Katarzyna Gach

1.5k total citations
64 papers, 1.2k citations indexed

About

Katarzyna Gach is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry. According to data from OpenAlex, Katarzyna Gach has authored 64 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 29 papers in Cellular and Molecular Neuroscience and 20 papers in Organic Chemistry. Recurrent topics in Katarzyna Gach's work include Neuropeptides and Animal Physiology (28 papers), Sesquiterpenes and Asteraceae Studies (10 papers) and Cancer, Stress, Anesthesia, and Immune Response (9 papers). Katarzyna Gach is often cited by papers focused on Neuropeptides and Animal Physiology (28 papers), Sesquiterpenes and Asteraceae Studies (10 papers) and Cancer, Stress, Anesthesia, and Immune Response (9 papers). Katarzyna Gach collaborates with scholars based in Poland, France and Hungary. Katarzyna Gach's co-authors include Anna Janecka, Jakub Fichna, Anna Wyrębska, Anna Janecka, Tomasz Janecki, Angelika Długosz-Pokorska, Janusz Szemraj, Renata Perlikowska, Jacek Szymański and Géza Tóth and has published in prestigious journals such as Journal of Neuroscience, International Journal of Molecular Sciences and Neuroscience.

In The Last Decade

Katarzyna Gach

62 papers receiving 1.2k citations

Peers

Katarzyna Gach
Anna Janecka Poland
Jean Peluso France
Yoshikazu Tasaki Japan
Anna Janecka Poland
Jianping Chen China
Soosung Kang South Korea
Heinz H. Pertz Germany
Vigilio Ballabeni Italy
Federico Monczor Argentina
Hassan Pajouhesh United States
Anna Janecka Poland
Katarzyna Gach
Citations per year, relative to Katarzyna Gach Katarzyna Gach (= 1×) peers Anna Janecka

Countries citing papers authored by Katarzyna Gach

Since Specialization
Citations

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

Fields of papers citing papers by Katarzyna Gach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katarzyna Gach

This figure shows the co-authorship network connecting the top 25 collaborators of Katarzyna Gach. A scholar is included among the top collaborators of Katarzyna Gach 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 Katarzyna Gach. Katarzyna Gach 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
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Gach, Katarzyna, et al.. (2025). Quinolin-4-ones: Methods of Synthesis and Application in Medicine. Molecules. 30(1). 163–163. 2 indexed citations
3.
Jastrzębska, Aneta, et al.. (2024). Synthesis of New Chiral β-Carbonyl Selenides with Antioxidant and Anticancer Activity Evaluation—Part I. Materials. 17(4). 899–899. 1 indexed citations
4.
Długosz-Pokorska, Angelika, Tomasz Janecki, Anna Janecka, & Katarzyna Gach. (2024). New uracil analog as inhibitor/modulator of ABC transporters or/and NF-κB in taxol-resistant MCF-7/Tx cell line. Journal of Cancer Research and Clinical Oncology. 150(6). 328–328. 1 indexed citations
5.
Celeda, Małgorzata, et al.. (2023). Trifluoromethylated 4,5-Dihydro-1,2,4-triazin-6(1H)-ones via (3+3)-Annulation of Nitrile Imines with α-Amino Esters. Materials. 16(2). 856–856. 4 indexed citations
6.
Jastrzębska, Aneta, et al.. (2023). Facile synthesis of chiral phenylselenides as novel antioxidants and cytotoxic agents. RSC Advances. 13(21). 14698–14702. 9 indexed citations
7.
8.
Gowing, Emma K., Raghavendra Y. Nagaraja, Pascale Quilichini, et al.. (2021). The Gliopeptide ODN, a Ligand for the Benzodiazepine Site of GABA A Receptors, Boosts Functional Recovery after Stroke. Journal of Neuroscience. 41(33). 7148–7159. 10 indexed citations
9.
Długosz-Pokorska, Angelika, et al.. (2018). Involvement of α-methylene-γ- and δ-lactones in the suppression of multidrug resistance in MCF-7 cells. Pharmacological Reports. 70(4). 631–638. 2 indexed citations
10.
Gach, Katarzyna, Iwona Grądzka, Sylwia Męczyńska‐Wielgosz, et al.. (2016). Anticancer activity and radiosensitization effect of methyleneisoxazolidin-5-ones in hepatocellular carcinoma HepG2 cells. Chemico-Biological Interactions. 248. 68–73. 4 indexed citations
11.
Gach, Katarzyna & Anna Janecka. (2014). α-Methylene-γ-lactones as a Novel Class of Anti-leukemic Agents. Anti-Cancer Agents in Medicinal Chemistry. 14(5). 688–694. 25 indexed citations
12.
Perlikowska, Renata, et al.. (2013). Cyclization in Opioid Peptides. Current Drug Targets. 14(7). 798–816. 27 indexed citations
13.
Bényei, Attila, Jakub Fichna, Katarzyna Gach, et al.. (2012). Synthesis and Opioid Activity of Novel 6-ketolevorphanol Derivatives. Medicinal Chemistry. 9(1). 1–10. 7 indexed citations
14.
Fichna, Jakub, Renata Perlikowska, Anna Wyrębska, et al.. (2011). Effect of 2′,6′-dimethyl-l-tyrosine (Dmt) on pharmacological activity of cyclic endomorphin-2 and morphiceptin analogs. Bioorganic & Medicinal Chemistry. 19(23). 6977–6981. 26 indexed citations
15.
Janecka, Anna, Renata Perlikowska, Katarzyna Gach, Anna Wyrębska, & Jakub Fichna. (2010). Development of Opioid Peptide Analogs for Pain Relief. Current Pharmaceutical Design. 16(9). 1126–1135. 40 indexed citations
16.
Czakó, Barbara, János Marton, Sándor Berényi, et al.. (2010). Synthesis and opioid activity of novel 6-substituted-6-demethoxy-ethenomorphinans. Bioorganic & Medicinal Chemistry. 18(10). 3535–3542. 2 indexed citations
17.
Fichna, Jakub, Katarzyna Gach, Renata Perlikowska, et al.. (2010). Novel endomorphin analogues with antagonist activity at the mu-opioid receptor in the gastrointestinal tract. Regulatory Peptides. 162(1-3). 109–114. 12 indexed citations
18.
Perlikowska, Renata, Katarzyna Gach, Jakub Fichna, et al.. (2009). Biological activity of endomorphin and [Dmt1]endomorphin analogs with six-membered proline surrogates in position 2. Bioorganic & Medicinal Chemistry. 17(11). 3789–3794. 27 indexed citations
19.
Fichna, Jakub, Katarzyna Gach, Renata Perlikowska, et al.. (2008). Identification of Endomorphin‐1 and Endomorphin‐2 Binding Sites in Human μ‐Opioid Receptor by Antisense Oligonucleotide Strategy. Chemical Biology & Drug Design. 72(6). 507–512. 3 indexed citations
20.
Fichna, Jakub, Katarzyna Gach, Jeroen Poels, et al.. (2006). [d-1-Nal4]endomorphin-2 is a potent μ-opioid receptor antagonist in the aequorin luminescence-based calcium assay. Life Sciences. 79(11). 1094–1099. 4 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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