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:

Dual recombinase fate mapping reveals a transient cholinergic phenotype in multiple populations of developing glutamatergic neurons
Nailyam Nasirova, Lely A. Quina, Ibis M. Agosto‐Marlin, et al.
The Journal of Comparative Neurology (2019) Vol. 528, Iss. 2, pp. 283-307
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

Molecular and anatomical characterization of parabrachial neurons and their axonal projections
Jordan L. Pauli, Jane Chen, Marcus L. Basiri, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 88

Breathing Rhythm and Pattern and Their Influence on Emotion
Sufyan Ashhad, Kaiwen Kam, Christopher A. Del Negro, et al.
Annual Review of Neuroscience (2022) Vol. 45, Iss. 1, pp. 223-247
Open Access | Times Cited: 84

Xanomeline restores endogenous nicotinic acetylcholine receptor signaling in mouse prefrontal cortex
Saige K. Power, Sridevi Venkatesan, Evelyn K. Lambe
Neuropsychopharmacology (2023) Vol. 48, Iss. 4, pp. 671-682
Open Access | Times Cited: 13

Neurochemistry of the Kölliker‐Fuse nucleus from a respiratory perspective
Adrienn G. Varga, Sebastian N. Maletz, Jordan T. Bateman, et al.
Journal of Neurochemistry (2020) Vol. 156, Iss. 1, pp. 16-37
Open Access | Times Cited: 38

Chrna5 is Essential for a Rapid and Protected Response to Optogenetic Release of Endogenous Acetylcholine in Prefrontal Cortex
Sridevi Venkatesan, Evelyn K. Lambe
Journal of Neuroscience (2020) Vol. 40, Iss. 38, pp. 7255-7268
Open Access | Times Cited: 35

Ontogenetic rules for the molecular diversification of hypothalamic neurons
Marco Benevento, Tomas Hökfelt, Tibor Harkany
Nature reviews. Neuroscience (2022) Vol. 23, Iss. 10, pp. 611-627
Closed Access | Times Cited: 17

Differential Expression of VGLUT2 in Mouse Mesopontine Cholinergic Neurons
Thomas Steinkellner, Ji Hoon Yoo, Thomas S. Hnasko
eNeuro (2019) Vol. 6, Iss. 4, pp. ENEURO.0161-19.2019
Open Access | Times Cited: 28

Heterogeneous expression of dopaminergic markers and Vglut2 in mouse mesodiencephalic dopaminergic nuclei A8–A13
Maxime Fougère, Cornelis Immanuel van der Zouwen, Joël Boutin, et al.
The Journal of Comparative Neurology (2020) Vol. 529, Iss. 7, pp. 1273-1292
Closed Access | Times Cited: 26

Endogenous Acetylcholine and Its Modulation of Cortical Microcircuits to Enhance Cognition
Sridevi Venkatesan, Ha‐Seul Jeoung, Tianhui Chen, et al.
Current topics in behavioral neurosciences (2020), pp. 47-69
Closed Access | Times Cited: 25

Transformation of Our Understanding of Breathing Control by Molecular Tools
Kevin Yackle
Annual Review of Physiology (2022) Vol. 85, Iss. 1, pp. 93-113
Open Access | Times Cited: 15

The organization of cholinergic projections in the visual thalamus of the mouse
Guela Sokhadze, Kyle L. Whyland, Martha E. Bickford, et al.
The Journal of Comparative Neurology (2021) Vol. 530, Iss. 7, pp. 1081-1098
Closed Access | Times Cited: 19

Impact of Prenatal Nicotine Exposure on Placental Function and Respiratory Neural Network Development
Sebastián Beltrán-Castillo, Karina Bravo, Jaime Eugenı́n
Advances in experimental medicine and biology (2023), pp. 233-244
Closed Access | Times Cited: 7

Forebrain and Hindbrain Projecting-neurons Target the Post-inspiratory Complex Cholinergic Neurons
Luíz M. Oliveira, Ana C. Takakura, Thiago S. Moreira
Neuroscience (2021) Vol. 476, pp. 102-115
Closed Access | Times Cited: 14

Alteration of the cholinergic system and motor deficits in cholinergic neuron-specific Dyt1 knockout mice
Yuning Liu, Hong Xing, Wanhui Sheng, et al.
Neurobiology of Disease (2021) Vol. 154, pp. 105342-105342
Open Access | Times Cited: 13

Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing
Angela M. Bard, Lindsay V. Clark, Erdal Coşgun, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Open Access | Times Cited: 1

The α7 and β2 nicotinic acetylcholine receptor subunits regulate apoptosis in the infant hippocampus, and in sudden infant death syndrome (SIDS)
Lauren Luijerink, Arunnjah Vivekanandarajah, Karen A. Waters, et al.
APOPTOSIS (2020) Vol. 25, Iss. 7-8, pp. 574-589
Closed Access | Times Cited: 10

Enhanced prefrontal nicotinic signaling as evidence of active compensation in Alzheimer’s disease models
Saige K. Power, Sridevi Venkatesan, Sarah Qu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3

Differential Subcellular Distribution and Release Dynamics of Cotransmitted Cholinergic and GABAergic Synaptic Inputs Modify Dopaminergic Neuronal Excitability
Keyrian Louis Le Gratiet, Christopher K. Anderson, Nagore Puente, et al.
Journal of Neuroscience (2022) Vol. 42, Iss. 46, pp. 8670-8693
Closed Access | Times Cited: 4

Afferent and Efferent Connections of the Postinspiratory Complex (PiCo) Revealed by AAV and Monosynaptic Rabies Viral Tracing
Luíz M. Oliveira, Alyssa Huff, Aguan Wei, et al.
The Journal of Comparative Neurology (2024) Vol. 532, Iss. 11
Closed Access

Enhanced prefrontal nicotinic signaling as evidence of active compensation in Alzheimer’s disease models
Saige K. Power, Sridevi Venkatesan, Sarah Qu, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access

Chrna5is essential for a rapid and protected response to optogenetic release of endogenous acetylcholine in prefrontal cortex
Sridevi Venkatesan, Evelyn K. Lambe
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2

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