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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:

GAF is essential for zygotic genome activation and chromatin accessibility in the early Drosophila embryo
Marissa M Gaskill, Tyler J. Gibson, Elizabeth D. Larson, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 113

Showing 1-25 of 113 citing articles:

Genome organization controls transcriptional dynamics during development
Philippe Batut, Xinyang Bing, Zachary Sisco, et al.
Science (2022) Vol. 375, Iss. 6580, pp. 566-570
Open Access | Times Cited: 183
Pioneer factors as master regulators of the epigenome and cell fate
Aurélio Balsalobre, Jacques Drouin
Nature Reviews Molecular Cell Biology (2022) Vol. 23, Iss. 7, pp. 449-464
Closed Access | Times Cited: 180
Transcriptional coupling of distant regulatory genes in living embryos
Michal Levo, João Raimundo, Xinyang Bing, et al.
Nature (2022) Vol. 605, Iss. 7911, pp. 754-760
Open Access | Times Cited: 127
Zygotic genome activation by the totipotency pioneer factor Nr5a2
Johanna Gassler, Wataru Kobayashi, Imre Gáspár, et al.
Science (2022) Vol. 378, Iss. 6626, pp. 1305-1315
Open Access | Times Cited: 98
OBOX regulates mouse zygotic genome activation and early development
Shu‐Yan Ji, Fengling Chen, Paula Stein, et al.
Nature (2023) Vol. 620, Iss. 7976, pp. 1047-1053
Open Access | Times Cited: 66
Chromatin expansion microscopy reveals nanoscale organization of transcription and chromatin
Mark E. Pownall, Liyun Miao, Charles E. Vejnar, et al.
Science (2023) Vol. 381, Iss. 6653, pp. 92-100
Open Access | Times Cited: 63
Chromosome-level organization of the regulatory genome in the Drosophila nervous system
Giriram Mohana, Julien Dorier, Xiao Li, et al.
Cell (2023) Vol. 186, Iss. 18, pp. 3826-3844.e26
Open Access | Times Cited: 51
GAGA-associated factor fosters loop formation in the Drosophila genome
Xiao Li, Xiaona Tang, Xinyang Bing, et al.
Molecular Cell (2023) Vol. 83, Iss. 9, pp. 1519-1526.e4
Open Access | Times Cited: 47
CLAMP and Zelda function together to promote Drosophila zygotic genome activation
Jingyue Duan, Leila E. Rieder, Megan M Colonnetta, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 72
Pioneering the developmental frontier
Elizabeth D. Larson, Audrey J. Marsh, Melissa M. Harrison
Molecular Cell (2021) Vol. 81, Iss. 8, pp. 1640-1650
Open Access | Times Cited: 62
Kinetic principles underlying pioneer function of GAGA transcription factor in live cells
Xiaona Tang, Taibo Li, Sheng Liu, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 7, pp. 665-676
Open Access | Times Cited: 53
The control of transcriptional memory by stable mitotic bookmarking
Maëlle Bellec, Jérémy Dufourt, George Hunt, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 39
Chromatin accessibility in the Drosophila embryo is determined by transcription factor pioneering and enhancer activation
Kaelan Brennan, Melanie Weilert, Sabrina Krueger, et al.
Developmental Cell (2023) Vol. 58, Iss. 19, pp. 1898-1916.e9
Open Access | Times Cited: 37
Pioneer factors: roles and their regulation in development
Amandine Barral, Kenneth S. Zaret
Trends in Genetics (2023) Vol. 40, Iss. 2, pp. 134-148
Open Access | Times Cited: 36
The miR-430 locus with extreme promoter density forms a transcription body during the minor wave of zygotic genome activation
Yavor Hadzhiev, Lucy Wheatley, Ledean Cooper, et al.
Developmental Cell (2023) Vol. 58, Iss. 2, pp. 155-170.e8
Open Access | Times Cited: 33
CBP and Gcn5 drive zygotic genome activation independently of their catalytic activity
Filippo Ciabrelli, Leily Rabbani, Francesco Cardamone, et al.
Science Advances (2023) Vol. 9, Iss. 16
Open Access | Times Cited: 30
Stepwise modifications of transcriptional hubs link pioneer factor activity to a burst of transcription
Chun-Yi Cho, Patrick H. O’Farrell
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 24
Protein-intrinsic properties and context-dependent effects regulate pioneer factor binding and function
Tyler J. Gibson, Elizabeth D. Larson, Melissa M. Harrison
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 3, pp. 548-558
Open Access | Times Cited: 13
Tissue-specific RNA Polymerase II promoter-proximal pause release and burst kinetics in a Drosophila embryonic patterning network
George Hunt, Roshan Vaid, S. A. Pirogov, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 9
Chromosome structure in Drosophila is determined by boundary pairing not loop extrusion
Xinyang Bing, Wenfan Ke, Miki Fujioka, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 9
GAGA factor: a multifunctional pioneering chromatin protein
Darya Chetverina, Maksim Erokhin, Paul Schedl
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 9, pp. 4125-4141
Open Access | Times Cited: 46
Histone variant H2A.Z regulates zygotic genome activation
Dafne Ibarra-Morales, Michael Rauer, Piergiuseppe Quarato, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 43
Mechanisms of Interaction between Enhancers and Promoters in Three Drosophila Model Systems
Olga Kyrchanova, Vladimir Sokolov, Pavel Georgiev
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 2855-2855
Open Access | Times Cited: 21
Localization of the Drosophila pioneer factor GAF to subnuclear foci is driven by DNA binding and required to silence satellite repeat expression
Marissa M Gaskill, Isabella V. Soluri, Annemarie E. Branks, et al.
Developmental Cell (2023) Vol. 58, Iss. 17, pp. 1610-1624.e8
Open Access | Times Cited: 14
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