Alina Wojda

414 total citations
15 papers, 291 citations indexed

About

Alina Wojda is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Alina Wojda has authored 15 papers receiving a total of 291 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Reproductive Medicine. Recurrent topics in Alina Wojda's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), DNA Repair Mechanisms (4 papers) and Sperm and Testicular Function (4 papers). Alina Wojda is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), DNA Repair Mechanisms (4 papers) and Sperm and Testicular Function (4 papers). Alina Wojda collaborates with scholars based in Poland and Portugal. Alina Wojda's co-authors include Ewa Ziętkiewicz, Michał Witt, Jadwiga Jaruzelska, Andrzej Pogorzelski, Anna Latos‐Bieleńska, Małgorzata Mossakowska, Maria Szarras‐Czapnik, Kamila Kusz-Zamelczyk, Maciej Kotecki and A Warenik-Szymankiewicz and has published in prestigious journals such as PLoS ONE, The Journals of Gerontology Series A and American Journal of Respiratory Cell and Molecular Biology.

In The Last Decade

Alina Wojda

15 papers receiving 269 citations

Peers

Alina Wojda

GENET

PRM

PPCH

Keiko Shioda United States

Magda Carolina Sánchez Colombia

Jianghan Qu United States

Marina Koltšina Estonia

Patrizia Doi Italy

Rebecca F. Lowdon United States

Zhibing Zhang China

Nina Mørup Denmark

Ghislain Auclair France

N. A. Egolina Russia

Keiko Shioda United States

Alina Wojda

272 ×1.6

142 ×1.0

GENET

43 ×0.6

14 ×0.3

PRM

21 ×0.6

PPCH

Citations per year, relative to Alina Wojda Alina Wojda (= 1×) peers Keiko Shioda

Countries citing papers authored by Alina Wojda

Since Specialization

Citations

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

Fields of papers citing papers by Alina Wojda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alina Wojda

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

All Works

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15 of 15 papers shown

Ziętkiewicz, Ewa, Zuzanna Bukowy‐Bieryłło, Patrycja Daca‐Roszak, et al.. (2019). CFAP300 : Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking. American Journal of Respiratory Cell and Molecular Biology. 61(4). 440–449. 18 indexed citations

Bukowy‐Bieryłło, Zuzanna, M Dabrowski, Andrzej Pogorzelski, et al.. (2019). Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms. Journal of Medical Genetics. 56(11). 769–777. 33 indexed citations

Kurkowiak, Małgorzata, Ewa Ziętkiewicz, Katarzyna Voelkel, et al.. (2016). ZMYND10 - Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia. PLoS ONE. 11(1). e0148067–e0148067. 10 indexed citations

Czyźyk, A, et al.. (2010). Analysis of Phenotype and Karyotype of Children Born From Mothers With 45,X/46,XX Mosaicism. The Endocrinologist. 20(6). 283–285. 2 indexed citations

Ziętkiewicz, Ewa, Alina Wojda, & Michał Witt. (2009). Cytogenetic perspective of ageing and longevity in men and women. Journal of Applied Genetics. 50(3). 261–273. 25 indexed citations

Wojda, Alina, Ewa Ziętkiewicz, & Michał Witt. (2007). Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects. Mutagenesis. 22(3). 195–200. 64 indexed citations

Wojda, Alina, et al.. (2006). Correlation Between the Level of Cytogenetic Aberrations in Cultured Human Lymphocytes and the Age and Gender of Donors. The Journals of Gerontology Series A. 61(8). 763–772. 34 indexed citations

Wojda, Alina, et al.. (2003). Manifestations of ageing at the cytogenetic level.. PubMed. 44(3). 383–99. 34 indexed citations

Wojda, Alina, et al.. (2003). The 102-year old woman with translocation (7;12) and infertility in anamnesis.. PubMed. 44(3). 425–7. 3 indexed citations

10.

Wiland, Ewa, Alina Wojda, Marzena Kamieniczna, Monika A. Szczygiel, & Maciej Kurpisz. (2002). Infertility status of male individuals with abnormal spermiogram evaluated by cytogenetic analysis and in vitro sperm penetration assay.. PubMed. 8(5). CR394–400. 11 indexed citations

11.

Kusz-Zamelczyk, Kamila, Alina Wojda, Marzena Wiśniewska, Anna Latos‐Bieleńska, & Jadwiga Jaruzelska. (2001). A familial X/Y translocation: cytogenetic and molecular study.. PubMed. 42(2). 237–40. 3 indexed citations

12.

Wiland, Ewa, Alina Wojda, Marzena Kamieniczna, et al.. (2001). Idiopathic infertility in married couples in the light of cytogenetic analysis and sperm penetration assay.. PubMed. 39(1). 35–41. 5 indexed citations

13.

Wojda, Alina, Piotr Jędrzejczak, Maciej Kotecki, et al.. (2001). [Importance of cytogenetic analysis in patients with azoospermia or severe oligozoospermia undergoing in vitro fertilization].. PubMed. 72(11). 847–53. 4 indexed citations

14.

Kusz-Zamelczyk, Kamila, Maciej Kotecki, Alina Wojda, et al.. (1999). Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome. Journal of Medical Genetics. 36(6). 452–456. 44 indexed citations

15.

Panasiuk, Barbara, et al.. (1999). [Turner syndrome in a girl with marker chromosome in karyotype].. PubMed. 70(5). 348–53. 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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