Ewelina Bukowska‐Olech

514 total citations
41 papers, 273 citations indexed

About

Ewelina Bukowska‐Olech is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Ewelina Bukowska‐Olech has authored 41 papers receiving a total of 273 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 24 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Ewelina Bukowska‐Olech's work include Cleft Lip and Palate Research (6 papers), Connective tissue disorders research (5 papers) and Craniofacial Disorders and Treatments (5 papers). Ewelina Bukowska‐Olech is often cited by papers focused on Cleft Lip and Palate Research (6 papers), Connective tissue disorders research (5 papers) and Craniofacial Disorders and Treatments (5 papers). Ewelina Bukowska‐Olech collaborates with scholars based in Poland, United States and Germany. Ewelina Bukowska‐Olech's co-authors include Aleksander Jamsheer, Anna Sowińska‐Seidler, Anna Latos‐Bieleńska, Magdalena Socha, Joanna Walczak‐Sztulpa, K. Kozlowski, Anna Wawrocka, Marek Niedziela, Tomasz Żemojtel and Anna Materna‐Kiryluk and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Ewelina Bukowska‐Olech

37 papers receiving 271 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ewelina Bukowska‐Olech Poland 11 157 147 33 25 23 41 273
Yu Ding China 12 219 1.4× 170 1.2× 24 0.7× 35 1.4× 35 1.5× 38 359
Eri Imagawa Japan 13 250 1.6× 170 1.2× 26 0.8× 17 0.7× 41 1.8× 30 418
Gökhan Yigit Germany 11 207 1.3× 132 0.9× 18 0.5× 25 1.0× 31 1.3× 24 355
Glenda M. Beaman United Kingdom 9 129 0.8× 86 0.6× 34 1.0× 26 1.0× 28 1.2× 20 278
Eva‐Lena Stattin Sweden 8 175 1.1× 133 0.9× 53 1.6× 27 1.1× 24 1.0× 11 307
Emma Hobson United Kingdom 9 213 1.4× 256 1.7× 42 1.3× 33 1.3× 40 1.7× 24 405
Louise A. Stephen United Kingdom 10 229 1.5× 120 0.8× 31 0.9× 60 2.4× 25 1.1× 23 349
Farooq Ahmad Pakistan 12 272 1.7× 227 1.5× 54 1.6× 15 0.6× 25 1.1× 38 421
Maryam Sedghi Iran 11 176 1.1× 80 0.5× 14 0.4× 19 0.8× 23 1.0× 46 338
Susanna Lemmelä Finland 12 225 1.4× 93 0.6× 31 0.9× 22 0.9× 29 1.3× 16 470

Countries citing papers authored by Ewelina Bukowska‐Olech

Since Specialization
Citations

This map shows the geographic impact of Ewelina Bukowska‐Olech'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 Ewelina Bukowska‐Olech with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ewelina Bukowska‐Olech more than expected).

Fields of papers citing papers by Ewelina Bukowska‐Olech

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ewelina Bukowska‐Olech. 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 Ewelina Bukowska‐Olech. The network helps show where Ewelina Bukowska‐Olech may publish in the future.

Co-authorship network of co-authors of Ewelina Bukowska‐Olech

This figure shows the co-authorship network connecting the top 25 collaborators of Ewelina Bukowska‐Olech. A scholar is included among the top collaborators of Ewelina Bukowska‐Olech 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 Ewelina Bukowska‐Olech. Ewelina Bukowska‐Olech is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Spadafora, Luigi, Federico Russo, Ewelina Bukowska‐Olech, et al.. (2025). Cardiovascular Safety of Bruton Tyrosine Kinase Inhibitors: From Ibrutinib to Next-Generation Agents. American Journal of Cardiovascular Drugs. 26(1). 21–34. 1 indexed citations
3.
Bukowska‐Olech, Ewelina, et al.. (2024). Chromatinopathies: insight in clinical aspects and underlying epigenetic changes. Journal of Applied Genetics. 65(2). 287–301. 2 indexed citations
4.
Jurek, Marta, Ewa Obersztyn, Monika Bekiesińska‐Figatowska, et al.. (2023). Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism. Journal of Applied Genetics. 64(3). 507–514. 2 indexed citations
5.
Bukowska‐Olech, Ewelina, Anna Sowińska‐Seidler, Jolanta Wierzba, & Aleksander Jamsheer. (2022). SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably. Orphanet Journal of Rare Diseases. 17(1). 325–325.
6.
Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Aleksander Jankowski, et al.. (2022). The pZRS non-coding regulatory mutation resulting in triphalangeal thumb–polysyndactyly syndrome changes the pattern of local interactions. Molecular Genetics and Genomics. 297(5). 1343–1352. 2 indexed citations
7.
Bukowska‐Olech, Ewelina, et al.. (2022). Rare multiple congenital anomalies-hypotonia-seizures syndrome type 1 (MCAHS1) – the clinical and molecular summary. European Journal of Medical Genetics. 66(1). 104668–104668. 1 indexed citations
8.
Bukowska‐Olech, Ewelina, et al.. (2021). Clinical and molecular characterization of craniofrontonasal syndrome: new symptoms and novel pathogenic variants in the EFNB1 gene. Orphanet Journal of Rare Diseases. 16(1). 286–286. 4 indexed citations
9.
Bukowska‐Olech, Ewelina, et al.. (2021). Hereditary Multiple Exostoses—A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies. Frontiers in Genetics. 12. 759129–759129. 28 indexed citations
10.
Bukowska‐Olech, Ewelina, et al.. (2020). Further phenotypic delineation of the auriculocondylar syndrome type 2 with literature review. Journal of Applied Genetics. 62(1). 107–113. 7 indexed citations
11.
Bukowska‐Olech, Ewelina, Delfina Popiel, Grzegorz Koczyk, et al.. (2020). Adapting SureSelect enrichment protocol to the Ion Torrent S5 platform in molecular diagnostics of craniosynostosis. Scientific Reports. 10(1). 4159–4159. 4 indexed citations
12.
Bukowska‐Olech, Ewelina, Anna Sowińska‐Seidler, Krzysztof Szczałuba, & Aleksander Jamsheer. (2020). A novel biallelic splice‐site variant in the LRP4 gene causes sclerosteosis 2. Birth Defects Research. 112(9). 652–659. 5 indexed citations
13.
Wawrocka, Anna, Joanna Walczak‐Sztulpa, Ewelina Bukowska‐Olech, et al.. (2020). Two sisters with microphthalmia and anterior segment dysgenesis secondary to a PAX6 pathogenic variant with clinically healthy parents: a case of gonadal mosaicism?. Japanese Journal of Ophthalmology. 64(2). 134–139. 3 indexed citations
14.
Walczak‐Sztulpa, Joanna, Renata Posmyk, Ewelina Bukowska‐Olech, et al.. (2020). Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease. Orphanet Journal of Rare Diseases. 15(1). 36–36. 12 indexed citations
15.
Walczak‐Sztulpa, Joanna, Anna Wawrocka, Heleen H. Arts, et al.. (2020). Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35. American Journal of Medical Genetics Part A. 182(10). 2417–2425. 8 indexed citations
16.
Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Magdalena Socha, et al.. (2019). Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia. Clinical Genetics. 96(5). 429–438. 16 indexed citations
17.
Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Magdalena Socha, Dawid Larysz, & Aleksander Jamsheer. (2018). Novel 1q22-q23.1 duplication in a patient with lambdoid and metopic craniosynostosis, muscular hypotonia, and psychomotor retardation. Journal of Applied Genetics. 59(3). 281–289. 5 indexed citations
18.
Bukowska‐Olech, Ewelina, Tomasz Żemojtel, Anna Sowińska‐Seidler, et al.. (2016). Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology. 1(1). 78–83. 4 indexed citations
19.
Jamsheer, Aleksander, Ewelina Bukowska‐Olech, K. Kozlowski, et al.. (2016). Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiency. Journal of Human Genetics. 61(7). 577–583. 15 indexed citations
20.
Sowińska‐Seidler, Anna, Monika Piwecka, Ewelina Bukowska‐Olech, et al.. (2014). Hyperosmia, ectrodactyly, mild intellectual disability, and other defects in a male patient with an X-linked partial microduplication and overexpression of the KAL1 gene. Journal of Applied Genetics. 56(2). 177–184. 12 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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