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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:

A taxonomy of transcriptomic cell types across the isocortex and hippocampal formation
Zizhen Yao, Cindy T. J. van Velthoven, Thuc Nghi Nguyen, et al.
Cell (2021) Vol. 184, Iss. 12, pp. 3222-3241.e26
Open Access | Times Cited: 807

Showing 1-25 of 807 citing articles:

Cell2location maps fine-grained cell types in spatial transcriptomics
Vitalii Kleshchevnikov, Artem Shmatko, Emma Dann, et al.
Nature Biotechnology (2022) Vol. 40, Iss. 5, pp. 661-671
Closed Access | Times Cited: 694
A multimodal cell census and atlas of the mammalian primary motor cortex
Edward M. Callaway, Hong‐Wei Dong, Joseph R. Ecker, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 86-102
Open Access | Times Cited: 464
Integrated Morphoelectric and Transcriptomic Classification of Cortical GABAergic Cells
Nathan W. Gouwens, Staci A. Sorensen, Fahimeh Baftizadeh, et al.
Cell (2020) Vol. 183, Iss. 4, pp. 935-953.e19
Open Access | Times Cited: 446
A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain
Zizhen Yao, Cindy T. J. van Velthoven, Michael Kunst, et al.
Nature (2023) Vol. 624, Iss. 7991, pp. 317-332
Open Access | Times Cited: 402
Spatially resolved cell atlas of the mouse primary motor cortex by MERFISH
Meng Zhang, Stephen W. Eichhorn, Brian Zingg, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 137-143
Open Access | Times Cited: 366
Morphological diversity of single neurons in molecularly defined cell types
Hanchuan Peng, Peng Xie, Lijuan Liu, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 174-181
Open Access | Times Cited: 295
What is a cell type and how to define it?
Hongkui Zeng
Cell (2022) Vol. 185, Iss. 15, pp. 2739-2755
Open Access | Times Cited: 278
Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells
Daniel Franjic, Mario Škarica, Shaojie Ma, et al.
Neuron (2021) Vol. 110, Iss. 3, pp. 452-469.e14
Open Access | Times Cited: 227
Molecularly defined and spatially resolved cell atlas of the whole mouse brain
Meng Zhang, Xingjie Pan, Won Jung, et al.
Nature (2023) Vol. 624, Iss. 7991, pp. 343-354
Open Access | Times Cited: 213
DNA methylation atlas of the mouse brain at single-cell resolution
Hanqing Liu, Jingtian Zhou, Wei Tian, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 120-128
Open Access | Times Cited: 212
An atlas of cortical arealization identifies dynamic molecular signatures
Aparna Bhaduri, Carmen Sandoval-Espinosa, Marcos Otero-García, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 200-204
Open Access | Times Cited: 206
Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data
Patrick Danaher, Young‐Mi Kim, Brenn Nelson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 199
Single-Cell Sequencing of Brain Cell Transcriptomes and Epigenomes
Ethan J. Armand, Junhao Li, Fangming Xie, et al.
Neuron (2021) Vol. 109, Iss. 1, pp. 11-26
Open Access | Times Cited: 189
Cerebellar nuclei evolved by repeatedly duplicating a conserved cell-type set
Justus M. Kebschull, Ethan B. Richman, Noam Ringach, et al.
Science (2020) Vol. 370, Iss. 6523
Open Access | Times Cited: 185
A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brain
Anoushka Joglekar, Andrey D. Prjibelski, Ahmed Mahfouz, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 184
Single-neuron projectome of mouse prefrontal cortex
Le Gao, Sang Liu, Lingfeng Gou, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 4, pp. 515-529
Closed Access | Times Cited: 172
Multi-omics integration in the age of million single-cell data
Zhen Miao, Benjamin D. Humphreys, Andrew P. McMahon, et al.
Nature Reviews Nephrology (2021) Vol. 17, Iss. 11, pp. 710-724
Open Access | Times Cited: 156
Single-cell and spatial transcriptomics: deciphering brain complexity in health and disease
Monika Piwecka, Nikolaus Rajewsky, Agnieszka Rybak‐Wolf
Nature Reviews Neurology (2023) Vol. 19, Iss. 6, pp. 346-362
Open Access | Times Cited: 151
Brain circuits for pain and its treatment
Nicole Mercer Lindsay, Chong Chen, Gadi Gilam, et al.
Science Translational Medicine (2021) Vol. 13, Iss. 619
Open Access | Times Cited: 144
Standardizing workflows in imaging transcriptomics with the abagen toolbox
Ross D. Markello, Aurina Arnatkevičiūtė, Jean‐Baptiste Poline, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 142
Gene regulation by gonadal hormone receptors underlies brain sex differences
Bruno Gegenhuber, Melody V. Wu, Robert Bronstein, et al.
Nature (2022) Vol. 606, Iss. 7912, pp. 153-159
Open Access | Times Cited: 141
Specialized astrocytes mediate glutamatergic gliotransmission in the CNS
Roberta De Ceglia, Ada Ledonne, David Litvin, et al.
Nature (2023) Vol. 622, Iss. 7981, pp. 120-129
Open Access | Times Cited: 141
Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data
Martin Jinye Zhang, Kangcheng Hou, Kushal K. Dey, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1572-1580
Open Access | Times Cited: 125
A transcriptomic axis predicts state modulation of cortical interneurons
Stéphane Bugeon, Joshua Duffield, Mario Dipoppa, et al.
Nature (2022) Vol. 607, Iss. 7918, pp. 330-338
Open Access | Times Cited: 123
Shared mechanisms across the major psychiatric and neurodegenerative diseases
Thomas S. Wingo, Yue Liu, Ekaterina S. Gerasimov, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 116
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