
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 efficacy of coenzyme Q10 treatment in alleviating the symptoms of primary coenzyme Q10 deficiency: A systematic review
Ying Wang, Siegfried Hekimi
Journal of Cellular and Molecular Medicine (2022) Vol. 26, Iss. 17, pp. 4635-4644
Open Access | Times Cited: 27
Ying Wang, Siegfried Hekimi
Journal of Cellular and Molecular Medicine (2022) Vol. 26, Iss. 17, pp. 4635-4644
Open Access | Times Cited: 27
Showing 1-25 of 27 citing articles:
Coenzyme Q biochemistry and biosynthesis
Rachel M. Guerra, David J. Pagliarini
Trends in Biochemical Sciences (2023) Vol. 48, Iss. 5, pp. 463-476
Open Access | Times Cited: 63
Rachel M. Guerra, David J. Pagliarini
Trends in Biochemical Sciences (2023) Vol. 48, Iss. 5, pp. 463-476
Open Access | Times Cited: 63
Primary Coenzyme Q10 Deficiency: An Update
David Mantle, Lauren Millichap, Jesús Castro‐Marrero, et al.
Antioxidants (2023) Vol. 12, Iss. 8, pp. 1652-1652
Open Access | Times Cited: 21
David Mantle, Lauren Millichap, Jesús Castro‐Marrero, et al.
Antioxidants (2023) Vol. 12, Iss. 8, pp. 1652-1652
Open Access | Times Cited: 21
Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment
Marivi V. Cascajo-Almenara, Natalia Juliá‐Palacios, Roser Urreizti, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 4, pp. 426-434
Open Access | Times Cited: 7
Marivi V. Cascajo-Almenara, Natalia Juliá‐Palacios, Roser Urreizti, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 4, pp. 426-434
Open Access | Times Cited: 7
Understanding Coenzyme Q
Ying Wang, Noah Lilienfeldt, Siegfried Hekimi
Physiological Reviews (2024) Vol. 104, Iss. 4, pp. 1533-1610
Open Access | Times Cited: 7
Ying Wang, Noah Lilienfeldt, Siegfried Hekimi
Physiological Reviews (2024) Vol. 104, Iss. 4, pp. 1533-1610
Open Access | Times Cited: 7
Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signs
Adriana Rebelo, Pedro José Tomaselli, Jessica Medina, et al.
Brain (2023) Vol. 146, Iss. 10, pp. 4191-4199
Closed Access | Times Cited: 12
Adriana Rebelo, Pedro José Tomaselli, Jessica Medina, et al.
Brain (2023) Vol. 146, Iss. 10, pp. 4191-4199
Closed Access | Times Cited: 12
Coenzyme Q4 is a functional substitute for coenzyme Q10 and can be targeted to the mitochondria
Laura Steenberge, Sean Rogers, Andrew Y. Sung, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 5, pp. 107269-107269
Open Access | Times Cited: 4
Laura Steenberge, Sean Rogers, Andrew Y. Sung, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 5, pp. 107269-107269
Open Access | Times Cited: 4
4-Hydroxybenzoic acid rescues multisystemic disease and perinatal lethality in a mouse model of mitochondrial disease
Julia Corral-Sarasa, Juan Manuel Martinez Galvez, Pilar González-García, et al.
Cell Reports (2024) Vol. 43, Iss. 5, pp. 114148-114148
Open Access | Times Cited: 4
Julia Corral-Sarasa, Juan Manuel Martinez Galvez, Pilar González-García, et al.
Cell Reports (2024) Vol. 43, Iss. 5, pp. 114148-114148
Open Access | Times Cited: 4
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
The effects of statins on mitochondria – the current state of knowledge
Małgorzata Belczyk, Małgorzata Knapik-Czajka, Anna Gawędzka, et al.
Farmacja Polska (2025) Vol. 80, Iss. 8, pp. 579-587
Open Access
Małgorzata Belczyk, Małgorzata Knapik-Czajka, Anna Gawędzka, et al.
Farmacja Polska (2025) Vol. 80, Iss. 8, pp. 579-587
Open Access
Two cases of neonatal hyperglycemia caused by a homozygous COQ9 stop‐gain variant
Russell Donis, Maryam Al Badi, Nadia Alhashmi, et al.
Journal of Diabetes Investigation (2025)
Open Access
Russell Donis, Maryam Al Badi, Nadia Alhashmi, et al.
Journal of Diabetes Investigation (2025)
Open Access
New Insights on the Uptake and Trafficking of Coenzyme Q
Michael D. Guile, Akash Jain, Kyle A. Anderson, et al.
Antioxidants (2023) Vol. 12, Iss. 7, pp. 1391-1391
Open Access | Times Cited: 10
Michael D. Guile, Akash Jain, Kyle A. Anderson, et al.
Antioxidants (2023) Vol. 12, Iss. 7, pp. 1391-1391
Open Access | Times Cited: 10
Hem25p is required for mitochondrial IPP transport in fungi
Jonathan Tai, Rachel M. Guerra, Sean Rogers, et al.
Nature Cell Biology (2023) Vol. 25, Iss. 11, pp. 1616-1624
Open Access | Times Cited: 8
Jonathan Tai, Rachel M. Guerra, Sean Rogers, et al.
Nature Cell Biology (2023) Vol. 25, Iss. 11, pp. 1616-1624
Open Access | Times Cited: 8
Primary Coenzyme Q10 Deficiency-Related Ataxias
Piervito Lopriore, Marco Vista, Alessandra Tessa, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 8, pp. 2391-2391
Open Access | Times Cited: 2
Piervito Lopriore, Marco Vista, Alessandra Tessa, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 8, pp. 2391-2391
Open Access | Times Cited: 2
Combined Supplementation of Coenzyme Q10 and Other Nutrients in Specific Medical Conditions
Torsak Tippairote, Geir Bjørklund, Amin Gasmi, et al.
Nutrients (2022) Vol. 14, Iss. 20, pp. 4383-4383
Open Access | Times Cited: 10
Torsak Tippairote, Geir Bjørklund, Amin Gasmi, et al.
Nutrients (2022) Vol. 14, Iss. 20, pp. 4383-4383
Open Access | Times Cited: 10
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization
Xiang Lin, Junyi Jiang, Daojun Hong, et al.
Movement Disorders (2023) Vol. 39, Iss. 1, pp. 152-163
Closed Access | Times Cited: 6
Xiang Lin, Junyi Jiang, Daojun Hong, et al.
Movement Disorders (2023) Vol. 39, Iss. 1, pp. 152-163
Closed Access | Times Cited: 6
Novel mitochondrial-related gene signature predicts prognosis and immunological status in glioma
Yongsheng Liu, Lize Cai, Hao Wang, et al.
Translational Cancer Research (2024) Vol. 13, Iss. 7, pp. 3338-3353
Open Access | Times Cited: 1
Yongsheng Liu, Lize Cai, Hao Wang, et al.
Translational Cancer Research (2024) Vol. 13, Iss. 7, pp. 3338-3353
Open Access | Times Cited: 1
4-Hydroxybenzoic acid restrains Nlrp3 inflammasome priming and activation via disrupting PU.1 DNA binding activity and direct antioxidation
Yanbo Kou, Qiyue Jing, Xiaoqing Yan, et al.
Chemico-Biological Interactions (2024) Vol. 404, pp. 111262-111262
Closed Access | Times Cited: 1
Yanbo Kou, Qiyue Jing, Xiaoqing Yan, et al.
Chemico-Biological Interactions (2024) Vol. 404, pp. 111262-111262
Closed Access | Times Cited: 1
Syndromic Retinitis Pigmentosa
Jessica S. Karuntu, Hind Almushattat, Xuan‐Thanh‐An Nguyen, et al.
Progress in Retinal and Eye Research (2024), pp. 101324-101324
Open Access | Times Cited: 1
Jessica S. Karuntu, Hind Almushattat, Xuan‐Thanh‐An Nguyen, et al.
Progress in Retinal and Eye Research (2024), pp. 101324-101324
Open Access | Times Cited: 1
Hem25p is a mitochondrial IPP transporter
Jonathan Tai, Rachel M. Guerra, Sean Rogers, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Jonathan Tai, Rachel M. Guerra, Sean Rogers, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Primary Coenzyme Q10 Deficiency (COQ10D)
Neluwa-Liyanage R. Indika, Udara D. Senarathne, Jannik Prasuhn
Springer eBooks (2024), pp. 1-7
Closed Access
Neluwa-Liyanage R. Indika, Udara D. Senarathne, Jannik Prasuhn
Springer eBooks (2024), pp. 1-7
Closed Access
Refractory Epilepsy in Adult Patient With COQ8A Variant Improves With CoQ10 Supplementation
Jonathan LoVoi, Don Q. Thai, Jennifer L. Han, et al.
Neurology Genetics (2024) Vol. 10, Iss. 5
Open Access
Jonathan LoVoi, Don Q. Thai, Jennifer L. Han, et al.
Neurology Genetics (2024) Vol. 10, Iss. 5
Open 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
Novel Coenzyme Q2 (CoQ2) Mutation in a Pediatric Patient With Primary Steroid-Resistant Nephrotic Syndrome Due to Coenzyme Q10 (CoQ10) Deficiency
Shahad Alwazzan, Osama Inweihi, Neetha Soma John, et al.
Cureus (2024)
Open Access
Shahad Alwazzan, Osama Inweihi, Neetha Soma John, et al.
Cureus (2024)
Open Access
Coenzyme Q4is a functional substitute for coenzyme Q10and can be targeted to the mitochondria
Laura Steenberge, Andrew Y. Sung, Jing Fan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Laura Steenberge, Andrew Y. Sung, Jing Fan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1