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:
Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies
Dan Sun, Yan Liu, Wei Cai, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 13
Dan Sun, Yan Liu, Wei Cai, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 13
Showing 13 citing articles:
A systematic literature review on the global epidemiology of Dravet syndrome and Lennox–Gastaut syndrome: Prevalence, incidence, diagnosis, and mortality
Joseph Sullivan, Arturo Benítez, Jeannine Roth, et al.
Epilepsia (2024) Vol. 65, Iss. 5, pp. 1240-1263
Open Access | Times Cited: 16
Joseph Sullivan, Arturo Benítez, Jeannine Roth, et al.
Epilepsia (2024) Vol. 65, Iss. 5, pp. 1240-1263
Open Access | Times Cited: 16
Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices
Yufeng Huang, Wenyue Deng, Hui Huang, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Yufeng Huang, Wenyue Deng, Hui Huang, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism
Yassine Zouaghi, Anbreen Mazhar Choudhary, Saba Irshad, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Yassine Zouaghi, Anbreen Mazhar Choudhary, Saba Irshad, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations
Liangliang Jiang, Shaohua Bi, Li Lin, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 12
Open Access | Times Cited: 3
Liangliang Jiang, Shaohua Bi, Li Lin, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 12
Open Access | Times Cited: 3
Genetic analysis using targeted exome sequencing of 53 Vietnamese children with developmental and epileptic encephalopathies
Nguyen Le Trung Hieu, Nguyen Thuy Minh Thu, Le Tran Anh Ngan, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2048-2060
Closed Access | Times Cited: 5
Nguyen Le Trung Hieu, Nguyen Thuy Minh Thu, Le Tran Anh Ngan, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2048-2060
Closed Access | Times Cited: 5
Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability
Jiacheng Hu, Mingming Xu, Xiaobo Zhu, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 813-813
Open Access | Times Cited: 4
Jiacheng Hu, Mingming Xu, Xiaobo Zhu, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 813-813
Open Access | Times Cited: 4
Prevalence and prognosis of molecularly defined familial hypercholesterolemia in patients with acute coronary syndrome
Cheng Wang, Puliang Yu, Lizhi Hu, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 4
Cheng Wang, Puliang Yu, Lizhi Hu, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 4
Genetic analysis of periventricular nodular heterotopia 7 caused by a novel NEDD4L missense mutation: Case and literature summary
Juan Liu, Jihong Hu, Yaqing Duan, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 7
Open Access | Times Cited: 2
Juan Liu, Jihong Hu, Yaqing Duan, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 7
Open Access | Times Cited: 2
Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
Min Zhou, Ningjie Shi, Juan Zheng, et al.
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 5
Min Zhou, Ningjie Shi, Juan Zheng, et al.
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 5
Prenatal Detection of Novel Compound Heterozygous Splice Site Variants of the KIAA0825 Gene in a Fetus with Postaxial Polydactyly Type A
Yanyi Yao, Shan Deng, Feng Zhu
Genes (2022) Vol. 13, Iss. 7, pp. 1230-1230
Open Access | Times Cited: 3
Yanyi Yao, Shan Deng, Feng Zhu
Genes (2022) Vol. 13, Iss. 7, pp. 1230-1230
Open Access | Times Cited: 3
Trends and hotspots in gene research of epilepsy in children: A review and bibliometric analysis from 2010 to 2022
Yu-Ling Tian, Xilian Zhang, Hanjiang Chen, et al.
Medicine (2023) Vol. 102, Iss. 30, pp. e34417-e34417
Open Access | Times Cited: 1
Yu-Ling Tian, Xilian Zhang, Hanjiang Chen, et al.
Medicine (2023) Vol. 102, Iss. 30, pp. e34417-e34417
Open Access | Times Cited: 1
A Novel Loss of Function Variant in HCN1 Gene Underlies Early Infantile Epileptic Encephalopathy 24 [EIEE24]
Mujahid, Ahmed Waqas, Ibrahim Abdullah Almazni, et al.
Molecular Syndromology (2024), pp. 1-13
Closed Access
Mujahid, Ahmed Waqas, Ibrahim Abdullah Almazni, et al.
Molecular Syndromology (2024), pp. 1-13
Closed Access
Diagnostic yields of genetic testing and related benefits in infantile epileptic spasms syndrome: A systematic review and meta-analysis
Xinyu Feng, Jie Yang, Ningning Chen, et al.
Seizure (2024) Vol. 124, pp. 18-24
Closed Access
Xinyu Feng, Jie Yang, Ningning Chen, et al.
Seizure (2024) Vol. 124, pp. 18-24
Closed Access
