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:
Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence Networks
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 5
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 5
Showing 5 citing articles:
Better understanding the phenotypic effects of drugs through shared targets in genetic disease networks
Elena Díaz-Santiago, Aurelio A. Moya‐García, José Manuel Pérez-García, et al.
Frontiers in Pharmacology (2025) Vol. 15
Open Access
Elena Díaz-Santiago, Aurelio A. Moya‐García, José Manuel Pérez-García, et al.
Frontiers in Pharmacology (2025) Vol. 15
Open Access
The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases
Dèlia Yubero, Daniel Natera‐de Benito, Jordi Pijuan, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4274-4274
Open Access | Times Cited: 16
Dèlia Yubero, Daniel Natera‐de Benito, Jordi Pijuan, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4274-4274
Open Access | Times Cited: 16
Hypermobile Ehlers–Danlos syndrome: A review and a critical appraisal of published genetic research to date
Kirsty Scicluna, Melissa M. Formosa, Rosienne Farrugia, et al.
Clinical Genetics (2021) Vol. 101, Iss. 1, pp. 20-31
Closed Access | Times Cited: 16
Kirsty Scicluna, Melissa M. Formosa, Rosienne Farrugia, et al.
Clinical Genetics (2021) Vol. 101, Iss. 1, pp. 20-31
Closed Access | Times Cited: 16
Network-Based Methods for Approaching Human Pathologies from a Phenotypic Point of View
Juan A. G. Ranea, James R. Perkins, Mónica Chagoyen, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1081-1081
Open Access | Times Cited: 7
Juan A. G. Ranea, James R. Perkins, Mónica Chagoyen, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1081-1081
Open Access | Times Cited: 7
Co-occurrence of CAPN3 homozygous mutation and CCTG expansion in the CNBP gene in a patient with muscular dystrophy
Wiktoria Radziwonik-Frączyk, Ewelina Elert‐Dobkowska, Jolanta Kubalska, et al.
Postępy Psychiatrii i Neurologii (2024) Vol. 33, Iss. 2, pp. 109-114
Open Access
Wiktoria Radziwonik-Frączyk, Ewelina Elert‐Dobkowska, Jolanta Kubalska, et al.
Postępy Psychiatrii i Neurologii (2024) Vol. 33, Iss. 2, pp. 109-114
Open Access
