Miha Modic

1.5k total citations
20 papers, 798 citations indexed

About

Miha Modic is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Miha Modic has authored 20 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Neurology and 2 papers in Genetics. Recurrent topics in Miha Modic's work include RNA Research and Splicing (10 papers), RNA modifications and cancer (7 papers) and CRISPR and Genetic Engineering (5 papers). Miha Modic is often cited by papers focused on RNA Research and Splicing (10 papers), RNA modifications and cancer (7 papers) and CRISPR and Genetic Engineering (5 papers). Miha Modic collaborates with scholars based in United Kingdom, Slovenia and Germany. Miha Modic's co-authors include Jernej Ule, Tomaž Curk, Nejc Haberman, Boris Rogelj, Gregor Rot, Christopher R. Sibley, Christopher E. Shaw, Yoichiro Sugimoto, Gireesh K. Bogu and Blaž Zupan and has published in prestigious journals such as Nature, Nucleic Acids Research and Nature Communications.

In The Last Decade

Miha Modic

20 papers receiving 792 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miha Modic United Kingdom 12 661 286 208 106 53 20 798
Danae Campos‐Melo Canada 15 443 0.7× 326 1.1× 244 1.2× 121 1.1× 119 2.2× 24 696
Anthony Q. Vu United States 11 998 1.5× 193 0.7× 147 0.7× 164 1.5× 77 1.5× 13 1.1k
Ze’ev Melamed United States 9 770 1.2× 492 1.7× 304 1.5× 153 1.4× 97 1.8× 10 1.0k
Mariah L. Hoye United States 7 261 0.4× 164 0.6× 145 0.7× 78 0.7× 51 1.0× 10 401
Julianne Aebischer France 9 249 0.4× 289 1.0× 184 0.9× 55 0.5× 82 1.5× 11 493
Sandra Camelo United States 5 518 0.8× 231 0.8× 122 0.6× 51 0.5× 111 2.1× 6 771
Matthew Wyles United Kingdom 11 474 0.7× 224 0.8× 397 1.9× 41 0.4× 65 1.2× 13 706
I‐Fang Wang Taiwan 9 219 0.3× 268 0.9× 116 0.6× 53 0.5× 67 1.3× 11 543
Julio Aguila Benitez Sweden 9 492 0.7× 93 0.3× 82 0.4× 90 0.8× 95 1.8× 11 633
Laura De Conti Italy 12 933 1.4× 728 2.5× 459 2.2× 86 0.8× 71 1.3× 20 1.3k

Countries citing papers authored by Miha Modic

Since Specialization
Citations

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

Fields of papers citing papers by Miha Modic

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miha Modic

This figure shows the co-authorship network connecting the top 25 collaborators of Miha Modic. A scholar is included among the top collaborators of Miha Modic 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 Miha Modic. Miha Modic 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.
Modic, Miha, Rupert Faraway, Igor Ruiz de los Mozos, et al.. (2024). Poised PABP–RNA hubs implement signal-dependent mRNA decay in development. Nature Structural & Molecular Biology. 31(9). 1439–1447. 3 indexed citations
2.
Miccolo, Claudia, Mirko Doni, Gerda Egger, et al.. (2024). The domesticated transposon protein L1TD1 associates with its ancestor L1 ORF1p to promote LINE-1 retrotransposition. eLife. 13. 2 indexed citations
3.
Modic, Miha, et al.. (2024). The impact of IDR phosphorylation on the RNA binding profiles of proteins. Trends in Genetics. 40(7). 580–586. 10 indexed citations
4.
Shi, Xianle, Yanjing Li, Hongwei Zhou, et al.. (2024). DDX18 coordinates nucleolus phase separation and nuclear organization to control the pluripotency of human embryonic stem cells. Nature Communications. 15(1). 10803–10803. 3 indexed citations
5.
Sideri, Theodora, Miha Modic, Charlotte Capitanchik, et al.. (2023). m6A-ELISA, a simple method for quantifying N6 -methyladenosine from mRNA populations. RNA. 29(5). 705–712. 21 indexed citations
6.
Hruscha, Alexander, Frauke van Bebber, Miha Modic, et al.. (2023). Loss of TDP-43 causes ectopic endothelial sprouting and migration defects through increased fibronectin, vcam 1 and integrin α4/β1. Frontiers in Cell and Developmental Biology. 11. 1169962–1169962. 5 indexed citations
7.
Qin, Weihua, Enes Ugur, Christopher B. Mulholland, et al.. (2021). Phosphorylation of the HP1β hinge region sequesters KAP1 in heterochromatin and promotes the exit from naïve pluripotency. Nucleic Acids Research. 49(13). 7406–7423. 11 indexed citations
8.
Mulholland, Christopher B., Franziska R. Traube, Enes Ugur, et al.. (2020). Distinct and stage-specific contributions of TET1 and TET2 to stepwise cytosine oxidation in the transition from naive to primed pluripotency. Scientific Reports. 10(1). 12066–12066. 16 indexed citations
9.
Schulte, Dorothea, Michael Kiebler, Julia A. Hasler, et al.. (2019). Choroid plexus‐derived miR‐204 regulates the number of quiescent neural stem cells in the adult brain. The EMBO Journal. 38(17). e100481–e100481. 54 indexed citations
10.
Modic, Miha, Markus Grosch, Gregor Rot, et al.. (2019). Cross-Regulation between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition. Molecular Cell. 74(5). 951–965.e13. 92 indexed citations
11.
Rusha, Ejona, Rizwan Rehimi, Miha Modic, et al.. (2019). Pathological ASXL1 Mutations and Protein Variants Impair Neural Crest Development. Stem Cell Reports. 12(5). 861–868. 12 indexed citations
12.
Modic, Miha, Davide Cacchiarelli, & Derk ten Berge. (2019). Integrative biology studies in pluripotent stem cells. Stem Cell Research. 42. 101686–101686. 1 indexed citations
13.
Mihevc, Sonja Prpar, Maja Štalekar, Helena Motaln, et al.. (2019). Nuclear RNA foci fromC9ORF72expansion mutation form paraspeckle-like bodies. Journal of Cell Science. 132(5). 35 indexed citations
14.
Tyzack, Giulia E., Raphaëlle Luisier, Doaa M. Taha, et al.. (2019). Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis. Brain. 142(9). 2572–2580. 108 indexed citations
15.
Bratkovič, Tomaž, et al.. (2018). Neuronal differentiation induces SNORD115 expression and is accompanied by post-transcriptional changes of serotonin receptor 2c mRNA. Scientific Reports. 8(1). 5101–5101. 21 indexed citations
16.
Modic, Miha, Gregor Rot, Markus Grosch, et al.. (2018). Cross-Regulation Between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition. SSRN Electronic Journal. 2 indexed citations
17.
Rot, Gregor, Zhen Wang, Ina Huppertz, et al.. (2017). High-Resolution RNA Maps Suggest Common Principles of Splicing and Polyadenylation Regulation by TDP-43. Cell Reports. 19(5). 1056–1067. 67 indexed citations
18.
Sibley, Christopher R., Warren Emmett, Lorea Blázquez, et al.. (2015). Recursive splicing in long vertebrate genes. Nature. 521(7552). 371–375. 102 indexed citations
19.
Modic, Miha, Jernej Ule, & Christopher R. Sibley. (2013). CLIPing the brain: Studies of protein–RNA interactions important for neurodegenerative disorders. Molecular and Cellular Neuroscience. 56. 429–435. 27 indexed citations
20.
Rogelj, Boris, Laura E. Easton, Gireesh K. Bogu, et al.. (2012). Widespread binding of FUS along nascent RNA regulates alternative splicing in the brain. Scientific Reports. 2(1). 603–603. 206 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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