Ivan Šubrt

1.2k total citations
52 papers, 641 citations indexed

About

Ivan Šubrt is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ivan Šubrt has authored 52 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in Ivan Šubrt's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (8 papers) and Congenital limb and hand anomalies (6 papers). Ivan Šubrt is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (8 papers) and Congenital limb and hand anomalies (6 papers). Ivan Šubrt collaborates with scholars based in Czechia, United States and Slovakia. Ivan Šubrt's co-authors include Dorothy Pettay, C Turleau, Mea Andersson, David C. Page, Albert de la Chapelle, J. de Grouchy, J. Pokorný, Jitka Seidlerová, Jana Hirmerová and Jaroslav Šimon and has published in prestigious journals such as International Journal of Cancer, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Ivan Šubrt

51 papers receiving 588 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ivan Šubrt Czechia 16 366 190 138 122 78 52 641
Emmanuelle Girodon France 22 226 0.6× 311 1.6× 30 0.2× 134 1.1× 116 1.5× 73 1.4k
Ashutosh Halder India 16 166 0.5× 194 1.0× 25 0.2× 243 2.0× 121 1.6× 84 684
Necat İmirzalıoğlu Türkiye 11 128 0.3× 159 0.8× 27 0.2× 146 1.2× 56 0.7× 31 429
Mohgah Elsheikh United Kingdom 11 616 1.7× 325 1.7× 34 0.2× 38 0.3× 120 1.5× 22 863
Cantú Jm Mexico 12 259 0.7× 165 0.9× 83 0.6× 104 0.9× 41 0.5× 67 405
Anahita Mohseni Meybodi Iran 15 250 0.7× 267 1.4× 46 0.3× 67 0.5× 29 0.4× 66 582
Michele Olivieri Italy 9 132 0.4× 486 2.6× 38 0.3× 72 0.6× 36 0.5× 11 784
M J Mahoney United States 21 435 1.2× 329 1.7× 43 0.3× 655 5.4× 184 2.4× 37 1.2k
P.R.L.C. Lam-Po-Tang Australia 14 219 0.6× 193 1.0× 75 0.5× 192 1.6× 35 0.4× 44 642
Dianne Nguyen United States 9 180 0.5× 122 0.6× 51 0.4× 127 1.0× 18 0.2× 16 480

Countries citing papers authored by Ivan Šubrt

Since Specialization
Citations

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

Fields of papers citing papers by Ivan Šubrt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivan Šubrt

This figure shows the co-authorship network connecting the top 25 collaborators of Ivan Šubrt. A scholar is included among the top collaborators of Ivan Šubrt 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 Ivan Šubrt. Ivan Šubrt 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.
Šubrt, Ivan, et al.. (2024). A recurrent synonymous L1CAM variant in a fetus with hydrocephalus. Human Genome Variation. 11(1). 4–4.
2.
Bitar, Ibrahim, et al.. (2024). Targeted long-read sequencing identified a causal structural variant in X-linked nephrogenic diabetes insipidus. BMC Medical Genomics. 17(1). 29–29. 1 indexed citations
3.
Pivovarčíková, Kristýna, Reza Alaghehbandan, Petr Šteiner, et al.. (2023). Lynch syndrome-associated upper tract urothelial carcinoma frequently occurs in patients older than 60 years: an opportunity to revisit urology clinical guidelines. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 483(4). 517–526. 3 indexed citations
4.
5.
Hirmerová, Jana, et al.. (2021). Prevalence of cancer in patients with superficial vein thrombosis and its clinical importance. Journal of Vascular Surgery Venous and Lymphatic Disorders. 10(1). 26–32. 9 indexed citations
6.
Hirmerová, Jana, et al.. (2017). Thrombophilia testing results in patients with a first venous thromboembolic event: should the selection criteria for testing be revisited?. International Angiology. 36(2). 167–173. 1 indexed citations
7.
Šubrt, Ivan. (2015). Concept of social time in sociology – promising approach or a theoretical impassė?. 3–11. 1 indexed citations
8.
Hirmerová, Jana, Jitka Seidlerová, & Ivan Šubrt. (2014). The association of factor V Leiden with various clinical patterns of venous thromboembolism--the factor V Leiden paradox. QJM. 107(9). 715–720. 9 indexed citations
9.
10.
Brožková, Dana Šafka, et al.. (2009). Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease. Genetic Testing and Molecular Biomarkers. 14(1). 3–7. 11 indexed citations
11.
Šubrt, Ivan, et al.. (2008). ORIGINAL ARTICLE: Recurrent Pregnancy Loss and Frequency of Eight Antiphospholipid Antibodies and Genetic Thrombophilic Factors in Czech Women. American Journal of Reproductive Immunology. 59(3). 193–200. 15 indexed citations
12.
Mayer, Otto, Jaroslav Šimon, L Holubec, Richard Pikner, & Ivan Šubrt. (2003). Fenofibrate-induced hyperhomocysteinemia may be prevented by folate co-administration. European Journal of Clinical Pharmacology. 59(5-6). 367–371. 25 indexed citations
13.
Mayer, Otto, et al.. (2002). The effects of folate supplementation on some coagulation parameters and oxidative status surrogates. European Journal of Clinical Pharmacology. 58(1). 1–5. 27 indexed citations
14.
Pettenati, Mark J., Ivan Šubrt, Nagesh Rao, et al.. (1991). 45,X/47,XYY mosaicism: Clinical discrepancy between prenatally and postnatally diagnosed cases. American Journal of Medical Genetics. 39(1). 42–47. 27 indexed citations
15.
Šubrt, Ivan, et al.. (1988). Frequency of tri- and multiradial configurations in fragile X chromosomes. Human Genetics. 78(2). 196–197. 1 indexed citations
16.
Andersson, Mea, David C. Page, Dorothy Pettay, et al.. (1988). Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11. Human Genetics. 79(1). 2–7. 104 indexed citations
17.
Šubrt, Ivan, et al.. (1988). Familial translocation t(17;22), including the segregation in five consecutive abortuses. Human Genetics. 80(2). 195–196. 1 indexed citations
18.
19.
Šubrt, Ivan, et al.. (1970). Chromosomal Abnormalities in a Girl with Physical and Mental Maldevelopment. Human Heredity. 20(3). 252–259. 1 indexed citations
20.
Šubrt, Ivan, et al.. (1968). Aberrant Chromosome 13–15 in a Patient with Down’s Syndrome, Diabetes Mellitus and Hyperthyroidism and in his Father. Human Heredity. 18(1). 38–44. 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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