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:

Distinct molecular programs regulate synapse specificity in cortical inhibitory circuits
Emilia Favuzzi, Rubén Deogracias, André Marques–Smith, et al.
Science (2019) Vol. 363, Iss. 6425, pp. 413-417
Open Access | Times Cited: 213

Showing 26-50 of 213 citing articles:

Transcriptional and morphological profiling of parvalbumin interneuron subpopulations in the mouse hippocampus
Lin Que, David Lukacsovich, Wenshu Luo, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 51

Microglia regulate chandelier cell axo-axonic synaptogenesis
Nicholas B. Gallo, Artan Berisha, Linda Van Aelst
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 11
Open Access | Times Cited: 38

Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders
David Exposito-Alonso, Beatriz Rico
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 391-422
Closed Access | Times Cited: 28

Single genomic enhancers drive experience-dependent GABAergic plasticity to maintain sensory processing in the adult cortex
Ori Roethler, Eran Zohar, Katayun Cohen-Kashi Malina, et al.
Neuron (2023) Vol. 111, Iss. 17, pp. 2693-2708.e8
Open Access | Times Cited: 19

Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons
Chad R. Camp, Anna Vlachos, Chiara Klöckner, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 19

LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neurons
Baptiste Libé‐Philippot, Amélie Lejeune, Keimpe Wierda, et al.
Cell (2023) Vol. 186, Iss. 26, pp. 5766-5783.e25
Open Access | Times Cited: 18

Oligodendrocyte-derived LGI3 and its receptor ADAM23 organize juxtaparanodal Kv1 channel clustering for short-term synaptic plasticity
Yuri Miyazaki, Takeshi Otsuka, Yoko Yamagata, et al.
Cell Reports (2024) Vol. 43, Iss. 1, pp. 113634-113634
Open Access | Times Cited: 7

Spatial and temporal pattern of structure–function coupling of human brain connectome with development
Guozheng Feng, Yiwen Wang, Weijie Huang, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 7

Shedding Light on Chandelier Cell Development, Connectivity, and Contribution to Neural Disorders
Nicholas B. Gallo, Anirban Paul, Linda Van Aelst
Trends in Neurosciences (2020) Vol. 43, Iss. 8, pp. 565-580
Open Access | Times Cited: 44

The essence of the engram: Cellular or synaptic?
Dae Hee Han, Pojeong Park, Dong Il Choi, et al.
Seminars in Cell and Developmental Biology (2021) Vol. 125, pp. 122-135
Open Access | Times Cited: 40

Enkephalin release from VIP interneurons in the hippocampal CA2/3a region mediates heterosynaptic plasticity and social memory
Félix Leroy, Christopher A. de Solis, Lara M. Boyle, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 6, pp. 2879-2900
Open Access | Times Cited: 36

Targeted proteoform mapping uncovers specific Neurexin-3 variants required for dendritic inhibition
David Hauser, Katharina Behr, Kohtarou Konno, et al.
Neuron (2022) Vol. 110, Iss. 13, pp. 2094-2109.e10
Open Access | Times Cited: 28

Identification of visual cortex cell types and species differences using single-cell RNA sequencing
Jia-Ru Wei, Zhao-Zhe Hao, Chuan Xu, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 28

Origin, Development, and Synaptogenesis of Cortical Interneurons
Alfredo Llorca, Rubén Deogracias
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 26

Activated somatostatin interneurons orchestrate memory microcircuits
TaeHyun Kim, Dong Il Choi, Ja Eun Choi, et al.
Neuron (2023) Vol. 112, Iss. 2, pp. 201-208.e4
Closed Access | Times Cited: 15

Cerebellin–neurexin complexes instructing synapse properties
Thomas C. Südhof
Current Opinion in Neurobiology (2023) Vol. 81, pp. 102727-102727
Open Access | Times Cited: 14

GluD1 binds GABA and controls inhibitory plasticity
Laura Piot, Christina Heroven, Simon Bossi, et al.
Science (2023) Vol. 382, Iss. 6677, pp. 1389-1394
Closed Access | Times Cited: 14

Astrocyte-Secreted Neurocan Controls Inhibitory Synapse Formation and Function
Dolores Irala, Shiyi Wang, Kristina Sakers, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 13

DSCAM gene triplication causes excessive GABAergic synapses in the neocortex in Down syndrome mouse models
Hao Liu, René N. Caballero-Florán, Ty Hergenreder, et al.
PLoS Biology (2023) Vol. 21, Iss. 4, pp. e3002078-e3002078
Open Access | Times Cited: 13

The role of microglia heterogeneity in synaptic plasticity and brain disorders: Will sequencing shed light on the discovery of new therapeutic targets?
Yi You, Zhong Chen, Weiwei Hu
Pharmacology & Therapeutics (2024) Vol. 255, pp. 108606-108606
Closed Access | Times Cited: 5

Nr4a1 regulates cell-specific transcriptional programs in inhibitory GABAergic interneurons
Min Huang, Simon Pieraut, Jasmine Cao, et al.
Neuron (2024) Vol. 112, Iss. 12, pp. 2031-2044.e7
Closed Access | Times Cited: 5

CTNND2 moderates the pace of synaptic maturation and links human evolution to synaptic neoteny
Nora Assendorp, Matteo Fossati, Baptiste Libé-Philippot, et al.
Cell Reports (2024) Vol. 43, Iss. 10, pp. 114797-114797
Open Access | Times Cited: 5

Robust perisomatic GABAergic self-innervation inhibits basket cells in the human and mouse supragranular neocortex
Viktor Szegedi, Melinda Paizs, Judith Baka, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 36

Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy
Andrew E. Fry, Christopher Marra, Anna V. Derrick, et al.
The American Journal of Human Genetics (2020) Vol. 108, Iss. 1, pp. 176-185
Open Access | Times Cited: 35

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