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:

Optimal Decoding of Cellular Identities in a Genetic Network
Mariela D. Petkova, Gašper Tkačik, William Bialek, et al.
Cell (2019) Vol. 176, Iss. 4, pp. 844-855.e15
Open Access | Times Cited: 166

Showing 1-25 of 166 citing articles:

Gene expression cartography
Mor Nitzan, Nikos Karaiskos, Nir Friedman, et al.
Nature (2019) Vol. 576, Iss. 7785, pp. 132-137
Open Access | Times Cited: 271

Control of Tissue Development by Morphogens
Anna Kicheva, James Briscoe
Annual Review of Cell and Developmental Biology (2023) Vol. 39, Iss. 1, pp. 91-121
Open Access | Times Cited: 61

Precise and scalable self-organization in mammalian pseudo-embryos
Mélody Merle, Leah Friedman, Corinne Chureau, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 6, pp. 896-902
Closed Access | Times Cited: 21

Self-Organization in Pattern Formation
François Schweisguth, Francis Corson
Developmental Cell (2019) Vol. 49, Iss. 5, pp. 659-677
Open Access | Times Cited: 124

Multimodal transcriptional control of pattern formation in embryonic development
Nicholas C Lammers, Vahe Galstyan, Armando Reimer, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 117, Iss. 2, pp. 836-847
Open Access | Times Cited: 98

Escherichia coli chemotaxis is information limited
Henry H. Mattingly, Keita Kamino, Benjamin B. Machta, et al.
Nature Physics (2021) Vol. 17, Iss. 12, pp. 1426-1431
Open Access | Times Cited: 77

Mechanical forces drive a reorientation cascade leading to biofilm self-patterning
Japinder Nijjer, Changhao Li, Qiuting Zhang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 62

Precision of tissue patterning is controlled by dynamical properties of gene regulatory networks
Katherine Exelby, Edgar Herrera-Delgado, Lorena Garcia Perez, et al.
Development (2021) Vol. 148, Iss. 4
Open Access | Times Cited: 60

The many bits of positional information
Gašper Tkačik, Thomas Gregor
Development (2021) Vol. 148, Iss. 2
Open Access | Times Cited: 56

Optogenetic control of the Bicoid morphogen reveals fast and slow modes of gap gene regulation
Anand Pratap Singh, Ping Wu, Sergey Ryabichko, et al.
Cell Reports (2022) Vol. 38, Iss. 12, pp. 110543-110543
Open Access | Times Cited: 38

Deriving a genetic regulatory network from an optimization principle
Thomas R. Sokolowski, Thomas Gregor, William Bialek, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 1
Open Access | Times Cited: 1

Growing Up in a Changing World: Environmental Regulation of Development in Insects
Christen K. Mirth, Timothy E. Saunders, Christopher Amourda
Annual Review of Entomology (2020) Vol. 66, Iss. 1, pp. 81-99
Closed Access | Times Cited: 53

Patterning principles of morphogen gradients
M. Fethullah Simsek, Ertuğrul M. Özbudak
Open Biology (2022) Vol. 12, Iss. 10
Open Access | Times Cited: 31

Precision of morphogen gradients in neural tube development
Roman Vetter, Dagmar Iber
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 29

Geometric control of myosin II orientation during axis elongation
Matthew F Lefebvre, Nikolas H Claussen, Noah Mitchell, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 21

Finding the Last Bits of Positional Information
Lauren McGough, Helena Casademunt, Miloš Nikolić, et al.
PRX Life (2024) Vol. 2, Iss. 1
Open Access | Times Cited: 8

Direct measurement of dynamic attractant gradients reveals breakdown of the Patlak–Keller–Segel chemotaxis model
Trung V. Phan, Henry H. Mattingly, Lam Vo, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 3
Open Access | Times Cited: 6

Optogenetic control of Nodal signaling patterns
Harold M. McNamara, Bill Jia, Alison Guyer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6

Shaping Organs: Shared Structural Principles Across Kingdoms
Olivier Hamant, Timothy E. Saunders
Annual Review of Cell and Developmental Biology (2020) Vol. 36, Iss. 1, pp. 385-410
Open Access | Times Cited: 48

Information-theoretic analysis of multivariate single-cell signaling responses
Tomasz Jetka, Karol Nienałtowski, Tomasz Winarski, et al.
PLoS Computational Biology (2019) Vol. 15, Iss. 7, pp. e1007132-e1007132
Open Access | Times Cited: 46

Zygotic pioneer factor activity of Odd-paired/Zic is necessary for late function of the Drosophila segmentation network
Isabella V. Soluri, Lauren M Zumerling, Omar A. Payán Parra, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 46

Does new physics lurk inside living matter?
Paul Davies
Physics Today (2020) Vol. 73, Iss. 8, pp. 34-40
Closed Access | Times Cited: 43

Bridging scales in a multiscale pattern-forming system
Laeschkir Würthner, Fridtjof Brauns, Grzegorz Pawlik, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 33
Open Access | Times Cited: 27

Aster repulsion drives short-ranged ordering in the Drosophila syncytial blastoderm
Jorge de‐Carvalho, Sham Tlili, Lars Hufnagel, et al.
Development (2022) Vol. 149, Iss. 2
Open Access | Times Cited: 27

Page 1 - Next Page

Scroll to top