Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Predicting functional effects of ion channel variants using new phenotypic machine learning methods
Christian M. Boßelmann, Ulrike B. S. Hedrich, Holger Lerche, et al.
PLoS Computational Biology (2023) Vol. 19, Iss. 3, pp. e1010959-e1010959
Open Access | Times Cited: 13

Showing 13 citing articles:

Cenobamate as add‐on treatment for SCN8A developmental and epileptic encephalopathy
Cathrine E. Gjerulfsen, Madeleine J. Oudin, Francesca Furia, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy
Shir Quinn, Nan Zhang, Timothy A. Fenton, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 5, pp. 167127-167127
Open Access | Times Cited: 5
The role of ion channels in T cell function and disease
Nicholas Manolios, John Papaemmanouil, David J. Adams
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 11
Genotype‐function‐phenotype correlations for SCN1A variants identified by clinical genetic testing
Andrew Knox, Christopher H. Thompson, Dillon Scott, et al.
Annals of Clinical and Translational Neurology (2025)
Open Access
Machine learning models reveal distinct disease subgroups and improve diagnostic and prognostic accuracy for individuals with pathogenic SCN8A gain-of-function variants
Joshua Hack, Joseph C. Watkins, Michael F. Hammer
Biology Open (2024) Vol. 13, Iss. 4
Open Access | Times Cited: 3
Mapping Structural Distribution and Gating-Property Impacts of Disease-Associated Mutations in Voltage-Gated Sodium Channels
Amin Akbari Ahangar, Eslam Elhanafy, Hayden Blanton, et al.
iScience (2024) Vol. 27, Iss. 9, pp. 110678-110678
Open Access | Times Cited: 3
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing
Woong‐Woo Lee, Cha Gon Lee, Chang‐Seok Ki
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024) Vol. 195, Iss. 7
Closed Access | Times Cited: 1
Respiratory Dysfunction in Epileptic Encephalopathies: Insights and Challenges
Muhammad Ali Khan, Shah Dev, Maneesha Kumari, et al.
Cureus (2023)
Open Access | Times Cited: 2
Artificial Intelligence and Machine Learning in Electrophysiology—a Short Review
Shahrukh Khan, Chanho Lim, Humza A Chaudhry, et al.
Current Treatment Options in Cardiovascular Medicine (2023) Vol. 25, Iss. 10, pp. 443-460
Closed Access | Times Cited: 1
Cenobamate as add-on treatment for SCN8A development and epileptic encephalopathy
Cathrine E. Gjerulfsen, Madeleine J. Oudin, Francesca Furia, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
STACKION: Ion Channel-Modulating Peptides Identification Using Stacking-Based Ensemble Machine Learning
Md. Mamun Ali, Kawsar Ahmed, Francis M. Bui, et al.
(2023), pp. 216-221
Closed Access
Complex biophysical changes and reduced neuronal firing in anSCN8Avariant associated with developmental delay and epilepsy
Shir Quinn, Nan Zhang, Timothy A. Fenton, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Time series-based hybrid ensemble learning model with multivariate multidimensional feature coding for DNA methylation prediction
Wu Yan, Li Tan, Mengshan Li, et al.
BMC Genomics (2023) Vol. 24, Iss. 1
Open Access
Page 1

Scroll to top