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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:

Restricting retrotransposons: a review
John L. Goodier
Mobile DNA (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 400

Showing 1-25 of 400 citing articles:

Ten things you should know about transposable elements
Guillaume Bourque, Kathleen H. Burns, Mary Gehring, et al.
Genome biology (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 1127
Measuring and interpreting transposable element expression
Sophie Lanciano, Gaël Cristofari
Nature Reviews Genetics (2020) Vol. 21, Iss. 12, pp. 721-736
Open Access | Times Cited: 296
Selective silencing of euchromatic L1s revealed by genome-wide screens for L1 regulators
Nian Liu, Cameron H. Lee, Tomek Swigut, et al.
Nature (2017) Vol. 553, Iss. 7687, pp. 228-232
Open Access | Times Cited: 295
The role of retrotransposable elements in ageing and age-associated diseases
Vera Gorbunova, Andrei Seluanov, Paolo Mita, et al.
Nature (2021) Vol. 596, Iss. 7870, pp. 43-53
Open Access | Times Cited: 293
ALS Genetics: Gains, Losses, and Implications for Future Therapies
Garam Kım, Olivia Gautier, Eduardo Tassoni-Tsuchida, et al.
Neuron (2020) Vol. 108, Iss. 5, pp. 822-842
Open Access | Times Cited: 292
Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of Neuroinflammation
Charles A. Thomas, Leon Tejwani, Cleber A. Trujillo, et al.
Cell stem cell (2017) Vol. 21, Iss. 3, pp. 319-331.e8
Open Access | Times Cited: 276
Roles of transposable elements in the regulation of mammalian transcription
Raquel Fueyo, Julius Judd, Cédric Feschotte, et al.
Nature Reviews Molecular Cell Biology (2022) Vol. 23, Iss. 7, pp. 481-497
Open Access | Times Cited: 259
Host–transposon interactions: conflict, cooperation, and cooption
Rachel Cosby, Ni‐Chen Chang, Cédric Feschotte
Genes & Development (2019) Vol. 33, Iss. 17-18, pp. 1098-1116
Open Access | Times Cited: 254
Mammalian transposable elements and their impacts on genome evolution
Roy N. Platt, Michael W. Vandewege, David A. Ray
Chromosome Research (2018) Vol. 26, Iss. 1-2, pp. 25-43
Open Access | Times Cited: 238
Transposable element expression in tumors is associated with immune infiltration and increased antigenicity
Yu Kong, Christopher M. Rose, Ashley Cass, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 208
The impact of transposable elements on mammalian development
José L. García-Pérez, Thomas J. Widmann, Ian R. Adams
Development (2016) Vol. 143, Iss. 22, pp. 4101-4114
Open Access | Times Cited: 196
Cytoplasmic DNA: sources, sensing, and role in aging and disease
Karl N. Miller, Stella Victorelli, Hanna Salmonowicz, et al.
Cell (2021) Vol. 184, Iss. 22, pp. 5506-5526
Open Access | Times Cited: 188
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons
Elaine Y. Liu, Jenny Russ, Christopher P. Cali, et al.
Cell Reports (2019) Vol. 27, Iss. 5, pp. 1409-1421.e6
Open Access | Times Cited: 184
Transgenic Mouse Models in Cancer Research
Urša Lampreht Tratar, Simon Horvat, Maja Čemažar
Frontiers in Oncology (2018) Vol. 8
Open Access | Times Cited: 181
Effect of aging on stem cells
Abu Ahmed, Matilda H.‐C. Sheng, Samiksha Wasnik, et al.
World Journal of Experimental Medicine (2017) Vol. 7, Iss. 1, pp. 1-1
Open Access | Times Cited: 173
Nanopore Sequencing Enables Comprehensive Transposable Element Epigenomic Profiling
Adam D. Ewing, Nathan Smits, Francisco J. Sánchez‐Luque, et al.
Molecular Cell (2020) Vol. 80, Iss. 5, pp. 915-928.e5
Open Access | Times Cited: 159
DNA methylation enables transposable element-driven genome expansion
Wanding Zhou, Gangning Liang, Peter L. Molloy, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 32, pp. 19359-19366
Open Access | Times Cited: 149
Endogenous retroviruses in the origins and treatment of cancer
Natasha Jansz, Geoffrey J. Faulkner
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 111
Chromatin modifier HUSH co-operates with RNA decay factor NEXT to restrict transposable element expression
William A. Garland, Iris Müller, Mengjun Wu, et al.
Molecular Cell (2022) Vol. 82, Iss. 9, pp. 1691-1707.e8
Open Access | Times Cited: 74
Antiaging agents: safe interventions to slow aging and healthy life span extension
Ji‐Kai Liu
Natural Products and Bioprospecting (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 70
Evolution of bird genomes—a transposon's‐eye view
Aurélie Kapusta, Alexander Suh
Annals of the New York Academy of Sciences (2016) Vol. 1389, Iss. 1, pp. 164-185
Closed Access | Times Cited: 159
Engineered LINE-1 retrotransposition in nondividing human neurons
Ángela Macia, Thomas J. Widmann, Sara R. Heras, et al.
Genome Research (2016) Vol. 27, Iss. 3, pp. 335-348
Open Access | Times Cited: 147
LINE-1 Evasion of Epigenetic Repression in Humans
Francisco J. Sánchez‐Luque, Marie-Jeanne H.C. Kempen, Patricia Gerdes, et al.
Molecular Cell (2019) Vol. 75, Iss. 3, pp. 590-604.e12
Open Access | Times Cited: 137
The Landscape of L1 Retrotransposons in the Human Genome Is Shaped by Pre-insertion Sequence Biases and Post-insertion Selection
Tania Sultana, Dominic van Essen, Oliver Siol, et al.
Molecular Cell (2019) Vol. 74, Iss. 3, pp. 555-570.e7
Open Access | Times Cited: 128
LINE-1 protein localization and functional dynamics during the cell cycle
Paolo Mita, Aleksandra Wudzinska, Xiaoji Sun, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 123
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