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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:

Coupling chromatin structure and dynamics by live super-resolution imaging
Roman Barth, Kerstin Bystricky, Haitham A. Shaban
Science Advances (2020) Vol. 6, Iss. 27
Open Access | Times Cited: 81

Showing 26-50 of 81 citing articles:

Nanoscale analysis of human G1 and metaphase chromatin in situ
Jon K. Chen, Tingsheng Liu, Shujun Cai, et al.
The EMBO Journal (2025)
Open Access
Navigating the crowd: visualizing coordination between genome dynamics, structure, and transcription
Haitham A. Shaban, Roman Barth, Kerstin Bystricky
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 30
Peptide‐PAINT Using a Transfected‐Docker Enables Live‐ and Fixed‐Cell Super‐Resolution Imaging
Barun Kumar Maity, Duncan Nall, Yongjae Lee, et al.
Small Methods (2023) Vol. 7, Iss. 4
Open Access | Times Cited: 10
Ras isoform-specific expression, chromatin accessibility, and signaling
Ruth Nussinov, Mingzhen Zhang, Ryan Maloney, et al.
Biophysical Reviews (2021) Vol. 13, Iss. 4, pp. 489-505
Open Access | Times Cited: 21
Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
Dennis May, Sangwon Yun, David G. Gonzalez, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 9
Super-resolution visualization of chromatin loop folding in human lymphoblastoid cells using interferometric photoactivated localization microscopy
Zofia Parteka-Tojek, Jacqueline Jufen Zhu, Byoungkoo Lee, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 14
Nanoscale analysis of human G1 and metaphase chromatinin situ
Jon K. Chen, Tingsheng Liu, Shujun Cai, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Genome-wide analysis of the biophysical properties of chromatin and nuclear proteins in living cells with Hi-D
César Augusto Valades-Cruz, Roman Barth, Marwan Abdellah, et al.
Nature Protocols (2024)
Closed Access | Times Cited: 2
Deciphering the Complexity of 3D Chromatin Organization Driving Lymphopoiesis and Lymphoid Malignancies
Laurianne Scourzic, Eralda Salataj, Effie Apostolou
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 13
Probing Chromatin Compaction and Its Epigenetic States in situ With Single-Molecule Localization-Based Super-Resolution Microscopy
Jianquan Xu, Yang Liu
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 13
A machine learning approach to elucidating PFOS-induced alterations of repressive epigenetic marks in kidney cancer cells with single-cell imaging
Wenjie Liu, Xiaohui Zhang, Yi Wen, et al.
Environmental Advances (2023) Vol. 11, pp. 100344-100344
Open Access | Times Cited: 5
Fluorescence-based super-resolution-microscopy strategies for chromatin studies
T.C.Q. Burgers, Rifka Vlijm
Chromosoma (2023) Vol. 132, Iss. 3, pp. 191-209
Open Access | Times Cited: 5
Dynamics as a cause for the nanoscale organization of the genome
Roman Barth, Geneviève Fourel, Haitham A. Shaban
Nucleus (2020) Vol. 11, Iss. 1, pp. 83-98
Open Access | Times Cited: 14
Nano-Surveillance: Tracking Individual Molecules in a Sea of Chromatin
Daniël P. Melters, Yamini Dalal
Journal of Molecular Biology (2020) Vol. 433, Iss. 6, pp. 166720-166720
Open Access | Times Cited: 12
Characterization of network hierarchy reflects cell state specificity in genome organization
Jingyao Wang, Yue Xue, Yueying He, et al.
Genome Research (2023) Vol. 33, Iss. 2, pp. 247-260
Open Access | Times Cited: 4
Sequence-specific DNA labelling for fluorescence microscopy
Shalini Pradhan, Sinem Apaydın, Jonas Bucevičius, et al.
Biosensors and Bioelectronics (2023) Vol. 230, pp. 115256-115256
Open Access | Times Cited: 4
Multi-Scale Imaging of the Dynamic Organization of Chromatin
Fabiola García Fernández, Sébastien Huet, Judith Miné-Hattab
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 21, pp. 15975-15975
Open Access | Times Cited: 4
Nuclear blebs are associated with destabilized chromatin packing domains
Emily M. Pujadas-Liwag, Nicolas Acosta, Luay M. Almassalha, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Tracing the Chromatin: From 3C to Live-Cell Imaging
Arianna N. Lacen, Hui-Ting Lee
Chemical & Biomedical Imaging (2024) Vol. 2, Iss. 10, pp. 659-682
Open Access | Times Cited: 1
Shear flow as a tool to distinguish microscopic activities of molecular machines in a chromatin loop
Sandeep Kumar, Ranjith Padinhateeri, Snigdha Thakur
Soft Matter (2024) Vol. 20, Iss. 32, pp. 6500-6506
Open Access | Times Cited: 1
Recent advancements in CRISPR-Cas toolbox for imaging applications
Vikram Singh, Mukesh Jain
Critical Reviews in Biotechnology (2021), pp. 1-24
Open Access | Times Cited: 10
Characterizing locus specific chromatin structure and dynamics with correlative conventional and super-resolution imaging in living cells
Dushyant Mehra, Santosh Adhikari, Chiranjib Banerjee, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 13, pp. e78-e78
Open Access | Times Cited: 7
Monitoring global chromatin dynamics in response to DNA damage
Haitham A. Shaban, Andrew Seeber
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (2020) Vol. 821, pp. 111707-111707
Closed Access | Times Cited: 10
The interplay of chromatin phase separation and lamina interactions in nuclear organization
Rabia Laghmach, Michele Di Pierro, Davit A. Potoyan
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 9
Spatially coherent diffusion of human RNA Pol II depends on transcriptional state rather than chromatin motion
Roman Barth, Haitham A. Shaban
Nucleus (2022) Vol. 13, Iss. 1, pp. 196-204
Open Access | Times Cited: 6

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