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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:

Inborn Metabolic Diseases
Jean‐Marie Saudubray, Matthias R. Baumgartner, John H. Walter
Springer eBooks (2016)
Closed Access | Times Cited: 115

Showing 1-25 of 115 citing articles:

An international classification of inherited metabolic disorders (ICIMD)
Carlos R. Ferreira, Shamima Rahman, Markus A. Keller, et al.
Journal of Inherited Metabolic Disease (2020) Vol. 44, Iss. 1, pp. 164-177
Open Access | Times Cited: 232
Fructose Metabolism in Cancer
Nils Krause, André Wegner
Cells (2020) Vol. 9, Iss. 12, pp. 2635-2635
Open Access | Times Cited: 71
Dyslipidemia Diagnosis and Treatment: Risk Stratification in Children and Adolescents
Sara Mosca, Graça Araújo, Vanessa Costa, et al.
Journal of Nutrition and Metabolism (2022) Vol. 2022, pp. 1-10
Open Access | Times Cited: 47
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies
René G. Feichtinger, Monika Oláhová, Yoshihito Kishita, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 4, pp. 525-538
Open Access | Times Cited: 73
The role of OXCT1 in the pathogenesis of cancer as a rate-limiting enzyme of ketone body metabolism
Song Zhang, Caifeng Xie
Life Sciences (2017) Vol. 183, pp. 110-115
Closed Access | Times Cited: 64
Neurological manifestations of organic acidurias
Moaçir Wajner
Nature Reviews Neurology (2019) Vol. 15, Iss. 5, pp. 253-271
Closed Access | Times Cited: 55
Anemia in Sports: A Narrative Review
Marc-Tudor Damian, Romana Vulturar, Cezar Login, et al.
Life (2021) Vol. 11, Iss. 9, pp. 987-987
Open Access | Times Cited: 47
An 8-Week Ketogenic Diet Alternated Interleukin-6, Ketolytic and Lipolytic Gene Expression, and Enhanced Exercise Capacity in Mice
Sihui Ma, Qingyi Huang, Takaki Tominaga, et al.
Nutrients (2018) Vol. 10, Iss. 11, pp. 1696-1696
Open Access | Times Cited: 50
Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of Metabolism
Dylan Mordaunt, David J. Cox, Maria Fuller
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 4, pp. 1195-1195
Open Access | Times Cited: 41
Inborn Errors of Metabolism
Kristen Lee
Elsevier eBooks (2024)
Closed Access | Times Cited: 5
Fast and accurate quantitative organic acid analysis with LC‐QTOF/MS facilitates screening of patients for inborn errors of metabolism
Irene M. L. W. Körver‐Keularts, Ping Wang, Huub W. A. H. Waterval, et al.
Journal of Inherited Metabolic Disease (2018) Vol. 41, Iss. 3, pp. 415-424
Open Access | Times Cited: 44
Genetic Disorders Associated with Metal Metabolism
Muhammad Umair, Majid Alfadhel
Cells (2019) Vol. 8, Iss. 12, pp. 1598-1598
Open Access | Times Cited: 40
Development of Strategies to Decrease False Positive Results in Newborn Screening
Sabrina Malvagia, G Forni, Daniela Ombrone, et al.
International Journal of Neonatal Screening (2020) Vol. 6, Iss. 4, pp. 84-84
Open Access | Times Cited: 38
Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome
Àngels García‐Cazorla, Edgard Verdura, Natalia Juliá‐Palacios, et al.
Acta Neuropathologica (2020) Vol. 140, Iss. 6, pp. 971-975
Open Access | Times Cited: 33
Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review
Federica Conte, Juda-El Sam, Dirk J. Lefeber, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 8632-8632
Open Access | Times Cited: 11
The natural history of dihydrolipoamide dehydrogenase deficiency in Israel
Ben Pode‐Shakked, Yuval E. Landau, Nava Shaul Lotan, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 895-902
Open Access | Times Cited: 4
An inborn error of metabolism presenting with apparently isolated subacute neuropsychiatric symptoms in an adolescent
Sarah Grace Engel, Ali Said Al-Beshri, Amitha Ananth, et al.
Translational Science of Rare Diseases (2025)
Open Access
Nutrition in Children with Inborn Errors of Metabolism

American Academy of PediatricsItasca, IL eBooks (2025)
Closed Access
The multifaceted challenges faced by women in the field of inherited metabolic disorders
Livia Lenzini, Sara Bianconi, Giorgia Gugelmo, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Biomarkers in Glycogen Storage Diseases: An Update
Alberto Molares-Vila, Alberte Corbalán-Rivas, Miguel Carnero-Gregorio, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4381-4381
Open Access | Times Cited: 24
Rapid and efficient LC-MS/MS diagnosis of inherited metabolic disorders: a semi-automated workflow for analysis of organic acids, acylglycines, and acylcarnitines in urine
Barbora Piskláková, Jaroslava Friedecká, Eliška Ivanovová, et al.
Clinical Chemistry and Laboratory Medicine (CCLM) (2023) Vol. 61, Iss. 11, pp. 2017-2027
Open Access | Times Cited: 9
Propionate hampers differentiation and modifies histone propionylation and acetylation in skeletal muscle cells
Bart Lagerwaard, Marjanne D. van der Hoek, Joris Hoeks, et al.
Mechanisms of Ageing and Development (2021) Vol. 196, pp. 111495-111495
Open Access | Times Cited: 21
Analysis of urinary oligosaccharide excretion patterns by UHPLC/HRAM mass spectrometry for screening of lysosomal storage disorders
Marne C. Hagemeijer, Jeroen C. van den Bosch, Michiel Bongaerts, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 46, Iss. 2, pp. 206-219
Open Access | Times Cited: 8
International practices in the dietary management of fructose 1-6 biphosphatase deficiency
Alex Pinto, Majid Alfadhel, R. Akroyd, et al.
Orphanet Journal of Rare Diseases (2018) Vol. 13, Iss. 1
Open Access | Times Cited: 26
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase Deficiency
Orna Staretz‐Chacham, Ben Pode‐Shakked, Eyal Kristal, et al.
Nutrients (2021) Vol. 13, Iss. 10, pp. 3523-3523
Open Access | Times Cited: 18
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