Open Access Helper

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:

Condensation of LINE-1 is critical for retrotransposition
Srinjoy Sil, Sarah Keegan, Farida Ettefa, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 19

Showing 19 citing articles:

Molecular determinants of condensate composition
Alex S. Holehouse, Simon Alberti
Molecular Cell (2025) Vol. 85, Iss. 2, pp. 290-308
Open Access | Times Cited: 4
LINE-1 retrotransposition and its deregulation in cancers: implications for therapeutic opportunities
Carlos Mendez‐Dorantes, Kathleen H. Burns
Genes & Development (2023) Vol. 37, Iss. 21-24, pp. 948-967
Open Access | Times Cited: 27
RNA: The Unsuspected Conductor in the Orchestra of Macromolecular Crowding
Elsa Zacco, Laura Broglia, Misuzu Kurihara, et al.
Chemical Reviews (2024) Vol. 124, Iss. 8, pp. 4734-4777
Open Access | Times Cited: 14
Dissolution of ribonucleoprotein condensates by the embryonic stem cell protein L1TD1
Sang Woo Jin, Youngmo Seong, Dayoung Yoon, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 6, pp. 3310-3326
Open Access | Times Cited: 6
RNA and condensates: Disease implications and therapeutic opportunities
Tina W. Han, Bede Portz, Richard A. Young, et al.
Cell chemical biology (2024) Vol. 31, Iss. 9, pp. 1593-1609
Open Access | Times Cited: 5
Retrotransposon LINE-1 bodies in the cytoplasm of piRNA-deficient mouse spermatocytes: Ribonucleoproteins overcoming the integrated stress response
Chiara De Luca, Anuj Gupta, Alex Bortvin
PLoS Genetics (2023) Vol. 19, Iss. 6, pp. e1010797-e1010797
Open Access | Times Cited: 11
Role of Polyadenylation in mRNA Genome Integration via LINE-1 Retrotransposons: An Opinion on mRNA Vaccine Safety
Isidoro Feliciello
Frontiers in Bioscience-Scholar (2025) Vol. 17, Iss. 1
Open Access
LINE-1 transposable element renaissance in aging and age-related diseases
Xiang Li, Huaxin Yu, Dong Li, et al.
Ageing Research Reviews (2024) Vol. 100, pp. 102440-102440
Closed Access | Times Cited: 3
Melatonin: Regulation of Viral Phase Separation and Epitranscriptomics in Post-Acute Sequelae of COVID-19
Doris Loh, Russel J. Reıter
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8122-8122
Open Access | Times Cited: 14
MOV10 recruits DCP2 to decap human LINE‐1 RNA by forming large cytoplasmic granules with phase separation properties
Qian Liu, Dongrong Yi, Jiwei Ding, et al.
EMBO Reports (2023) Vol. 24, Iss. 9
Open Access | Times Cited: 8
LINE-1: an emerging initiator of cGAS-STING signalling and inflammation that is dysregulated in disease
Sabateeshan Mathavarajah, Graham Dellaire
Biochemistry and Cell Biology (2023) Vol. 102, Iss. 1, pp. 38-46
Open Access | Times Cited: 7
From the cauldron of conflict: Endogenous gene regulation by piRNA and other modes of adaptation enabled by selfish transposable elements
Justin P. Blumenstiel
Seminars in Cell and Developmental Biology (2024) Vol. 164, pp. 1-12
Open Access | Times Cited: 2
Synchronous L1 retrotransposition events promote chromosomal crossover early in human tumorigenesis
Sonia Zumalave, Martín Santamarina, Nuria P. Espasandín, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Elevated expression of the retrotransposon LINE-1 drives Alzheimer’s disease-associated microglial dysfunction
Nainika Roy, Imdadul Haq, Jason C. Ngo, et al.
Acta Neuropathologica (2024) Vol. 148, Iss. 1
Open Access | Times Cited: 2
From the genome's perspective: Bearing somatic retrotransposition to leverage the regulatory potential of L1 RNAs
Damiano Mangoni, Anna P. Mazzetti, Federico Ansaloni, et al.
BioEssays (2024)
Open Access | Times Cited: 1
ZCCHC3 is a stress granule zinc knuckle protein that strongly suppresses LINE-1 retrotransposition
John Goodier, Han Wan, Alisha O. Soares, et al.
PLoS Genetics (2023) Vol. 19, Iss. 7, pp. e1010795-e1010795
Open Access | Times Cited: 3
The L1-ORF1p coiled coil enables formation of a tightly compacted nucleic acid-bound complex that is associated with retrotransposition
Ben A Cashen, M. Nabuan Naufer, Michael Morse, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 15, pp. 8690-8699
Open Access | Times Cited: 5
Technology to the rescue: how to uncover the role of transposable elements in preimplantation development
Lauryn A. Deaville, Rebecca V. Berrens
Biochemical Society Transactions (2024) Vol. 52, Iss. 3, pp. 1349-1362
Open Access
A prion-like domain in Gag capsid protein drives retrotransposon particle assembly and mobility
Pascale Lesage, Patrick H. Maxwell
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 35
Open Access
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