Linda Berná

579 total citations
11 papers, 420 citations indexed

About

Linda Berná is a scholar working on Physiology, Epidemiology and Organic Chemistry. According to data from OpenAlex, Linda Berná has authored 11 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 6 papers in Epidemiology and 4 papers in Organic Chemistry. Recurrent topics in Linda Berná's work include Lysosomal Storage Disorders Research (9 papers), Trypanosoma species research and implications (6 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Linda Berná is often cited by papers focused on Lysosomal Storage Disorders Research (9 papers), Trypanosoma species research and implications (6 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Linda Berná collaborates with scholars based in Czechia, Germany and Australia. Linda Berná's co-authors include J. Ledvinová, M. Elleder, Helena Poupětová, Lenka Dvořáková, Viktor Kožich, Befekadu Asfaw, Martin Hřebı́ček, Helena Hůlková, Barbara C. Paton and K. Harzer and has published in prestigious journals such as Analytical Biochemistry, Clinica Chimica Acta and FEBS Journal.

In The Last Decade

Linda Berná

11 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Linda Berná Czechia 10 361 152 135 107 96 11 420
Kristiane Michelin‐Tirelli Brazil 11 288 0.8× 123 0.8× 98 0.7× 88 0.8× 83 0.9× 23 347
Hadhami Ben Turkia Tunisia 13 417 1.2× 151 1.0× 171 1.3× 153 1.4× 151 1.6× 46 524
Carmela Zizzo Italy 14 384 1.1× 140 0.9× 137 1.0× 117 1.1× 122 1.3× 34 490
Jessica de Ruijter Netherlands 8 333 0.9× 162 1.1× 68 0.5× 99 0.9× 64 0.7× 11 405
Yasmina Amraoui Germany 10 297 0.8× 79 0.5× 109 0.8× 50 0.5× 88 0.9× 15 382
Marie T. Vanier France 8 496 1.4× 94 0.6× 183 1.4× 120 1.1× 193 2.0× 9 611
Xinying Hong United States 12 303 0.8× 107 0.7× 136 1.0× 53 0.5× 63 0.7× 41 441
Marie Jackson United Kingdom 11 233 0.6× 92 0.6× 124 0.9× 89 0.8× 64 0.7× 21 384
Carole Elbin United States 6 321 0.9× 112 0.7× 53 0.4× 53 0.5× 59 0.6× 8 373
Rebecca Soska United States 7 429 1.2× 166 1.1× 160 1.2× 171 1.6× 201 2.1× 11 506

Countries citing papers authored by Linda Berná

Since Specialization
Citations

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

Fields of papers citing papers by Linda Berná

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linda Berná

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

All Works

11 of 11 papers shown
1.
Kuchař, Ladislav, Linda Berná, Helena Poupětová, et al.. (2024). LysoGb3 quantification facilitates phenotypic categorization of Fabry disease patients: Insights gained by a novel MS/MS method. Clinica Chimica Acta. 561. 119824–119824. 2 indexed citations
2.
Poupětová, Helena, J. Ledvinová, Linda Berná, et al.. (2010). The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations. Journal of Inherited Metabolic Disease. 33(4). 387–396. 149 indexed citations
3.
Kuchař, Ladislav, J. Ledvinová, Martin Hřebı́ček, et al.. (2009). Prosaposin deficiency and saposin B deficiency (activator‐deficient metachromatic leukodystrophy): Report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations. American Journal of Medical Genetics Part A. 149A(4). 613–621. 60 indexed citations
4.
Beesley, Clare, Linda Berná, Hana Vlášková, et al.. (2009). Mucopolysaccharidosis type I in 21 Czech and Slovak patients: Mutation analysis suggests a functional importance of C‐terminus of the IDUA protein. American Journal of Medical Genetics Part A. 149A(5). 965–974. 29 indexed citations
5.
Hůlková, Helena, Robert Dobrovolný, Befekadu Asfaw, et al.. (2008). Replacement of α-galactosidase A in Fabry disease: effect on fibroblast cultures compared with biopsied tissues of treated patients. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 452(6). 651–665. 27 indexed citations
6.
Vyleťal, Petr, Helena Hůlková, Martina Živná, et al.. (2008). Abnormal expression and processing of uromodulin in Fabry disease reflects tubular cell storage alteration and is reversible by enzyme replacement therapy. Journal of Inherited Metabolic Disease. 31(4). 508–517. 24 indexed citations
7.
Marcão, Ana, et al.. (2005). Missense mutations as a cause of metachromatic leukodystrophy. FEBS Journal. 272(5). 1179–1188. 24 indexed citations
8.
Ługowska, Agnieszka, Olga Amaral, Johannes Berger, et al.. (2005). Mutations c.459 + 1G > A and p.P426L in the ARSA gene: Prevalence in metachromatic leukodystrophy patients from European countries. Molecular Genetics and Metabolism. 86(3). 353–359. 23 indexed citations
9.
Elleder, M., Martin Hřebı́ček, Linda Berná, et al.. (2005). Prosaposin Deficiency - a Rarely Diagnosed, Rapidly Progressing, Neonatal Neurovisceral Lipid Storage Disease. Report of a Further Patient. Neuropediatrics. 36(3). 171–180. 40 indexed citations
10.
Berná, Linda, Volkmar Gieselmann, Helena Poupětová, et al.. (2004). Novel mutations associated with metachromatic leukodystrophy: Phenotype and expression studies in nine Czech and Slovak patients. American Journal of Medical Genetics Part A. 129A(3). 277–281. 13 indexed citations
11.
Berná, Linda, et al.. (1999). Determination of Urinary Sulfatides and Other Lipids by Combination of Reversed-Phase and Thin-Layer Chromatographies. Analytical Biochemistry. 269(2). 304–311. 29 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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