Felix Votava

805 total citations
30 papers, 582 citations indexed

About

Felix Votava is a scholar working on Molecular Biology, Clinical Biochemistry and Hematology. According to data from OpenAlex, Felix Votava has authored 30 papers receiving a total of 582 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 8 papers in Hematology. Recurrent topics in Felix Votava's work include Sexual Differentiation and Disorders (12 papers), Metabolism and Genetic Disorders (10 papers) and Neonatal Respiratory Health Research (7 papers). Felix Votava is often cited by papers focused on Sexual Differentiation and Disorders (12 papers), Metabolism and Genetic Disorders (10 papers) and Neonatal Respiratory Health Research (7 papers). Felix Votava collaborates with scholars based in Czechia, Austria and Germany. Felix Votava's co-authors include Franz Waldhauser, Jan Lebl, J. Sólyom, Georg Heinze, Tadej Battelino, József Kovács, H Frisch, Adolf Mühl, Sylvia Stöckler‐Ipsiroglu and Sabina Baumgartner‐Parzer and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Clinical Chemistry.

In The Last Decade

Felix Votava

28 papers receiving 560 citations

Peers

Felix Votava

EDM

PRM

GENET

J. Sólyom Hungary

Dina Ramadan Kuwait

Keiichi Hara Japan

Ariadna González‐del Angel Mexico

Miller Wl United States

Suzanne K. Cordovado United States

Fernanda Caroline Soardi Brazil

Susanna Porcu Italy

Yasuyuki Shinozaki Japan

Cristina Martín-Higueras Spain

J. Sólyom Hungary

Felix Votava

610 ×1.9

173 ×1.1

508 ×3.5

EDM

30 ×0.3

PRM

258 ×2.2

GENET

Citations per year, relative to Felix Votava Felix Votava (= 1×) peers J. Sólyom

Countries citing papers authored by Felix Votava

Since Specialization

Citations

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

Fields of papers citing papers by Felix Votava

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Felix Votava

This figure shows the co-authorship network connecting the top 25 collaborators of Felix Votava. A scholar is included among the top collaborators of Felix Votava 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 Felix Votava. Felix Votava 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

Anderlová, Kateřina, Jan Krátký, Drahomíra Springer, et al.. (2024). Iodine supply and thyroid function in women with gestational diabetes mellitus: a cohort study. Endocrine Connections. 13(11).

Honzík, Tomáš, Viktor Kožich, Karolína Pešková, & Felix Votava. (2022). Laboratory newborn screening. 77(1). 12–18. 2 indexed citations

Potůčková, Eliška, Lucie Šrámková, Jan Starý, et al.. (2018). Two novel fusion genes, AIF1L‐ETV6 and ABL1‐AIF1L, result together with ETV6‐ABL1 from a single chromosomal rearrangement in acute lymphoblastic leukemia with prenatal origin. Genes Chromosomes and Cancer. 57(9). 471–477. 4 indexed citations

Chrastina, Petr, et al.. (2018). Neonatal screening in the Czech Republic: increased prevalence of selected diseases in low birthweight neonates. European Journal of Pediatrics. 177(11). 1697–1704. 6 indexed citations

Stopsack, Konrad H., J. Hammermann, Olaf Sommerburg, et al.. (2016). A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening. Journal of Cystic Fibrosis. 15(6). 752–758. 15 indexed citations

Froňková, Eva, Adam Klocperk, Michael Svatoň, et al.. (2014). The TREC/KREC Assay for the Diagnosis and Monitoring of Patients with DiGeorge Syndrome. PLoS ONE. 9(12). e114514–e114514. 24 indexed citations

Sommerburg, Olaf, J. Hammermann, Martin Lindner, et al.. (2013). Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations. Journal of Cystic Fibrosis. 13(1). 15–23. 36 indexed citations

Malíková, Jana, et al.. (2012). Genetic analysis of the CYP21A2 gene in neonatal dried blood spots from children with transiently elevated 17‐hydroxyprogesterone. Clinical Endocrinology. 77(2). 187–194. 4 indexed citations

Votava, Felix, et al.. (2012). Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance. European Journal of Pediatrics. 171(6). 935–940. 11 indexed citations

10.

Zuna, Jan, Markéta Žaliová, Kateřina Mužíková, et al.. (2010). Acute leukemias with ETV6/ABL1 (TEL/ABL) fusion: Poor prognosis and prenatal origin. Genes Chromosomes and Cancer. 49(10). 873–884. 25 indexed citations

11.

Votava, Felix, et al.. (2010). Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia. European Journal of Medical Genetics. 54(2). 112–117. 27 indexed citations

12.

Balaščaková, M., Veronika Skalická, D Zemková, et al.. (2009). Pilot newborn screening project for cystic fibrosis in the Czech Republic: Defining role of the delay in its symptomatic diagnosis and influence of ultrasound-based prenatal diagnosis on the incidence of the disease. Journal of Cystic Fibrosis. 8(3). 224–227. 7 indexed citations

13.

Votava, Felix, Jan Lebl, Adolf Mühl, et al.. (2006). Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria. European Journal of Pediatrics. 166(1). 1–4. 26 indexed citations

14.

Burjanivová, Tatiana, Jozef Madžo, Kateřina Mužíková, et al.. (2006). Prenatal origin of childhood AML occurs less frequently than in childhood ALL. BMC Cancer. 6(1). 100–100. 21 indexed citations

15.

Sólyom, J., G. Fekete, József Kovács, et al.. (2005). Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia. European Journal of Endocrinology. 153(1). 99–106. 78 indexed citations

16.

Votava, Felix, Dóra Török, József Kovács, et al.. (2005). Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia. European Journal of Endocrinology. 152(6). 869–874. 44 indexed citations

17.

Kovács, József, Felix Votava, Georg Heinze, et al.. (2001). Lessons From 30 Years of Clinical Diagnosis and Treatment of Congenital Adrenal Hyperplasia in Five Middle European Countries¹. The Journal of Clinical Endocrinology & Metabolism. 86(7). 2958–2964. 61 indexed citations

18.

Pohunek, Petr, et al.. (2001). Serum ECP Taken in the Acute Episode of Bronchial Obstruction Can Predict the Development of Bronchial Asthma in Young Children. Allergy and Asthma Proceedings. 22(2). 75–79. 3 indexed citations

19.

Aufricht, Christoph, et al.. (1997). Intratracheal furosemide in infants after cardiac surgery: its effects on lung mechanics and urinary output, and its levels in plasma and tracheal aspirate. Intensive Care Medicine. 23(9). 992–997. 11 indexed citations

20.

Aufricht, Christoph, et al.. (1995). Quasistatic Volume-Pressure Curve to Predict the Effects of Positive End-Expiratory Pressure on Lung Mechanics and Gas Exchange in Neonates Ventilated for Respiratory Distress Syndrome. American Journal of Perinatology. 12(1). 67–72. 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.

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