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 diverse network of pericoerulear neurons control arousal states
Andrew T. Luskin, Li Li, Xiaonan Fu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 36
Andrew T. Luskin, Li Li, Xiaonan Fu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 36
Showing 1-25 of 36 citing articles:
Noradrenergic and cholinergic systems take centre stage in neuropsychiatric diseases of ageing
Isabella F. Orlando, James M. Shine, Trevor W. Robbins, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 149, pp. 105167-105167
Open Access | Times Cited: 31
Isabella F. Orlando, James M. Shine, Trevor W. Robbins, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 149, pp. 105167-105167
Open Access | Times Cited: 31
Neuromodulatory control of complex adaptive dynamics in the brain
James M. Shine
Interface Focus (2023) Vol. 13, Iss. 3
Open Access | Times Cited: 24
James M. Shine
Interface Focus (2023) Vol. 13, Iss. 3
Open Access | Times Cited: 24
Cellular composition and circuit organization of the locus coeruleus of adult mice
Andrew McKinney, Ming Hu, Amber Hoskins, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 23
Andrew McKinney, Ming Hu, Amber Hoskins, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 23
Sleep and vigilance states: Embracing spatiotemporal dynamics
Yuval Nir, Luı́s de Lecea
Neuron (2023) Vol. 111, Iss. 13, pp. 1998-2011
Closed Access | Times Cited: 22
Yuval Nir, Luı́s de Lecea
Neuron (2023) Vol. 111, Iss. 13, pp. 1998-2011
Closed Access | Times Cited: 22
Inputs to the locus coeruleus from the periaqueductal gray and rostroventral medulla shape opioid-mediated descending pain modulation
Susan T. Lubejko, Giulia Livrizzi, Stanley A. Buczynski, et al.
Science Advances (2024) Vol. 10, Iss. 17
Open Access | Times Cited: 14
Susan T. Lubejko, Giulia Livrizzi, Stanley A. Buczynski, et al.
Science Advances (2024) Vol. 10, Iss. 17
Open Access | Times Cited: 14
Two types of locus coeruleus norepinephrine neurons drive reinforcement learning
Zhixiao Su, Jeremiah Y. Cohen
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 37
Zhixiao Su, Jeremiah Y. Cohen
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 37
Neuronal diversity of neuropeptide signaling, including galanin, in the mouse locus coeruleus
Martino Caramia, Roman A. Romanov, Spyridon Sideromenos, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 31
Open Access | Times Cited: 17
Martino Caramia, Roman A. Romanov, Spyridon Sideromenos, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 31
Open Access | Times Cited: 17
The gene expression landscape of the human locus coeruleus revealed by single-nucleus and spatially-resolved transcriptomics
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
eLife (2024) Vol. 12
Open Access | Times Cited: 7
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
eLife (2024) Vol. 12
Open Access | Times Cited: 7
A single-vector intersectional AAV strategy for interrogating cellular diversity and brain function
Alex C. Hughes, Brittany G. Pittman, Beisi Xu, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 7, pp. 1400-1410
Closed Access | Times Cited: 7
Alex C. Hughes, Brittany G. Pittman, Beisi Xu, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 7, pp. 1400-1410
Closed Access | Times Cited: 7
A pontomesencephalic PACAPergic pathway underlying panic-like behavioral and somatic symptoms in mice
SukJae Joshua Kang, Jong–Hyun Kim, Dong‐Il Kim, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 1, pp. 90-101
Open Access | Times Cited: 6
SukJae Joshua Kang, Jong–Hyun Kim, Dong‐Il Kim, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 1, pp. 90-101
Open Access | Times Cited: 6
Properties and modulation of excitatory inputs to the locus coeruleus
Kelsey Barcomb, Samantha S. Olah, Matthew J. Kennedy, et al.
The Journal of Physiology (2022) Vol. 600, Iss. 22, pp. 4897-4916
Open Access | Times Cited: 24
Kelsey Barcomb, Samantha S. Olah, Matthew J. Kennedy, et al.
The Journal of Physiology (2022) Vol. 600, Iss. 22, pp. 4897-4916
Open Access | Times Cited: 24
Bidirectional emotional regulation through prefrontal innervation of the locus coeruleus
Mayumi Watanabe, Akira Uematsu, Joshua P. Johansen
Molecular Psychiatry (2025)
Open Access
Mayumi Watanabe, Akira Uematsu, Joshua P. Johansen
Molecular Psychiatry (2025)
Open Access
Activity-dependent constraints on catecholamine signaling
Li Li, Akshay N. Rana, Esther M. Li, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113566-113566
Open Access | Times Cited: 12
Li Li, Akshay N. Rana, Esther M. Li, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113566-113566
Open Access | Times Cited: 12
Neural circuit-selective, multiplexed pharmacological targeting of prefrontal cortex-projecting locus coeruleus neurons drives antinociception
Chao‐Cheng Kuo, Jordan G. McCall
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Chao‐Cheng Kuo, Jordan G. McCall
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Cellular and Circuit Organization of the Locus Coeruleus of Adult Mice
Andrew McKinney, Ming Hu, Amber Hoskins, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 16
Andrew McKinney, Ming Hu, Amber Hoskins, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 16
The gene expression landscape of the human locus coeruleus revealed by single-nucleus and spatially-resolved transcriptomics
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 9
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 9
Bidirectional emotional regulation through prefrontal innervation of the locus coeruleus
Mayumi Watanabe, Akira Uematsu, Joshua P. Johansen
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Mayumi Watanabe, Akira Uematsu, Joshua P. Johansen
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Juxtacellular recordings from identified neurons in the mouse locus coeruleus
Ioannis S. Zouridis, Lisa Schmors, Kathrin Maite Fischer, et al.
European Journal of Neuroscience (2024) Vol. 60, Iss. 1, pp. 3659-3676
Open Access | Times Cited: 2
Ioannis S. Zouridis, Lisa Schmors, Kathrin Maite Fischer, et al.
European Journal of Neuroscience (2024) Vol. 60, Iss. 1, pp. 3659-3676
Open Access | Times Cited: 2
Locus coeruleus noradrenaline depletion and its differential impact on CO2-induced panic and hyperventilation in male and female mice
Gabriel C. Ripamonte, Elisa M. Fonseca, Alana Tercino Frias, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2024) Vol. 134, pp. 111063-111063
Closed Access | Times Cited: 2
Gabriel C. Ripamonte, Elisa M. Fonseca, Alana Tercino Frias, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2024) Vol. 134, pp. 111063-111063
Closed Access | Times Cited: 2
Substance P, NPY, CCK and their receptors in five brain regions in major depressive disorder with transcriptomic analysis of locus coeruleus neurons
Swapnali Barde, Julio Águila, Wen Zhong, et al.
European Neuropsychopharmacology (2023) Vol. 78, pp. 54-63
Open Access | Times Cited: 6
Swapnali Barde, Julio Águila, Wen Zhong, et al.
European Neuropsychopharmacology (2023) Vol. 78, pp. 54-63
Open Access | Times Cited: 6
A Novel Single Vector Intersectional AAV Strategy for Interrogating Cellular Diversity and Brain Function
Alex C. Hughes, Brittany G. Pollard, Beisi Xu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Alex C. Hughes, Brittany G. Pollard, Beisi Xu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Shining light on the noradrenergic system
Emmeraude Tanguay, Sarah-Julie Bouchard, Martin Lévesque, et al.
Neurophotonics (2023) Vol. 10, Iss. 04
Open Access | Times Cited: 3
Emmeraude Tanguay, Sarah-Julie Bouchard, Martin Lévesque, et al.
Neurophotonics (2023) Vol. 10, Iss. 04
Open Access | Times Cited: 3
Localization and neurochemical identity of alpha1-adrenergic receptor-containing elements in the mouse locus coeruleus
Zachary N. M. Luyo, Abigail B. Lawrence, Theodore G. Stathopoulos, et al.
Journal of Chemical Neuroanatomy (2023) Vol. 133, pp. 102343-102343
Open Access | Times Cited: 2
Zachary N. M. Luyo, Abigail B. Lawrence, Theodore G. Stathopoulos, et al.
Journal of Chemical Neuroanatomy (2023) Vol. 133, pp. 102343-102343
Open Access | Times Cited: 2
Endogenous opioids gate the locus coeruleus pain generator
Makenzie R. Norris, Chao‐Cheng Kuo, Samantha S. Dunn, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Makenzie R. Norris, Chao‐Cheng Kuo, Samantha S. Dunn, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
The gene expression landscape of the human locus coeruleus revealed by single-nucleus and spatially-resolved transcriptomics
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Lukas M. Weber, Heena R. Divecha, Matthew N. Tran, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
