M. Wisniewska

1.8k total citations
35 papers, 1.4k citations indexed

About

M. Wisniewska is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, M. Wisniewska has authored 35 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in M. Wisniewska's work include Wnt/β-catenin signaling in development and cancer (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Axon Guidance and Neuronal Signaling (5 papers). M. Wisniewska is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Axon Guidance and Neuronal Signaling (5 papers). M. Wisniewska collaborates with scholars based in Poland, France and Spain. M. Wisniewska's co-authors include Jacek Kuźnicki, Jonathan B Weitzman, Maya Ameyar, Joanna Gruszczynska‐Biegala, Latifa Bakiri, Andrzej Nagalski, Moshé Yaniv, Erwin F. Wagner, Koichi Matsuo and Katarzyna Misztal and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

M. Wisniewska

33 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Wisniewska Poland 18 879 369 222 165 134 35 1.4k
Tiemo J. Klisch United States 21 1.1k 1.2× 128 0.3× 276 1.2× 185 1.1× 206 1.5× 35 2.2k
Robert Beattie United Kingdom 25 1.1k 1.3× 624 1.7× 97 0.4× 98 0.6× 116 0.9× 45 1.6k
Akira Futatsugi Japan 17 903 1.0× 540 1.5× 186 0.8× 73 0.4× 44 0.3× 22 1.4k
Hideki Hiyama Japan 14 1.0k 1.2× 371 1.0× 54 0.2× 204 1.2× 56 0.4× 16 1.7k
Motohiko Takemura Japan 20 650 0.7× 520 1.4× 107 0.5× 53 0.3× 46 0.3× 70 1.3k
Tae‐Ju Park United States 23 772 0.9× 269 0.7× 46 0.2× 135 0.8× 63 0.5× 45 1.3k
Saki Shimizu Japan 29 810 0.9× 708 1.9× 53 0.2× 246 1.5× 104 0.8× 91 2.0k
Marcel D. Payet Canada 28 1.1k 1.3× 489 1.3× 107 0.5× 111 0.7× 64 0.5× 51 1.8k
Rodrigo Herrera‐Molina Chile 23 603 0.7× 303 0.8× 49 0.2× 80 0.5× 77 0.6× 32 1.2k
Hideaki Ando Japan 22 1.9k 2.2× 441 1.2× 134 0.6× 166 1.0× 632 4.7× 37 2.6k

Countries citing papers authored by M. Wisniewska

Since Specialization
Citations

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

Fields of papers citing papers by M. Wisniewska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Wisniewska

This figure shows the co-authorship network connecting the top 25 collaborators of M. Wisniewska. A scholar is included among the top collaborators of M. Wisniewska 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 M. Wisniewska. M. Wisniewska 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.
Iñiguez, L., Luis Pardo-Marín, J. M. Castro Cerón, et al.. (2025). Timing of exercise differentially impacts adipose tissue gain in male adolescent rats. Molecular Metabolism. 93. 102100–102100.
2.
Czopowicz, Michał, et al.. (2024). Astaxanthin Supplementation Does Not Alter Training-Related Changes in Inflammatory Cytokine Profile in Arabian Racing Horses. Antioxidants. 13(8). 905–905. 1 indexed citations
3.
Liszewska, Ewa, Ksenia Meyza, Joanna Urban‐Ciećko, et al.. (2023). Astrocytic β-catenin signaling via TCF7L2 regulates synapse development and social behavior. Molecular Psychiatry. 29(1). 57–73. 12 indexed citations
4.
5.
Balcerak, Anna, Rafał Tomecki, Krzysztof Goryca, et al.. (2022). The RNA-Binding Landscape of HAX1 Protein Indicates Its Involvement in Translation and Ribosome Assembly. Cells. 11(19). 2943–2943. 3 indexed citations
6.
Wisniewska, M. & Andrzej Kulig. (2022). Concept of Questionnaire Surveys in an Urban Agglomeration as an Essential Element of Identifying the Sources of Odour Nuisance. SHILAP Revista de lepidopterología. 1 indexed citations
7.
Koziński, Kamil, Magdalena J. Ślusarz, Jarosław Ruczyński, et al.. (2021). PTD4 Peptide Increases Neural Viability in an In Vitro Model of Acute Ischemic Stroke. International Journal of Molecular Sciences. 22(11). 6086–6086. 8 indexed citations
8.
Misztal, Katarzyna, et al.. (2016). TCF7L2 mediates the cellular and behavioral response to chronic lithium treatment in animal models. Neuropharmacology. 113(Pt A). 490–501. 12 indexed citations
9.
Wisniewska, M.. (2013). Physiological Role of β-Catenin/TCF Signaling in Neurons of the Adult Brain. Neurochemical Research. 38(6). 1144–1155. 71 indexed citations
10.
Wisniewska, M., Andrzej Nagalski, Michał Dąbrowski, Katarzyna Misztal, & Jacek Kuźnicki. (2012). Novel β-catenin target genes identified in thalamic neurons encode modulators of neuronal excitability. BMC Genomics. 13(1). 635–635. 36 indexed citations
11.
Nagalski, Andrzej, Manuel Irimia, José Luis Ferrán, et al.. (2012). Postnatal isoform switch and protein localization of LEF1 and TCF7L2 transcription factors in cortical, thalamic, and mesencephalic regions of the adult mouse brain. Brain Structure and Function. 218(6). 1531–1549. 30 indexed citations
12.
Misztal, Katarzyna, M. Wisniewska, Mateusz C. Ambrozkiewicz, Andrzej Nagalski, & Jacek Kuźnicki. (2011). WNT Protein-independent Constitutive Nuclear Localization of β-Catenin Protein and Its Low Degradation Rate in Thalamic Neurons. Journal of Biological Chemistry. 286(36). 31781–31788. 16 indexed citations
13.
Michowski, Wojciech, Roberta Ferretti, M. Wisniewska, et al.. (2010). Morgana/CHP-1 is a novel chaperone able to protect cells from stress. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1803(9). 1043–1049. 24 indexed citations
14.
Błażejczyk, Magdalena, Adam Sobczak, M. Wisniewska, et al.. (2009). Biochemical characterization and expression analysis of a novel EF-hand Ca2+ binding protein calmyrin2 (Cib2) in brain indicates its function in NMDA receptor mediated Ca2+ signaling. Archives of Biochemistry and Biophysics. 487(1). 66–78. 32 indexed citations
15.
Gruszczynska‐Biegala, Joanna, M. Wisniewska, Katarzyna Misztal, et al.. (2008). Expression of STIM1 in brain and puncta-like co-localization of STIM1 and ORAI1 upon depletion of Ca2+ store in neurons. Neurochemistry International. 54(1). 49–55. 86 indexed citations
16.
Wisniewska, M., Beata Pyrzyńska, & Bożena Kamińska. (2004). Impaired AP‐1 dimers and NFAT complex formation in immature thymocytes during in vivo glucocorticoid‐induced apoptosis. Cell Biology International. 28(11). 773–780. 7 indexed citations
17.
Ameyar, Maya, M. Wisniewska, & Jonathan B Weitzman. (2003). A role for AP-1 in apoptosis: the case for and against. Biochimie. 85(8). 747–752. 255 indexed citations
18.
Kamińska, Bożena, Beata Pyrzyńska, Iwona A. Ciechomska, & M. Wisniewska. (2000). Modulation of the composition of AP-1 complex and its impact on transcriptional activity. Acta Neurobiologiae Experimentalis. 60(3). 395–402. 67 indexed citations
19.
Wisniewska, M., et al.. (1999). Cloning, characterisation and regulation of the ornithine transaminase (otaA) gene of Aspergillus nidulans. Current Genetics. 35(2). 118–126. 20 indexed citations
20.
Wisniewska, M., et al.. (1997). NUCLEAR FACTOR OF ACTIVATED T CELLS (NFAT) IS A POSSIBLE TARGET FOR DEXAMETHASONE IN THYMOCYTE APOPTOSIS. Cell Biology International. 21(3). 127–132. 14 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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