Andrej Zupan

627 total citations
26 papers, 311 citations indexed

About

Andrej Zupan is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Andrej Zupan has authored 26 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Pulmonary and Respiratory Medicine and 6 papers in Rheumatology. Recurrent topics in Andrej Zupan's work include Bone Tumor Diagnosis and Treatments (5 papers), Sarcoma Diagnosis and Treatment (4 papers) and Glioma Diagnosis and Treatment (3 papers). Andrej Zupan is often cited by papers focused on Bone Tumor Diagnosis and Treatments (5 papers), Sarcoma Diagnosis and Treatment (4 papers) and Glioma Diagnosis and Treatment (3 papers). Andrej Zupan collaborates with scholars based in Slovenia, United Kingdom and France. Andrej Zupan's co-authors include Damjan Glavač, Jože Pižem, Chaim O. Jacob, David S. Ludwig, Richard A. Finkelstein, W S Dallas, Emanuela Boštjančič, Blaž Mavčič, Vladka Salapura and Mara Popović and has published in prestigious journals such as Clinical Infectious Diseases, International Journal of Molecular Sciences and The American Journal of Surgical Pathology.

In The Last Decade

Andrej Zupan

24 papers receiving 301 citations

Peers

Andrej Zupan

PRM

RHEUM

ENDOC

GENET

Andrea Hasenfus Germany

Gang Sun China

C.W. Thesingh Netherlands

Jorge Zárate Argentina

Melvin I. Roat United States

Glenda Mernaugh United States

Chia Ching Chan United States

Rebecca G. Pomerantz United States

Inmaculada de Prada Spain

Andrea Hasenfus Germany

Andrej Zupan

58 ×0.6

PRM

135 ×1.4

28 ×0.4

RHEUM

19 ×0.4

ENDOC

18 ×0.4

GENET

Citations per year, relative to Andrej Zupan Andrej Zupan (= 1×) peers Andrea Hasenfus

Countries citing papers authored by Andrej Zupan

Since Specialization

Citations

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

Fields of papers citing papers by Andrej Zupan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrej Zupan

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

Zupan, Andrej, et al.. (2024). Role of Targeted Sequencing in Routine Diagnostics of Spitz Melanocytic Neoplasms—An Analysis of 70 Cases. Journal of Cutaneous Pathology. 52(2). 141–153. 1 indexed citations

Majc, Bernarda, Marta Malavolta, Miloš Vittori, et al.. (2024). Patient-derived tumor organoids mimic treatment-induced DNA damage response in glioblastoma. iScience. 27(9). 110604–110604.

Pižem, Jože, Emanuela Boštjančič, Andrej Zupan, et al.. (2024). Multifocal vascular neoplasm with an EWSR1::NFATC2 gene fusion and progression to epithelioid angiosarcoma – a case report. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 485(6). 1175–1181. 1 indexed citations

Zupan, Andrej, et al.. (2023). Subcutaneous chondromyxoid fibroma with a novel PNISR::GRM1 fusion—report of a primary soft tissue tumour without connection to an underlying bone. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 482(5). 917–921. 3 indexed citations

Stražar, Klemen, et al.. (2021). Intraarticular nodular fasciitis—detection of USP6 gene fusions in three cases by targeted RNA sequencing. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 478(6). 1117–1124. 5 indexed citations

Pižem, Jože, Andrej Zupan, Emanuela Boštjančič, et al.. (2021). The role of molecular diagnostics in aneurysmal and simple bone cysts – a prospective analysis of 19 lesions. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 479(4). 795–802. 8 indexed citations

Zupan, Andrej, et al.. (2021). Associations of Single-Nucleotide Polymorphisms in Slovenian Patients with Acute Central Serous Chorioretinopathy. Genes. 13(1). 55–55. 3 indexed citations

Pižem, Jože, et al.. (2021). Fibroma of tendon sheath is defined by a USP6 gene fusion—morphologic and molecular reappraisal of the entity. Modern Pathology. 34(10). 1876–1888. 9 indexed citations

Sorokin, Maxim, Alja Zottel, Neja Šamec, et al.. (2021). Large-Scale Transcriptomics-Driven Approach Revealed Overexpression of CRNDE as a Poor Survival Prognosis Biomarker in Glioblastoma. Cancers. 13(14). 3419–3419. 14 indexed citations

10.

Zupan, Andrej, et al.. (2020). A case of MV2K subtype of sporadic Creutzfeldt–Jakob disease with florid‐like plaques: Similarities and differences to variant Creutzfeldt–Jakob disease. Neuropathology. 40(4). 389–398. 3 indexed citations

11.

Zupan, Andrej, et al.. (2020). Novel ASAP1‐USP6, FAT1‐USP6, SAR1A‐USP6, and TNC‐USP6 fusions in primary aneurysmal bone cyst. Genes Chromosomes and Cancer. 59(6). 357–365. 30 indexed citations

12.

Pižem, Jože, Andrej Zupan, Emanuela Boštjančič, et al.. (2020). FUS-NFATC2 or EWSR1-NFATC2 Fusions Are Present in a Large Proportion of Simple Bone Cysts. The American Journal of Surgical Pathology. 44(12). 1623–1634. 35 indexed citations

13.

Fakin, Ana, Maja Šuštar, Jelka Brecelj, et al.. (2019). Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy. Genes. 10(12). 956–956. 12 indexed citations

14.

Zupan, Andrej, et al.. (2019). A novel PTPRZ1‐ETV1 fusion in gliomas. Brain Pathology. 30(2). 226–234. 9 indexed citations

15.

Lumi, Xhevat, Andrej Zupan, Emanuela Boštjančič, et al.. (2019). SINGLE NUCLEOTIDE POLYMORPHISMS IN RETINAL DETACHMENT PATIENTS WITH AND WITHOUT PROLIFERATIVE VITREORETINOPATHY. Retina. 40(5). 811–818. 6 indexed citations

16.

Koritnik, Blaž, et al.. (2017). Familial tauopathy with P364S MAPT mutation: clinical course, neuropathology and ultrastructure of neuronal tau inclusions. Neuropathology and Applied Neurobiology. 44(6). 550–562. 10 indexed citations

17.

Zupan, Andrej, Nina Hauptman, & Damjan Glavač. (2015). The maternal perspective for five Slovenian regions: The importance of regional sampling. Annals of Human Biology. 43(1). 57–66. 3 indexed citations

18.

Zupan, Andrej, et al.. (2013). The paternal perspective of the Slovenian population and its relationship with other populations. Annals of Human Biology. 40(6). 515–526. 17 indexed citations

19.

Fakin, Ana, Andrej Zupan, Damjan Glavač, & Marko Hawlina. (2012). Combination of retinitis pigmentosa and hearing loss caused by a novel mutation in PRPH2 and a known mutation in GJB2: Importance for differential diagnosis of Usher syndrome. Vision Research. 75. 71–76. 5 indexed citations

20.

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

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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