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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:

DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber’s hereditary optic neuropathy and optic atrophy
Sinja Kieninger, Ting Xiao, Nicole Weisschuh, et al.
Journal of Medical Genetics (2022) Vol. 59, Iss. 10, pp. 1027-1034
Open Access | Times Cited: 21

Showing 21 citing articles:

Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial
Patrick Yu‐Wai‐Man, Valério Carelli, Nancy J. Newman, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 3, pp. 101437-101437
Open Access | Times Cited: 17
Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and management
Nancy J. Newman, Patrick Yu‐Wai‐Man, Valérie Biousse, et al.
The Lancet Neurology (2022) Vol. 22, Iss. 2, pp. 172-188
Open Access | Times Cited: 57
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
Leber’s hereditary optic neuropathy – current status of idebenone and gene replacement therapies
Thomas Klopstock, Li Zeng, Claudia Priglinger
Medizinische Genetik (2025) Vol. 37, Iss. 1, pp. 57-63
Closed Access | Times Cited: 1
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands
Aude Rocatcher, Valérie Desquiret‐Dumas, Majida Charif, et al.
Brain (2022) Vol. 146, Iss. 2, pp. 455-460
Open Access | Times Cited: 28
The value of genetic testing in pediatric and adult ophthalmology
Ulrich Kellner, Simone Kellner, Silke Weinitz, et al.
Medizinische Genetik (2025) Vol. 37, Iss. 1, pp. 11-18
Closed Access
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree
Sonia Emperador, Mouna Habbane, Ester López‐Gallardo, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 3
Modifier variants in metabolic pathways are associated with an increased penetrance of Leber’s Hereditary Optic Neuropathy
Eszter Sára Arany, Catarina Olimpio, Ida Paramonov, et al.
European Journal of Human Genetics (2025)
Open Access
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
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
Optic Nerve Structural and Functional Changes in LHON-Affected and Asymptomatic Maternal Relatives: Association with H and HV Mitochondrial Haplogroups
Clare Quigley, Kirk Stephenson, Paul F. Kenna, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1068-1068
Open Access | Times Cited: 4
Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series
Sanja Petrović Pajić, Martina Jarc-Vidmar, Ana Fakin, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 6
Neuromuscular disease: 2022 update.
Marta Margeta
DOAJ (DOAJ: Directory of Open Access Journals) (2022) Vol. 3
Closed Access | Times Cited: 5
Autosomal recessive Leber's hereditary optic neuropathy caused by a homozygous variant in DNAJC30 gene
L. Mauring, Sanna Puusepp, M. Parik, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 9, pp. 104821-104821
Closed Access | Times Cited: 2
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes
Yuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Brain (2024)
Open Access
Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON)
Paula Buonfiglio, Sebastián Menazzi, Liliana Francipane, et al.
PLoS ONE (2023) Vol. 18, Iss. 2, pp. e0275703-e0275703
Open Access | Times Cited: 1
Leber’s hereditary optic neuropathy: Update on the novel genes and therapeutic options
Jui-Lin Hu, Chih-Chien Hsu, Yu‐Jer Hsiao, et al.
Journal of the Chinese Medical Association (2023)
Open Access | Times Cited: 1
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
Phenotypic Variation of Autosomal Recessive Leber Hereditary Optic Neuropathy (arLHON) in One Family
Dorota Pojda‐Wilczek, Justyna Wójcik, Bożena Kmak, et al.
Diagnostics (2022) Vol. 12, Iss. 11, pp. 2701-2701
Open Access | Times Cited: 2
La génétique et physiopathologie de la neuropathie optique de Leber
V.M. Smimov
Journal Français d Ophtalmologie (2022) Vol. 45, Iss. 8, pp. S17-S23
Closed Access | Times Cited: 1
Current and Emerging Therapies for Leber Hereditary Optic Neuropathy
Pamela Davila-Siliezar, Noor Laylani, Konstantinos A. A. Douglas, et al.
touchREVIEWS in Ophthalmology (2023) Vol. 17, Iss. 1, pp. 21-21
Open Access
Long-term changes in morphological and functional parameters of the optic nerve in patients with various genetic variants of hereditary optic neuropathies
Yu K Murakhovskaya, N A Andreeva, Polina G. Tsygankova, et al.
Russian Annals of Ophthalmology (2023) Vol. 139, Iss. 6, pp. 77-77
Closed Access
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