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:

The role of sodium channels in sudden unexpected death in pediatrics
Anne Rochtus, Richard D. Goldstein, Ingrid A. Holm, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 8
Open Access | Times Cited: 19

Showing 19 citing articles:

Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 433-513
Open Access | Times Cited: 96
SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
Jiangwei Ding, Xinxiao Li, Haiyan Tian, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 74
Cardiac morbidity and mortality associated with the use of lamotrigine
Jakob Christensen, Betina B. Trabjerg, Julie Werenberg Dreier
Epilepsia (2022) Vol. 63, Iss. 9, pp. 2371-2380
Open Access | Times Cited: 23
The Genetics of Sudden and Unexpected Death
Monica H. Wojcik, Richard D. Goldstein
(2025), pp. 51-73
Closed Access
Genetic variants associated with sudden cardiac death in the young: a systematic review
Ghadeer M. M. Abdelaal, Shaimaa A. Shehata, Shrouk Ali, et al.
Egyptian Journal of Forensic Sciences (2025) Vol. 15, Iss. 1
Open Access
Genetic Factors Underlying Sudden Infant Death Syndrome
Christine Keywan, Annapurna Poduri, Richard D. Goldstein, et al.
The Application of Clinical Genetics (2021) Vol. Volume 14, pp. 61-76
Open Access | Times Cited: 21
Brainstem depolarization–induced lethal apnea associated with gain-of-function SCN1A L263V is prevented by sodium channel blockade
Nico A. Jansen, Sandrine Cestèle, Silvia Sanchez Marco, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 14
Closed Access | Times Cited: 3
Idiopathic generalized epilepsy in a family with SCN4A‐related myotonia
Mariagrazia Talarico, Francesco Fortunato, Audrey Labalme, et al.
Epilepsia Open (2024) Vol. 9, Iss. 3, pp. 951-959
Open Access | Times Cited: 2
Seizure‐related deaths in children: The expanding spectrum
Jenna Harowitz, Laura Gould, Declan McGuone, et al.
Epilepsia (2021) Vol. 62, Iss. 3, pp. 570-582
Open Access | Times Cited: 14
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing
Angela M. Bard, Lindsay V. Clark, Erdal Coşgun, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Open Access | Times Cited: 1
Sudden unexpected infant death, sudden unexplained death in childhood, and sudden unexpected death in epilepsy
Suvasini Sharma, Robyn Whitney, Sayoni Roy Chowdhury, et al.
Developmental Medicine & Child Neurology (2024)
Open Access | Times Cited: 1
The Genetics of Sudden Infant Death Syndrome—Towards a Gene Reference Resource
Emma B. Johannsen, Linda B. Baughn, Neeraj Sharma, et al.
Genes (2021) Vol. 12, Iss. 2, pp. 216-216
Open Access | Times Cited: 8
Yield of exome sequencing in patients with developmental and epileptic encephalopathies and inconclusive targeted gene panel
Lucie Sedláčková, Katalin Štěrbová, Markéta Vlčková, et al.
European Journal of Paediatric Neurology (2023) Vol. 48, pp. 17-29
Open Access | Times Cited: 3
New Challenges Resulting From the Loss of Function of Nav1.4 in Neuromuscular Diseases
Sophie Nicole, Philippe Lory
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 7
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age
Catherine A. Brownstein, Élise Douard, Robin L. Haynes, et al.
Advanced Genetics (2022) Vol. 4, Iss. 1
Open Access | Times Cited: 4
Genetic Landscape of <b><i>SCN1A</i></b> Variants in a Turkish Cohort with GEFS+ Spectrum and Dravet Syndrome
Ayberk Türkyılmaz, Emine Tekin, Oğuzhan Yaralı, et al.
Molecular Syndromology (2022), pp. 1-12
Open Access | Times Cited: 3
Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism
Agnieszka Szmigielska
American Journal of Case Reports (2022) Vol. 23
Open Access | Times Cited: 1
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome Sequencing
Angela M. Bard, Lindsay V. Clark, Erdal Coşgun, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Rare Genetic Variants Associated with Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study
Lauri Holmström, Ninad S. Chaudhary, Kotoka Nakamura, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Page 1

Scroll to top