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:
Novel Homozygous Variant inCOQ7in Siblings With Hereditary Motor Neuropathy
Ian C. P. Smith, Chantal A. Pileggi, Ying Wang, et al.
Neurology Genetics (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 8
Ian C. P. Smith, Chantal A. Pileggi, Ying Wang, et al.
Neurology Genetics (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 8
Showing 8 citing articles:
Understanding Coenzyme Q
Ying Wang, Noah Lilienfeldt, Siegfried Hekimi
Physiological Reviews (2024) Vol. 104, Iss. 4, pp. 1533-1610
Open Access | Times Cited: 6
Ying Wang, Noah Lilienfeldt, Siegfried Hekimi
Physiological Reviews (2024) Vol. 104, Iss. 4, pp. 1533-1610
Open Access | Times Cited: 6
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez‐Cuesta, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 938-946
Open Access | Times Cited: 5
Ilaria Pettenuzzo, Sara Carli, Ana Sánchez‐Cuesta, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 938-946
Open Access | Times Cited: 5
Mutations of the Electron Transport Chain Affect Lifespan and ROS Levels in C. elegans
Fanni Ősz, Aamir Nazir, Krisztina Takács‐Vellai, et al.
Antioxidants (2025) Vol. 14, Iss. 1, pp. 76-76
Open Access
Fanni Ősz, Aamir Nazir, Krisztina Takács‐Vellai, et al.
Antioxidants (2025) Vol. 14, Iss. 1, pp. 76-76
Open Access
New variants expand the neurological phenotype of COQ7 deficiency
María Alcázar‐Fabra, Abraham J. Paredes‐Fuentes, Manuel Torralba Carnerero, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 1047-1068
Open Access | Times Cited: 2
María Alcázar‐Fabra, Abraham J. Paredes‐Fuentes, Manuel Torralba Carnerero, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 1047-1068
Open Access | Times Cited: 2
Axonal Charcot-Marie-Tooth disease due to COQ7 mutation: expanding the genetic and clinical spectrum
Xinyun Zhang, Hai‐Lin Dong, Zhi‐Ying Wu
Brain (2023) Vol. 146, Iss. 12, pp. e117-e119
Closed Access | Times Cited: 2
Xinyun Zhang, Hai‐Lin Dong, Zhi‐Ying Wu
Brain (2023) Vol. 146, Iss. 12, pp. e117-e119
Closed Access | Times Cited: 2
COQ7 splice site variant causing a spastic paraparesis phenotype in siblings
Haseena Sait, Manmohan Pandey, Shubha R. Phadke
Journal of Genetics (2024) Vol. 103, Iss. 2
Closed Access
Haseena Sait, Manmohan Pandey, Shubha R. Phadke
Journal of Genetics (2024) Vol. 103, Iss. 2
Closed Access
COQ7-Related Juvenile-Onset Motor Neuronopathy: A New Pathogenetic Dysfunction Associated with Motor Neuron Disease
Paulo Victor Sgobbi de Souza, Igor Braga Farias, Paulo de Lima Serrano, et al.
Sclerosis (2023) Vol. 1, Iss. 1, pp. 22-26
Open Access
Paulo Victor Sgobbi de Souza, Igor Braga Farias, Paulo de Lima Serrano, et al.
Sclerosis (2023) Vol. 1, Iss. 1, pp. 22-26
Open Access
Distal hereditary motor neuropathy caused by coenzyme Q deficiency due to COQ7 variants
María Andrea Desbats, Leonardo Salviati
Brain (2023) Vol. 146, Iss. 10, pp. 3958-3959
Open Access
María Andrea Desbats, Leonardo Salviati
Brain (2023) Vol. 146, Iss. 10, pp. 3958-3959
Open Access
