Tomasz Roszkowski

415 total citations
41 papers, 242 citations indexed

About

Tomasz Roszkowski is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Tomasz Roszkowski has authored 41 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Pediatrics, Perinatology and Child Health, 16 papers in Genetics and 11 papers in Surgery. Recurrent topics in Tomasz Roszkowski's work include Prenatal Screening and Diagnostics (24 papers), Fetal and Pediatric Neurological Disorders (9 papers) and Gestational Trophoblastic Disease Studies (9 papers). Tomasz Roszkowski is often cited by papers focused on Prenatal Screening and Diagnostics (24 papers), Fetal and Pediatric Neurological Disorders (9 papers) and Gestational Trophoblastic Disease Studies (9 papers). Tomasz Roszkowski collaborates with scholars based in Poland, Belgium and United States. Tomasz Roszkowski's co-authors include Grzegorz Jakiel, Janusz Zimowski, Grzegorz Panek, Beata Nowakowska, Krystyna Szymańska, Kathleen A. Williamson, B Schmidt-Sidor, Teresa Wierzba‐Bobrowicz, Veronica van Heyningen and Jacek Zaremba and has published in prestigious journals such as Ultrasound in Obstetrics and Gynecology, Clinical Genetics and Prenatal Diagnosis.

In The Last Decade

Tomasz Roszkowski

39 papers receiving 236 citations

Peers

Tomasz Roszkowski

PPCH

GENET

SURGE

PHEOH

Feodora Stipoljev Croatia

A. Michiels Belgium

B Rösing Germany

Denise Molina‐Gomes France

Nicholas J. Ahn United States

Vicki M. Park United States

S. SenGupta United Kingdom

Judy F.C. Chow Hong Kong

Qingwei Qi China

Feodora Stipoljev Croatia

Tomasz Roszkowski

126 ×0.9

PPCH

104 ×1.2

GENET

50 ×0.8

42 ×0.7

SURGE

54 ×0.9

PHEOH

Citations per year, relative to Tomasz Roszkowski Tomasz Roszkowski (= 1×) peers Feodora Stipoljev

Countries citing papers authored by Tomasz Roszkowski

Since Specialization

Citations

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

Fields of papers citing papers by Tomasz Roszkowski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomasz Roszkowski

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

All Works

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20 of 20 papers shown

Geremek, Maciej, Tomasz Roszkowski, Michał Ciebiera, et al.. (2022). Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience. Genes. 13(5). 724–724. 12 indexed citations

Nowakowska, Beata, et al.. (2022). Prenatal diagnosis of acrania/exencephaly/anencephaly sequence (AEAS): additional structural and genetic anomalies. Archives of Gynecology and Obstetrics. 307(1). 293–299. 8 indexed citations

Zimowski, Janusz, et al.. (2021). Triploid pregnancy–Clinical implications. Clinical Genetics. 100(4). 368–375. 15 indexed citations

Roszkowski, Tomasz, et al.. (2021). Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing — an up-to-date review and new case report. Ginekologia Polska. 92(1). 51–56.

Zimowski, Janusz, et al.. (2021). Twin pregnancies discordant for digynic triploidy – A case series. Taiwanese Journal of Obstetrics and Gynecology. 60(1). 139–141. 1 indexed citations

Deperas-Kamińska, Marta, Ewa Obersztyn, Nathalie Brison, et al.. (2021). A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC). Molecular Cytogenetics. 14(1). 18–18. 2 indexed citations

Roszkowski, Tomasz, et al.. (2021). Distribution of diandric and digynic triploidy depending on gestational age. Journal of Assisted Reproduction and Genetics. 38(9). 2391–2395. 8 indexed citations

Zimowski, Janusz, et al.. (2020). Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review. Archives of Gynecology and Obstetrics. 301(5). 1139–1145. 8 indexed citations

Panek, Grzegorz, et al.. (2020). In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland. Journal of Assisted Reproduction and Genetics. 37(8). 1999–2006. 2 indexed citations

10.

Panek, Grzegorz, et al.. (2020). Ultrasound evaluation of a bilobed placenta with ‘battledore cord insertion’ — a report of an unusual case. Ginekologia Polska. 91(2). 100–100. 2 indexed citations

11.

Roszkowski, Tomasz, et al.. (2020). Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy. Journal of Human Genetics. 65(10). 889–894. 5 indexed citations

12.

Ciebiera, Michał, et al.. (2016). Blue Rubber Bleb Nevus Syndrome Diagnosed Prenatally as an Epignathus. Journal of Craniofacial Surgery. 27(8). e737–e738. 3 indexed citations

13.

Roszkowski, Tomasz, et al.. (2013). Increased nuchal translucency in chromosomally normal fetuses and pregnancy outcomes – a retrospective study. Ginekologia Polska. 84(3). 172–9. 2 indexed citations

14.

Jakiel, Grzegorz, et al.. (2013). Noninvasive prenatal diagnosis of trisomy 21, 18 and 13 using cel – free fetal DNA. Ginekologia Polska. 84(8). 714–9. 2 indexed citations

15.

Jakiel, Grzegorz, et al.. (2013). Multiplex Ligation-dependent Probe Amplification (MLPA) – new possibilities of prenatal diagnosis. Ginekologia Polska. 84(6). 461–4. 8 indexed citations

16.

Schmidt-Sidor, B, Krystyna Szymańska, Kathleen A. Williamson, et al.. (2009). Malformations of the brain in two fetuses with a compound heterozygosity for two PAX6 mutations.. PubMed. 47(4). 372–82. 21 indexed citations

17.

Roszkowski, Tomasz, et al.. (2006). Harlequin ichthyosis — difficulties in prenatal diagnosis. Journal of Applied Genetics. 47(2). 195–197. 10 indexed citations

18.

Roszkowski, Tomasz, et al.. (2005). P01.20: Prenatal ultrasound findings in trisomy 18: report of 38 cases. Ultrasound in Obstetrics and Gynecology. 26(4). 381–381. 1 indexed citations

19.

Roszkowski, Tomasz, et al.. (2001). [Prenatal diagnosis of a brain tumour--an example of diagnostic and therapeutical algorithm].. PubMed. 5(1). 59–64. 1 indexed citations

20.

Roszkowski, Tomasz, et al.. (2000). Adenosine Triphosphate for Cardioversion of Supraventricular Tachycardia in Two Hydropic Fetuses. Fetal Diagnosis and Therapy. 15(6). 326–330. 6 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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