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OpenAlex Citation Counts

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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:

Gene therapy for glycogen storage diseases
Dwight D. Koeberl, Rebecca L. Koch, Jeong‐A Lim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 93-118
Closed Access | Times Cited: 19

Showing 19 citing articles:

Glycogen storage diseases
William B. Hannah, Terry G. J. Derks, Mitchell L. Drumm, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Closed Access | Times Cited: 40
Liver‐directed gene therapy for inherited metabolic diseases
Julien Baruteau, Nicola Brunetti‐Pierri, Paul Gissen
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 1, pp. 9-21
Open Access | Times Cited: 14
IMPC impact on preclinical mouse models
Sabine M. Hölter, Pilar Cacheiro, Damian Smedley, et al.
Mammalian Genome (2025)
Open Access
Gene Therapy with Gene Delivery Systems and Therapeutic Strategies: A New Frontier in Cancer Treatment
Thippenahalli Narasimhaiah Ramakrishnaiah, Sowbhagya Ramachandregowda, Harsha Muktha, et al.
Journal of Drug Delivery Science and Technology (2025), pp. 106798-106798
Closed Access
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7
Juan Zhu, Hongping Yu, Jing Zou, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Mission possible: Gene therapy for inherited metabolic diseases
Julien Baruteau, Nandaki Keshavan, Charles P. Venditti
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 1, pp. 5-6
Open Access | Times Cited: 2
Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases
Colin Walsh, Sha Jin
Cells (2024) Vol. 13, Iss. 12, pp. 1052-1052
Open Access | Times Cited: 2
Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs)
Kumudesh Mishra, Or Kakhlon
(2024)
Open Access | Times Cited: 1
Precision medicine in action for Pompe disease
Antonietta Tarallo, Giancarlo Parenti, Nicola Brunetti‐Pierri
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 3, pp. 102265-102265
Open Access | Times Cited: 1
Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs)
Kumudesh Mishra, Or Kakhlon
Biomolecules (2024) Vol. 14, Iss. 9, pp. 1096-1096
Open Access | Times Cited: 1
The Autophagic Activator GHF-201 Can Alleviate Pathology in a Mouse Model and in Patient Fibroblasts of Type III Glycogenosis
Kumudesh Mishra, Sahar Sweetat, Saja Baraghithy, et al.
Biomolecules (2024) Vol. 14, Iss. 8, pp. 893-893
Open Access | Times Cited: 1
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort
Parinaz Moghimi, Feyzollah Hashemi‐Gorji, Sanaz Jamshidi, et al.
Biochemical Genetics (2024)
Closed Access
Detailed Insights into Heart Histology and Cardiomyocyte Molecular Architecture
maha hammady, Lamia A Heikal, Nadia Amin, et al.
Deleted Journal (2024), pp. 61-78
Open Access
Functional impairments, known genetic disorders, and review reports of established and possible therapies for specific genetic diseases
Moyra Smith
Elsevier eBooks (2024), pp. 159-205
Closed Access
In silico analysis of point mutation (c.687dupC; p. Met230Hisfs*6) in PGAM2 gene that causes Glycogen Storage Disease (GSD) Type X
Ayesha Abid, Elwalid Fadul Nasir, Hassaan Mehboob Awan
Kuwait Journal of Science (2024) Vol. 52, Iss. 1, pp. 100344-100344
Open Access
Consequences of COVID-19 on Imports and Exports of China with Forecasted Error and Future Trends
Muneeb Ahmad, Muhammad Umer Quddoos, Yousaf Ali Khan, et al.
Gurukul Business Review (2020) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Enfermedades por depósito de glucógeno hepático: clínica, manejo y mutaciones asociadas
Catalina Grez, Magdalena Araya, Juan Francisco Cabello
Andes pediatrica (2021) Vol. 92, Iss. 3, pp. 461-461
Open Access | Times Cited: 1
Glomerulopatia colapsante idiopática: bases moleculares e correlações entre parâmetros moleculares, proteômicos, clínicos e histológicos
Precil Diego Miranda de Menezes Neves
(2023)
Open Access
Βιοχημικές μελέτες στο μεταβολισμό του γλυκογόνου
Ευθύμιος Κυριάκης
(2020)
Closed Access
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