Jiří Šantavý

611 total citations
17 papers, 439 citations indexed

About

Jiří Šantavý is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jiří Šantavý has authored 17 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jiří Šantavý's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Sexual Differentiation and Disorders (4 papers) and Prenatal Screening and Diagnostics (4 papers). Jiří Šantavý is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Sexual Differentiation and Disorders (4 papers) and Prenatal Screening and Diagnostics (4 papers). Jiří Šantavý collaborates with scholars based in Czechia, Yemen and Netherlands. Jiří Šantavý's co-authors include Ishraq Dhaifalah, Gudrun Boysen, Juha Kere, C. P. J. Maury, Albert de la Chapelle, Liesbeth M. Bleeker-Wagemakers, Martin Procházka, Marek Ľubušký, Radek Vodička and Radek Vrtěl and has published in prestigious journals such as Nature Genetics, Reproductive BioMedicine Online and American Journal of Medical Genetics.

In The Last Decade

Jiří Šantavý

17 papers receiving 421 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiří Šantavý Czechia 9 141 137 76 65 55 17 439
Sarah Dickson United Kingdom 8 222 1.6× 33 0.2× 57 0.8× 24 0.4× 14 0.3× 17 524
Hirohiko Watanabe Japan 9 121 0.9× 46 0.3× 32 0.4× 5 0.1× 9 0.2× 15 442
Jaswinder Kaur India 11 172 1.2× 18 0.1× 34 0.4× 4 0.1× 50 0.9× 35 564
Habiba Al Safar United Arab Emirates 9 128 0.9× 39 0.3× 14 0.2× 10 0.2× 19 0.3× 20 331
Jing Leng China 9 63 0.4× 40 0.3× 9 0.1× 4 0.1× 74 1.3× 21 303
Torsten Frambach Germany 12 202 1.4× 64 0.5× 110 1.4× 9 0.1× 39 0.7× 23 689
Koumudi Godbole India 10 102 0.7× 36 0.3× 82 1.1× 48 0.9× 22 295
Felix Schreiner Germany 13 215 1.5× 215 1.6× 111 1.5× 43 0.8× 35 546
Kathleen Rewers‐Felkins United States 13 61 0.4× 16 0.1× 79 1.0× 8 0.1× 29 0.5× 36 457
Meike L. Uhler United States 13 48 0.3× 80 0.6× 144 1.9× 7 0.1× 61 1.1× 29 598

Countries citing papers authored by Jiří Šantavý

Since Specialization
Citations

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

Fields of papers citing papers by Jiří Šantavý

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiří Šantavý

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

All Works

17 of 17 papers shown
1.
Vodička, Radek, et al.. (2011). SEQUENCE RECOMBINATION IN EXON 1 OF THE TSPY GENE IN MEN WITH IMPAIRED FERTILITY. Biomedical Papers. 155(3). 287–298. 3 indexed citations
2.
Šantavý, Jiří. (2010). HEMOLYTIC DISEASE IN THE NEWBORN - HISTORY AND PREVENTION IN THE WORLD AND THE CZECH REPUBLIC. Biomedical Papers. 154(2). 147–151. 4 indexed citations
3.
Vodička, Radek, Radek Vrtěl, Ladislav Dušek, et al.. (2008). Refined fluorescent STR quantification of cell‐free fetal DNA during pregnancy in physiological and Down syndrome fetuses. Prenatal Diagnosis. 28(5). 425–433. 10 indexed citations
4.
Ľubušký, Marek, et al.. (2007). Single umbilical artery and its siding in the second trimester of pregnancy: relation to chromosomal defects. Prenatal Diagnosis. 27(4). 327–331. 31 indexed citations
5.
Vodička, Radek, Radek Vrtěl, Ladislav Dušek, et al.. (2007). TSPY gene copy number as a potential new risk factor for male infertility. Reproductive BioMedicine Online. 14(5). 579–587. 54 indexed citations
6.
Dhaifalah, Ishraq, Jiří Šantavý, & Jana Zapletalová. (2006). SCREENING FOR CHROMOSOMAL ANOMALIES IN THE FIRST TRIMESTER: A REPORT ON THE FIRST YEAR OF PROSPECTIVE SCREENING FOR CHROMOSOMAL ANOMALIES IN THE FIRST TRIMESTER IN THE CZECH REPUBLIC. Biomedical Papers. 150(2). 275–278. 3 indexed citations
7.
Dhaifalah, Ishraq, Jiří Šantavý, & H Fingerová. (2006). Uterine rupture during pregnancy and delivery among women attending the Al-Tthawra Hospital in Sana'a City Yemen Republic. Biomedical Papers. 150(2). 279–283. 22 indexed citations
8.
Ľubušký, Marek, et al.. (2006). Concordant partial urorectal septum malformation sequence in monozygotic twins. American Journal of Medical Genetics Part A. 140A(24). 2828–2831. 6 indexed citations
9.
Ľubušký, Marek, Martin Procházka, Ishraq Dhaifalah, et al.. (2006). Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence. Prenatal Diagnosis. 26(4). 345–349. 30 indexed citations
10.
Singh, Arvind R., et al.. (2006). Comparative Study of AZF Deletions and TSPY Gene Variation in Czech and Indian Infertile Men. International Journal of Human Genetics. 6(3). 209–217. 1 indexed citations
11.
Singh, Arvind R., et al.. (2006). Genetic Factors in Male Infertility and their Implications. International Journal of Human Genetics. 6(2). 163–169. 7 indexed citations
12.
Singh, Arvind R., et al.. (2005). Y Chromosome and Male Infertility. International Journal of Human Genetics. 5(4). 225–235. 3 indexed citations
13.
Vodička, Radek, Radek Vrtěl, Jiřina Zapletalová, et al.. (2004). Refined quantitative fluorescent PCR of Y-chromosome DNA sequences mosaics in Turner's syndrome patients—alternative to real-time PCR. Journal of Biochemical and Biophysical Methods. 60(2). 151–162. 9 indexed citations
14.
Dhaifalah, Ishraq & Jiří Šantavý. (2004). KHAT HABIT AND ITS HEALTH EFFECT. A NATURAL AMPHETAMINE. Biomedical Papers. 148(1). 11–15. 106 indexed citations
15.
Drábek, Jir̆ı́, et al.. (1997). Familial hydronephrosis unlinked to the HLA complex. American Journal of Medical Genetics. 70(2). 118–120. 3 indexed citations
16.
Zapletalová, Jiřina, et al.. (1994). Spondyloepiphyseal dysplasia with nephrotic syndrome (Schimke immunoosseous dysplasia). American Journal of Medical Genetics. 49(3). 270–273. 12 indexed citations
17.
Chapelle, Albert de la, Gudrun Boysen, Jiří Šantavý, et al.. (1992). Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. Nature Genetics. 2(2). 157–160. 135 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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