Liisa Arike

4.6k total citations · 4 hit papers
36 papers, 2.9k citations indexed

About

Liisa Arike is a scholar working on Molecular Biology, Surgery and Food Science. According to data from OpenAlex, Liisa Arike has authored 36 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Surgery and 10 papers in Food Science. Recurrent topics in Liisa Arike's work include Gut microbiota and health (10 papers), Probiotics and Fermented Foods (9 papers) and Helicobacter pylori-related gastroenterology studies (9 papers). Liisa Arike is often cited by papers focused on Gut microbiota and health (10 papers), Probiotics and Fermented Foods (9 papers) and Helicobacter pylori-related gastroenterology studies (9 papers). Liisa Arike collaborates with scholars based in Sweden, Estonia and United Kingdom. Liisa Arike's co-authors include Gunnar C. Hansson, Malin Johansson, George Birchenough, Fredrik Bäckhed, Jessica Holmén‐Larsson, Kaarel Adamberg, Bjoern O. Schroeder, Marcus Ståhlman, Raivo Vilu and Lauri Peil and has published in prestigious journals such as Science, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Liisa Arike

32 papers receiving 2.8k citations

Hit Papers

Bifidobacteria or Fiber Protects against Diet-Induced Mic... 2015 2026 2018 2022 2017 2015 2019 2021 100 200 300 400 500

Peers

Liisa Arike
Chin Wen Png Singapore
Liisa Arike
Citations per year, relative to Liisa Arike Liisa Arike (= 1×) peers Chin Wen Png

Countries citing papers authored by Liisa Arike

Since Specialization
Citations

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

Fields of papers citing papers by Liisa Arike

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liisa Arike

This figure shows the co-authorship network connecting the top 25 collaborators of Liisa Arike. A scholar is included among the top collaborators of Liisa Arike 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 Liisa Arike. Liisa Arike 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.
Yılmaz, Bahtiyar, Elisabeth Nyström, Elena Layunta, et al.. (2025). Neonatal microbiota colonization primes maturation of goblet cell–mediated protection in the pre-weaning colon. The Journal of Experimental Medicine. 222(8).
2.
Svensson, Frida, Liisa Arike, Jenny K. Gustafsson, et al.. (2025). EatA mediated degradation of intestinal mucus is species-specific and driven by MUC2 structural features. Nature Communications. 17(1). 158–158.
3.
Layunta, Elena, et al.. (2024). MUC17 is an essential small intestinal glycocalyx component that is disrupted in Crohn’s disease. JCI Insight. 10(3). 7 indexed citations
4.
Song, Ran, William McAlpine, Evan Nair‐Gill, et al.. (2023). Trans-Golgi protein TVP23B regulates host-microbe interactions via Paneth cell homeostasis and Goblet cell glycosylation. Nature Communications. 14(1). 3652–3652. 8 indexed citations
5.
Nyström, Elisabeth, Beatriz Martínez‐Abad, Liisa Arike, et al.. (2021). An intercrypt subpopulation of goblet cells is essential for colonic mucus barrier function. Science. 372(6539). 224 indexed citations breakdown →
6.
Layunta, Elena, et al.. (2021). IL-22 promotes the formation of a MUC17 glycocalyx barrier in the postnatal small intestine during weaning. Cell Reports. 34(7). 108757–108757. 29 indexed citations
7.
Arike, Liisa, Gunnar C. Hansson, & Christian V. Recktenwald. (2020). Identifying transglutaminase reaction products via mass spectrometry as exemplified by the MUC2 mucin - Pitfalls and traps. Analytical Biochemistry. 597. 113668–113668. 8 indexed citations
8.
Arike, Liisa, Andrus Seiman, Sjoerd van der Post, et al.. (2020). Protein Turnover in Epithelial Cells and Mucus along the Gastrointestinal Tract Is Coordinated by the Spatial Location and Microbiota. Cell Reports. 30(4). 1077–1087.e3. 53 indexed citations
9.
Post, Sjoerd van der, Karolina S. Jabbar, George Birchenough, et al.. (2019). Structural weakening of the colonic mucus barrier is an early event in ulcerative colitis pathogenesis. Gut. 68(12). 2142–2151. 364 indexed citations breakdown →
10.
Johansson, Malin, Liisa Arike, Beatriz Martínez‐Abad, et al.. (2019). Normal Calcium-Activated Anion Secretion in a Mouse Selectively Lacking TMEM16A in Intestinal Epithelium. Frontiers in Physiology. 10. 694–694. 7 indexed citations
11.
Arike, Liisa, Ana M. Rodríguez‐Piñeiro, Beatriz Martínez‐Abad, et al.. (2018). Attached stratified mucus separates bacteria from the epithelial cells in COPD lungs. JCI Insight. 3(17). 37 indexed citations
12.
Nyström, Elisabeth, George Birchenough, Sjoerd van der Post, et al.. (2018). Calcium-activated Chloride Channel Regulator 1 (CLCA1) Controls Mucus Expansion in Colon by Proteolytic Activity. EBioMedicine. 33. 134–143. 75 indexed citations
13.
Schroeder, Bjoern O., George Birchenough, Marcus Ståhlman, et al.. (2017). Bifidobacteria or Fiber Protects against Diet-Induced Microbiota-Mediated Colonic Mucus Deterioration. Cell Host & Microbe. 23(1). 27–40.e7. 545 indexed citations breakdown →
14.
Arike, Liisa & Gunnar C. Hansson. (2016). The Densely O-Glycosylated MUC2 Mucin Protects the Intestine and Provides Food for the Commensal Bacteria. Journal of Molecular Biology. 428(16). 3221–3229. 157 indexed citations
15.
Johansson, Malin, Hedvig E. Jakobsson, Jessica Holmén‐Larsson, et al.. (2015). Normalization of Host Intestinal Mucus Layers Requires Long-Term Microbial Colonization. Cell Host & Microbe. 18(5). 582–592. 381 indexed citations breakdown →
16.
Moisan, Annick, Hélène Chiapello, Liisa Arike, et al.. (2015). Genome-wide investigation of mRNA lifetime determinants in Escherichia coli cells cultured at different growth rates. BMC Genomics. 16(1). 275–275. 26 indexed citations
17.
Nyström, Elisabeth, Lars Mundhenk, Liisa Arike, et al.. (2015). The Goblet Cell Protein Clca1 (Alias mClca3 or Gob-5) Is Not Required for Intestinal Mucus Synthesis, Structure and Barrier Function in Naive or DSS-Challenged Mice. PLoS ONE. 10(7). e0131991–e0131991. 18 indexed citations
18.
Arike, Liisa & Lauri Peil. (2014). Spectral Counting Label-Free Proteomics. Methods in molecular biology. 1156. 213–222. 75 indexed citations
19.
Olspert, Allan, Liisa Arike, Lauri Peil, & Erkki Truve. (2011). Sobemovirus RNA linked to VPg over a threonine residue. FEBS Letters. 585(19). 2979–2985. 12 indexed citations
20.
Arike, Liisa, et al.. (2008). Single bioreactor gastrointestinal tract simulator for study of survival of probiotic bacteria. Applied Microbiology and Biotechnology. 80(2). 317–324. 39 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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