Beata Stasiewicz‐Jarocka

548 citations
16 papers · 195 indexed · h-index 7
Topics
Genomic variations and chromosomal abnormalities (9 papers)Prenatal Screening and Diagnostics (8 papers)Genetic Syndromes and Imprinting (3 papers)
Partner nations
PolandCzechiaCroatia

In The Last Decade

Beata Stasiewicz‐Jarocka

16 papers receiving 147 citations

Peers

Beata Stasiewicz‐Jarocka
Comparison fields: 5 of 64
  • Genetics 107
  • Molecular Biology 68
  • Pediatrics, Perinatology and Child Health 52
  • Plant Science 43
  • Physiology 25
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Citations per field
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Citations per year

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

16 of 16 papers shown
#WorkIndexed citations
1 51
2 6
3 3
4 12
5 7
6 4
7 1
8
[Thrombosis in the course of ovarian hyperstimulation syndrome].
2
9 19
10
[The results of cytogenetic and molecular genetic examinations in 35 couples with primary sterility].
4
11 22
12 26
13 30
14
[Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH].
2
15
[Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH].
3
16
[Jaeken's (CDG) syndrome in two sisters].
3

About Beata Stasiewicz‐Jarocka

Beata Stasiewicz‐Jarocka is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 16 papers that have together received 195 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Genetics (107 citations), Pediatrics, Perinatology and Child Health (52 citations) and Clinical Biochemistry (17 citations). Beata Stasiewicz‐Jarocka has collaborated with scholars based in Poland, Czechia and Croatia. Frequent 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. Their work appears in journals such as Nutrients, Clinical Genetics and American Journal of Medical Genetics Part A.

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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