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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:

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation
Viorica Chelban, Matthew P. Wilson, Jodi Warman‐Chardon, et al.
Annals of Neurology (2019) Vol. 86, Iss. 2, pp. 225-240
Open Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

Critical illness polyneuropathy, myopathy and neuronal biomarkers in COVID-19 patients: A prospective study
Robert Frithiof, Elham Rostami, Eva Kumlien, et al.
Clinical Neurophysiology (2021) Vol. 132, Iss. 7, pp. 1733-1740
Open Access | Times Cited: 118
Vitamin B-6-Induced Neuropathy: Exploring the Mechanisms of Pyridoxine Toxicity
Felix Hadtstein, Misha F. Vrolijk
Advances in Nutrition (2021) Vol. 12, Iss. 5, pp. 1911-1929
Open Access | Times Cited: 77
The Rationale for Vitamin, Mineral, and Cofactor Treatment in the Precision Medical Care of Autism Spectrum Disorder
Neluwa-Liyanage R. Indika, Richard E. Frye, Daniel A. Rossignol, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 2, pp. 252-252
Open Access | Times Cited: 32
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes
Chiara Cappelletti, Sandra Pilar Henriksen, Hanneke Geut, et al.
Acta Neuropathologica (2023) Vol. 146, Iss. 2, pp. 227-244
Open Access | Times Cited: 28
The Role of Vitamin B6 in Peripheral Neuropathy: A Systematic Review
Raman Muhamad, Alexandra Akrivaki, Georgia Papagiannopoulou, et al.
Nutrients (2023) Vol. 15, Iss. 13, pp. 2823-2823
Open Access | Times Cited: 24
Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities
Brett A. McCray, Steven S. Scherer
Neurotherapeutics (2021) Vol. 18, Iss. 4, pp. 2269-2285
Open Access | Times Cited: 46
B vitamin supply in plants and humans: the importance of vitamer homeostasis
Zeguang Liu, Péter Farkas, Kai Wang, et al.
The Plant Journal (2022) Vol. 111, Iss. 3, pp. 662-682
Open Access | Times Cited: 37
IGF1 deficiency integrates stunted growth and neurodegeneration in Down syndrome
Paula Araya, Kohl T. Kinning, Christina Coughlan, et al.
Cell Reports (2022) Vol. 41, Iss. 13, pp. 111883-111883
Open Access | Times Cited: 31
Clinical genetics of Charcot–Marie–Tooth disease
Yujiro Higuchi, Hiroshi Takashima
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 199-214
Closed Access | Times Cited: 30
Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery
Kym M. Boycott, Taila Hartley, Kristin D. Kernohan, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 11, pp. 1947-1959
Open Access | Times Cited: 29
Vitamin B6 regulates IL-33 homeostasis to alleviate type 2 inflammation
Songling Zhu, Shufen Zhong, Kebin Cheng, et al.
Cellular and Molecular Immunology (2023) Vol. 20, Iss. 7, pp. 794-807
Open Access | Times Cited: 17
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases
Yoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Vida Baratang, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 2, pp. 384-394
Open Access | Times Cited: 48
The multifaceted role of vitamin B 6 in cancer: Drosophila as a model system to investigate DNA damage
Roberto Contestabile, Martino L. di Salvo, Victoria I. Bunik, et al.
Open Biology (2020) Vol. 10, Iss. 3
Open Access | Times Cited: 29
CoExp: A Web Tool for the Exploitation of Co-expression Networks
Sonia García-Ruiz, Ana Luisa Gil-Martínez, Alejandro Cisterna‐García, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 26
Simplifying the B Complex: How Vitamins B6 and B9 Modulate One Carbon Metabolism in Cancer and Beyond
Carolina N. Franco, Laurence J. Seabrook, Steven T. Nguyen, et al.
Metabolites (2022) Vol. 12, Iss. 10, pp. 961-961
Open Access | Times Cited: 17
SLC25A38 is required for mitochondrial pyridoxal 5’-phosphate (PLP) accumulation
Izabella A. Pena, Ju Shi, Sarah Chang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
PhenomeCentral: 7 years of rare disease matchmaking
Matthew Osmond, Taila Hartley, Brittney Johnstone, et al.
Human Mutation (2022)
Open Access | Times Cited: 15
Nutritional peripheral neuropathies
Caroline Kramarz, Elaine Murphy, Mary M. Reilly, et al.
Journal of Neurology Neurosurgery & Psychiatry (2023) Vol. 95, Iss. 1, pp. 61-72
Closed Access | Times Cited: 8
Vitamin B6 and diabetes and its role in counteracting advanced glycation end products
Fiammetta Vernı̀
Vitamins and hormones (2024), pp. 401-438
Closed Access | Times Cited: 3
Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada
Matthew Osmond, Taila Hartley, David A. Dyment, et al.
Genetics in Medicine (2021) Vol. 24, Iss. 1, pp. 100-108
Closed Access | Times Cited: 20
Orphan Peripheral Neuropathies
Josef Finsterer, Wolfgang N. Löscher, Julia Wanschitz, et al.
Journal of Neuromuscular Diseases (2020) Vol. 8, Iss. 1, pp. 1-23
Open Access | Times Cited: 19
Inborn errors in the vitamin B6 salvage enzymes associated with neonatal epileptic encephalopathy and other pathologies
Mohini S. Ghatge, Mohammed Al Mughram, Abdelsattar M. Omar, et al.
Biochimie (2021) Vol. 183, pp. 18-29
Open Access | Times Cited: 17
The Therapeutic Potential of Vitamins B1, B3 and B6 in Charcot–Marie–Tooth Disease with the Compromised Status of Vitamin-Dependent Processes
Victoria I. Bunik
Biology (2023) Vol. 12, Iss. 7, pp. 897-897
Open Access | Times Cited: 7
Mouse models for inherited monoamine neurotransmitter disorders
Beat Thöny, Joanne Ng, Manju A. Kurian, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 3, pp. 533-550
Open Access | Times Cited: 2
Rare disease genomics and precision medicine
Juhyeon Hong, D. Lee, A. Hwang, et al.
Genomics & Informatics (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
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