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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:

Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier
Bigna K. Bölsterli, Eugen Boltshauser, Luigi Palmieri, et al.
Nutrients (2022) Vol. 14, Iss. 17, pp. 3605-3605
Open Access | Times Cited: 22

Showing 22 citing articles:

The malate-aspartate shuttle is important for de novo serine biosynthesis
Melissa H. Broeks, Nils W. F. Meijer, Denise Westland, et al.
Cell Reports (2023) Vol. 42, Iss. 9, pp. 113043-113043
Open Access | Times Cited: 26
Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition
Jun Kido, Georgios Makris, Saikat Santra, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 6, pp. 1144-1156
Open Access | Times Cited: 9
Fifty years of the mitochondrial pyruvate carrier: New insights into its structure, function, and inhibition
Sotiria Tavoulari, Maximilian Sichrovsky, Edmund R.S. Kunji
Acta Physiologica (2023) Vol. 238, Iss. 4
Open Access | Times Cited: 21
The effects of probiotics on gastrointestinal symptoms and microbiota in patients with celiac disease: a systematic review and meta-analysis on clinical trials
MohammadHossein MozafaryBazargany, Mohammadian Khonsari, Leily Sokoty, et al.
Clinical and Experimental Medicine (2023) Vol. 23, Iss. 6, pp. 2773-2788
Open Access | Times Cited: 20
Ketogenic diet in children and adolescents: The effects on growth and nutritional status
Antonio Corsello, Chiara Maria Trovato, Elisabetta Di Profio, et al.
Pharmacological Research (2023) Vol. 191, pp. 106780-106780
Open Access | Times Cited: 14
Spotlight on GOT2 in Cancer Metabolism
Samuel A. Kerk, Javier García‐Bermúdez, Kıvanç Birsoy, et al.
OncoTargets and Therapy (2023) Vol. Volume 16, pp. 695-702
Open Access | Times Cited: 13
Citrin deficiency—The East‐side story
Johannes Häberle
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 6, pp. 1129-1133
Open Access | Times Cited: 4
Effect of the ketogenic diet as a treatment for refractory epilepsy in children and adolescents: a systematic review of reviews
Cristina Díez-Arroyo, Mónica García, María José Soto‐Méndez, et al.
Nutrition Reviews (2023) Vol. 82, Iss. 4, pp. 487-502
Closed Access | Times Cited: 10
Current Understanding of Pathogenic Mechanisms and Disease Models of Citrin Deficiency
Denis Lacabanne, Alice P. Sowton, Bosco Jose, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Genetic aetiologies in relation to response to the ketogenic diet in 226 children with epilepsy
Maria Dahlin, Tommy Stödberg, Elisabet Ekman, et al.
Brain Communications (2025) Vol. 7, Iss. 2
Open Access
Molecular basis of pyruvate transport and inhibition of the human mitochondrial pyruvate carrier
Maximilian Sichrovsky, Denis Lacabanne, Jonathan J. Ruprecht, et al.
Science Advances (2025) Vol. 11, Iss. 16
Open Access
Deciphering the Mutational Background in Citrin Deficiency Through a Nationwide Study in Japan and Literature Review
Jun Kido, Keishin Sugawara, Sotiria Tavoulari, et al.
Human Mutation (2025) Vol. 2025, Iss. 1
Open Access
Efficacy and Safety of Ketogenic Diet Treatment in Pediatric Patients with Mitochondrial Disease
Dorota Wesół‐Kucharska, Milena Greczan, Magdalena Kaczor, et al.
Nutrients (2024) Vol. 16, Iss. 6, pp. 812-812
Open Access | Times Cited: 2
Inborn errors of the malate aspartate shuttle – Update on patients and cellular models
J Koch, Melissa H. Broeks, Matthias Gautschi, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 4, pp. 108520-108520
Open Access | Times Cited: 2
The Role of Mitochondrial Pyruvate Carrier in Neurological Disorders
Yue Liu, Xiying Yu, Wei Jiang
Molecular Neurobiology (2024)
Closed Access | Times Cited: 2
Induced pluripotent stem cell-derived hepatocytes reveal TCA cycle disruption and the potential basis for triheptanoin treatment for malate dehydrogenase 2 deficiency
Déborah Mathis, J Koch, S. Koller, et al.
Molecular Genetics and Metabolism Reports (2024) Vol. 39, pp. 101066-101066
Open Access | Times Cited: 1
My path to citrin deficiency
John E. Walker
Journal of Inherited Metabolic Disease (2024)
Open Access | Times Cited: 1
Editorial for “The Role of Ketogenic Diet in Human Health and Diseases”: The Multifaceted Impact of Ketogenic Diets on Health and Disease
Mikiko Watanabe, Silvia Savastano, Carla Lubrano, et al.
Nutrients (2023) Vol. 15, Iss. 18, pp. 4027-4027
Open Access | Times Cited: 1
Fourteenth Jesús Culebras Lecture. Ketogenic diet, a half-discovered treatment
Consuelo Carmen Pedrón Giner
Nutrición Hospitalaria (2024)
Open Access
The mitochondrial aspartate/glutamate carrier does not transport GABA
Vito Porcelli, Serena Barile, Loredana Capobianco, et al.
Biochimica et Biophysica Acta (BBA) - Bioenergetics (2024) Vol. 1865, Iss. 4, pp. 149487-149487
Closed Access
MITOCHONDRIAL DISORDER DIAGNOSIS AND MANAGEMENT– WHAT THE PEDIATRIC NEUROLOGIST WANTS TO KNOW
Oliver Heath, René G. Feichtinger, Melanie T. Achleitner, et al.
European Journal of Paediatric Neurology (2024) Vol. 54, pp. 75-88
Closed Access
Tracing metabolic pathways in a spectrum of inherited diseases
Melissa H. Broeks
(2023)
Open Access
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