Vĕra Malinová

1.2k total citations
24 papers, 573 citations indexed

About

Vĕra Malinová is a scholar working on Physiology, Epidemiology and Cell Biology. According to data from OpenAlex, Vĕra Malinová has authored 24 papers receiving a total of 573 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Physiology, 5 papers in Epidemiology and 5 papers in Cell Biology. Recurrent topics in Vĕra Malinová's work include Lysosomal Storage Disorders Research (20 papers), Trypanosoma species research and implications (5 papers) and Cellular transport and secretion (4 papers). Vĕra Malinová is often cited by papers focused on Lysosomal Storage Disorders Research (20 papers), Trypanosoma species research and implications (5 papers) and Cellular transport and secretion (4 papers). Vĕra Malinová collaborates with scholars based in Czechia, United States and France. Vĕra Malinová's co-authors include Eugen Mengel, Miriam Kolníková, Reena Sharma, Soňa Nevšímalová, Gregory M. Enns, Jörg Reinke, Vassili Valayannopoulos, Tatiana Brémovà-Ertl, Anthony Quinn and Patrick Deegan and has published in prestigious journals such as Hepatology, Neurology and Analytical Biochemistry.

In The Last Decade

Vĕra Malinová

24 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vĕra Malinová Czechia 15 400 135 126 84 83 24 573
Helena Jahnová Czechia 10 381 1.0× 73 0.5× 191 1.5× 170 2.0× 55 0.7× 18 545
Christine í Dali Denmark 14 323 0.8× 115 0.9× 199 1.6× 63 0.8× 39 0.5× 28 532
Ana Carolina Brusius‐Facchin Brazil 12 308 0.8× 163 1.2× 79 0.6× 80 1.0× 19 0.2× 39 408
Fernanda de Souza Teixeira Spain 12 326 0.8× 99 0.7× 237 1.9× 116 1.4× 38 0.5× 28 698
P. Santavuori Finland 11 329 0.8× 67 0.5× 243 1.9× 126 1.5× 43 0.5× 11 551
Hernán Amartino Argentina 15 400 1.0× 139 1.0× 102 0.8× 67 0.8× 11 0.1× 47 596
C. Iturriaga Spain 8 195 0.5× 73 0.5× 188 1.5× 40 0.5× 19 0.2× 8 464
Lars Schlotawa Germany 13 260 0.7× 173 1.3× 215 1.7× 118 1.4× 32 0.4× 29 621
Takahito Inoue Japan 12 211 0.5× 79 0.6× 185 1.5× 38 0.5× 9 0.1× 30 604
Johanna M. P. van den Hout Netherlands 12 634 1.6× 150 1.1× 144 1.1× 61 0.7× 38 0.5× 31 729

Countries citing papers authored by Vĕra Malinová

Since Specialization
Citations

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

Fields of papers citing papers by Vĕra Malinová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vĕra Malinová

This figure shows the co-authorship network connecting the top 25 collaborators of Vĕra Malinová. A scholar is included among the top collaborators of Vĕra Malinová 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 Vĕra Malinová. Vĕra Malinová 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.
Malinová, Vĕra, et al.. (2023). Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients. International Journal of Molecular Sciences. 24(19). 14440–14440. 3 indexed citations
2.
Brémovà-Ertl, Tatiana, Larry A. Abel, Mark Walterfang, et al.. (2021). A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C. European Journal of Neurology. 28(9). 3040–3050. 9 indexed citations
3.
Ješina, Pavel, et al.. (2020). Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis. International Journal of Pediatric Otorhinolaryngology. 135. 110137–110137. 13 indexed citations
4.
Malinová, Vĕra, Manisha Balwani, Reena Sharma, et al.. (2020). Sebelipase alfa for lysosomal acid lipase deficiency: 5‐year treatment experience from a phase 2 open‐label extension study. Liver International. 40(9). 2203–2214. 15 indexed citations
5.
Pineda, M., Parvaneh Karimzadeh, Miriam Kolníková, et al.. (2019). Evaluation of different suspicion indices in identifying patients with Niemann-Pick disease Type C in clinical practice: a post hoc analysis of a retrospective chart review. Orphanet Journal of Rare Diseases. 14(1). 161–161. 6 indexed citations
6.
Brémovà-Ertl, Tatiana, Raphael Schiffmann, Marc C. Patterson, et al.. (2018). Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their Correlation with Neurological Findings. Frontiers in Neurology. 8. 711–711. 14 indexed citations
7.
Kuchař, Ladislav, Jakub Sikora, Maria Gulinello, et al.. (2017). Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases. Analytical Biochemistry. 525. 73–77. 52 indexed citations
8.
Brémovà-Ertl, Tatiana, Vĕra Malinová, Yasmina Amraoui, et al.. (2015). Acetyl- dl -leucine in Niemann-Pick type C. Neurology. 85(16). 1368–1375. 62 indexed citations
9.
Nevšímalová, Soňa & Vĕra Malinová. (2014). Cataplexy and Sleep Disorders in Niemann-Pick Type C Disease. Current Neurology and Neuroscience Reports. 15(1). 522–522. 21 indexed citations
10.
Balwani, Manisha, Catherine Breen, Gregory M. Enns, et al.. (2013). Clinical Effect And Safety Profile of Recombinant Human Lysosomal Acid Lipase in Patients With Cholesteryl Ester Storage Disease. Hepatology. 58(3). 950–957. 77 indexed citations
11.
Jurecka, Agnieszka, et al.. (2013). Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature. Clinical Rheumatology. 33(5). 725–731. 9 indexed citations
12.
Jurecka, Agnieszka, Ekaterina Zakharova, Loreta Cimbalistienė, et al.. (2013). Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe. Pediatrics International. 56(4). 520–525. 19 indexed citations
13.
Enns, Gregory M., Manisha Balwani, Patrick Deegan, et al.. (2012). Initial Human Experience with SBC-102, a Recombinant Enzyme Replacement Therapy in Adults with Lysosomal Acid Lipase Deficiency. Molecular Genetics and Metabolism. 105(2). S29–S29. 5 indexed citations
14.
Malinová, Vĕra, Grzegorz Węgrzyn, & Magdalena Narajczyk. (2011). The Use of Elevated Doses of Genistein-Rich Soy Extract in the Gene Expression-Targeted Isoflavone Therapy for Sanfilippo Disease Patients. JIMD Reports. 5. 21–25. 25 indexed citations
15.
Kayserová, Jana, et al.. (2010). Serum Immunoglobulin Free Light Chains in Severe Forms of Atopic Dermatitis. Scandinavian Journal of Immunology. 71(4). 312–316. 15 indexed citations
16.
Malinová, Vĕra, Helena Poupětová, Lenka Dvořáková, & J Zeman. (2009). Enzyme replacement therapy for Gaucher disease in twin pregnancy. International Journal of Gynecology & Obstetrics. 106(1). 64–66. 1 indexed citations
17.
Zimran, Ari, Eugen Mengel, Paige Kaplan, et al.. (2009). The female Gaucher patient: The impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause). Blood Cells Molecules and Diseases. 43(3). 264–288. 43 indexed citations
18.
Hůlková, Helena, et al.. (2009). Autopsy case of Gaucher disease type I in a patient on enzyme replacement therapy. Comments on the dynamics of persistent storage process. Journal of Inherited Metabolic Disease. 32(4). 551–559. 16 indexed citations
19.
Dezortová, Monika, Filip Jírů, Jan Petrášek, et al.. (2008). 1H MR spectroscopy as a diagnostic tool for cerebral creatine deficiency. Magnetic Resonance Materials in Physics Biology and Medicine. 21(5). 327–332. 21 indexed citations
20.
Malinová, Vĕra, et al.. (1989). [A case of Pelger-Huet anomaly in a premature infant].. PubMed. 116(1). 145–9. 1 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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