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:
Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
Helena Martins Custodio, Lisa M. Clayton, Ravishankara Bellampalli, et al.
Brain (2023) Vol. 146, Iss. 9, pp. 3885-3897
Open Access | Times Cited: 33
Helena Martins Custodio, Lisa M. Clayton, Ravishankara Bellampalli, et al.
Brain (2023) Vol. 146, Iss. 9, pp. 3885-3897
Open Access | Times Cited: 33
Showing 1-25 of 33 citing articles:
Developmental and epileptic encephalopathies
Ingrid E. Scheffer, Sameer M. Zuberi, Heather C. Mefford, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 21
Ingrid E. Scheffer, Sameer M. Zuberi, Heather C. Mefford, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 21
Genotype–phenotype associations in 1018 individuals with SCN1A‐related epilepsies
D.S. Gallagher, Eduardo Pérez‐Palma, Tobias Bruenger, et al.
Epilepsia (2024) Vol. 65, Iss. 4, pp. 1046-1059
Open Access | Times Cited: 16
D.S. Gallagher, Eduardo Pérez‐Palma, Tobias Bruenger, et al.
Epilepsia (2024) Vol. 65, Iss. 4, pp. 1046-1059
Open Access | Times Cited: 16
Zebrafish: unraveling genetic complexity through duplicated genes
Maliha Tasnim, Preston Wahlquist, Jonathon T. Hill
Development Genes and Evolution (2024)
Open Access | Times Cited: 7
Maliha Tasnim, Preston Wahlquist, Jonathon T. Hill
Development Genes and Evolution (2024)
Open Access | Times Cited: 7
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
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Guidance for estimating penetrance of monogenic disease-causing variants in population cohorts
Caroline F. Wright, Luke N Sharp, Leigh Jackson, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1772-1779
Closed Access | Times Cited: 5
Caroline F. Wright, Luke N Sharp, Leigh Jackson, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1772-1779
Closed Access | Times Cited: 5
Are Genetic Therapies for Epilepsy Ready for the Clinic?
James S. Street, Yichen Qiu, Gabriele Lignani
Epiliepsy currents/Epilepsy currents (2023) Vol. 23, Iss. 4, pp. 245-250
Open Access | Times Cited: 13
James S. Street, Yichen Qiu, Gabriele Lignani
Epiliepsy currents/Epilepsy currents (2023) Vol. 23, Iss. 4, pp. 245-250
Open Access | Times Cited: 13
Steps to Improve Precision Medicine in Epilepsy
Simona Balestrini, Davide Mei, Sanjay M. Sisodiya, et al.
Molecular Diagnosis & Therapy (2023) Vol. 27, Iss. 6, pp. 661-672
Open Access | Times Cited: 12
Simona Balestrini, Davide Mei, Sanjay M. Sisodiya, et al.
Molecular Diagnosis & Therapy (2023) Vol. 27, Iss. 6, pp. 661-672
Open Access | Times Cited: 12
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
Hang Lyu, Christian M. Boßelmann, Katrine M. Johannesen, et al.
EBioMedicine (2023) Vol. 98, pp. 104855-104855
Open Access | Times Cited: 11
Hang Lyu, Christian M. Boßelmann, Katrine M. Johannesen, et al.
EBioMedicine (2023) Vol. 98, pp. 104855-104855
Open Access | Times Cited: 11
Merritt-Putnam Symposium | Developmental and Epileptic Encephalopathies—Current Concepts and Novel Approaches
Rod C. Scott, Jenny Hsieh, Amy McTague, et al.
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Rod C. Scott, Jenny Hsieh, Amy McTague, et al.
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Delphi consensus on referral criteria for pediatric patients with suspected Dravet syndrome
Ángel Aledo‐Serrano, Susana Boronat, Juan José Garcı́a-Peñas, et al.
Epilepsy & Behavior (2025) Vol. 167, pp. 110401-110401
Closed Access
Ángel Aledo‐Serrano, Susana Boronat, Juan José Garcı́a-Peñas, et al.
Epilepsy & Behavior (2025) Vol. 167, pp. 110401-110401
Closed Access
Developmental and epileptic encephalopathy in patients with epilepsy due to hypothalamic hamartomas
Kathrin Wagner, Theo Demerath, Sarah M. Metzger, et al.
Epilepsia (2025)
Open Access
Kathrin Wagner, Theo Demerath, Sarah M. Metzger, et al.
Epilepsia (2025)
Open Access
From All to One: Can a Large Cohort of Individuals with SCN1A-Related Epilepsy Offer Predictions for Other Individuals With SCN1A Variants?
Elizabeth E. Gerard
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Elizabeth E. Gerard
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Phenotypic Spectrum of KATNIP-Associated Joubert Syndrome: Possible Association with Esophageal Atresia and Review of the Literature
Maria Giovanna Tedesco, Ilaria Donati, Chiara Romeo, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 524-524
Open Access
Maria Giovanna Tedesco, Ilaria Donati, Chiara Romeo, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 524-524
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
Takafumi Kubota, Irma Wati Ngadimon, Hisashi Ohseto, et al.
Epilepsy & Behavior (2025) Vol. 169, pp. 110438-110438
Open Access
Monogenic Epilepsies in Adult Epilepsy Clinics and Gene-Driven Approaches to Treatment
Lisa M. Clayton, Angeliki Vakrinou, Simona Balestrini, et al.
Current Neurology and Neuroscience Reports (2025) Vol. 25, Iss. 1
Open Access
Lisa M. Clayton, Angeliki Vakrinou, Simona Balestrini, et al.
Current Neurology and Neuroscience Reports (2025) Vol. 25, Iss. 1
Open Access
PRRT 2 -Related Epilepsy
Madeline Komar, J. Sidhu, J. Joseph, et al.
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access
Madeline Komar, J. Sidhu, J. Joseph, et al.
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
Benedetta Kassabian, Christina Fenger, Marjolaine Willems, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
Benedetta Kassabian, Christina Fenger, Marjolaine Willems, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
Voltage‐gated calcium channels in genetic epilepsies
Robert J. Lauerer, Holger Lerche
Journal of Neurochemistry (2023)
Open Access | Times Cited: 7
Robert J. Lauerer, Holger Lerche
Journal of Neurochemistry (2023)
Open Access | Times Cited: 7
The influence of temperature and genomic variation on intracranial EEG measures in people with epilepsy
Olivia C McNicholas, Diego Jiménez‐Jiménez, Joana F. A. Oliveira, et al.
Brain Communications (2024) Vol. 6, Iss. 5
Open Access | Times Cited: 2
Olivia C McNicholas, Diego Jiménez‐Jiménez, Joana F. A. Oliveira, et al.
Brain Communications (2024) Vol. 6, Iss. 5
Open Access | Times Cited: 2
Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects
Fulya Kürekçi, Mehmet Akif Kılıç, Sinan Akbaş, et al.
Epilepsy & Behavior (2024) Vol. 158, pp. 109930-109930
Closed Access | Times Cited: 2
Fulya Kürekçi, Mehmet Akif Kılıç, Sinan Akbaş, et al.
Epilepsy & Behavior (2024) Vol. 158, pp. 109930-109930
Closed Access | Times Cited: 2
The Biallelic Inheritance of Two Novel SCN1A Variants Results in Developmental and Epileptic Encephalopathy Responsive to Levetiracetam
Giorgia Dinoi, Elena Conte, Orazio Palumbo, et al.
Biomedicines (2024) Vol. 12, Iss. 8, pp. 1698-1698
Open Access | Times Cited: 2
Giorgia Dinoi, Elena Conte, Orazio Palumbo, et al.
Biomedicines (2024) Vol. 12, Iss. 8, pp. 1698-1698
Open Access | Times Cited: 2
Two epilepsy‐associated variants in KCNA2 (KV1.2) at position H310 oppositely affect channel functional expression
Teresa Minguez, Varsha Prakash, Kaiqian Wang, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 23, pp. 5367-5389
Open Access | Times Cited: 5
Teresa Minguez, Varsha Prakash, Kaiqian Wang, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 23, pp. 5367-5389
Open Access | Times Cited: 5
Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report
Hinde El Mouhi, Nada Amllal, Meriame Abbassi, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access | Times Cited: 1
Hinde El Mouhi, Nada Amllal, Meriame Abbassi, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access | Times Cited: 1
In vitro human cell culture models in a bench‐to‐bedside approach to epilepsy
Šárka Danačíková, Barbora Straka, Jan Daněk, et al.
Epilepsia Open (2024) Vol. 9, Iss. 3, pp. 865-890
Open Access | Times Cited: 1
Šárka Danačíková, Barbora Straka, Jan Daněk, et al.
Epilepsia Open (2024) Vol. 9, Iss. 3, pp. 865-890
Open Access | Times Cited: 1
The epilepsy phenotype of KCNK4-related neurodevelopmental disease
Magdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
Seizure (2024) Vol. 121, pp. 114-122
Closed Access | Times Cited: 1
Magdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
Seizure (2024) Vol. 121, pp. 114-122
Closed Access | Times Cited: 1
