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:

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery
Karen Oliver, Colin A. Ellis, Ingrid E. Scheffer, et al.
EBioMedicine (2022) Vol. 81, pp. 104079-104079
Open Access | Times Cited: 22

Showing 22 citing articles:

The current landscape of epilepsy genetics: where are we, and where are we going?
Sarah M. Ruggiero, Julie Xian, Ingo Helbig
Current Opinion in Neurology (2023)
Open Access | Times Cited: 28
Protective effect of CACNA1A deficiency in oligogenic refractory epilepsy with CACNA1A‐CELSR2 digenic mutations
ChengYan Liu, Mingyang Sun, Yansong Lin, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview
Florian P. Fischer, Robin A. Karge, Yvonne G. Weber, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 21
Polygenic Risk in Families With Spontaneous Coronary Artery Dissection
Ingrid Tarr, Stephanie Hesselson, Michael Troup, et al.
JAMA Cardiology (2024) Vol. 9, Iss. 3, pp. 254-254
Closed Access | Times Cited: 6
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: 6
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture
Rebekah V. Harris, Karen Oliver, Piero Perucca, et al.
Annals of Neurology (2023) Vol. 94, Iss. 5, pp. 825-835
Open Access | Times Cited: 11
Genetic Testing in Epilepsy: Improving Outcomes and Informing Gaps in Research
Christa W. Habela, Krista Schatz, Sarah A. Kelley
Epiliepsy currents/Epilepsy currents (2024)
Open Access | Times Cited: 4
Phenotypic heterogeneity in familial epilepsies is influenced by polygenic risk for generalized and focal epilepsies
Colin A. Ellis, Ruth Ottman, Michael P. Epstein, et al.
Epilepsia (2025)
Open Access
Genome-wide association meta-analyses of drug-resistant epilepsy
Costin Leu, Andreja Avberšek, Remi Stevelink, et al.
EBioMedicine (2025), pp. 105675-105675
Open Access
Predictive value of the polygenic risk score for developing epilepsy: a systematic review and meta-analysis
Takafumi Kubota, Irma Wati Ngadimon, Hisashi Ohseto, et al.
Epilepsy & Behavior (2025) Vol. 169, pp. 110438-110438
Open Access
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability
Lea Urpa, Mitja Kurki, Elisa Rahikkala, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 5, pp. 576-583
Open Access | Times Cited: 3
Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families
Karen Oliver, Ingrid E. Scheffer, Colin A. Ellis, et al.
EBioMedicine (2024) Vol. 109, pp. 105404-105404
Closed Access | Times Cited: 3
Adolescent-onset epilepsy and deterioration associated with CAD deficiency: A case report
Sebastián Silva, M.J. Rosas, Benjamín Guerra, et al.
Brain and Development (2024) Vol. 46, Iss. 7, pp. 250-253
Closed Access | Times Cited: 2
Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias
Colin A. Ellis, Karen Oliver, Rebekah V. Harris, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 9, pp. 1805-1809
Closed Access | Times Cited: 2
Dynamic convergence of autism disorder risk genes across neurodevelopment
Meilín Fernández García, Kayla G. Townsley, April Pruitt, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Polygenic Risk of Epilepsy and Poststroke Epilepsy
Santiago Clocchiatti‐Tuozzo, Cyprien Rivier, Shubham Misra, et al.
Stroke (2024) Vol. 55, Iss. 12, pp. 2835-2843
Open Access | Times Cited: 2
Molecular Genetics of Acquired Temporal Lobe Epilepsy
Anne‐Marie Neumann, Stefan Britsch
Biomolecules (2024) Vol. 14, Iss. 6, pp. 669-669
Open Access | Times Cited: 1
Polygenic Risk of Epilepsy and Post-Stroke Epilepsy
Cyprien Rivier, Santiago Clocchiatti‐Tuozzo, Shubham Misra, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
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.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Exploration von Zusammenhängen zwischen polygenem Risikoscore und phänotypischer Ausprägung bei Patienten mit genetisch generalisierter Epilepsie
Nils Kristian Hartung
(2024)
Open Access
“I am not a number!” Opinions and preferences of people with intellectual disability about genomic healthcare.
Elizabeth E. Palmer, Joanne Danker, Iva Strnadová, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 1
Channeling the Future of Pathogenicity Prediction for Genetic Variants in Epilepsy
Jacy L. Wagnon
Epiliepsy currents/Epilepsy currents (2023) Vol. 23, Iss. 2, pp. 118-120
Open Access
Page 1

Scroll to top