OpenAlex Citation Counts

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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:

Toxic PR Poly-Dipeptides Encoded by the C9orf72 Repeat Expansion Target LC Domain Polymers
Yi Lin, Eiichiro Mori, Masato Kato, et al.
Cell (2016) Vol. 167, Iss. 3, pp. 789-802.e12
Open Access | Times Cited: 431

Showing 26-50 of 431 citing articles:

Functional Implications of Intracellular Phase Transitions
Alex S. Holehouse, Rohit V. Pappu
Biochemistry (2018) Vol. 57, Iss. 17, pp. 2415-2423
Open Access | Times Cited: 237

Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions
Julia K. Nussbacher, Ricardos Tabet, G Yeo, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 294-320
Open Access | Times Cited: 230

FUS and TDP-43 Phases in Health and Disease
Bede Portz, Bo Lim Lee, James Shorter
Trends in Biochemical Sciences (2021) Vol. 46, Iss. 7, pp. 550-563
Open Access | Times Cited: 230

Toxic PR n poly-dipeptides encoded by the C9orf72 repeat expansion block nuclear import and export
Kevin Shi, Eiichiro Mori, Zehra F. Nizami, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 7
Open Access | Times Cited: 226

A gel phase promotes condensation of liquid P granules in Caenorhabditis elegans embryos
Andrea Putnam, Madeline Cassani, Jarrett Smith, et al.
Nature Structural & Molecular Biology (2019) Vol. 26, Iss. 3, pp. 220-226
Open Access | Times Cited: 225

CRISPR–Cas9 screens in human cells and primary neurons identify modifiers of C9ORF72 dipeptide-repeat-protein toxicity
Nicholas J. Kramer, Michael S. Haney, David W. Morgens, et al.
Nature Genetics (2018) Vol. 50, Iss. 4, pp. 603-612
Open Access | Times Cited: 222

Clusters of bacterial RNA polymerase are biomolecular condensates that assemble through liquid–liquid phase separation
Anne‐Marie Ladouceur, Baljyot Parmar, Stefan Biedzinski, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 31, pp. 18540-18549
Open Access | Times Cited: 208

RNA-binding proteins in neurodegeneration: mechanisms in aggregate
Erin G. Conlon, James L. Manley
Genes & Development (2017) Vol. 31, Iss. 15, pp. 1509-1528
Open Access | Times Cited: 204

C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation
Weiwei Cheng, Shaopeng Wang, Alexander A. Mestre, et al.
Nature Communications (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 195

Phase Separation of Intrinsically Disordered Proteins
Ammon E. Posey, Alex S. Holehouse, Rohit V. Pappu
Methods in enzymology on CD-ROM/Methods in enzymology (2018), pp. 1-30
Closed Access | Times Cited: 194

Bridging biophysics and neurology: aberrant phase transitions in neurodegenerative disease
Natalia B. Nedelsky, J. Paul Taylor
Nature Reviews Neurology (2019) Vol. 15, Iss. 5, pp. 272-286
Closed Access | Times Cited: 187

Biological phase separation: cell biology meets biophysics
Takuya Yoshizawa, Ryu‐Suke Nozawa, Tony Z. Jia, et al.
Biophysical Reviews (2020) Vol. 12, Iss. 2, pp. 519-539
Open Access | Times Cited: 176

C9orf72 Poly(PR) Dipeptide Repeats Disturb Biomolecular Phase Separation and Disrupt Nucleolar Function
Michael R. White, Diana M. Mitrea, Peipei Zhang, et al.
Molecular Cell (2019) Vol. 74, Iss. 4, pp. 713-728.e6
Open Access | Times Cited: 174

Bridging-induced phase separation induced by cohesin SMC protein complexes
Je‐Kyung Ryu, Céline Bouchoux, Hon Wing Liu, et al.
Science Advances (2021) Vol. 7, Iss. 7
Open Access | Times Cited: 145

1,6-Hexanediol, commonly used to dissolve liquid–liquid phase separated condensates, directly impairs kinase and phosphatase activities
Robert Düster, Ines H. Kaltheuner, Maximilian Schmitz, et al.
Journal of Biological Chemistry (2021) Vol. 296, pp. 100260-100260
Open Access | Times Cited: 128

Selective sorting of microRNAs into exosomes by phase-separated YBX1 condensates
Xiao‐Man Liu, Liang Ma, Randy Schekman
eLife (2021) Vol. 10
Open Access | Times Cited: 112

A brief guideline for studies of phase-separated biomolecular condensates
Yifei Gao, Xi Li, Pilong Li, et al.
Nature Chemical Biology (2022) Vol. 18, Iss. 12, pp. 1307-1318
Closed Access | Times Cited: 107

Mutations linked to neurological disease enhance self-association of low-complexity protein sequences
Xiaoming Zhou, Lily Sumrow, Kyuto Tashiro, et al.
Science (2022) Vol. 377, Iss. 6601
Open Access | Times Cited: 76

Bacteria require phase separation for fitness in the mammalian gut
Emilia Krypotou, Guy E. Townsend, Xiaohui Gao, et al.
Science (2023) Vol. 379, Iss. 6637, pp. 1149-1156
Open Access | Times Cited: 59

Vimentin filaments integrate low-complexity domains in a complex helical structure
Matthias Eibauer, Miriam S. Weber, Rafael Kronenberg‐Tenga, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 6, pp. 939-949
Open Access | Times Cited: 31

Signal-induced NLRP3 phase separation initiates inflammasome activation
Guijin Zou, Young Tang, Jie Yang, et al.
Cell Research (2025)
Open Access | Times Cited: 2

Dysregulated molecular pathways in amyotrophic lateral sclerosis–frontotemporal dementia spectrum disorder
Fen‐Biao Gao, Sandra Almeida, Rodrigo López‐González
The EMBO Journal (2017) Vol. 36, Iss. 20, pp. 2931-2950
Open Access | Times Cited: 166

Methods for Physical Characterization of Phase-Separated Bodies and Membrane-less Organelles
Diana M. Mitrea, Bappaditya Chandra, Mylene C. Ferrolino, et al.
Journal of Molecular Biology (2018) Vol. 430, Iss. 23, pp. 4773-4805
Open Access | Times Cited: 151

Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells
Mikołaj Ogrodnik, Hanna Salmonowicz, Vadim N. Gladyshev
Aging Cell (2018) Vol. 18, Iss. 1
Open Access | Times Cited: 150

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