Barbara Panasiuk

768 total citations
29 papers, 307 citations indexed

About

Barbara Panasiuk is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Barbara Panasiuk has authored 29 papers receiving a total of 307 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 8 papers in Plant Science. Recurrent topics in Barbara Panasiuk's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Barbara Panasiuk is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Barbara Panasiuk collaborates with scholars based in Poland, Germany and United States. Barbara Panasiuk's co-authors include Alina T. Midro, Ewa Wiland, Maciej Kurpisz, R Leśniewicz, Beata Stasiewicz‐Jarocka, D Prokopowicz, Anna Sawicka, K Michalová, Thomas Eggermann and Vaidutis Kučinskas and has published in prestigious journals such as Journal of Andrology, Clinical Genetics and Journal of Assisted Reproduction and Genetics.

In The Last Decade

Barbara Panasiuk

28 papers receiving 234 citations

Peers

Barbara Panasiuk
Marcos Iuri Roos Kulmann Brazil
Arundhati S. Athalye India
W. Hammans Germany
T. Hassold United States
M. Benkhalifa France
Ewa Wiland Poland
Martha Hentemann Norway
A. Babu United States
D. Wells United Kingdom
Simona De Toffol Italy
Marcos Iuri Roos Kulmann Brazil
Barbara Panasiuk
Citations per year, relative to Barbara Panasiuk Barbara Panasiuk (= 1×) peers Marcos Iuri Roos Kulmann

Countries citing papers authored by Barbara Panasiuk

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Panasiuk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Panasiuk

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

All Works

20 of 20 papers shown
1.
Panasiuk, Barbara, et al.. (2026). Hereditary ovarian cancer. Discover Oncology. 17(1). 260–260.
2.
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
3.
4.
Midro, Alina T., Marcella Zollino, Ewa Wiland, et al.. (2015). Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1. Journal of Assisted Reproduction and Genetics. 33(2). 189–197. 2 indexed citations
5.
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
6.
Wiland, Ewa, Marta Olszewska, Andrew Georgiadis, et al.. (2014). Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male. Molecular Cytogenetics. 7(1). 14–14. 3 indexed citations
7.
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
8.
Olszewska, Marta, Monika Frączek, Ewa Wiland, et al.. (2013). Chromatin structure analysis of spermatozoa from reciprocal chromosome translocation (RCT) carriers with known meiotic segregation patterns. Reproductive Biology. 13(3). 209–220. 12 indexed citations
9.
10.
Iwanowski, Piotr, Barbara Panasiuk, Griet Van Buggenhout, et al.. (2011). Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter. American Journal of Medical Genetics Part A. 155(8). 1833–1847. 4 indexed citations
11.
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
12.
Engels, Hartmut, Thomas Eggermann, Almuth Caliebe, et al.. (2008). Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees. American Journal of Medical Genetics Part A. 146A(20). 2611–2616. 45 indexed citations
13.
14.
Midro, Alina T., Barbara Panasiuk, Griet Van Buggenhout, et al.. (2007). Simple and translation forms of monosomy 4p16.1↔ pter: quantitative syndrome definition and cytogenetic evaluation by FISH. Medizinische Genetik. 19(1). 64. 1 indexed citations
15.
Midro, Alina T., Ewa Wiland, Barbara Panasiuk, R Leśniewicz, & Maciej Kurpisz. (2006). Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa. American Journal of Medical Genetics Part A. 140A(3). 245–256. 33 indexed citations
16.
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
17.
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
18.
Panasiuk, Barbara, et al.. (2003). Immunological Response in HIV-Positive Patients Vaccinated against Tick-Borne Encephalitis. Infection. 31(1). 45–46. 25 indexed citations
19.
Panasiuk, Barbara, et al.. (1997). Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother. Clinical Genetics. 52(2). 120–125. 5 indexed citations
20.
Midro, Alina T., et al.. (1988). Familial occurrence of isodicentric X chromosomes with different breakpoints. Clinical Genetics. 34(3). 153–160. 4 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marcos Iuri Roos Kulmann Breakdown of academic impact, for papers by Arundhati S. Athalye Breakdown of academic impact, for papers by W. Hammans Breakdown of academic impact, for papers by T. Hassold Breakdown of academic impact, for papers by M. Benkhalifa Breakdown of academic impact, for papers by Ewa Wiland Breakdown of academic impact, for papers by Martha Hentemann Breakdown of academic impact, for papers by A. Babu Breakdown of academic impact, for papers by D. Wells Breakdown of academic impact, for papers by Simona De Toffol
Rankless by CCL
2026