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:
Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery
Elisa Calì, Clarissa Rocca, Vincenzo Salpietro, et al.
Frontiers in Neurology (2022) Vol. 12
Open Access | Times Cited: 16
Elisa Calì, Clarissa Rocca, Vincenzo Salpietro, et al.
Frontiers in Neurology (2022) Vol. 12
Open Access | Times Cited: 16
Showing 16 citing articles:
Energetics, kinetics, and pathways of SNARE assembly in membrane fusion
Yongli Zhang, Lu Ma, Huan Bao
Critical Reviews in Biochemistry and Molecular Biology (2022) Vol. 57, Iss. 4, pp. 443-460
Open Access | Times Cited: 25
Yongli Zhang, Lu Ma, Huan Bao
Critical Reviews in Biochemistry and Molecular Biology (2022) Vol. 57, Iss. 4, pp. 443-460
Open Access | Times Cited: 25
STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy
Mirella Vinci, Carola Costanza, Rosanna Galati Rando, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16436-16436
Open Access | Times Cited: 13
Mirella Vinci, Carola Costanza, Rosanna Galati Rando, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16436-16436
Open Access | Times Cited: 13
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
Nora I. Strom, Brad Verhulst, Silviu‐Alin Bacanu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5
Nora I. Strom, Brad Verhulst, Silviu‐Alin Bacanu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5
Developmental and Epileptic Encephalopathy: Pathogenesis of Intellectual Disability Beyond Channelopathies
Alexandra D. Medyanik, Polina E. Anisimova, Angelina Kustova, et al.
Biomolecules (2025) Vol. 15, Iss. 1, pp. 133-133
Open Access
Alexandra D. Medyanik, Polina E. Anisimova, Angelina Kustova, et al.
Biomolecules (2025) Vol. 15, Iss. 1, pp. 133-133
Open Access
Mendelian Randomization Study Using Dopaminergic Neuron‐Specific eQTL Nominates Potential Causal Genes for Parkinson's Disease
Xinglun Dang, Zhijun Zhang, Xiong‐Jian Luo
Movement Disorders (2022) Vol. 37, Iss. 12, pp. 2451-2456
Closed Access | Times Cited: 18
Xinglun Dang, Zhijun Zhang, Xiong‐Jian Luo
Movement Disorders (2022) Vol. 37, Iss. 12, pp. 2451-2456
Closed Access | Times Cited: 18
Recent Developments in Autism Genetic Research: A Scientometric Review from 2018 to 2022
Mengyu Lim, Alessandro Carollo, Dagmara Dimitriou, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1646-1646
Open Access | Times Cited: 17
Mengyu Lim, Alessandro Carollo, Dagmara Dimitriou, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1646-1646
Open Access | Times Cited: 17
Syntabulin regulates neuronal excitation/inhibition balance and epileptic seizures by transporting syntaxin 1B
Pingyang Ke, Juan Gu, Jing Liu, et al.
Cell Death Discovery (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 10
Pingyang Ke, Juan Gu, Jing Liu, et al.
Cell Death Discovery (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 10
Clocking Epilepsies: A Chronomodulated Strategy-Based Therapy for Rhythmic Seizures
Sha Sun, Han Wang
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4223-4223
Open Access | Times Cited: 8
Sha Sun, Han Wang
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4223-4223
Open Access | Times Cited: 8
STXBP1-Related Disorders: Clinical Presentation, Molecular Function, Treatment, and Future Directions
Alexander Freibauer, Mikayla Wohlleben, Cyrus Boelman
Genes (2023) Vol. 14, Iss. 12, pp. 2179-2179
Open Access | Times Cited: 8
Alexander Freibauer, Mikayla Wohlleben, Cyrus Boelman
Genes (2023) Vol. 14, Iss. 12, pp. 2179-2179
Open Access | Times Cited: 8
A Mutual Nexus Between Epilepsy and α-Synuclein: A Puzzle Pathway
Naif H. Ali, Hayder M. Al‐kuraishy, Ali I. Al‐Gareeb, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 12, pp. 10198-10215
Closed Access | Times Cited: 1
Naif H. Ali, Hayder M. Al‐kuraishy, Ali I. Al‐Gareeb, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 12, pp. 10198-10215
Closed Access | Times Cited: 1
Gene Expression at the Tripartite Synapse: Bridging the Gap Between Neurons and Astrocytes
Gillian Imrie, Madison B Gray, Vishnuvasan Raghuraman, et al.
Advances in neurobiology (2024), pp. 95-136
Closed Access | Times Cited: 1
Gillian Imrie, Madison B Gray, Vishnuvasan Raghuraman, et al.
Advances in neurobiology (2024), pp. 95-136
Closed Access | Times Cited: 1
Unraveling the molecular landscape of lead-induced cochlear synaptopathy: a quantitative proteomics analysis
Pankaj Bhatia, Shomaila Mehmood, Nicole Doyon-Reale, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access
Pankaj Bhatia, Shomaila Mehmood, Nicole Doyon-Reale, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access
Synaptic Vesicle Cycling Disorders: Cross-Sectional Phenotyping Study of a Gene Functional Network
Josefine Eck, Tess A. Smith, Anna Kolesnik, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Josefine Eck, Tess A. Smith, Anna Kolesnik, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Quantitative EEG biomarkers for STXBP1 ‐related disorders
Alberto Cossu, Francesca Furia, Jacopo Proietti, et al.
Epilepsia (2024)
Open Access
Alberto Cossu, Francesca Furia, Jacopo Proietti, et al.
Epilepsia (2024)
Open Access
Angelman Syndrome causing UBE3A ligase displays predominantly synaptic ubiquitination activity in the mouse brain
Ugo Mayor, Unai Alduntzin, Benoît Lectez, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
Ugo Mayor, Unai Alduntzin, Benoît Lectez, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss
Amal Abu Rayyan, Ryan J. Carlson, Grace Rabie, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2265-2268
Open Access
Amal Abu Rayyan, Ryan J. Carlson, Grace Rabie, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2265-2268
Open Access
