Beata Stasiewicz‐Jarocka
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- Genomic variations and chromosomal abnormalities 9
- Genetic Syndromes and Imprinting 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- Prenatal Screening and Diagnostics 8
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- Chromosomal and Genetic Variations 3
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- Alcoholism and Thiamine Deficiency 1
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- RNA modifications and cancer 1
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- Muscle and Compartmental Disorders 1
Beata Stasiewicz‐Jarocka
16 papers receiving 147 citations
Peers
Comparison fields: 5 of 64
- Genetics 107
- Pediatrics, Perinatology and Child Health 52
- Clinical Biochemistry 17
- Biological Psychiatry 4
- Plant Science 43
Countries citing papers authored by Beata Stasiewicz‐Jarocka
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
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
The 25 scholars most cited alongside Beata Stasiewicz‐Jarocka, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 51 | |
| 2 | 2020 | 6 | |
| 3 | 2018 | 3 | |
| 4 | 2017 | 12 | |
| 5 | 2014 | 7 | |
| 6 | 2014 | 4 | |
| 7 | 2013 | 1 | |
| 8 | [Thrombosis in the course of ovarian hyperstimulation syndrome]. | 2013 | 2 |
| 9 | 2009 | 19 | |
| 10 | [The results of cytogenetic and molecular genetic examinations in 35 couples with primary sterility]. | 2006 | 4 |
| 11 | 2004 | 22 | |
| 12 | 2004 | 26 | |
| 13 | 2003 | 30 | |
| 14 | [Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH]. | 2000 | 2 |
| 15 | [Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH]. | 1998 | 3 |
| 16 | [Jaeken's (CDG) syndrome in two sisters]. | 1996 | 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), Genetic Syndromes and Imprinting (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers), Alcoholism and Thiamine Deficiency (1 paper), RNA modifications and cancer (1 paper) and Muscle and Compartmental Disorders (1 paper). 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.