Lukasz Swiech

4.6k total citations · 1 hit paper
17 papers, 1.9k citations indexed

About

Lukasz Swiech is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lukasz Swiech has authored 17 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lukasz Swiech's work include Neuroscience and Neuropharmacology Research (3 papers), Microtubule and mitosis dynamics (3 papers) and RNA and protein synthesis mechanisms (3 papers). Lukasz Swiech is often cited by papers focused on Neuroscience and Neuropharmacology Research (3 papers), Microtubule and mitosis dynamics (3 papers) and RNA and protein synthesis mechanisms (3 papers). Lukasz Swiech collaborates with scholars based in Poland, United States and Netherlands. Lukasz Swiech's co-authors include Jacek Jaworski, Matthias Heidenreich, John J. Trombetta, Yinqing Li, Naomi Habib, Anna R. Malik, Małgorzata Perycz, Feng Zhang, Mriganka Sur and Abhishek Banerjee and has published in prestigious journals such as Science, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Lukasz Swiech

16 papers receiving 1.9k citations

Hit Papers

In vivo interrogation of gene function in the mammalian b... 2014 2026 2018 2022 2014 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lukasz Swiech Poland 14 1.3k 389 319 184 177 17 1.9k
Paul S. Amieux United States 20 1.6k 1.2× 593 1.5× 264 0.8× 160 0.9× 228 1.3× 31 2.3k
Yi‐Shuian Huang Taiwan 25 1.7k 1.3× 463 1.2× 219 0.7× 134 0.7× 177 1.0× 69 2.3k
Rosanna Parlato Germany 28 1.5k 1.1× 879 2.3× 428 1.3× 132 0.7× 155 0.9× 63 2.4k
Konstantin Khodosevich Denmark 29 1.2k 0.9× 559 1.4× 284 0.9× 257 1.4× 99 0.6× 57 2.1k
Chantal M. Longo-Guess United States 18 1.5k 1.1× 234 0.6× 291 0.9× 224 1.2× 173 1.0× 24 2.2k
Sohyun Ahn United States 15 1.1k 0.8× 762 2.0× 209 0.7× 154 0.8× 155 0.9× 22 1.8k
Jason D. Berndt United States 25 1.6k 1.2× 347 0.9× 195 0.6× 98 0.5× 318 1.8× 47 2.4k
Marie‐Christine Birling France 25 1.0k 0.8× 477 1.2× 403 1.3× 64 0.3× 185 1.0× 61 1.8k
Daniel P. Seeburg United States 16 1.4k 1.1× 570 1.5× 380 1.2× 146 0.8× 259 1.5× 26 2.2k
Shinichiro Taya Japan 25 1.5k 1.1× 391 1.0× 343 1.1× 213 1.2× 110 0.6× 36 2.1k

Countries citing papers authored by Lukasz Swiech

Since Specialization
Citations

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

Fields of papers citing papers by Lukasz Swiech

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lukasz Swiech

This figure shows the co-authorship network connecting the top 25 collaborators of Lukasz Swiech. A scholar is included among the top collaborators of Lukasz Swiech 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 Lukasz Swiech. Lukasz Swiech is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Bustos, Fernando J., Jianping Zhao, Matthias Heidenreich, et al.. (2023). Removal of a partial genomic duplication restores synaptic transmission and behavior in the MyosinVA mutant mouse Flailer. BMC Biology. 21(1). 232–232. 6 indexed citations
2.
Choi, Eugene, Walker S. Lahr, Emily J. Pomeroy, et al.. (2021). Engineering CD70-Directed CAR-NK Cells for the Treatment of Hematological and Solid Malignancies. Blood. 138(Supplement 1). 1691–1691. 20 indexed citations
3.
Waight, Jeremy D., Dhan Chand, Thomas Horn, et al.. (2018). Selective FcγR Co-engagement on APCs Modulates the Activity of Therapeutic Antibodies Targeting T Cell Antigens. Cancer Cell. 33(6). 1033–1047.e5. 64 indexed citations
4.
Habib, Naomi, Yinqing Li, Matthias Heidenreich, et al.. (2016). Div-Seq: Single-nucleus RNA-Seq reveals dynamics of rare adult newborn neurons. Science. 353(6302). 925–928. 382 indexed citations
5.
Malik, Anna R., Ewa Liszewska, Agnieszka Skalecka, et al.. (2015). Tuberous sclerosis complex neuropathology requires glutamate-cysteine ligase. Acta Neuropathologica Communications. 3(1). 48–48. 14 indexed citations
6.
Konopka, Anna, Paweł Trzaskoma, Josephine Labus, et al.. (2014). CD44 regulates dendrite morphogenesis through Src tyrosine kinase-dependent positioning of the Golgi apparatus. Journal of Cell Science. 127(Pt 23). 5038–51. 34 indexed citations
7.
Swiech, Lukasz, Matthias Heidenreich, Abhishek Banerjee, et al.. (2014). In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9. Nature Biotechnology. 33(1). 102–106. 608 indexed citations breakdown →
8.
Konopka, Anna, Paweł Trzaskoma, Josephine Labus, et al.. (2014). CD44 regulates dendrite morphogenesis through Src tyrosine kinase-dependent positioning of the Golgi. Development. 141(24). e2407–e2407. 10 indexed citations
9.
Malik, Anna R., Małgorzata Urbańska, Agata Góźdź, et al.. (2013). Cyr61, a Matricellular Protein, Is Needed for Dendritic Arborization of Hippocampal Neurons. Journal of Biological Chemistry. 288(12). 8544–8559. 38 indexed citations
10.
Urbańska, Małgorzata, Agata Góźdź, Lukasz Swiech, & Jacek Jaworski. (2012). Mammalian Target of Rapamycin Complex 1 (mTORC1) and 2 (mTORC2) Control the Dendritic Arbor Morphology of Hippocampal Neurons. Journal of Biological Chemistry. 287(36). 30240–30256. 122 indexed citations
11.
Urbańska, Małgorzata, Lukasz Swiech, & Jacek Jaworski. (2012). Developmental Plasticity of the Dendritic Compartment: Focus on the Cytoskeleton. Advances in experimental medicine and biology. 970. 265–284. 30 indexed citations
12.
Swiech, Lukasz, Magdalena Błażejczyk, Małgorzata Urbańska, et al.. (2011). CLIP-170 and IQGAP1 Cooperatively Regulate Dendrite Morphology. Journal of Neuroscience. 31(12). 4555–4568. 76 indexed citations
13.
Stefaniuk, Marzena, Lukasz Swiech, Joanna Dzwonek, & Katarzyna Łukasiuk. (2010). Expression of Ttyh1, a member of the Tweety family in neurons in vitro and in vivo and its potential role in brain pathology. Journal of Neurochemistry. 115(5). 1183–1194. 31 indexed citations
14.
Piechota, Marcin, Michał Korostyński, Wojciech Solecki, et al.. (2010). The dissection of transcriptional modules regulated by various drugs of abuse in the mouse striatum. Genome biology. 11(5). R48–R48. 129 indexed citations
15.
Perycz, Małgorzata, Lukasz Swiech, Anna R. Malik, & Jacek Jaworski. (2007). mTOR w fizjologii i patologii ukladu nerwowego. Postepy Biologii Komorki. 34(3). 511–525. 2 indexed citations
16.
Swiech, Lukasz, et al.. (2007). Accumulation and dynamics of proteins of the MCM family during mouse oogenesis and the first embryonic cell cycle. The International Journal of Developmental Biology. 51(4). 283–295. 22 indexed citations
17.
Swiech, Lukasz, Małgorzata Perycz, Anna R. Malik, & Jacek Jaworski. (2007). Role of mTOR in physiology and pathology of the nervous system. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1784(1). 116–132. 284 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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