Helena Hůlková

3.2k total citations
51 papers, 1.5k citations indexed

About

Helena Hůlková is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Helena Hůlková has authored 51 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Physiology, 22 papers in Molecular Biology and 16 papers in Cell Biology. Recurrent topics in Helena Hůlková's work include Lysosomal Storage Disorders Research (24 papers), Cellular transport and secretion (14 papers) and Mitochondrial Function and Pathology (8 papers). Helena Hůlková is often cited by papers focused on Lysosomal Storage Disorders Research (24 papers), Cellular transport and secretion (14 papers) and Mitochondrial Function and Pathology (8 papers). Helena Hůlková collaborates with scholars based in Czechia, United States and Germany. Helena Hůlková's co-authors include M. Elleder, Robert J. Desnick, Martin G. Bialer, Donna L. Bernstein, Stanislav Kmoch, J Zeman, Veronika Barešová, Helena Jahnová, Viktor Stránecký and Hana Hartmannová and has published in prestigious journals such as Journal of Clinical Investigation, Neurology and Cell Metabolism.

In The Last Decade

Helena Hůlková

50 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helena Hůlková Czechia 20 692 692 347 181 179 51 1.5k
Filippo Pinto e Vairo Brazil 20 569 0.8× 602 0.9× 207 0.6× 211 1.2× 30 0.2× 111 1.4k
Kyle Trudeau United States 17 794 1.1× 306 0.4× 124 0.4× 273 1.5× 58 0.3× 25 1.3k
Julian Raiman Canada 24 559 0.8× 738 1.1× 127 0.4× 331 1.8× 61 0.3× 58 1.5k
Viktor Stránecký Czechia 18 642 0.9× 225 0.3× 177 0.5× 107 0.6× 41 0.2× 66 1.3k
Eduard Paschke Austria 27 800 1.2× 1.3k 1.9× 396 1.1× 493 2.7× 54 0.3× 91 2.2k
Mina Mirzaian Netherlands 20 481 0.7× 1.3k 1.9× 533 1.5× 577 3.2× 96 0.5× 35 1.6k
Masaru Kuriyama Japan 19 676 1.0× 669 1.0× 263 0.8× 371 2.0× 17 0.1× 53 1.7k
Rongrong Cui China 25 885 1.3× 198 0.3× 87 0.3× 290 1.6× 18 0.1× 59 1.8k
Keishi Yamauchi Japan 21 986 1.4× 206 0.3× 178 0.5× 156 0.9× 31 0.2× 83 1.8k
Angela Wirth Germany 15 856 1.2× 327 0.5× 162 0.5× 57 0.3× 25 0.1× 26 1.4k

Countries citing papers authored by Helena Hůlková

Since Specialization
Citations

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

Fields of papers citing papers by Helena Hůlková

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helena Hůlková

This figure shows the co-authorship network connecting the top 25 collaborators of Helena Hůlková. A scholar is included among the top collaborators of Helena Hůlková 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 Helena Hůlková. Helena Hůlková 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.
Kuchař, Ladislav, Ondřej Lukšan, Befekadu Asfaw, et al.. (2020). Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations. Orphanet Journal of Rare Diseases. 15(1). 85–85. 4 indexed citations
2.
Marek, Josef, Petr Kuchynka, Tomáš Paleček, et al.. (2020). Combined valve replacement and aortocoronary bypass in an adult mucopolysaccharidosis type VII patient. Cardiovascular Pathology. 50. 107297–107297. 5 indexed citations
3.
Jedličková, Ivana, Maxime Cadieux‐Dion, Anna Přistoupilová, et al.. (2020). Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing. European Journal of Human Genetics. 28(6). 783–789. 11 indexed citations
4.
Ameele, Jelle van den, Ivana Jedličková, Anna Přistoupilová, et al.. (2018). Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion. Neurology. 90(8). e658–e663. 8 indexed citations
5.
Yu, Samuel Mon-Wei, Anthony J. Bleyer, Leal Herlitz, et al.. (2017). Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation. American Journal of Kidney Diseases. 71(4). 495–500. 8 indexed citations
6.
Jahnová, Helena, Lenka Dvořáková, Hana Vlášková, et al.. (2014). Observational, retrospective study of a large cohort of patients with Niemann-Pick disease type C in the Czech Republic: a surprisingly stable diagnostic rate spanning almost 40 years. Orphanet Journal of Rare Diseases. 9(1). 140–140. 45 indexed citations
7.
Kuchař, Ladislav, Lukáš Krásný, Robert Dobrovolný, et al.. (2014). Fabry disease: renal sphingolipid distribution in the α-Gal A knockout mouse model by mass spectrometric and immunohistochemical imaging. Analytical and Bioanalytical Chemistry. 407(8). 2283–2291. 17 indexed citations
8.
Stibůrková, Blanka, Ivan Šebesta, Kimiyoshi Ichida, et al.. (2013). Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis. European Journal of Human Genetics. 21(10). 1067–1073. 50 indexed citations
9.
Lukáš, J., Eva Svobodová, Ladislav Kuchař, et al.. (2013). Rapid Isolation of Lysosomal Membranes from Cultured Cells. Folia Biologica. 59(1). 41–46. 2 indexed citations
10.
Bernstein, Donna L., Helena Hůlková, Martin G. Bialer, & Robert J. Desnick. (2013). Cholesteryl ester storage disease: Review of the findings in 135 reported patients with an underdiagnosed disease. Journal of Hepatology. 58(6). 1230–1243. 235 indexed citations
11.
Nosková, Lenka, Viktor Stránecký, Hana Hartmannová, et al.. (2011). Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis. The American Journal of Human Genetics. 89(4). 589–589. 10 indexed citations
12.
Bleyer, Anthony J., Martina Živná, Helena Hůlková, et al.. (2010). Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone. Clinical Nephrology. 74(12). 411–422. 30 indexed citations
13.
Hůlková, Helena, Helena Poupětová, K. Harzer, et al.. (2010). Abnormal nonstoring capillary endothelium: a novel feature of Gaucher disease. Ultrastructural study of dermal capillaries. Journal of Inherited Metabolic Disease. 33(1). 69–78. 10 indexed citations
14.
Stibůrek, Lukáš, Kateřina Veselá, Hana Hansı́ková, Helena Hůlková, & J Zeman. (2009). Loss of function of Sco1 and its interaction with cytochrome c oxidase. American Journal of Physiology-Cell Physiology. 296(5). C1218–C1226. 83 indexed citations
15.
Elleder, M., Lenka Dvořáková, Hana Vlášková, et al.. (2008). Atypical CLN2 with later onset and prolonged course: a neuropathologic study showing different sensitivity of neuronal subpopulations to TPP1 deficiency. Acta Neuropathologica. 116(1). 119–124. 29 indexed citations
16.
Veselá, Kateřina, Helena Hůlková, Hana Hansíková, J Zeman, & M. Elleder. (2008). Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene. Apmis. 116(1). 41–49. 14 indexed citations
17.
Hůlková, Helena, et al.. (2005). Lactosylceramide in lysosomal storage disorders. A comparative immunohistochemical and biochemical study. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 447(1). 31–44. 11 indexed citations
18.
Hodaňová, Kateřina, Jacek Majewski, Petr Vyleťal, et al.. (2005). Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41. Kidney International. 68(4). 1472–1482. 26 indexed citations
19.
20.
Zeman, J, H Houst'ková, Hana Hansíková, et al.. (1999). [Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome].. PubMed. 138(13). 401–5. 8 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Filippo Pinto e Vairo Breakdown of academic impact, for papers by Kyle Trudeau Breakdown of academic impact, for papers by Julian Raiman Breakdown of academic impact, for papers by Viktor Stránecký Breakdown of academic impact, for papers by Eduard Paschke Breakdown of academic impact, for papers by Mina Mirzaian Breakdown of academic impact, for papers by Masaru Kuriyama Breakdown of academic impact, for papers by Rongrong Cui Breakdown of academic impact, for papers by Keishi Yamauchi Breakdown of academic impact, for papers by Angela Wirth
Rankless by CCL
2026