
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:
Channelopathies in fragile X syndrome
Pan‐Yue Deng, Vitaly A. Klyachko
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 5, pp. 275-289
Open Access | Times Cited: 86
Pan‐Yue Deng, Vitaly A. Klyachko
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 5, pp. 275-289
Open Access | Times Cited: 86
Showing 1-25 of 86 citing articles:
Fragile X Syndrome: From Molecular Aspect to Clinical Treatment
Dragana Protić, Ramkumar Aishworiya, María Jimena Salcedo‐Arellano, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 4, pp. 1935-1935
Open Access | Times Cited: 61
Dragana Protić, Ramkumar Aishworiya, María Jimena Salcedo‐Arellano, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 4, pp. 1935-1935
Open Access | Times Cited: 61
Hyperexcitability and Homeostasis in Fragile X Syndrome
Xiaopeng Liu, Vipendra Kumar, Nien‐Pei Tsai, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 14
Open Access | Times Cited: 40
Xiaopeng Liu, Vipendra Kumar, Nien‐Pei Tsai, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 14
Open Access | Times Cited: 40
The multifaceted role of Fragile X-Related Protein 1 (FXR1) in cellular processes: an updated review on cancer and clinical applications
Faiz Ali Khan, Na Fang, Weijuan Zhang, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Faiz Ali Khan, Na Fang, Weijuan Zhang, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Ca2+- and Voltage-Activated K+ (BK) Channels in the Nervous System: One Gene, a Myriad of Physiological Functions
Carlos Ancatén-González, Ignacio Segura, Rosangelina Alvarado-Sánchez, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3407-3407
Open Access | Times Cited: 22
Carlos Ancatén-González, Ignacio Segura, Rosangelina Alvarado-Sánchez, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3407-3407
Open Access | Times Cited: 22
Potassium channelopathies associated with epilepsy-related syndromes and directions for therapeutic intervention
Valentin K. Gribkoff, Raymond J. Winquist
Biochemical Pharmacology (2023) Vol. 208, pp. 115413-115413
Closed Access | Times Cited: 19
Valentin K. Gribkoff, Raymond J. Winquist
Biochemical Pharmacology (2023) Vol. 208, pp. 115413-115413
Closed Access | Times Cited: 19
Genetic modifiers of repeat expansion disorders
Sangeerthana Rajagopal, Jasmine Donaldson, Michael Flower, et al.
Emerging Topics in Life Sciences (2023) Vol. 7, Iss. 3, pp. 325-337
Open Access | Times Cited: 19
Sangeerthana Rajagopal, Jasmine Donaldson, Michael Flower, et al.
Emerging Topics in Life Sciences (2023) Vol. 7, Iss. 3, pp. 325-337
Open Access | Times Cited: 19
Large conductance voltage-and calcium-activated K+ (BK) channel in health and disease
Felipe Echeverría, Naileth González-Sanabria, Rosangelina Alvarado-Sánchez, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 8
Felipe Echeverría, Naileth González-Sanabria, Rosangelina Alvarado-Sánchez, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 8
Neocortical localization and thalamocortical modulation of neuronal hyperexcitability contribute to Fragile X Syndrome
Ernest V. Pedapati, Lauren Schmitt, Lauren E. Ethridge, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 27
Ernest V. Pedapati, Lauren Schmitt, Lauren E. Ethridge, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 27
BK Channelopathies and KCNMA1-Linked Disease Models
Andrea L. Meredith
Annual Review of Physiology (2023) Vol. 86, Iss. 1, pp. 277-300
Closed Access | Times Cited: 16
Andrea L. Meredith
Annual Review of Physiology (2023) Vol. 86, Iss. 1, pp. 277-300
Closed Access | Times Cited: 16
Astrocytes mediate cell non-autonomous correction of aberrant firing in human FXS neurons
Shreya Das Sharma, K. R. Bharath Kumar Reddy, Rakhi Pal, et al.
Cell Reports (2023) Vol. 42, Iss. 4, pp. 112344-112344
Open Access | Times Cited: 15
Shreya Das Sharma, K. R. Bharath Kumar Reddy, Rakhi Pal, et al.
Cell Reports (2023) Vol. 42, Iss. 4, pp. 112344-112344
Open Access | Times Cited: 15
The enigmatic HCN channels: A cellular neurophysiology perspective
Poonam Mishra, Rishikesh Narayanan
Proteins Structure Function and Bioinformatics (2023) Vol. 93, Iss. 1, pp. 72-92
Open Access | Times Cited: 12
Poonam Mishra, Rishikesh Narayanan
Proteins Structure Function and Bioinformatics (2023) Vol. 93, Iss. 1, pp. 72-92
Open Access | Times Cited: 12
Roles of Rac1-Dependent Intrinsic Forgetting in Memory-Related Brain Disorders: Demon or Angel
Wei Wang, Zixu Wang, Jing Cao, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 10736-10736
Open Access | Times Cited: 11
Wei Wang, Zixu Wang, Jing Cao, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 10736-10736
Open Access | Times Cited: 11
Early expression of GluN2A-containing NMDA receptors in a model of fragile X syndrome
Tue G. Banke, Stephen F. Traynelis, Andrés Barría
Journal of Neurophysiology (2024) Vol. 131, Iss. 4, pp. 768-777
Closed Access | Times Cited: 4
Tue G. Banke, Stephen F. Traynelis, Andrés Barría
Journal of Neurophysiology (2024) Vol. 131, Iss. 4, pp. 768-777
Closed Access | Times Cited: 4
Neurophysiological effects of a combined treatment of lovastatin and minocycline in patients with fragile X syndrome: Ancillary results of the LOVAMIX randomized clinical trial
Florence Morin‐Parent, Camille Champigny, Samantha Côté, et al.
Autism Research (2024) Vol. 17, Iss. 9, pp. 1944-1956
Open Access | Times Cited: 4
Florence Morin‐Parent, Camille Champigny, Samantha Côté, et al.
Autism Research (2024) Vol. 17, Iss. 9, pp. 1944-1956
Open Access | Times Cited: 4
Brain Network Alterations in Fragile X Syndrome
Flavia Venetucci Gouveia, Jürgen Gernmann, George M. Ibrahim
Neuroscience & Biobehavioral Reviews (2025), pp. 106101-106101
Closed Access
Flavia Venetucci Gouveia, Jürgen Gernmann, George M. Ibrahim
Neuroscience & Biobehavioral Reviews (2025), pp. 106101-106101
Closed Access
mGluR5 Negative Modulators for Fragile X: Treatment Resistance and Persistence
David C. Stoppel, Patrick K. McCamphill, Rebecca K. Senter, et al.
Frontiers in Psychiatry (2021) Vol. 12
Open Access | Times Cited: 26
David C. Stoppel, Patrick K. McCamphill, Rebecca K. Senter, et al.
Frontiers in Psychiatry (2021) Vol. 12
Open Access | Times Cited: 26
Phenotypic variability to medication management: an update on fragile X syndrome
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 10
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 10
Neuronal potassium channel activity triggers initiation of mRNA translation through binding of translation regulators
Taylor J. Malone, Jing Wu, Yalan Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Taylor J. Malone, Jing Wu, Yalan Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
FMRP Regulates Neuronal RNA Granules Containing Stalled Ribosomes, Not Where Ribosomes Stall
Jewel T-Y. Li, Mehdi Amiri, Senthilkumar Kailasam, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Jewel T-Y. Li, Mehdi Amiri, Senthilkumar Kailasam, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
FMRP Controls Neuronal Architecture and Synaptic Content of NMDA Receptors in Cultured Hippocampal Neurons
Elisa Corti, Carlos B. Duarte
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 2
Open Access
Elisa Corti, Carlos B. Duarte
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 2
Open Access
Altered integration of excitatory inputs onto the basal dendrites of layer 5 pyramidal neurons in a mouse model of Fragile X syndrome
Diana Mitchell, Soledad Miranda‐Rottmann, Maxime G. Blanchard, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 2
Open Access | Times Cited: 9
Diana Mitchell, Soledad Miranda‐Rottmann, Maxime G. Blanchard, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 2
Open Access | Times Cited: 9
Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome
Cristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9206-9206
Open Access | Times Cited: 9
Cristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9206-9206
Open Access | Times Cited: 9
Plasticity manifolds and degeneracy govern circadian oscillations of neuronal intrinsic properties in the suprachiasmatic nucleus
H.S. Nagaraj, Rishikesh Narayanan
iScience (2023) Vol. 26, Iss. 4, pp. 106503-106503
Open Access | Times Cited: 8
H.S. Nagaraj, Rishikesh Narayanan
iScience (2023) Vol. 26, Iss. 4, pp. 106503-106503
Open Access | Times Cited: 8
The Fragile X Protein Family in Amyotrophic Lateral Sclerosis
Sarah B. Mueller, Lorena Decker, Sonja Menge, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 7, pp. 3898-3910
Open Access | Times Cited: 8
Sarah B. Mueller, Lorena Decker, Sonja Menge, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 7, pp. 3898-3910
Open Access | Times Cited: 8
Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome
YeEun Tak, Andrea Schneider, Ellery Santos, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 331-331
Open Access | Times Cited: 3
YeEun Tak, Andrea Schneider, Ellery Santos, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 331-331
Open Access | Times Cited: 3