Specialization

Citations

This map shows the geographic impact of Katarzyna Borg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Katarzyna Borg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katarzyna Borg more than expected).

Fields of papers citing papers by Katarzyna Borg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katarzyna Borg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Katarzyna Borg. The network helps show where Katarzyna Borg may publish in the future.

Co-authorship network of co-authors of Katarzyna Borg

This figure shows the co-authorship network connecting the top 25 collaborators of Katarzyna Borg. A scholar is included among the top collaborators of Katarzyna Borg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Katarzyna Borg. Katarzyna Borg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Patkowska, Elżbieta, et al.. (2021). Trudności w leczeniu chorego na ostrą białaczkę szpikową z mutacją FLT3-ITD i wysokim stosunkiem allelicznym — oporność na standardową chemioterapię indukującą w połączeniu z midostauryną. 11(4). 253–258.

Barankiewicz, Joanna, et al.. (2020). The impact of cytogenetic evolution and acquisition of del(17p) on the prognosis of multiple myeloma patients. Polskie Archiwum Medycyny Wewnętrznej. 130(6). 483–491. 3 indexed citations

Białopiotrowicz, Emilia, Ewa Jabłońska, Anna Szumera‐Ciećkiewicz, et al.. (2020). SIRT1 and HSP90alpha Are Functionally Linked and Control Mitotic Chromosome Segregation and Cell Viability in a Subset of Dlbcls. Blood. 136(Supplement 1). 28–29. 1 indexed citations

Semenova, Ekaterina, et al.. (2017). Isolation and Characteristics of Mesenchymal Stromal Cells from Different Parts of Placenta. Journal of Stem Cell Research & Therapy. 7(2). 2 indexed citations

Białopiotrowicz, Emilia, Patryk Górniak, Bartosz Puła, et al.. (2016). Microenvironment-Induced Expression of PIM Kinases Supports Chronic Lymphocytic Leukemia Cells Survival and Promotes CXCR4-mTOR Pathway Dependent Migration. Blood. 128(22). 3239–3239. 3 indexed citations

Bujko, Mateusz, Paulina Kober, Marta Libura, et al.. (2015). Promoter DNA methylation and expression levels of HOXA4, HOXA5 and MEIS1 in acute myeloid leukemia. Molecular Medicine Reports. 11(5). 3948–3954. 16 indexed citations

Górniak, Patryk, Anna Ejduk, Katarzyna Borg, et al.. (2015). Comparison of high‐resolution melting analysis with direct sequencing for the detection of recurrent mutations in DNA methyltransferase 3A and isocitrate dehydrogenase 1 and 2 genes in acute myeloid leukemia patients. European Journal Of Haematology. 96(2). 181–187. 11 indexed citations

Czyż, Anna, Kazimierz Hałaburda, Mirosław Markiewicz, et al.. (2015). Mild chronic graft-versus-host disease may alleviate poor prognosis associated with FLT3-internal tandem duplication for adult acute myeloid leukemia following allogeneic stem cell transplantation with myeloablative conditioning in first complete remission; a retrospective study. Acta Haematologica Polonica. 46. 143–144.

Czyż, Anna, Mirosław Markiewicz, Piotr Rzepecki, et al.. (2015). Mild chronic graft‐versus‐host disease may alleviate poor prognosis associated with FLT3 internal tandem duplication for adult acute myeloid leukemia following allogeneic stem cell transplantation with myeloablative conditioning in first complete remission: a retrospective study. European Journal Of Haematology. 96(3). 236–244. 6 indexed citations

10.

Bujko, Mateusz, Paulina Kober, Marta Libura, et al.. (2014). Comparison of promoter DNA methylation and expression levels of genes encoding CCAAT/enhancer binding proteins in AML patients. Leukemia Research. 38(7). 850–856. 18 indexed citations

11.

Windak, Renata, Maciej Szydłowski, Emilia Białopiotrowicz, et al.. (2014). Abstract 1749: Preclinical characterization of SEL24-B489, a dual PIM/FLT3 inhibitor for the treatment of hematological malignancies. Cancer Research. 74(19_Supplement). 1749–1749. 1 indexed citations

12.

Ejduk, Anna, Katarzyna Borg, Ilona Seferyńska, et al.. (2013). Aberracje cytogenetyczne długiego ramienia chromosomu 3 w nowotworach układu krwiotwórczego — opis trzech chorych. 4(3). 271–278.

13.

Grygalewicz, Beata, et al.. (2012). Acute panmyelosis with myelofibrosis with EVI1 amplification. Cancer Genetics. 205(5). 255–260. 3 indexed citations

14.

Borg, Katarzyna, Ewa Bocian, Beata Nowakowska, et al.. (2009). [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].. PubMed. 13(2). 81–93.

15.

Nowakowska, Beata, Paweł Stankiewicz, Ewa Obersztyn, et al.. (2008). Application of metaphase HR‐CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features. American Journal of Medical Genetics Part A. 146A(18). 2361–2369. 12 indexed citations

16.

Nawara, Magdalena, Jakub Klapecki, Katarzyna Borg, et al.. (2008). Novel mutation of IL1RAPL1 gene in a nonspecific X‐linked mental retardation (MRX) family. American Journal of Medical Genetics Part A. 146A(24). 3167–3172. 38 indexed citations

17.

Borg, Katarzyna, Beata Nowakowska, Ewa Obersztyn, et al.. (2007). Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation. American Journal of Medical Genetics Part A. 143A(22). 2738–2743. 11 indexed citations

18.

Bocian, Ewa, Beata Nowakowska, Ewa Obersztyn, et al.. (2007). [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].. PubMed. 10(1 Pt 2). 211–25. 1 indexed citations

19.

Borg, Katarzyna, Paweł Stankiewicz, Ewa Bocian, et al.. (2005). Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a ∼0.5-Mb submicroscopic deletion in a patient with mild mental retardation. Human Genetics. 118(2). 267–275. 28 indexed citations

20.

Terracio, Louis, et al.. (1988). Cellular hypertrophy can be included by cyclical mechanical stretch in vitro. 51–56. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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