Beata Stasiewicz‐Jarocka

548 total citations
16 papers, 195 citations indexed

About

Beata Stasiewicz‐Jarocka is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Beata Stasiewicz‐Jarocka has authored 16 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Beata Stasiewicz‐Jarocka's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Genetic Syndromes and Imprinting (3 papers). Beata Stasiewicz‐Jarocka is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Genetic Syndromes and Imprinting (3 papers). Beata Stasiewicz‐Jarocka collaborates with scholars based in Poland, Czechia and Croatia. Beata Stasiewicz‐Jarocka's co-authors include Alina T. Midro, Barbara Panasiuk, Sylwia Chojnowska, Napoleon Waszkiewicz, Alina Kępka, Małgorzata Borzym‐Κluczyk, K Michalová, Vaidutis Kučinskas, Barbara Pieńkowska‐Grela and Anna Sawicka and has published in prestigious journals such as Nutrients, Clinical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Beata Stasiewicz‐Jarocka

16 papers receiving 147 citations

Peers

Beata Stasiewicz‐Jarocka

GENET

PPCH

PHYSI

Celia Medrano Spain

Shawn Fayer United States

Mari‐Anne Vals Estonia

Ayumi Uematsu Japan

Shu-Min Kao Taiwan

Meral Yirmibeş Karaoğuz Türkiye

Meryl Altree Australia

Magalie Boguenet France

Solenn Pruvost Switzerland

Mitsukazu Mamada Japan

Celia Medrano Spain

Beata Stasiewicz‐Jarocka

67 ×0.6

GENET

100 ×1.5

33 ×0.6

PPCH

17 ×0.4

30 ×1.2

PHYSI

Citations per year, relative to Beata Stasiewicz‐Jarocka Beata Stasiewicz‐Jarocka (= 1×) peers Celia Medrano

Countries citing papers authored by Beata Stasiewicz‐Jarocka

Since Specialization

Citations

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

Fields of papers citing papers by Beata Stasiewicz‐Jarocka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beata Stasiewicz‐Jarocka. 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 Beata Stasiewicz‐Jarocka. The network helps show where Beata Stasiewicz‐Jarocka may publish in the future.

Co-authorship network of co-authors of Beata Stasiewicz‐Jarocka

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

All Works

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16 of 16 papers shown

Kępka, Alina, et al.. (2020). Preventive Role of L-Carnitine and Balanced Diet in Alzheimer’s Disease. Nutrients. 12(7). 1987–1987. 51 indexed citations

Midro, Alina T., Beata Stasiewicz‐Jarocka, Jan Borys, et al.. (2020). Two unrelated families with variable expression of Fraser syndrome due to the same pathogenic variant in the FRAS1 gene. American Journal of Medical Genetics Part A. 182(4). 773–779. 6 indexed citations

Midro, Alina T., Beata Stasiewicz‐Jarocka, Jan Borys, et al.. (2018). A 23‐year follow‐up of a male with Hajdu‐Cheney syndrome due to NOTCH2 mutation. American Journal of Medical Genetics Part A. 176(11). 2382–2388. 3 indexed citations

Lozić, Bernarda, Piotr Iwanowski, Tatijana Zemunik, et al.. (2017). Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations. Molecular Cytogenetics. 10(1). 29–29. 12 indexed citations

Stasiewicz‐Jarocka, Beata, et al.. (2014). Complex balanced chromosomal translocation t(2;5;13) (p21;p15;q22) in a woman with four reproductive failures. Molecular Cytogenetics. 7(1). 83–83. 7 indexed citations

Midro, Alina T., Barbara Panasiuk, Beata Stasiewicz‐Jarocka, et al.. (2014). Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2). Journal of Human Genetics. 59(12). 667–674. 4 indexed citations

Stasiewicz‐Jarocka, Beata, et al.. (2013). Risk estimation of different pregnancy outcomes in the families of carriers of reciprocal chromosomal translocations involving chromosome 20. Ginekologia Polska. 84(6). 422–9. 1 indexed citations

Mrugacz, Grzegorz, et al.. (2013). [Thrombosis in the course of ovarian hyperstimulation syndrome].. PubMed. 16(4). 303–6. 2 indexed citations

Panasiuk, Barbara, Jacqueline Suk Danik, Beata Stasiewicz‐Jarocka, et al.. (2009). Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2. Advances in Medical Sciences. 54(2). 203–10. 19 indexed citations

10.

Haus, Olga, Ryszard Ślężak, Alina T. Midro, et al.. (2006). [The results of cytogenetic and molecular genetic examinations in 35 couples with primary sterility].. PubMed. 59(1-2). 38–43. 4 indexed citations

11.

Stasiewicz‐Jarocka, Beata, Olga Haus, E. Van Assche, et al.. (2004). Genetic counseling in carriers of reciprocal chromosomal translocations involving long arm of chromosome 16. Clinical Genetics. 66(3). 189–207. 22 indexed citations

12.

Panasiuk, Barbara, Beata Stasiewicz‐Jarocka, Barbara Pieńkowska‐Grela, et al.. (2004). Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X. Annales de Génétique. 47(1). 11–28. 26 indexed citations

13.

Midro, Alina T., Barbara Panasiuk, Zeynep Tümer, et al.. (2003). Interstitial deletion 9q22.32‐q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin–Goltz syndrome and features of Nail‐Patella syndrome. American Journal of Medical Genetics Part A. 124A(2). 179–191. 30 indexed citations

14.

Stasiewicz‐Jarocka, Beata, et al.. (2000). [Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH].. PubMed. 71(10). 1262–72. 2 indexed citations

15.

Sawicka, Anna, R Leśniewicz, M Zawada, Beata Stasiewicz‐Jarocka, & Alina T. Midro. (1998). [Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH].. PubMed. 69(4). 200–6. 3 indexed citations

16.

Midro, Alina T., et al.. (1996). [Jaeken's (CDG) syndrome in two sisters].. PubMed. 71(7). 621–8. 3 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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