Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Congenital myopathies: an update
Kristl G. Claeys
Developmental Medicine & Child Neurology (2019) Vol. 62, Iss. 3, pp. 297-302
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort
Maryke Schoonen, Mahmoud R. Fassad, Krutik Patel, et al.
European Journal of Human Genetics (2025)
Open Access | Times Cited: 1
The widening genetic and myopathologic spectrum of Congenital Myopathies (CMYOs): a narrative review
Marion Onnée, E. Malfatti
Neuromuscular Disorders (2025), pp. 105338-105338
Closed Access | Times Cited: 1
Special Issue: The Actin-Myosin Interaction in Muscle: Background and Overview
John M. Squire
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 22, pp. 5715-5715
Open Access | Times Cited: 70
Reissner fibre-induced urotensin signalling from cerebrospinal fluid-contacting neurons prevents scoliosis of the vertebrate spine
Hao Lu, Aidana Shagirova, Julian Goggi, et al.
Biology Open (2020) Vol. 9, Iss. 5
Open Access | Times Cited: 53
Progressive external ophthalmoplegia
Michio Hirano, Robert D. S. Pitceathly
Handbook of clinical neurology (2023), pp. 9-21
Open Access | Times Cited: 19
Nutritional Strategies for Muscle Atrophy: Current Evidence and Underlying Mechanisms
Yuntian Shen, Chen Zhang, Chaolun Dai, et al.
Molecular Nutrition & Food Research (2024) Vol. 68, Iss. 10
Closed Access | Times Cited: 7
A review of major causative genes in congenital myopathies
Masashi Ogasawara, Ichizo Nishino
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 215-225
Closed Access | Times Cited: 27
MyoSight—semi-automated image analysis of skeletal muscle cross sections
Lyle W. Babcock, Amy D. Hanna, Nadia H. Agha, et al.
Skeletal Muscle (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 36
Case study on the applicability of the international classification of functioning, disability, and health in a patient with mitochondrial myopathy treated in the rehabilitation service
Mihaela Taranu, Daniel Borda, Jorge Eduardo Rivadeneira, et al.
Journal of the International Society of Physical and Rehabilitation Medicine (2025)
Open Access
The Hypotonic Infant: Recognition and Investigation
Louise Hartley, Laura Hyrapetian
Elsevier eBooks (2025)
Closed Access
A Systematic Review and Meta-Analysis of the Prevalence of Congenital Myopathy
Kun Huang, Fangfang Bi, Huan Yang
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 25
Therapeutic approaches in different congenital myopathies
Charlotte Gineste, Jocelyn Laporte
Current Opinion in Pharmacology (2022) Vol. 68, pp. 102328-102328
Open Access | Times Cited: 17
Congenital Myopathies
Ruchee Patel, Carsten G. Bönnemann
Elsevier eBooks (2025)
Closed Access
Precision Medicine in Rare Diseases
Irene Villalón-García, Mónica Álvarez-Córdoba, Juan M. Suárez-Rivero, et al.
Diseases (2020) Vol. 8, Iss. 4, pp. 42-42
Open Access | Times Cited: 25
MR imaging of inherited myopathies: a review and proposal of imaging algorithms
Laís Uyeda Aivazoglou, Júlio Brandão Guimarães, Thomas M. Link, et al.
European Radiology (2021) Vol. 31, Iss. 11, pp. 8498-8512
Closed Access | Times Cited: 16
Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India
Ganaraja Valakunja Harikrishna, Hansashree Padmanabha, Kiran Polavarapu, et al.
Journal of Neuromuscular Diseases (2024) Vol. 11, Iss. 5, pp. 935-957
Open Access | Times Cited: 2
ALDH2 mutation promotes skeletal muscle atrophy in mice via accumulation of oxidative stress
Hiroki Kobayashi, Satoshi Nakamura, Yuiko Sato, et al.
Bone (2020) Vol. 142, pp. 115739-115739
Open Access | Times Cited: 17
Molecular signatures of inherited and acquired sporadic late onset nemaline myopathies
Stefan Nicolau, Aneesha Dasgupta, Surendra Dasari, et al.
Acta Neuropathologica Communications (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 6
The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort
Daniel Natera‐de Benito, C. Ortez, Cristina Jou, et al.
Pediatric Neurology (2020) Vol. 115, pp. 50-65
Open Access | Times Cited: 16
Tissue Engineering Applied to Skeletal Muscle: Strategies and Perspectives
Ana Luisa Lopes Martins, Luciana Pastena Giorno, Arnaldo Rodrigues Santos
Bioengineering (2022) Vol. 9, Iss. 12, pp. 744-744
Open Access | Times Cited: 9
Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress
Marie-Céline François-Heude, Ulrike Walther‐Louvier, Caroline Espil‐Taris, et al.
European Journal of Paediatric Neurology (2021) Vol. 31, pp. 78-87
Open Access | Times Cited: 12
A novel frameshift ACTN2 variant causes a rare adult‐onset distal myopathy with multi‐minicores
Lei Chen, Dian‐Fu Chen, Hai‐Lin Dong, et al.
CNS Neuroscience & Therapeutics (2021) Vol. 27, Iss. 10, pp. 1198-1205
Open Access | Times Cited: 12
Correlation of Phenotype–Genotype and Protein Structure in RYR1-Related Myopathy
Xingzhi Chang, Risheng Wei, Cuijie Wei, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 9
A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy
Nathalie Laflamme, Baiba Lāce, Samarth Thonta Setty, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 11
Update on Congenital Myopathies in Adulthood
George K. Papadimas, Sophia Xirou, Evangelia Kararizou, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 10, pp. 3694-3694
Open Access | Times Cited: 11
Page 1 - Next Page

Scroll to top