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OpenAlex Citation Counts

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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:

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

Showing 12 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: 7
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
Lipid metabolism alterations in peripheral neuropathies
Alessio Silva, Robert Prior, Maurizio D’Antonio, et al.
Neuron (2025)
Closed Access
Hereditary spastic paraplegia: Novel insights into the pathogenesis and management
Wireko Andrew Awuah, Joecelyn Kirani Tan, Anastasiia D. Shkodina, et al.
SAGE Open Medicine (2023) Vol. 12
Open Access | Times Cited: 9
Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia
Yusen Qiu, Ying Xiong, Lulu Wang, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 4, pp. 1067-1074
Open Access | Times Cited: 3
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
Reticulon 2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity
Reza Maroofian, Payam Sarraf, Thomas J O’Brien, et al.
Brain (2024) Vol. 147, Iss. 7, pp. 2334-2343
Open Access | Times Cited: 1
The GENESIS database and tools: A decade of discovery in Mendelian genomics
Matt C. Danzi, Eric Powell, Adriana Rebelo, et al.
Experimental Neurology (2024) Vol. 382, pp. 114978-114978
Closed Access | Times Cited: 1
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
Hereditary Motor Neuropathy
Jonathan De Winter, Jonathan Baets
Elsevier eBooks (2024)
Closed Access
Primary CoQ10 deficiency: treatable heterogeneous group of disorders
Ronen Spiegel
European Journal of Human Genetics (2024)
Open Access
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
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
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