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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:

Expanding the phenotype of DNAJC30‐associated Leigh syndrome
Marta Zawadzka, Magdalena Krygier, Małgorzata Pawłowicz, et al.
Clinical Genetics (2022) Vol. 102, Iss. 5, pp. 438-443
Closed Access | Times Cited: 12

Showing 12 citing articles:

Autosomal recessive Leber hereditary optic neuropathy, a new neuro-ophthalmo-genetic paradigm
Guy Lenaers, Cléis Beaulieu, Majida Charif, et al.
Brain (2023) Vol. 146, Iss. 8, pp. 3156-3161
Open Access | Times Cited: 23
Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant
Beryll Blickhäuser, Sarah L. Stenton, Christiane Neuhofer, et al.
Brain (2024) Vol. 147, Iss. 6, pp. 1967-1974
Open Access | Times Cited: 5
Response to: DNAJC30 variants can also manifest phenotypically as Leigh/LHON overlap syndrome
Karol Chojnowski, Kamil Dzwilewski, Magdalena Krygier, et al.
Neurologia i Neurochirurgia Polska (2025)
Closed Access
Emerging Roles of NDUFS8 Located in Mitochondrial Complex I in Different Diseases
Sifan Wang, Yuanbo Kang, Ruifeng Wang, et al.
Molecules (2022) Vol. 27, Iss. 24, pp. 8754-8754
Open Access | Times Cited: 13
Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome
Claudia Nesti, Chiara Ticci, Anna Rubegni, et al.
Journal of Neurology (2023) Vol. 270, Iss. 6, pp. 3266-3269
Closed Access | Times Cited: 7
Digenic Inheritance in Rare Disorders and Mitochondrial Disease—Crossing the Frontier to a More Comprehensive Understanding of Etiology
Christiane Neuhofer, Holger Prokisch
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4602-4602
Open Access | Times Cited: 2
DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients
Anna Skorczyk‐Werner, Katarzyna Tońska, Aleksandra Maciejczuk, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17496-17496
Open Access | Times Cited: 4
Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191T>C in MT-ND3
Shaundra M. Newstead, Josef Finsterer
Annals of African Medicine (2024) Vol. 23, Iss. 3, pp. 512-513
Open Access | Times Cited: 1
Effects of idebenone treatment in a patient with DNAJC30-associated Leigh Syndrome
Kamil Dzwilewski, Karol Chojnowski, Magdalena Krygier, et al.
Neurologia i Neurochirurgia Polska (2024) Vol. 58, Iss. 4, pp. 468-470
Open Access | Times Cited: 1
Dystonia
Katja Lohmann, Christine Klein
Elsevier eBooks (2024), pp. 133-170
Closed Access
An Unusual Presentation of Leber Hereditary Optic Neuropathy‐Plus Case Caused by a Novel DNAJC30 Variant
Hüseyin Bahadır Şenol, Didem Soydemir, Ayşe İpek Polat, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals
Toby Charles Major, Eszter Sára Arany, Katherine Schon, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 1
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