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:
Treating pediatric neuromuscular disorders: The future is now
James J. Dowling, Hernán Gonorazky, Ronald D. Cohn, et al.
American Journal of Medical Genetics Part A (2017) Vol. 176, Iss. 4, pp. 804-841
Open Access | Times Cited: 115
James J. Dowling, Hernán Gonorazky, Ronald D. Cohn, et al.
American Journal of Medical Genetics Part A (2017) Vol. 176, Iss. 4, pp. 804-841
Open Access | Times Cited: 115
Showing 1-25 of 115 citing articles:
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 3, pp. 466-483
Open Access | Times Cited: 208
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 3, pp. 466-483
Open Access | Times Cited: 208
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 5, pp. 1007-1007
Open Access | Times Cited: 193
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 5, pp. 1007-1007
Open Access | Times Cited: 193
Emery‐Dreifuss muscular dystrophy
Scott Heller, Renata Shih, Raghav Kalra, et al.
Muscle & Nerve (2019) Vol. 61, Iss. 4, pp. 436-448
Open Access | Times Cited: 134
Scott Heller, Renata Shih, Raghav Kalra, et al.
Muscle & Nerve (2019) Vol. 61, Iss. 4, pp. 436-448
Open Access | Times Cited: 134
The genetics of congenital myopathies
Hernán Gonorazky, Carsten G. Bönnemann, James J. Dowling
Handbook of clinical neurology (2018), pp. 549-564
Closed Access | Times Cited: 82
Hernán Gonorazky, Carsten G. Bönnemann, James J. Dowling
Handbook of clinical neurology (2018), pp. 549-564
Closed Access | Times Cited: 82
Congenital myopathies: an update
Kristl G. Claeys
Developmental Medicine & Child Neurology (2019) Vol. 62, Iss. 3, pp. 297-302
Open Access | Times Cited: 74
Kristl G. Claeys
Developmental Medicine & Child Neurology (2019) Vol. 62, Iss. 3, pp. 297-302
Open Access | Times Cited: 74
Ryanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature
Tokunbor A. Lawal, Joshua J. Todd, Jessica W. Witherspoon, et al.
Skeletal Muscle (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 65
Tokunbor A. Lawal, Joshua J. Todd, Jessica W. Witherspoon, et al.
Skeletal Muscle (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 65
Neonatal encephalopathy: Etiologies other than hypoxic-ischemic encephalopathy
Amanda G. Sandoval Karamian, Saadet Mercimek‐Andrews, Khorshid Mohammad, et al.
Seminars in Fetal and Neonatal Medicine (2021) Vol. 26, Iss. 5, pp. 101272-101272
Closed Access | Times Cited: 42
Amanda G. Sandoval Karamian, Saadet Mercimek‐Andrews, Khorshid Mohammad, et al.
Seminars in Fetal and Neonatal Medicine (2021) Vol. 26, Iss. 5, pp. 101272-101272
Closed Access | Times Cited: 42
Collagen VI is required for the structural and functional integrity of the neuromuscular junction
Matilde Cescon, Di Gregorio, Nane Eiber, et al.
Acta Neuropathologica (2018) Vol. 136, Iss. 3, pp. 483-499
Closed Access | Times Cited: 47
Matilde Cescon, Di Gregorio, Nane Eiber, et al.
Acta Neuropathologica (2018) Vol. 136, Iss. 3, pp. 483-499
Closed Access | Times Cited: 47
Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy
Lorenzo Maggi, Silvia Bonanno, Concetta Altamura, et al.
Cells (2021) Vol. 10, Iss. 6, pp. 1521-1521
Open Access | Times Cited: 33
Lorenzo Maggi, Silvia Bonanno, Concetta Altamura, et al.
Cells (2021) Vol. 10, Iss. 6, pp. 1521-1521
Open Access | Times Cited: 33
Complexity of skeletal muscle degeneration: multi-systems pathophysiology and organ crosstalk in dystrophinopathy
Kay Ohlendieck, Dieter Swandulla
Pflügers Archiv - European Journal of Physiology (2021) Vol. 473, Iss. 12, pp. 1813-1839
Open Access | Times Cited: 33
Kay Ohlendieck, Dieter Swandulla
Pflügers Archiv - European Journal of Physiology (2021) Vol. 473, Iss. 12, pp. 1813-1839
Open Access | Times Cited: 33
Update on Muscular Dystrophies with Focus on Novel Treatments and Biomarkers
Neil Datta, Partha S. Ghosh
Current Neurology and Neuroscience Reports (2020) Vol. 20, Iss. 6
Closed Access | Times Cited: 36
Neil Datta, Partha S. Ghosh
Current Neurology and Neuroscience Reports (2020) Vol. 20, Iss. 6
Closed Access | Times Cited: 36
Gastrointestinal and nutritional care in pediatric neuromuscular disorders
Valeria Dipasquale, Rossella Morello, Claudio Romano
World Journal of Clinical Pediatrics (2023) Vol. 12, Iss. 4, pp. 197-204
Open Access | Times Cited: 12
Valeria Dipasquale, Rossella Morello, Claudio Romano
World Journal of Clinical Pediatrics (2023) Vol. 12, Iss. 4, pp. 197-204
Open Access | Times Cited: 12
Treating neuromuscular diseases: unveiling gene therapy breakthroughs and pioneering future applications
Yu‐Fu Wu, Jun‐An Chen, Yuh‐Jyh Jong
Journal of Biomedical Science (2025) Vol. 32, Iss. 1
Open Access
Yu‐Fu Wu, Jun‐An Chen, Yuh‐Jyh Jong
Journal of Biomedical Science (2025) Vol. 32, Iss. 1
Open Access
Recent advances in understanding congenital myopathies
Gianina Ravenscroft, Robert J. Bryson‐Richardson, Kristen L. Nowak, et al.
F1000Research (2018) Vol. 7, pp. 1921-1921
Open Access | Times Cited: 35
Gianina Ravenscroft, Robert J. Bryson‐Richardson, Kristen L. Nowak, et al.
F1000Research (2018) Vol. 7, pp. 1921-1921
Open Access | Times Cited: 35
From Doubt to Diagnosis: Canadian Patient Perspectives on a Limb‐Girdle Muscular Dystrophy Diagnosis
Homira Osman, Zainab Adamji, Gerald Pfeffer, et al.
Health Expectations (2025) Vol. 28, Iss. 3
Open Access
Homira Osman, Zainab Adamji, Gerald Pfeffer, et al.
Health Expectations (2025) Vol. 28, Iss. 3
Open Access
Mouse model of severe recessive RYR1-related myopathy
Stephanie Brennan, Maricela García‐Castañeda, Antonio Michelucci, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 18, pp. 3024-3036
Open Access | Times Cited: 28
Stephanie Brennan, Maricela García‐Castañeda, Antonio Michelucci, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 18, pp. 3024-3036
Open Access | Times Cited: 28
Clinical exome sequencing in the diagnosis of pediatric neuromuscular disease
Isabella Herman, Michael A. Lopez, Dana Marafi, et al.
Muscle & Nerve (2020) Vol. 63, Iss. 3, pp. 304-310
Closed Access | Times Cited: 27
Isabella Herman, Michael A. Lopez, Dana Marafi, et al.
Muscle & Nerve (2020) Vol. 63, Iss. 3, pp. 304-310
Closed Access | Times Cited: 27
Emerging proteomic biomarkers of X-linked muscular dystrophy
Paul Dowling, Sandra Murphy, Margit Zweyer, et al.
Expert Review of Molecular Diagnostics (2019) Vol. 19, Iss. 8, pp. 739-755
Open Access | Times Cited: 26
Paul Dowling, Sandra Murphy, Margit Zweyer, et al.
Expert Review of Molecular Diagnostics (2019) Vol. 19, Iss. 8, pp. 739-755
Open Access | Times Cited: 26
Respiratory considerations in patients with neuromuscular disorders
Nina Patel, Ileana M. Howard, Ahmet Baydur
Muscle & Nerve (2023) Vol. 68, Iss. 2, pp. 122-141
Closed Access | Times Cited: 8
Nina Patel, Ileana M. Howard, Ahmet Baydur
Muscle & Nerve (2023) Vol. 68, Iss. 2, pp. 122-141
Closed Access | Times Cited: 8
Pathological Involvement of Protein Phase Separation and Aggregation in Neurodegenerative Diseases
Y. Wu, Biao Ma, Chang Yu Liu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 10187-10187
Open Access | Times Cited: 3
Y. Wu, Biao Ma, Chang Yu Liu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 10187-10187
Open Access | Times Cited: 3
ATS Core Curriculum 2022. Pediatric Pulmonary Medicine: Updates in pediatric neuromuscular disease
Carmen Leon‐Astudillo, Caroline U. A. Okorie, Michael McCown, et al.
Pediatric Pulmonology (2023) Vol. 58, Iss. 7, pp. 1866-1874
Closed Access | Times Cited: 8
Carmen Leon‐Astudillo, Caroline U. A. Okorie, Michael McCown, et al.
Pediatric Pulmonology (2023) Vol. 58, Iss. 7, pp. 1866-1874
Closed Access | Times Cited: 8
Cored in the act: the use of models to understand core myopathies
Aurora Fusto, Louise A. Moyle, Penney M. Gilbert, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 12
Open Access | Times Cited: 20
Aurora Fusto, Louise A. Moyle, Penney M. Gilbert, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 12
Open Access | Times Cited: 20
Peak Cough Flow in Children with Neuromuscular Disorders
Nidhi Kotwal, Prateek Shukla, Geovanny F. Pérez
Lung (2020) Vol. 198, Iss. 2, pp. 371-375
Closed Access | Times Cited: 20
Nidhi Kotwal, Prateek Shukla, Geovanny F. Pérez
Lung (2020) Vol. 198, Iss. 2, pp. 371-375
Closed Access | Times Cited: 20
New diagnostic and therapeutic modalities in neuromuscular disorders in children
Mahesh Chikkannaiah, Irma Reyes
Current problems in pediatric and adolescent health care (2021) Vol. 51, Iss. 7, pp. 101033-101033
Closed Access | Times Cited: 17
Mahesh Chikkannaiah, Irma Reyes
Current problems in pediatric and adolescent health care (2021) Vol. 51, Iss. 7, pp. 101033-101033
Closed Access | Times Cited: 17
