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:
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Andrea Cortese, Sarah J. Beecroft, Stefano Facchini, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Andrea Cortese, Sarah J. Beecroft, Stefano Facchini, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Showing 13 citing articles:
Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis
Elisa Vegezzi, Hiroyuki Ishiura, D. Cristopher Bragg, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 7, pp. 725-739
Closed Access | Times Cited: 12
Elisa Vegezzi, Hiroyuki Ishiura, D. Cristopher Bragg, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 7, pp. 725-739
Closed Access | Times Cited: 12
Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies
Elsa Leitão, Christopher Schröder, Christel Depienne
Revue Neurologique (2024) Vol. 180, Iss. 5, pp. 383-392
Open Access | Times Cited: 9
Elsa Leitão, Christopher Schröder, Christel Depienne
Revue Neurologique (2024) Vol. 180, Iss. 5, pp. 383-392
Open Access | Times Cited: 9
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability
Bharati Jadhav, Paras Garg, Joke J.F.A. van Vugt, et al.
Nature Genetics (2024)
Closed Access | Times Cited: 5
Bharati Jadhav, Paras Garg, Joke J.F.A. van Vugt, et al.
Nature Genetics (2024)
Closed Access | Times Cited: 5
CGG/CCG Repeat Expansions in LOC642361/NUTM2B-AS1 in Thai Patients With Oculopharyngodistal Myopathy
Sunsanee Pongpakdee, Metha Apiwattanakul, Thanes Termglinchan, et al.
Neurology Genetics (2024) Vol. 10, Iss. 4
Open Access | Times Cited: 4
Sunsanee Pongpakdee, Metha Apiwattanakul, Thanes Termglinchan, et al.
Neurology Genetics (2024) Vol. 10, Iss. 4
Open Access | Times Cited: 4
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Wouter De Coster, Ida Höijer, Inge Bruggeman, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 2074-2080
Open Access | Times Cited: 4
Wouter De Coster, Ida Höijer, Inge Bruggeman, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 2074-2080
Open Access | Times Cited: 4
A case report of oculopharyngodistal myopathy with 126 CGG repeat expansions in RILPL1
Wenjing Wang, Tielun Yin, Xinyu Zhang, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Wenjing Wang, Tielun Yin, Xinyu Zhang, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Microsatellite expansions hidden within the human dark genome are translated in novel and toxic proteins causing muscle and neurodegenerative diseases
Nicolas Charlet‐Berguerand, Manon Boivin, Jiaxi Yu, et al.
Research Square (Research Square) (2025)
Closed Access
Nicolas Charlet‐Berguerand, Manon Boivin, Jiaxi Yu, et al.
Research Square (Research Square) (2025)
Closed Access
Long-read sequencing for diagnosis of genetic myopathies
Dennis Yeow, Laura Ivete Rudaks, Ryan L. Davis, et al.
BMJ Neurology Open (2025) Vol. 7, Iss. 1, pp. e000990-e000990
Open Access
Dennis Yeow, Laura Ivete Rudaks, Ryan L. Davis, et al.
BMJ Neurology Open (2025) Vol. 7, Iss. 1, pp. e000990-e000990
Open Access
Double vision: 2D and 3D mosquito trajectories can be as valuable for behaviour analysis via machine learning
Yasser M. Qureshi, Vitaly Voloshin, Catherine E. Towers, et al.
Parasites & Vectors (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 3
Yasser M. Qureshi, Vitaly Voloshin, Catherine E. Towers, et al.
Parasites & Vectors (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 3
Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies
Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, et al.
Movement Disorders (2025)
Open Access
Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, et al.
Movement Disorders (2025)
Open Access
Identification of New Repeat Expansion Diseases
Hiroyuki Ishiura
Neurology and Clinical Neuroscience (2025)
Closed Access
Hiroyuki Ishiura
Neurology and Clinical Neuroscience (2025)
Closed Access
RNA Gain-of-Function Mechanisms in Short Tandem Repeat Diseases
Mackenzie L. Davenport, Maurice S. Swanson
RNA (2024), pp. rna.080277.124-rna.080277.124
Closed Access | Times Cited: 2
Mackenzie L. Davenport, Maurice S. Swanson
RNA (2024), pp. rna.080277.124-rna.080277.124
Closed Access | Times Cited: 2
Current advance on distal myopathy genetics
Johanna Ranta‐aho, Mridul Johari, B. Udd
Current Opinion in Neurology (2024) Vol. 37, Iss. 5, pp. 515-522
Closed Access | Times Cited: 1
Johanna Ranta‐aho, Mridul Johari, B. Udd
Current Opinion in Neurology (2024) Vol. 37, Iss. 5, pp. 515-522
Closed Access | Times Cited: 1
