Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

MobiDB 3.0: more annotations for intrinsic disorder, conformational diversity and interactions in proteins
Damiano Piovesan, Francesco Tabaro, Lisanna Paladin, et al.
Nucleic Acids Research (2017) Vol. 46, Iss. D1, pp. D471-D476
Open Access | Times Cited: 212

Showing 1-25 of 212 citing articles:

Pfam: The protein families database in 2021
Jaina Mistry, Sara Chuguransky, Lowri Williams, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D412-D419
Open Access | Times Cited: 5737
The InterPro protein families and domains database: 20 years on
Matthias Blum, Hsin-Yu Chang, Sara Chuguransky, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D344-D354
Open Access | Times Cited: 1906
InterPro in 2019: improving coverage, classification and access to protein sequence annotations
Alex Mitchell, Teresa K. Attwood, Patricia C. Babbitt, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D351-D360
Open Access | Times Cited: 1369
IUPred2A: context-dependent prediction of protein disorder as a function of redox state and protein binding
Bálint Mészáros, Gábor Erdős, Zsuzsanna Dosztányi
Nucleic Acids Research (2018) Vol. 46, Iss. W1, pp. W329-W337
Open Access | Times Cited: 1325
Phase Separation of Zonula Occludens Proteins Drives Formation of Tight Junctions
Oliver Beutel, Riccardo Maraspini, Karina Pombo‐García, et al.
Cell (2019) Vol. 179, Iss. 4, pp. 923-936.e11
Open Access | Times Cited: 375
Nuclear condensates of the Polycomb protein chromobox 2 (CBX2) assemble through phase separation
Roubina Tatavosian, Samantha Kent, Kyle Brown, et al.
Journal of Biological Chemistry (2018) Vol. 294, Iss. 5, pp. 1451-1463
Open Access | Times Cited: 313
Critical assessment of protein intrinsic disorder prediction
Marco Necci, Damiano Piovesan, Md Tamjidul Hoque, et al.
Nature Methods (2021) Vol. 18, Iss. 5, pp. 472-481
Open Access | Times Cited: 282
ELM—the eukaryotic linear motif resource in 2020
Manjeet Kumar, Marc Gouw, Sushama Michael, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 278
SIFTS: updated Structure Integration with Function, Taxonomy and Sequences resource allows 40-fold increase in coverage of structure-based annotations for proteins
Jose M Dana, Aleksandras Gutmanas, Nidhi Tyagi, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D482-D489
Open Access | Times Cited: 232
Modulating biomolecular condensates: a novel approach to drug discovery
Diana M. Mitrea, Matthäus Mittasch, Beatriz Ferreira Gomes, et al.
Nature Reviews Drug Discovery (2022) Vol. 21, Iss. 11, pp. 841-862
Open Access | Times Cited: 232
DisProt: intrinsic protein disorder annotation in 2020
András Hatos, Borbála Hajdu-Soltész, Alexander Miguel Monzón, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 224
PhaSepDB: a database of liquid–liquid phase separation related proteins
Kaiqiang You, Qi Huang, Chunyu Yu, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D354-D359
Open Access | Times Cited: 196
Wnt/Beta-Catenin Signaling Regulation and a Role for Biomolecular Condensates
Kristina N. Schaefer, Mark Peifer
Developmental Cell (2019) Vol. 48, Iss. 4, pp. 429-444
Open Access | Times Cited: 185
Metapredict: a fast, accurate, and easy-to-use predictor of consensus disorder and structure
Ryan J. Emenecker, Daniel Griffith, Alex S. Holehouse
Biophysical Journal (2021) Vol. 120, Iss. 20, pp. 4312-4319
Open Access | Times Cited: 185
The ZSWIM8 ubiquitin ligase mediates target-directed microRNA degradation
Charlie Y. Shi, Elena R. Kingston, Benjamin Kleaveland, et al.
Science (2020) Vol. 370, Iss. 6523
Open Access | Times Cited: 184
LLPSDB: a database of proteins undergoing liquid–liquid phase separation in vitro
Qian Li, Xiaojun Peng, Yuanqing Li, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D320-D327
Open Access | Times Cited: 165
DrLLPS: a data resource of liquid–liquid phase separation in eukaryotes
Wanshan Ning, Yaping Guo, Shaofeng Lin, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D288-D295
Open Access | Times Cited: 162
Liquid–Liquid Phase Separation by Intrinsically Disordered Protein Regions of Viruses: Roles in Viral Life Cycle and Control of Virus–Host Interactions
Stefania Brocca, Rita Grandori, Sonia Longhi, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 23, pp. 9045-9045
Open Access | Times Cited: 155
A prion-like protein regulator of seed germination undergoes hydration-dependent phase separation
Yanniv Dorone, Steven Boeynaems, Eduardo Flores, et al.
Cell (2021) Vol. 184, Iss. 16, pp. 4284-4298.e27
Open Access | Times Cited: 148
MobiDB: 10 years of intrinsically disordered proteins
Damiano Piovesan, Alessio Del Conte, Damiano Clementel, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D438-D444
Open Access | Times Cited: 125
PED in 2021: a major update of the protein ensemble database for intrinsically disordered proteins
Tamás Lázár, Elizabeth Martínez‐Pérez, Federica Quaglia, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D404-D411
Open Access | Times Cited: 127
Intrinsically disordered proteins and structured proteins with intrinsically disordered regions have different functional roles in the cell
Antonio Deiana, Sergio Forcelloni, Alessandro Porrello, et al.
PLoS ONE (2019) Vol. 14, Iss. 8, pp. e0217889-e0217889
Open Access | Times Cited: 118
PDBe-KB: a community-driven resource for structural and functional annotations
Mihály Váradi, John M. Berrisford, Mandar Deshpande, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D344-D353
Open Access | Times Cited: 112
Biological Phase Separation and Biomolecular Condensates in Plants
Ryan J. Emenecker, Alex S. Holehouse, Lucia C. Strader
Annual Review of Plant Biology (2021) Vol. 72, Iss. 1, pp. 17-46
Open Access | Times Cited: 104
Pan-retroviral Nucleocapsid-Mediated Phase Separation Regulates Genomic RNA Positioning and Trafficking
Anne Monette, Meijuan Niu, Lois Chen, et al.
Cell Reports (2020) Vol. 31, Iss. 3, pp. 107520-107520
Open Access | Times Cited: 103
Page 1 - Next Page

Scroll to top