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:
Primary Coenzyme Q10 Deficiency-7 and Pathogenic COQ4 Variants: Clinical Presentation, Biochemical Analyses, and Treatment
Jieqiong Xie, Jiayang Jiang, Qiwei Guo
Frontiers in Genetics (2022) Vol. 12
Open Access | Times Cited: 8
Jieqiong Xie, Jiayang Jiang, Qiwei Guo
Frontiers in Genetics (2022) Vol. 12
Open Access | Times Cited: 8
Showing 8 citing articles:
Clinical features and genotype in COQ4 associated hereditary spastic paraplegia: a case report and a literature reanalysis
Zhe Yu, Rongfei Wang, Xiang Feng, et al.
Neurological Sciences (2025)
Closed Access
Zhe Yu, Rongfei Wang, Xiang Feng, et al.
Neurological Sciences (2025)
Closed Access
Updated Gene Therapy for Renal Inborn Errors of Metabolism
Sean Hergenrother, Mustafa Husein, C Ward Thompson, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 516-516
Open Access
Sean Hergenrother, Mustafa Husein, C Ward Thompson, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 516-516
Open Access
Beneficial antioxidant effects of Coenzyme Q10 on reproduction
Maria Fernanda Hornos Carneiro, Mónica P. Colaiácovo
Vitamins and hormones (2022), pp. 143-167
Closed Access | Times Cited: 8
Maria Fernanda Hornos Carneiro, Mónica P. Colaiácovo
Vitamins and hormones (2022), pp. 143-167
Closed Access | Times Cited: 8
Ethnically unique disease burden and limitations of current expanded carrier screening panels
Chih‐Ling Chen, Ni‐Chung Lee, Yin‐Hsiu Chien, et al.
International Journal of Gynecology & Obstetrics (2023) Vol. 164, Iss. 3, pp. 918-924
Closed Access | Times Cited: 4
Chih‐Ling Chen, Ni‐Chung Lee, Yin‐Hsiu Chien, et al.
International Journal of Gynecology & Obstetrics (2023) Vol. 164, Iss. 3, pp. 918-924
Closed Access | Times Cited: 4
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype
Qiao Wei, Hao Yu, Pei‐Shan Wang, et al.
CNS Neuroscience & Therapeutics (2023) Vol. 30, Iss. 4
Open Access | Times Cited: 4
Qiao Wei, Hao Yu, Pei‐Shan Wang, et al.
CNS Neuroscience & Therapeutics (2023) Vol. 30, Iss. 4
Open Access | Times Cited: 4
Metabolic etiologies in children with infantile epileptic spasm syndrome: Experience at a tertiary pediatric neurology center
Merve Feyza Yüksel, Neslihan Doğulu, Miraç Yıldırım, et al.
Brain and Development (2024) Vol. 46, Iss. 6, pp. 213-218
Closed Access | Times Cited: 1
Merve Feyza Yüksel, Neslihan Doğulu, Miraç Yıldırım, et al.
Brain and Development (2024) Vol. 46, Iss. 6, pp. 213-218
Closed Access | Times Cited: 1
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engi̇n Köse, et al.
Journal of Pediatric Endocrinology and Metabolism (2024) Vol. 37, Iss. 3, pp. 260-270
Closed Access
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engi̇n Köse, et al.
Journal of Pediatric Endocrinology and Metabolism (2024) Vol. 37, Iss. 3, pp. 260-270
Closed Access
The Spectrum of clinical manifestations in newborns with the COQ4 mutation: case series and literature review
Pianpian Pan, Na Zhou, Yi Sun, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access
Pianpian Pan, Na Zhou, Yi Sun, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access
Blended Phenotypes of Sexual Development Disorder and Coenzyme Q10 Deficiency, Together with a Sibling with Homozygous Variants in the AHI1 Gene
Rumeysa Atasay, Leyla Nur Yilmaz, Ayten Güleç, et al.
Molecular Syndromology (2024), pp. 1-7
Closed Access
Rumeysa Atasay, Leyla Nur Yilmaz, Ayten Güleç, et al.
Molecular Syndromology (2024), pp. 1-7
Closed Access
