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:
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
Showing 16 citing articles:
Genetic landscape of Charcot–Marie–Tooth disease in Vietnam: A prospective multicenter study
Hoang Tien Trong Nghia, Thirugnanam Umapathi, Nguyen Minh Duc, et al.
Journal of Neuromuscular Diseases (2025) Vol. 12, Iss. 1
Closed Access
Hoang Tien Trong Nghia, Thirugnanam Umapathi, Nguyen Minh Duc, et al.
Journal of Neuromuscular Diseases (2025) Vol. 12, Iss. 1
Closed Access
Neuromuscular disorders: finding the missing genetic diagnoses
Katherine Koczwara, Nicole J. Lake, Alec M. DeSimone, et al.
Trends in Genetics (2022) Vol. 38, Iss. 9, pp. 956-971
Closed Access | Times Cited: 11
Katherine Koczwara, Nicole J. Lake, Alec M. DeSimone, et al.
Trends in Genetics (2022) Vol. 38, Iss. 9, pp. 956-971
Closed Access | Times Cited: 11
Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease
Berta Estévez‐Arias, Laura Carrera‐García, A. Nascimento, et al.
Journal of Translational Genetics and Genomics (2022) Vol. 6, pp. 333-352
Open Access | Times Cited: 8
Berta Estévez‐Arias, Laura Carrera‐García, A. Nascimento, et al.
Journal of Translational Genetics and Genomics (2022) Vol. 6, pp. 333-352
Open Access | Times Cited: 8
Genetic Profile of Patients with Limb-Girdle Muscle Weakness in the Chilean Population
Mathieu Cérino, Patricio González‐Hormazábal, Mario Abaji, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1076-1076
Open Access | Times Cited: 7
Mathieu Cérino, Patricio González‐Hormazábal, Mario Abaji, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1076-1076
Open Access | Times Cited: 7
The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics
Laynie Dratch, Tanya Bardakjian, Kelsey Johnson, et al.
(2024)
Open Access | Times Cited: 1
Laynie Dratch, Tanya Bardakjian, Kelsey Johnson, et al.
(2024)
Open Access | Times Cited: 1
The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics
Laynie Dratch, Tanya M. Bardakjian, Kelsey Johnson, et al.
Biology (2024) Vol. 13, Iss. 2, pp. 93-93
Open Access | Times Cited: 1
Laynie Dratch, Tanya M. Bardakjian, Kelsey Johnson, et al.
Biology (2024) Vol. 13, Iss. 2, pp. 93-93
Open Access | Times Cited: 1
Improving Diagnostic Precision: Phenotype-Driven Analysis Uncovers a Maternal Mosaicism in an Individual with RYR1-Congenital Myopathy
Berta Estévez‐Arias, Leslie Matalonga, Loreto Martorell, et al.
Journal of Neuromuscular Diseases (2024) Vol. 11, Iss. 3, pp. 647-653
Open Access | Times Cited: 1
Berta Estévez‐Arias, Leslie Matalonga, Loreto Martorell, et al.
Journal of Neuromuscular Diseases (2024) Vol. 11, Iss. 3, pp. 647-653
Open Access | Times Cited: 1
Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies
Sofía Gouveia, M.E. Vázquez-Mosquera, Emiliano Gonzaléz‐Vioque, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 10, pp. 2750-2750
Open Access | Times Cited: 6
Sofía Gouveia, M.E. Vázquez-Mosquera, Emiliano Gonzaléz‐Vioque, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 10, pp. 2750-2750
Open Access | Times Cited: 6
Current Status of Genetic Counselling for Rare Diseases in Spain
Sara Álvaro-Sánchez, Irene Abreu‐Rodríguez, Anna Abulí, et al.
Diagnostics (2021) Vol. 11, Iss. 12, pp. 2320-2320
Open Access | Times Cited: 7
Sara Álvaro-Sánchez, Irene Abreu‐Rodríguez, Anna Abulí, et al.
Diagnostics (2021) Vol. 11, Iss. 12, pp. 2320-2320
Open Access | Times Cited: 7
Diagnostic strategies in patients with undiagnosed and rare diseases
Dídac Casas‐Alba, Janet Hoenicka, Alba Vilanova‐Adell, et al.
Journal of Translational Genetics and Genomics (2022) Vol. 6, pp. 322-332
Open Access | Times Cited: 3
Dídac Casas‐Alba, Janet Hoenicka, Alba Vilanova‐Adell, et al.
Journal of Translational Genetics and Genomics (2022) Vol. 6, pp. 322-332
Open Access | Times Cited: 3
Bialelic Pathogenic (c.830G>A(p.R277Q)) Variant Disrupting the GNE Gene Function and Causes Nonaka myopathy Phenotype
Mustafa Doğan, Ekrem Akbulut, Alper Gezdirici, et al.
Cytology and Genetics (2023) Vol. 57, Iss. 4, pp. 347-355
Closed Access | Times Cited: 1
Mustafa Doğan, Ekrem Akbulut, Alper Gezdirici, et al.
Cytology and Genetics (2023) Vol. 57, Iss. 4, pp. 347-355
Closed Access | Times Cited: 1
Las enfermedades minoritarias en España: una mirada hacia adelante
Antoni Riera-Mestre
Medicina Clínica (2022) Vol. 158, Iss. 6, pp. 274-276
Open Access | Times Cited: 1
Antoni Riera-Mestre
Medicina Clínica (2022) Vol. 158, Iss. 6, pp. 274-276
Open Access | Times Cited: 1
Whole genome and transcriptome sequencing in neuromuscular disorders: a diagnostic and health economic analysis
Ziying Yang, Xiaoru Yang, Yunmei Chen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Ziying Yang, Xiaoru Yang, Yunmei Chen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Rare diseases in Spain: a look into the future
Antoni Riera-Mestre
Medicina Clínica (English Edition) (2022) Vol. 158, Iss. 6, pp. 274-276
Closed Access
Antoni Riera-Mestre
Medicina Clínica (English Edition) (2022) Vol. 158, Iss. 6, pp. 274-276
Closed Access
