Mojca Stražišar

1.5k total citations
32 papers, 863 citations indexed

About

Mojca Stražišar is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Mojca Stražišar has authored 32 papers receiving a total of 863 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Oncology. Recurrent topics in Mojca Stražišar's work include Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (5 papers) and MicroRNA in disease regulation (4 papers). Mojca Stražišar is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (5 papers) and MicroRNA in disease regulation (4 papers). Mojca Stražišar collaborates with scholars based in Belgium, Slovenia and Sweden. Mojca Stražišar's co-authors include Damjan Glavač, Peter De Rijk, Jurgen Del‐Favero, Marko Hawlina, Wouter De Coster, Tim De Pooter, Vid Mlakar, Metka Ravnik‐Glavač, Svenn D’Hert and Kristel Sleegers and has published in prestigious journals such as Nucleic Acids Research, Bioinformatics and PLoS ONE.

In The Last Decade

Mojca Stražišar

31 papers receiving 842 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mojca Stražišar Belgium 17 486 212 200 159 89 32 863
Shengqian Dou China 15 378 0.8× 108 0.5× 30 0.1× 158 1.0× 65 0.7× 41 650
Anne‐Marie Brun‐Zinkernagel United States 10 408 0.8× 15 0.1× 235 1.2× 74 0.5× 146 1.6× 11 652
Thomas R. Sundermeier United States 13 703 1.4× 279 1.3× 139 0.7× 16 0.1× 53 0.6× 16 807
Ye Yin China 17 467 1.0× 53 0.3× 250 1.3× 77 0.5× 246 2.8× 35 962
Lucy H. Williams United States 7 633 1.3× 89 0.4× 227 1.1× 39 0.2× 23 0.3× 9 807
Marc Pauper Netherlands 11 186 0.4× 53 0.3× 104 0.5× 64 0.4× 115 1.3× 13 529
Alla V. Ivanova United States 18 472 1.0× 80 0.4× 49 0.2× 37 0.2× 3 0.0× 41 937
Martin P. Keough United States 10 326 0.7× 87 0.4× 146 0.7× 94 0.6× 15 0.2× 11 747
Manuela Roldán Pallarés Spain 15 198 0.4× 24 0.1× 68 0.3× 261 1.6× 366 4.1× 31 703
Derek M. Pavelec United States 13 814 1.7× 149 0.7× 39 0.2× 20 0.1× 11 0.1× 23 1.1k

Countries citing papers authored by Mojca Stražišar

Since Specialization
Citations

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

Fields of papers citing papers by Mojca Stražišar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mojca Stražišar

This figure shows the co-authorship network connecting the top 25 collaborators of Mojca Stražišar. A scholar is included among the top collaborators of Mojca Stražišar 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 Mojca Stražišar. Mojca Stražišar 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.
Dewaele, Barbara, Bert Callewaert, Olivier Vanakker, et al.. (2024). Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping. Scientific Reports. 14(1). 29142–29142. 5 indexed citations
2.
Rombauts, Stéphane, Lisanne de Vries, Tim De Pooter, et al.. (2023). Suppression of the Arabidopsis cinnamoyl-CoA reductase 1-6 intronic T-DNA mutation by epigenetic modification. PLANT PHYSIOLOGY. 192(4). 3001–3016. 5 indexed citations
3.
Ibrahim, Joe, Ligia Mateiu, Tim De Pooter, et al.. (2023). Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy. International Journal of Molecular Sciences. 24(22). 16412–16412. 10 indexed citations
4.
Coster, Wouter De, Endre Bakken Stovner, & Mojca Stražišar. (2020). Methplotlib: analysis of modified nucleotides from nanopore sequencing. Bioinformatics. 36(10). 3236–3238. 18 indexed citations
5.
Coster, Wouter De, Peter De Rijk, Arne De Roeck, et al.. (2019). Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome. Genome Research. 29(7). 1178–1187. 100 indexed citations
6.
Roeck, Arne De, Wouter De Coster, Rita Cacace, et al.. (2019). NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION. Genome biology. 20(1). 239–239. 68 indexed citations
7.
Stražišar, Mojca, et al.. (2015). Genetic variants in microRNA genes: impact on microRNA expression, function, and disease. Frontiers in Genetics. 6. 186–186. 104 indexed citations
8.
Stražišar, Mojca, Bart Smets, Sarah Weckhuysen, et al.. (2015). Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets. PLoS ONE. 10(12). e0144428–e0144428. 10 indexed citations
9.
Stražišar, Mojca, Karlijn van der Ven, Diego A. Forero, et al.. (2014). MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets. Molecular Psychiatry. 20(4). 472–481. 83 indexed citations
10.
Bossche, Maarten Van Den, Mojca Stražišar, Anthony Liekens, et al.. (2013). Identification of rare copy number variants in high burden schizophrenia families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(3). 273–282. 20 indexed citations
11.
Bossche, Maarten Van Den, et al.. (2012). Co-occurrence of Marfan syndrome and schizophrenia: What can be learned?. European Journal of Medical Genetics. 55(4). 252–255. 10 indexed citations
12.
Bossche, Maarten Van Den, Lise Docx, Manuel Morrens, et al.. (2012). Less Cognitive and Neurological Deficits in Schizophrenia Patients Carrying Risk Variant in <b><i>ZNF804A</i></b>. Neuropsychobiology. 66(3). 158–166. 13 indexed citations
13.
Bossche, Maarten Van Den, Mandy Johnstone, Mojca Stražišar, et al.. (2012). Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(7). 812–822. 26 indexed citations
14.
Stražišar, Mojca, et al.. (2010). Genetics and clinical characteristics of keratoconus.. PubMed. 19(2). 3–10. 42 indexed citations
15.
Stražišar, Mojca, et al.. (2010). Absence of Pathogenic Mutations in VSX1 and SOD1 Genes in Patients With Keratoconus. Cornea. 29(2). 172–176. 58 indexed citations
16.
Godić, Aleksandar, et al.. (2010). Darier disease in Slovenia: spectrum of ATP2A2 mutations and relation to patients’ phenotypes. European Journal of Dermatology. 20(3). 271–275. 6 indexed citations
17.
Stražišar, Mojca, Vid Mlakar, T Rott, & Damjan Glavač. (2009). Somatic Alterations of the Serine/Threonine KinaseLKB1Gene in Squamous Cell (SCC) and Large Cell (LCC) Lung Carcinoma. Cancer Investigation. 27(4). 407–416. 15 indexed citations
18.
Stražišar, Mojca, Vid Mlakar, & Damjan Glavač. (2008). LATS2 tumour specific mutations and down-regulation of the gene in non-small cell carcinoma. Lung Cancer. 64(3). 257–262. 48 indexed citations
19.
Stražišar, Mojca, T Rott, & Damjan Glavač. (2008). K‐RAS and P53 Mutations in Association with COX‐2 and Htert Expression and Clinico‐Pathological Status of Nsclc Patients. Disease Markers. 25(2). 97–106. 3 indexed citations
20.
Stražišar, Mojca, T Rott, & Damjan Glavač. (2008). Frequent polymorphic variations but rare tumour specific mutations of the S100A2 on 1q21 in non-small cell lung cancer. Lung Cancer. 63(3). 354–359. 9 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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