Lenka Nosková

1.7k total citations
25 papers, 743 citations indexed

About

Lenka Nosková is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Lenka Nosková has authored 25 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Physiology and 5 papers in Genetics. Recurrent topics in Lenka Nosková's work include Cellular transport and secretion (4 papers), Lysosomal Storage Disorders Research (4 papers) and Mitochondrial Function and Pathology (3 papers). Lenka Nosková is often cited by papers focused on Cellular transport and secretion (4 papers), Lysosomal Storage Disorders Research (4 papers) and Mitochondrial Function and Pathology (3 papers). Lenka Nosková collaborates with scholars based in Czechia, United States and Slovakia. Lenka Nosková's co-authors include Hana Hartmannová, Stanislav Kmoch, Viktor Stránecký, Anna Přistoupilová, M Jirsa, Martin Hřebı́ček, Eva Sticová, Els Wagenaar, A. S. Knisely and Kathryn E. Kenworthy and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Lenka Nosková

24 papers receiving 732 citations

Peers

Lenka Nosková

MB

ONCOL

PHYSI

PPCH

CB

Yu Deng China

Kizzie Manning Germany

Lei Lei China

Junko Sawada United States

Xia Mao United States

Shaohui Zhang China

Kuniaki Suzuki Japan

Flavie Sicard France

Elena‐Raluca Nicoli United States

Yu Deng China

Lenka Nosková

600 ×2.2

MB

77 ×0.4

ONCOL

54 ×0.3

PHYSI

113 ×0.8

PPCH

45 ×0.3

CB

Citations per year, relative to Lenka Nosková Lenka Nosková (= 1×) peers Yu Deng

Countries citing papers authored by Lenka Nosková

Since Specialization

Citations

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

Fields of papers citing papers by Lenka Nosková

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lenka Nosková

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

1.

Přistoupilová, Anna, Ivana Jedličková, Hana Hartmannová, et al.. (2024). Increased burden of rare protein‐truncating variants in constrained, brain‐specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder. Genes Brain & Behavior. 23(1). e12882–e12882. 5 indexed citations

2.

Škopková, Martina, Viktor Stránecký, Miriam Kolníková, et al.. (2023). ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability. Orphanet Journal of Rare Diseases. 18(1). 92–92. 6 indexed citations

3.

Bruel, Ange‐Line, Lenka Nosková, Irene Valenzuela, et al.. (2023). Pathogenic RAB34 variants impair primary cilium assembly and cause a novel oral-facial-digital syndrome. Human Molecular Genetics. 32(18). 2822–2831. 8 indexed citations

4.

Stawarski, Michał, Lenka Nosková, Martin Magner, et al.. (2022). GABBR1 monoallelic de novo variants linked to neurodevelopmental delay and epilepsy. The American Journal of Human Genetics. 109(10). 1885–1893. 14 indexed citations

5.

Jedličková, Ivana, Anna Přistoupilová, Lenka Nosková, et al.. (2020). Spinal muscular atrophy caused by a novel Alu‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing. Molecular Genetics & Genomic Medicine. 8(7). e1238–e1238. 9 indexed citations

6.

Zikánová, Marie, A Baxová, Lenka Nosková, et al.. (2020). Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene. SHILAP Revista de lepidopterología. 121(3). 153–162. 3 indexed citations

7.

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

8.

Vevera, Jan, Mehdi Zarrei, Hana Hartmannová, et al.. (2018). Rare copy number variation in extremely impulsively violent males. Genes Brain & Behavior. 18(6). e12536–e12536. 10 indexed citations

9.

Ehling, Rainer, Lenka Nosková, Viktor Stránecký, et al.. (2013). Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V. Journal of the Neurological Sciences. 326(1-2). 75–82. 17 indexed citations

10.

Hejzlarová, Kateřina, Tomáš Mráček, Markéta Tesařová, et al.. (2012). Localization and orientation of TMEM70 protein in the inner mitochondrial membrane. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1817. S15–S15. 1 indexed citations

11.

Steeg, Evita van de, Viktor Stránecký, Hana Hartmannová, et al.. (2012). Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver. Journal of Clinical Investigation. 122(2). 519–528. 260 indexed citations

12.

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

13.

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(2). 241–252. 201 indexed citations

14.

Hejzlarová, Kateřina, Markéta Tesařová, Marek Vrbacký, et al.. (2010). Expression and processing of the TMEM70 protein. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1807(1). 144–149. 23 indexed citations

15.

Šíp, Miroslav, et al.. (2010). Detection of viral infections by an oligonucleotide microarray. Journal of Virological Methods. 165(1). 64–70. 7 indexed citations

16.

Stránecký, Viktor, Robert Ivánek, Hana Hartmannová, et al.. (2008). Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency. BMC Genomics. 9(1). 38–38. 22 indexed citations

17.

Bačáková, Lucie, Andrei Choukourov, H. Boldyryeva, et al.. (2008). Nanocomposite Ti/hydrocarbon plasma polymer films from reactive magnetron sputtering as growth support for osteoblast‐like and endothelial cells. Journal of Biomedical Materials Research Part A. 88A(4). 952–966. 12 indexed citations

18.

Pamuła, Elżbieta, Lucie Bačáková, Elena Filová, et al.. (2007). The influence of pore size on colonization of poly(l-lactide-glycolide) scaffolds with human osteoblast-like MG 63 cells in vitro. Journal of Materials Science Materials in Medicine. 19(1). 425–435. 59 indexed citations

19.

Hřebı́ček, Martin, Tomáš Jirásek, Hana Hartmannová, et al.. (2007). Rotor‐type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump. Liver International. 27(4). 485–491. 9 indexed citations

20.

Kraml, J, et al.. (2003). Glucocorticoid agonistic and antagonistic effects of mifepristone and onapristone on thymocyte subset composition and CD26/dipeptidyl peptidase IV activity in infant male rats. The Journal of Steroid Biochemistry and Molecular Biology. 87(1). 85–96. 7 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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