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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:

Studying Brain Circuit Function with Dynamic Causal Modeling for Optogenetic fMRI
David Bernal‐Casas, Hyun Joo Lee, Andrew J. Weitz, et al.
Neuron (2017) Vol. 93, Iss. 3, pp. 522-532.e5
Open Access | Times Cited: 68

Showing 1-25 of 68 citing articles:

Novel electrode technologies for neural recordings
Guosong Hong, Charles M. Lieber
Nature reviews. Neuroscience (2019) Vol. 20, Iss. 6, pp. 330-345
Open Access | Times Cited: 591
Brain circuit dysfunction in post-traumatic stress disorder: from mouse to man
Robert J. Fenster, Lauren A. M. Lebois, Kerry J. Ressler, et al.
Nature reviews. Neuroscience (2018) Vol. 19, Iss. 9, pp. 535-551
Open Access | Times Cited: 389
Inferring neural signalling directionality from undirected structural connectomes
Caio Seguin, Adeel Razi, Andrew Zalesky
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 101
Solving brain circuit function and dysfunction with computational modeling and optogenetic fMRI
Jin Hyung Lee, Qin Liu, Ehsan Dadgar‐Kiani
Science (2022) Vol. 378, Iss. 6619, pp. 493-499
Open Access | Times Cited: 39
Whole-brain mapping of effective connectivity by fMRI with cortex-wide patterned optogenetics
Seonghoon Kim, Hyun Seok Moon, Thanh Tan Vo, et al.
Neuron (2023) Vol. 111, Iss. 11, pp. 1732-1747.e6
Open Access | Times Cited: 27
The emergence of multiscale connectomics-based approaches in stroke recovery
Shahrzad Latifi, S. Thomas Carmichael
Trends in Neurosciences (2024) Vol. 47, Iss. 4, pp. 303-318
Open Access | Times Cited: 11
Advances in optogenetic and chemogenetic methods to study brain circuits in non-human primates
Adriana Galván, Michael Caiola, Daniel L. Albaugh
Journal of Neural Transmission (2017) Vol. 125, Iss. 3, pp. 547-563
Open Access | Times Cited: 74
Causal evidence for lateral prefrontal cortex dynamics supporting cognitive control
Derek Evan Nee, Mark D’Esposito
eLife (2017) Vol. 6
Open Access | Times Cited: 68
Optogenetic fUSI for brain-wide mapping of neural activity mediating collicular-dependent behaviors
Arnau Sans-Dublanc, Anna Chrzanowska, Katja Reinhard, et al.
Neuron (2021) Vol. 109, Iss. 11, pp. 1888-1905.e10
Open Access | Times Cited: 55
Contribution of Excitatory and Inhibitory Neuronal Activity to BOLD fMRI
Hyun Seok Moon, Haiyan Jiang, Thanh Tan Vo, et al.
Cerebral Cortex (2021)
Open Access | Times Cited: 53
Quantifying the axonal pathways directly stimulated in therapeutic subcallosal cingulate deep brain stimulation
Bryan Lad Howell, Ki Sueng Choi, Kabilar Gunalan, et al.
Human Brain Mapping (2018) Vol. 40, Iss. 3, pp. 889-903
Open Access | Times Cited: 54
Generic dynamic causal modelling: An illustrative application to Parkinson's disease
Bernadette C.M. van Wijk, Hayriye Cagnan, Vladimir Litvak, et al.
NeuroImage (2018) Vol. 181, pp. 818-830
Open Access | Times Cited: 51
Multimodal Functional Neuroimaging by Simultaneous BOLD fMRI and Fiber-Optic Calcium Recordings and Optogenetic Control
Franziska Albers, Lydia Wachsmuth, Timo Mauritz van Alst, et al.
Molecular Imaging and Biology (2017) Vol. 20, Iss. 2, pp. 171-182
Closed Access | Times Cited: 46
Optogenetic fMRI and electrophysiological identification of region-specific connectivity between the cerebellar cortex and forebrain
Katrina Y. Choe, C.F. Sánchez, Neil G. Harris, et al.
NeuroImage (2018) Vol. 173, pp. 370-383
Open Access | Times Cited: 46
Hierarchical Dynamic Causal Modeling of Resting-State fMRI Reveals Longitudinal Changes in Effective Connectivity in the Motor System after Thalamotomy for Essential Tremor
Hae‐Jeong Park, Chongwon Pae, Karl Friston, et al.
Frontiers in Neurology (2017) Vol. 8
Open Access | Times Cited: 43
Comparing dynamic causal models of neurovascular coupling with fMRI and EEG/MEG
Amirhossein Jafarian, Vladimir Litvak, Hayriye Cagnan, et al.
NeuroImage (2020) Vol. 216, pp. 116734-116734
Open Access | Times Cited: 38
Functional and Optogenetic Approaches to Discovering Stable Subtype-Specific Circuit Mechanisms in Depression
Logan Grosenick, Tracey C. Shi, Faith M. Gunning, et al.
Biological Psychiatry Cognitive Neuroscience and Neuroimaging (2019) Vol. 4, Iss. 6, pp. 554-566
Open Access | Times Cited: 37
Individual variability in functional connectivity architecture of the mouse brain
Eyal Bergmann, Xenia Gofman, Alexandra Kavushansky, et al.
Communications Biology (2020) Vol. 3, Iss. 1
Open Access | Times Cited: 37
Structurally informed resting-state effective connectivity recapitulates cortical hierarchy
Matthew D. Greaves, Leonardo Novelli, Adeel Razi
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Optogenetic activation of striatal D1R and D2R cells differentially engages downstream connected areas beyond the basal ganglia
Christina Grimm, Stefan Frässle, Céline Steger, et al.
Cell Reports (2021) Vol. 37, Iss. 13, pp. 110161-110161
Open Access | Times Cited: 24
Optogenetic fMRI for Brain-Wide Circuit Analysis of Sensory Processing
Jeong-Yun Lee, Taeyi You, Choong‐Wan Woo, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12268-12268
Open Access | Times Cited: 17
Mapping effective connectivity by virtually perturbing a surrogate brain
Zixiang Luo, Kaining Peng, Zhichao Liang, et al.
Nature Methods (2025)
Closed Access
Whole-brain effective connectivity of the sensorimotor system using 7T fMRI with electrical microstimulation in non-human primates
Min‐Jun Han, Young Lyun Oh, Yejin Ann, et al.
Progress in Neurobiology (2025), pp. 102760-102760
Open Access
fMRI detects bilateral brain network activation following unilateral chemogenetic activation of direct striatal projection neurons
Yuki Nakamura, Yukari Nakamura, Assunta Pelosi, et al.
NeuroImage (2020) Vol. 220, pp. 117079-117079
Open Access | Times Cited: 26
Mapping the Brain-Wide Network Effects by Optogenetic Activation of the Corpus Callosum
Yi Chen, Filip Sobczak, Patricia Pais‐Roldán, et al.
Cerebral Cortex (2020) Vol. 30, Iss. 11, pp. 5885-5898
Open Access | Times Cited: 26
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