Ewa Bocian

1.2k total citations
51 papers, 683 citations indexed

About

Ewa Bocian is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Ewa Bocian has authored 51 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 31 papers in Molecular Biology and 14 papers in Plant Science. Recurrent topics in Ewa Bocian's work include Genomic variations and chromosomal abnormalities (24 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Chromosomal and Genetic Variations (14 papers). Ewa Bocian is often cited by papers focused on Genomic variations and chromosomal abnormalities (24 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Chromosomal and Genetic Variations (14 papers). Ewa Bocian collaborates with scholars based in Poland, United States and United Kingdom. Ewa Bocian's co-authors include Paweł Stankiewicz, Ewa Obersztyn, Tadeusz Mazurczak, Beata Nowakowska, Sau Wai Cheung, Krzysztof Szczałuba, Marta Smyk, Magdalena Nawara, Katarzyna Derwińska and Anna Kutkowska‐Kaźmierczak and has published in prestigious journals such as British Journal of Cancer, International Journal of Radiation Oncology*Biology*Physics and Journal of Histochemistry & Cytochemistry.

In The Last Decade

Ewa Bocian

50 papers receiving 648 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ewa Bocian Poland	16	479	346	144	108	62	51	683
Marsha Speevak Canada	17	420 0.9×	302 0.9×	96 0.7×	141 1.3×	54 0.9×	37	636
Roel Hordijk Netherlands	15	520 1.1×	409 1.2×	100 0.7×	184 1.7×	42 0.7×	22	739
Lukrecija Brečević Switzerland	17	479 1.0×	361 1.0×	161 1.1×	174 1.6×	57 0.9×	31	749
Benno Röthlisberger Switzerland	17	462 1.0×	313 0.9×	92 0.6×	163 1.5×	68 1.1×	34	729
Martine Doco‐Fenzy France	15	302 0.6×	349 1.0×	70 0.5×	80 0.7×	59 1.0×	29	690
Joanna Wiszniewska United States	12	360 0.8×	348 1.0×	67 0.5×	106 1.0×	38 0.6×	22	607
Carolina Sismani Cyprus	19	735 1.5×	515 1.5×	184 1.3×	266 2.5×	54 0.9×	75	984
Nicole Maas Belgium	7	351 0.7×	191 0.6×	120 0.8×	101 0.9×	21 0.3×	13	455
Sophia Kitsiou‐Tzeli Greece	16	407 0.8×	422 1.2×	69 0.5×	77 0.7×	15 0.2×	39	656
Hiba Risheg United States	10	403 0.8×	374 1.1×	53 0.4×	164 1.5×	21 0.3×	13	640

Countries citing papers authored by Ewa Bocian

Since Specialization

Citations

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

Fields of papers citing papers by Ewa Bocian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ewa Bocian. 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 Ewa Bocian. The network helps show where Ewa Bocian may publish in the future.

Co-authorship network of co-authors of Ewa Bocian

This figure shows the co-authorship network connecting the top 25 collaborators of Ewa Bocian. A scholar is included among the top collaborators of Ewa Bocian 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 Ewa Bocian. Ewa Bocian 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

Szczałuba, Krzysztof, Beata Nowakowska, Marta Smyk, et al.. (2016). Application of Array Comparative Genomic Hybridization in Newborns with Multiple Congenital Anomalies. Advances in experimental medicine and biology. 912. 1–9. 4 indexed citations

Szczałuba, Krzysztof, Beata Nowakowska, Marta Smyk, et al.. (2015). High-Resolution Array Comparative Genomic Hybridization Utility in Polish Newborns with Isolated Cleft Lip and Palate. Neonatology. 107(3). 173–178. 7 indexed citations

Bartnik, Magdalena, Beata Nowakowska, Katarzyna Derwińska, et al.. (2013). Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability. Journal of Applied Genetics. 55(1). 125–144. 26 indexed citations

Derwińska, Katarzyna, Hanna Mierzewska, Elżbieta Szczepanik, et al.. (2012). Clinical improvement of the aggressive neurobehavioral phenotype in a patient with a deletion of PITX3 and the absence of L‐DOPA in the cerebrospinal fluid. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(2). 236–242. 15 indexed citations

Bartnik, Magdalena, Katarzyna Derwińska, Monika Goś, et al.. (2011). Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females. Genetics in Medicine. 13(5). 447–452. 38 indexed citations

Nowakowska, Beata, Ewa Obersztyn, Krystyna Szymańska, et al.. (2010). Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(5). 1042–1051. 71 indexed citations

Szczałuba, Krzysztof, Katarzyna Derwińska, Barbara Wiśniowiecka‐Kowalnik, et al.. (2008). Clinical and molecular‐cytogenetic evaluation of a family with partial Jacobsen syndrome without thrombocytopenia caused by an ∼5 Mb deletion del(11)(q24.3). American Journal of Medical Genetics Part A. 146A(19). 2449–2454. 28 indexed citations

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Different‐sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 799–806. 47 indexed citations

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Recurrent SOX9 deletion campomelic dysplasia due to somatic mosaicism in the father. American Journal of Medical Genetics Part A. 143A(8). 866–870. 25 indexed citations

10.

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

11.

Nowakowska, Beata, Anna Kutkowska‐Kaźmierczak, Paweł Stankiewicz, et al.. (2007). A girl with deletion 9q22.1–q22.32 including thePTCHandROR2genes identified by genome‐wide array‐CGH. American Journal of Medical Genetics Part A. 143A(16). 1885–1889. 17 indexed citations

12.

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

13.

Dmochowska, Aleksandra, Paweł Stankiewicz, Paweł Golik, et al.. (1998). Assignment<footref rid="foot01"><sup>1</sup></footref> of SUPV3L1 to human chromosome band 10q22.1 by in situ hybridization. Cytogenetic and Genome Research. 83(1-2). 84–85. 6 indexed citations

14.

Bocian, Ewa, et al.. (1996). Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH). Journal of Applied Genetics. 37(3). 313–324. 1 indexed citations

15.

Mazurczak, Tadeusz, Ewa Bocian, Michał Milewski, et al.. (1996). Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland. American Journal of Medical Genetics. 64(1). 184–186. 10 indexed citations

16.

Milewski, Michał, Jerzy Bal, Wout H. Deelen, et al.. (1996). Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.. Acta Biochimica Polonica. 43(2). 383–388. 1 indexed citations

17.

Bocian, Ewa, et al.. (1982). Chromosomal Aberrations Induced by X-rays in Two Mouse Lymphoma (L5178Y) Sublines of Different Radiosensitivity. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine. 42(3). 347–351. 17 indexed citations

18.

Bocian, Ewa, et al.. (1980). Chromosome Aberrations Induced by Low Doses of X-rays in Human Lymphocytes in Vitro. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine. 37(2). 231–236. 8 indexed citations

19.

Bocian, Ewa, et al.. (1978). Chromosome aberrations in human lymphocytes exposed to tritiated water in vitro.. PubMed. 12(1-4). 168–81. 14 indexed citations

20.

Bocian, Ewa, et al.. (1978). Post-irradiation treatment of human lymphocytes with spermidine reduces frequency of chromatid breaks.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 26(9). 639–43. 2 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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