Iakowos Karakesisoglou

3.2k total citations
39 papers, 2.6k citations indexed

About

Iakowos Karakesisoglou is a scholar working on Molecular Biology, Cell Biology and Biophysics. According to data from OpenAlex, Iakowos Karakesisoglou has authored 39 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 21 papers in Cell Biology and 3 papers in Biophysics. Recurrent topics in Iakowos Karakesisoglou's work include Nuclear Structure and Function (26 papers), RNA Research and Splicing (22 papers) and Cellular Mechanics and Interactions (16 papers). Iakowos Karakesisoglou is often cited by papers focused on Nuclear Structure and Function (26 papers), RNA Research and Splicing (22 papers) and Cellular Mechanics and Interactions (16 papers). Iakowos Karakesisoglou collaborates with scholars based in Germany, United Kingdom and United States. Iakowos Karakesisoglou's co-authors include Angelika A. Noegel, Elaine Fuchs, Wenshu Lu, V. C. Padmakumar, Sabu Abraham, Maria Schneider, Josef Gotzmann, Atsuko Kodama, Alec Vaezi and Ellen Wong and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Genes & Development.

In The Last Decade

Iakowos Karakesisoglou

37 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iakowos Karakesisoglou Germany 25 1.9k 1.1k 130 127 105 39 2.6k
Masakazu Yamazaki Japan 22 1.6k 0.8× 1.0k 0.9× 140 1.1× 244 1.9× 279 2.7× 36 2.4k
Melissa G. Mendez United States 13 1.9k 1.0× 1.1k 1.0× 115 0.9× 156 1.2× 105 1.0× 17 3.0k
Ryan Schreiner United States 22 847 0.4× 588 0.5× 132 1.0× 204 1.6× 134 1.3× 43 1.5k
Gregor Kirfel Germany 24 709 0.4× 400 0.4× 95 0.7× 157 1.2× 121 1.2× 47 1.5k
Tomonori Hirose Japan 21 2.1k 1.1× 1.3k 1.2× 176 1.4× 118 0.9× 247 2.4× 43 2.9k
Heike Fölsch United States 27 2.1k 1.1× 1.7k 1.5× 254 2.0× 364 2.9× 276 2.6× 37 2.9k
Satomi Nadanaka Japan 27 1.4k 0.7× 1.7k 1.6× 199 1.5× 76 0.6× 228 2.2× 51 2.3k
Masashi Kusubata Japan 22 819 0.4× 470 0.4× 136 1.0× 105 0.8× 206 2.0× 49 1.5k
Franz Wendler United Kingdom 22 1.8k 0.9× 862 0.8× 167 1.3× 201 1.6× 175 1.7× 26 2.4k
Ichiro Izawa Japan 27 2.0k 1.0× 1.5k 1.4× 403 3.1× 73 0.6× 150 1.4× 45 2.8k

Countries citing papers authored by Iakowos Karakesisoglou

Since Specialization
Citations

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

Fields of papers citing papers by Iakowos Karakesisoglou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iakowos Karakesisoglou

This figure shows the co-authorship network connecting the top 25 collaborators of Iakowos Karakesisoglou. A scholar is included among the top collaborators of Iakowos Karakesisoglou 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 Iakowos Karakesisoglou. Iakowos Karakesisoglou 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
2.
Young, Natalie, Christoph S. Clemen, Rolf Schröder, et al.. (2024). An Intronic Heterozygous SYNE2 Splice Site Mutation: A Rare Cause for Myalgia and hyperCKemia?. SHILAP Revista de lepidopterología. 3(1). 100–109.
4.
Costello, Lydia, Daniel J. Maltman, Pamela Ritchie, et al.. (2023). Quantitative morphometric analysis of intrinsic and extrinsic skin ageing in individuals with Fitzpatrick skin types II–III. Experimental Dermatology. 32(5). 620–631. 9 indexed citations
5.
Young, Natalie, Maria Asif, Matthew P. Jackson, et al.. (2021). Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism. Genes. 12(9). 1294–1294. 9 indexed citations
6.
Roger, Mathilde, Nicola Fullard, Lydia Costello, et al.. (2019). Bioengineering the microanatomy of human skin. Journal of Anatomy. 234(4). 438–455. 115 indexed citations
7.
Karakesisoglou, Iakowos, et al.. (2018). Functional Analysis of LINC Complexes in the Skin. Methods in molecular biology. 1840. 295–306. 2 indexed citations
8.
Karakesisoglou, Iakowos, et al.. (2013). Nesprins in health and disease. Seminars in Cell and Developmental Biology. 29. 169–179. 70 indexed citations
9.
Eckes, Beate, Gernot Glöckner, Marco Groth, et al.. (2012). The nuclear envelope protein Nesprin-2 has roles in cell proliferation and differentiation during wound healing. Nucleus. 3(2). 172–186. 54 indexed citations
10.
Meinke, Peter, Sabu Abraham, Liu Yang, et al.. (2012). LINC complex alterations in DMD and EDMD/CMT fibroblasts. European Journal of Cell Biology. 91(8). 614–628. 48 indexed citations
11.
Stinchcombe, Jane C., et al.. (2012). Cytotoxic T lymphocyte effector function is independent of nucleus–centrosome dissociation. European Journal of Immunology. 42(8). 2132–2141. 15 indexed citations
12.
Schneider, Maria, Wenshu Lu, Sascha Neumann, et al.. (2010). Molecular mechanisms of centrosome and cytoskeleton anchorage at the nuclear envelope. Cellular and Molecular Life Sciences. 68(9). 1593–1610. 73 indexed citations
13.
Olins, Ada L., Van T. Hoang, Monika Zwerger, et al.. (2008). The LINC-less granulocyte nucleus. European Journal of Cell Biology. 88(4). 203–214. 84 indexed citations
14.
Stoffel, Wilhelm, Barbara Holz, Britta Jenke, et al.. (2008). Δ6‐Desaturase (FADS2) deficiency unveils the role of ω3‐ and ω6‐polyunsaturated fatty acids. The EMBO Journal. 27(17). 2281–2292. 187 indexed citations
15.
Lu, Wenshu, Josef Gotzmann, Lucia Sironi, et al.. (2008). Sun1 forms immobile macromolecular assemblies at the nuclear envelope. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783(12). 2415–2426. 79 indexed citations
17.
Neumann, Sascha, Wenshu Lu, Martina Munck, et al.. (2007). Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells. Human Molecular Genetics. 16(23). 2944–2959. 58 indexed citations
18.
Peche, Vivek S., Rolf Schröder, Michael Schleicher, et al.. (2007). CAP2, cyclase-associated protein 2, is a dual compartment protein. Cellular and Molecular Life Sciences. 64(19-20). 2702–2715. 70 indexed citations
19.
Padmakumar, V. C., Wenshu Lu, Sabu Abraham, et al.. (2005). The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope. Journal of Cell Science. 118(15). 3419–3430. 348 indexed citations
20.
Gottwald, Ulrich, et al.. (1996). Identification of a cyclase-associated protein (CAP) homologue in Dictyostelium discoideum and characterization of its interaction with actin.. Molecular Biology of the Cell. 7(2). 261–272. 72 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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