Katarzyna Borg
Impact in
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- Acute Myeloid Leukemia Research
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Hematology 12
- Acute Myeloid Leukemia Research 9
- Chronic Myeloid Leukemia Treatments 5
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- Epigenetics and DNA Methylation 4
- Co-authors
- Tadeusz Mazurczak (7 shared papers)Ewa Bocian (6 shared papers)Paweł Stankiewicz (4 shared papers)Ewa Obersztyn (6 shared papers)Przemysław Juszczyński (6 shared papers)Marta Jurek (1 shared paper)Jakub Klapecki (1 shared paper)Sarah Moreno (1 shared paper)
- Journals
- European Journal Of Haematology (3 papers)Blood (2 papers)Human Genetics (1 paper)Cancer Research (1 paper)Leukemia Research (1 paper)
- Partner nations
- PolandUnited StatesUnited Kingdom
In The Last Decade
Katarzyna Borg
19 papers receiving 169 citations
Peers
Comparison fields: 5 of 38
- Hematology 37
- Genetics 72
- Genetics 23
- Molecular Biology 80
- Developmental Biology 2
Countries citing papers authored by Katarzyna Borg
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
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-authors
The 25 scholars most cited alongside Katarzyna Borg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 38 | |
| 2 | 2005 | 28 | |
| 3 | 2014 | 18 | |
| 4 | 2015 | 16 | |
| 5 | 2008 | 12 | |
| 6 | 2015 | 12 | |
| 7 | 2007 | 11 | |
| 8 | 2018 | 8 | |
| 9 | 2015 | 6 | |
| 10 | 2020 | 4 | |
| 11 | 2017 | 3 | |
| 12 | 2016 | 3 | |
| 13 | 2012 | 3 | |
| 14 | 2017 | 3 | |
| 15 | [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities]. | 2007 | 2 |
| 16 | 2017 | 2 | |
| 17 | 2014 | 1 | |
| 18 | [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations]. | 2007 | 1 |
| 19 | 2020 | 1 | |
| 20 | Cellular hypertrophy can be included by cyclical mechanical stretch in vitro | 1988 | 1 |
About Katarzyna Borg
Katarzyna Borg is a scholar working on Hematology, Molecular Biology, Genetics, Pathology and Forensic Medicine and Genetics, having authored 24 papers that have together received 173 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (9 papers), Chronic Myeloid Leukemia Treatments (5 papers), Chronic Lymphocytic Leukemia Research (5 papers), Epigenetics and DNA Methylation (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Cancer Mechanisms and Therapy (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Hematology (37 citations), Genetics (72 citations), Genetics (23 citations), Molecular Biology (80 citations) and Developmental Biology (2 citations). Katarzyna Borg has collaborated with scholars based in Poland, United States and United Kingdom. Frequent co-authors include Tadeusz Mazurczak, Ewa Bocian, Paweł Stankiewicz, Ewa Obersztyn, Przemysław Juszczyński, Marta Jurek, Jakub Klapecki, Sarah Moreno, Jerzy Bal and Jamel Chelly. Their work appears in journals such as European Journal Of Haematology, Blood, Human Genetics, Cancer Research and Leukemia Research.
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.