
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:
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 88
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 88
Showing 1-25 of 88 citing articles:
Karen Oliver, Ingrid E. Scheffer, Mark F. Bennett, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1368-1375
Open Access | Times Cited: 68
A concerted neuron–astrocyte program declines in ageing and schizophrenia
Emi Ling, James Nemesh, Melissa Goldman, et al.
Nature (2024) Vol. 627, Iss. 8004, pp. 604-611
Open Access | Times Cited: 54
Emi Ling, James Nemesh, Melissa Goldman, et al.
Nature (2024) Vol. 627, Iss. 8004, pp. 604-611
Open Access | Times Cited: 54
Rare copy-number variants as modulators of common disease susceptibility
Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 23
Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 23
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Ludovica Montanucci, David Lewis‐Smith, Ryan L. Collins, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 30
Ludovica Montanucci, David Lewis‐Smith, Ryan L. Collins, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 30
Identification of novel genomic risk loci shared between common epilepsies and psychiatric disorders
Naz Karadag, Alexey Shadrin, Kevin S. O’Connell, et al.
Brain (2023) Vol. 146, Iss. 8, pp. 3392-3403
Open Access | Times Cited: 28
Naz Karadag, Alexey Shadrin, Kevin S. O’Connell, et al.
Brain (2023) Vol. 146, Iss. 8, pp. 3392-3403
Open Access | Times Cited: 28
An integrated single-nucleus and spatial transcriptomics atlas reveals the molecular landscape of the human hippocampus
Erik D. Nelson, Madhavi Tippani, Anthony D. Ramnauth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 8
Erik D. Nelson, Madhavi Tippani, Anthony D. Ramnauth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 8
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1864-1879
Closed Access | Times Cited: 8
Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1864-1879
Closed Access | Times Cited: 8
Deep learning predicts DNA methylation regulatory variants in specific brain cell types and enhances fine mapping for brain disorders
Jiyun Zhou, Daniel R. Weinberger, Shizhong Han
Science Advances (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
Jiyun Zhou, Daniel R. Weinberger, Shizhong Han
Science Advances (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
Holistic Exome-Based Genetic Testing in Adults With Epilepsy
Martin Krenn, Matias Wagner, Karin Trimmel, et al.
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access | Times Cited: 1
Martin Krenn, Matias Wagner, Karin Trimmel, et al.
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access | Times Cited: 1
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries
Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
Idiopathic Generalized Epilepsy
Orrin Devinsky, Christopher Elder, Shobi Sivathamboo, et al.
Neurology (2023) Vol. 102, Iss. 3
Open Access | Times Cited: 17
Orrin Devinsky, Christopher Elder, Shobi Sivathamboo, et al.
Neurology (2023) Vol. 102, Iss. 3
Open Access | Times Cited: 17
Breaking down causes, consequences, and mediating effects of telomere length variation on human health
Samuel Moix, Marie C. Sadler, Zoltán Kutalik, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Samuel Moix, Marie C. Sadler, Zoltán Kutalik, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants
Dina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 1222-1238
Open Access | Times Cited: 7
Dina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 1222-1238
Open Access | Times Cited: 7
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
Remi Stevelink, Dania Al‐Toma, Floor E. Jansen, et al.
EClinicalMedicine (2022) Vol. 53, pp. 101732-101732
Open Access | Times Cited: 26
Remi Stevelink, Dania Al‐Toma, Floor E. Jansen, et al.
EClinicalMedicine (2022) Vol. 53, pp. 101732-101732
Open Access | Times Cited: 26
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Integrative analysis of epilepsy-associated genes reveals expression-phenotype correlations
Wanhao Chi, Evangelos Kiskinis
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Wanhao Chi, Evangelos Kiskinis
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Extensive long-range polycomb interactions and weak compartmentalization are hallmarks of human neuronal 3D genome
Ilya A. Pletenev, Maria Bazarevich, Diana Zagirova, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 11, pp. 6234-6252
Open Access | Times Cited: 4
Ilya A. Pletenev, Maria Bazarevich, Diana Zagirova, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 11, pp. 6234-6252
Open Access | Times Cited: 4
Integrated Mendelian Randomization and Single‐Cell Transcriptomics Analysis Identifies Critical Blood Biomarkers and Potential Mechanisms in Epilepsy
Jianwei Shi, Jing Xie, Yanfeng Yang, et al.
CNS Neuroscience & Therapeutics (2025) Vol. 31, Iss. 1
Open Access
Jianwei Shi, Jing Xie, Yanfeng Yang, et al.
CNS Neuroscience & Therapeutics (2025) Vol. 31, Iss. 1
Open Access
Associations between epilepsy-related polygenic risk and brain morphology in childhood
Alexander Ngo, L W Liu, Sara Larivière, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Alexander Ngo, L W Liu, Sara Larivière, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Identification and verification of autophagy-related gene signatures and their association with immune infiltration and drug responsiveness in epilepsy
H. He, X Zhang, Fenfang Chen
Frontiers in Neurology (2025) Vol. 15
Open Access
H. He, X Zhang, Fenfang Chen
Frontiers in Neurology (2025) Vol. 15
Open Access
Association Between GABRG2 and Self-Rating of the Effects of Alcohol in a French Young Adult Sample
Jenny Skumsnes Moe, Jørgen G. Bramness, Ingeborg Bolstad, et al.
Risk Management and Healthcare Policy (2025) Vol. Volume 18, pp. 291-304
Open Access
Jenny Skumsnes Moe, Jørgen G. Bramness, Ingeborg Bolstad, et al.
Risk Management and Healthcare Policy (2025) Vol. Volume 18, pp. 291-304
Open Access
Multi-ancestry genome-wide meta-analysis with 472,819 individuals identifies 32 novel risk loci for psoriasis
Min Zhang, Wenting Su, Jun Deng, et al.
Journal of Translational Medicine (2025) Vol. 23, Iss. 1
Open Access
Min Zhang, Wenting Su, Jun Deng, et al.
Journal of Translational Medicine (2025) Vol. 23, Iss. 1
Open Access
Genome-Wide Association Study Identifying a Novel Gene Related to a History of Febrile Convulsions in Patients With Focal Epilepsy
Joon-Ho Kim, Hye Jeong Lee, Hyung Jun Park, et al.
Journal of Clinical Neurology (2025) Vol. 21
Open Access
Joon-Ho Kim, Hye Jeong Lee, Hyung Jun Park, et al.
Journal of Clinical Neurology (2025) Vol. 21
Open Access
Risk of epilepsy following first unprovoked and acute seizures: Cohort study
Isaac J. Egesa, Symon M. Kariuki, Collins Kipkoech, et al.
Epilepsia (2025)
Open Access
Isaac J. Egesa, Symon M. Kariuki, Collins Kipkoech, et al.
Epilepsia (2025)
Open Access
Global incidence, prevalence, deaths, and disability-adjusted life-years (DALYs) for idiopathic epilepsy, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021
Lin Chen, Yang Miao, Tianxiang Zhang
Research Square (Research Square) (2025)
Closed Access
Lin Chen, Yang Miao, Tianxiang Zhang
Research Square (Research Square) (2025)
Closed Access