Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Methods for mapping 3D chromosome architecture
Rieke Kempfer, Ana Pombo
Nature Reviews Genetics (2019) Vol. 21, Iss. 4, pp. 207-226
Closed Access | Times Cited: 452

Showing 26-50 of 452 citing articles:

Cell type–specific 3D-genome organization and transcription regulation in the brain
Shiwei Liu, Cosmos Yuqi Wang, Pu Zheng, et al.
Science Advances (2025) Vol. 11, Iss. 9
Open Access | Times Cited: 2
Unraveling Hematopoiesis through the Lens of Genomics
L. Alexander Liggett, Vijay G. Sankaran
Cell (2020) Vol. 182, Iss. 6, pp. 1384-1400
Open Access | Times Cited: 122
Impact of Lineage Plasticity to and from a Neuroendocrine Phenotype on Progression and Response in Prostate and Lung Cancers
Mark A. Rubin, Robert G. Bristow, Phillip Thienger, et al.
Molecular Cell (2020) Vol. 80, Iss. 4, pp. 562-577
Open Access | Times Cited: 103
Transcriptional Control of Circadian Rhythms and Metabolism: A Matter of Time and Space
Yong Hoon Kim, Mitchell A Lazar
Endocrine Reviews (2020) Vol. 41, Iss. 5, pp. 707-732
Open Access | Times Cited: 101
Cohesin residency determines chromatin loop patterns
Lorenzo Costantino, Tsung-Han S. Hsieh, Rebecca Lamothe, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 92
CTCF as a boundary factor for cohesin-mediated loop extrusion: evidence for a multi-step mechanism
Anders S. Hansen
Nucleus (2020) Vol. 11, Iss. 1, pp. 132-148
Open Access | Times Cited: 91
Nuclear speckles: dynamic hubs of gene expression regulation
İbrahim Ilik, Tuğçe Aktaş
FEBS Journal (2021) Vol. 289, Iss. 22, pp. 7234-7245
Open Access | Times Cited: 88
Unraveling the 3D Genome Architecture in Plants: Present and Future
Weizhi Ouyang, Dan Xiong, Guoliang Li, et al.
Molecular Plant (2020) Vol. 13, Iss. 12, pp. 1676-1693
Open Access | Times Cited: 73
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
Qingbo Wang, David R. Kelley, Jacob C. Ulirsch, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 72
Loop-extrusion and polymer phase-separation can co-exist at the single-molecule level to shape chromatin folding
Mattia Conte, Ehsan Irani, Andrea M. Chiariello, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 70
High-resolution, genome-wide mapping of positive supercoiling in chromosomes
Monica S. Guo, Ryo Kawamura, Megan L. Littlehale, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 67
Nuclear speckles – a driving force in gene expression
Gabriel P. Faber, Shani Nadav-Eliyahu, Yaron Shav‐Tal
Journal of Cell Science (2022) Vol. 135, Iss. 13
Open Access | Times Cited: 67
Phase separation of DNA: From past to present
John T. King, Anisha Shakya
Biophysical Journal (2021) Vol. 120, Iss. 7, pp. 1139-1149
Open Access | Times Cited: 65
Genome-wide maps of nucleolus interactions reveal distinct layers of repressive chromatin domains
Cristiana Bersaglieri, Jelena Kresoja‐Rakic, Shivani Gupta, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 64
Coming full circle: On the origin and evolution of the looping model for enhancer–promoter communication
Tessa M. Popay, Jesse R. Dixon
Journal of Biological Chemistry (2022) Vol. 298, Iss. 8, pp. 102117-102117
Open Access | Times Cited: 62
Long reads and Hi‐C sequencing illuminate the two‐compartment genome of the model arbuscular mycorrhizal symbiont Rhizophagus irregularis
Gökalp Yildirir, Jana Sperschneider, Mathu Malar C, et al.
New Phytologist (2021) Vol. 233, Iss. 3, pp. 1097-1107
Open Access | Times Cited: 61
Comparison of the Hi-C, GAM and SPRITE methods using polymer models of chromatin
Luca Fiorillo, Francesco Musella, Mattia Conte, et al.
Nature Methods (2021) Vol. 18, Iss. 5, pp. 482-490
Open Access | Times Cited: 59
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: 59
The Nuclear Lamina
Xianrong Wong, Ashley J. Melendez-Perez, Karen L. Reddy
Cold Spring Harbor Perspectives in Biology (2021) Vol. 14, Iss. 2, pp. a040113-a040113
Open Access | Times Cited: 58
Large-scale chromatin reorganization reactivates placenta-specific genes that drive cellular aging
Zunpeng Liu, Qianzhao Ji, Jie Ren, et al.
Developmental Cell (2022) Vol. 57, Iss. 11, pp. 1347-1368.e12
Open Access | Times Cited: 53
The era of 3D and spatial genomics
Britta A. M. Bouwman, Nicola Crosetto, Magda Bienko
Trends in Genetics (2022) Vol. 38, Iss. 10, pp. 1062-1075
Open Access | Times Cited: 53
Integrative genome modeling platform reveals essentiality of rare contact events in 3D genome organizations
Lorenzo Boninsegna, Aslı Yıldırım, Guido Polles, et al.
Nature Methods (2022) Vol. 19, Iss. 8, pp. 938-949
Open Access | Times Cited: 49
Capture-C: a modular and flexible approach for high-resolution chromosome conformation capture
Damien J. Downes, Alastair Smith, Magdalena A. Karpińska, et al.
Nature Protocols (2022) Vol. 17, Iss. 2, pp. 445-475
Open Access | Times Cited: 46
Comparative 3D genome architecture in vertebrates
Diyan Li, Mengnan He, Qianzi Tang, et al.
BMC Biology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 39
Beyond assembly: the increasing flexibility of single-molecule sequencing technology
Paul W. Hook, Winston Timp
Nature Reviews Genetics (2023) Vol. 24, Iss. 9, pp. 627-641
Open Access | Times Cited: 38

Scroll to top