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:

Transposable Element Domestication As an Adaptation to Evolutionary Conflicts
Diwash Jangam, Cédric Feschotte, Esther Betrán
Trends in Genetics (2017) Vol. 33, Iss. 11, pp. 817-831
Open Access | Times Cited: 230

Showing 1-25 of 230 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

Regulation of transposable elements by DNA modifications
Özgen Deniz, Jennifer M. Frost, Miguel R. Branco
Nature Reviews Genetics (2019) Vol. 20, Iss. 7, pp. 417-431
Open Access | Times Cited: 404

The impact of transposable elements in adaptive evolution
Lukas Schrader, Jürgen Schmitz
Molecular Ecology (2018) Vol. 28, Iss. 6, pp. 1537-1549
Closed Access | Times Cited: 266

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

Transposition favors the generation of large effect mutations that may facilitate rapid adaption
Leandro Quadrana, Mathilde Etcheverry, Arthur Gilly, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 174

The chromatin remodeler DDM1 prevents transposon mobility through deposition of histone variant H2A.W
Akihisa Osakabe, Bhagyshree Jamge, Elin Axelsson, et al.
Nature Cell Biology (2021) Vol. 23, Iss. 4, pp. 391-400
Closed Access | Times Cited: 104

Taming transposable elements in vertebrates: from epigenetic silencing to domestication
Miguel Vasconcelos Almeida, Grégoire Vernaz, Audrey L. K. Putman, et al.
Trends in Genetics (2022) Vol. 38, Iss. 6, pp. 529-553
Closed Access | Times Cited: 97

Horizontal acquisition of transposable elements and viral sequences: patterns and consequences
Clément Gilbert, Cédric Feschotte
Current Opinion in Genetics & Development (2018) Vol. 49, pp. 15-24
Open Access | Times Cited: 139

Transposon molecular domestication and the evolution of the RAG recombinase
Yuhang Zhang, Tat Cheung Cheng, Guangrui Huang, et al.
Nature (2019) Vol. 569, Iss. 7754, pp. 79-84
Open Access | Times Cited: 138

Retrotranspositional landscape of Asian rice revealed by 3000 genomes
Marie‐Christine Carpentier, Ernandes Manfroi, Fu‐Jin Wei, et al.
Nature Communications (2018) Vol. 10, Iss. 1
Open Access | Times Cited: 129

Evolution of the RNA N6-Methyladenosine Methylome Mediated by Genomic Duplication
Zhenyan Miao, Ting Zhang, Yuhong Qi, et al.
PLANT PHYSIOLOGY (2019) Vol. 182, Iss. 1, pp. 345-360
Open Access | Times Cited: 120

On the Population Dynamics of Junk: A Review on the Population Genomics of Transposable Elements
Yann Bourgeois, Stéphane Boissinot
Genes (2019) Vol. 10, Iss. 6, pp. 419-419
Open Access | Times Cited: 119

Plant Pan-Genomics Comes of Age
Lei Li, Eugene Goltsman, David Goodstein, et al.
Annual Review of Plant Biology (2021) Vol. 72, Iss. 1, pp. 411-435
Closed Access | Times Cited: 77

Transposable element-derived sequences in vertebrate development
Ema Etchegaray, Magali Naville, Jean‐Nicolas Volff, et al.
Mobile DNA (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 65

Transposon-triggered innate immune response confers cancer resistance to the blind mole rat
Yang Zhao, Ena Oreskovic, Quanwei Zhang, et al.
Nature Immunology (2021) Vol. 22, Iss. 10, pp. 1219-1230
Open Access | Times Cited: 61

Parallel pathways for recruiting effector proteins determine centromere drive and suppression
Tomohiro Kumon, Jun Ma, R. Brian Akins, et al.
Cell (2021) Vol. 184, Iss. 19, pp. 4904-4918.e11
Open Access | Times Cited: 60

The Structural, Functional and Evolutionary Impact of Transposable Elements in Eukaryotes
Dareen Almojil, Yann Bourgeois, Marcin Falis, et al.
Genes (2021) Vol. 12, Iss. 6, pp. 918-918
Open Access | Times Cited: 59

Mammalian genome innovation through transposon domestication
A Modzelewski, Johnny Gan Chong, Ting Wang, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 9, pp. 1332-1340
Open Access | Times Cited: 58

Epigenetic Reprogramming in Early Animal Development
Zhenhai Du, Ke Zhang, Wei Xie
Cold Spring Harbor Perspectives in Biology (2021) Vol. 14, Iss. 6, pp. a039677-a039677
Open Access | Times Cited: 57

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

Mammalian PIWI–piRNA–target complexes reveal features for broad and efficient target silencing
Zhiqing Li, Zhenzhen Li, Yuqi Zhang, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 8, pp. 1222-1231
Closed Access | Times Cited: 12

Transposable Elements Adaptive Role in Genome Plasticity, Pathogenicity and Evolution in Fungal Phytopathogens
Nurhani Mat Razali, Boon Huat Cheah, Kalaivani Nadarajah
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 14, pp. 3597-3597
Open Access | Times Cited: 75

Exaptation of transposable element coding sequences
Zoé Joly‐Lopez, Thomas E. Bureau
Current Opinion in Genetics & Development (2018) Vol. 49, pp. 34-42
Closed Access | Times Cited: 73

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