Elvir Bećirović

2.0k total citations
50 papers, 1.1k citations indexed

About

Elvir Bećirović is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Elvir Bećirović has authored 50 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 9 papers in Genetics. Recurrent topics in Elvir Bećirović's work include Retinal Development and Disorders (23 papers), CRISPR and Genetic Engineering (8 papers) and Virus-based gene therapy research (7 papers). Elvir Bećirović is often cited by papers focused on Retinal Development and Disorders (23 papers), CRISPR and Genetic Engineering (8 papers) and Virus-based gene therapy research (7 papers). Elvir Bećirović collaborates with scholars based in Germany, Bosnia and Herzegovina and Switzerland. Elvir Bećirović's co-authors include Martin Biel, Stylianos Michalakis, Hanno J. Bolz, Mathias W. Seeliger, Inga Ebermann, Sybille Böhm, Naoyuki Tanimoto, Susanne Beck, J. Lamprecht and Elena Aller and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Elvir Bećirović

48 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elvir Bećirović Germany	20	850	264	182	172	132	50	1.1k
Judith Mosinger Ogilvie United States	17	818 1.0×	318 1.2×	171 0.9×	124 0.7×	146 1.1×	36	1.2k
Arpad Palfi Ireland	23	1.5k 1.8×	424 1.6×	315 1.7×	58 0.3×	405 3.1×	49	1.8k
Teresa Jaijo Spain	22	984 1.2×	196 0.7×	201 1.1×	597 3.5×	151 1.1×	58	1.4k
Gretel Beck United States	8	837 1.0×	166 0.6×	280 1.5×	117 0.7×	362 2.7×	8	1.4k
Saskia Biskup Germany	17	771 0.9×	264 1.0×	137 0.8×	17 0.1×	358 2.7×	37	1.1k
Eberhart Zrenner Germany	16	727 0.9×	257 1.0×	433 2.4×	44 0.3×	47 0.4×	67	1.1k
Henri Leinonen United States	15	515 0.6×	202 0.8×	133 0.7×	15 0.1×	84 0.6×	32	704
Klaus Rüther Germany	21	1.3k 1.6×	549 2.1×	624 3.4×	36 0.2×	158 1.2×	67	1.7k
Nancy J. Mangini United States	18	669 0.8×	385 1.5×	139 0.8×	63 0.4×	33 0.3×	30	1.0k
Haibo Zhou China	12	583 0.7×	176 0.7×	18 0.1×	106 0.6×	184 1.4×	14	921

Countries citing papers authored by Elvir Bećirović

Since Specialization

Citations

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

Fields of papers citing papers by Elvir Bećirović

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elvir Bećirović

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

Gerhardt, Maximilian, St. Engel, Isabelle Meneau, et al.. (2025). CRISPR/Cas-mediated activation of genes associated with inherited retinal dystrophies in human cells for diagnostic purposes. JCI Insight. 10(22).

Bećirović, Elvir, et al.. (2025). Retina-directed gene therapy: Achievements and remaining challenges. Pharmacology & Therapeutics. 271. 108862–108862. 2 indexed citations

Bećirović, Elvir, et al.. (2023). Role of transgenerational transmission of trauma in development of schizophrenia: A case report of a patient whose parents survived genocide in Srebrenica. European Psychiatry. 66(S1). S632–S633. 1 indexed citations

Bećirović, Elvir. (2022). Maybe you can turn me on: CRISPRa-based strategies for therapeutic applications. Cellular and Molecular Life Sciences. 79(2). 130–130. 30 indexed citations

Pavlou, Marina, Sybille Böhm, Gilles Gasparoni, et al.. (2020). Antisense Oligonucleotide- and CRISPR-Cas9-Mediated Rescue of mRNA Splicing for a Deep Intronic CLRN1 Mutation. Molecular Therapy — Nucleic Acids. 21. 1050–1061. 24 indexed citations

Falk, Nathalie, Kristin Kessler, Karsten Boldt, et al.. (2018). Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis. Journal of Cell Science. 131(16). 8 indexed citations

Wagner, Johanna, Christian Schön, Elvir Bećirović, Martin Biel, & Stylianos Michalakis. (2018). In Vitro Evaluation of AAV Vectors for Retinal Gene Therapy. Methods in molecular biology. 1834. 383–390. 4 indexed citations

Fenske, Stefanie, Verena Hammelmann, Elvir Bećirović, et al.. (2018). Disturbed Processing of Contextual Information in HCN3 Channel Deficient Mice. Frontiers in Molecular Neuroscience. 10. 436–436. 19 indexed citations

Böhm, Sybille, et al.. (2018). Construction and Cloning of Minigenes for in vivo Analysis of Potential Splice Mutations. BIO-PROTOCOL. 8(5). e2760–e2760. 5 indexed citations

10.

Petersen‐Jones, Simon M., Laurence M. Occelli, Paige A. Winkler, et al.. (2017). Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach. Journal of Clinical Investigation. 128(1). 190–206. 46 indexed citations

11.

Schön, Christian, Elvir Bećirović, Martin Biel, & Stylianos Michalakis. (2017). Design and Development of AAV-based Gene Supplementation Therapies for Achromatopsia and Retinitis Pigmentosa. Methods in molecular biology. 1715. 33–46. 5 indexed citations

12.

Böhm, Sybille, Ong Nam Phuong Nguyen, Andreas Gießl, et al.. (2017). Peripherin-2 and Rom-1 have opposing effects on rod outer segment targeting of retinitis pigmentosa-linked peripherin-2 mutants. Scientific Reports. 7(1). 2321–2321. 11 indexed citations

13.

Nguyen, Ong Nam Phuong, Sybille Böhm, Andreas Gießl, et al.. (2016). Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors. Human Molecular Genetics. 25(12). ddw103–ddw103. 10 indexed citations

14.

Michalakis, Stylianos, Susanne Koch, Vithiyanjali Sothilingam, et al.. (2014). Gene Therapy Restores Vision and Delays Degeneration in the CNGB1−/− Mouse Model of Retinitis Pigmentosa. Advances in experimental medicine and biology. 801. 733–739. 29 indexed citations

15.

Michalakis, Stylianos, Susanne Koch, Regine Muehlfriedel, et al.. (2012). Three-dimensional magnetic resonance analysis of extraocular muscles demonstrates gaze-specific contractile shape changes. Investigative Ophthalmology & Visual Science. 53(14). 1924–1924. 1 indexed citations

16.

Michalakis, Stylianos, Regine Mühlfriedel, Naoyuki Tanimoto, et al.. (2011). Gene Therapy Restores Missing Cone-Mediated Vision in the CNGA3−/− Mouse Model of Achromatopsia. Advances in experimental medicine and biology. 723. 183–189. 20 indexed citations

17.

Bećirović, Elvir, et al.. (2010). The Retinitis Pigmentosa Mutation c.3444+1G>A in CNGB1 Results in Skipping of Exon 32. PLoS ONE. 5(1). e8969–e8969. 11 indexed citations

18.

Michalakis, Stylianos, Naoyuki Tanimoto, M. Dominik Fischer, et al.. (2010). Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice. Cellular and Molecular Life Sciences. 67(18). 3173–3186. 26 indexed citations

19.

Dostović, Zikrija, et al.. (2009). DELIRIUM AFTER STROKE. 38(1). 26–29. 2 indexed citations

20.

Bećirović, Elvir, et al.. (2008). Usher syndrome type 1 due to missense mutations on bothCDH23 alleles: investigation of mRNA splicing. Human Mutation. 29(3). 452–452. 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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