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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:

Multi-Omic Approach to Identify Phenotypic Modifiers Underlying Cerebral Demyelination in X-Linked Adrenoleukodystrophy
Phillip A. Richmond, Frans van der Kloet, Frédéric M. Vaz, et al.
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 19

Showing 19 citing articles:

The expanding diagnostic toolbox for rare genetic diseases
Kristin D. Kernohan, Kym M. Boycott
Nature Reviews Genetics (2024) Vol. 25, Iss. 6, pp. 401-415
Closed Access | Times Cited: 29
Lipidomic biomarkers in plasma correlate with disease severity in adrenoleukodystrophy
Yorrick R. J. Jaspers, Hemmo A. F. Yska, Caroline G. Bergner, et al.
Communications Medicine (2024) Vol. 4, Iss. 1
Open Access | Times Cited: 6
Proteomics in Inherited Metabolic Disorders
María del Pilar Chantada‐Vázquez, Susana B. Bravo, Sofía Gouveia, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 23, pp. 14744-14744
Open Access | Times Cited: 22
Four-dimensional Lipidomics Profiling in X-linked Adrenoleukodystrophy using Trapped Ion Mobility Mass Spectrometry
Yorrick R. J. Jaspers, Sven W Meyer, Mia L Pras-Raves, et al.
Journal of Lipid Research (2024) Vol. 65, Iss. 6, pp. 100567-100567
Open Access | Times Cited: 3
ABCD1 and X‐linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models
Joshua Manor, Hyunglok Chung, Pranjali Bhagwat, et al.
Journal of Neuroscience Research (2021) Vol. 99, Iss. 12, pp. 3170-3181
Open Access | Times Cited: 20
Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need
Madison I. J. Honey, Yorrick R. J. Jaspers, Marc Engelen, et al.
Cells (2021) Vol. 10, Iss. 12, pp. 3427-3427
Open Access | Times Cited: 20
Personalized medicine for rare neurogenetic disorders: can we make it happen?
Agnies M. van Eeghen, Hilgo Bruining, Nicole I. Wolf, et al.
PubMed (2022) Vol. 8, Iss. 2
Closed Access | Times Cited: 13
Endocrine dysfunction in adrenoleukodystrophy
Marc Engelen, Stephan Kemp, Florian Eichler
Handbook of clinical neurology (2021), pp. 257-267
Closed Access | Times Cited: 16
Generation and characterization of a zebrafish gain-of-function ACOX1 Mitchell disease model
Quentin Raas, Austin Wood, Tamara J. Stevenson, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access | Times Cited: 2
Dosage Compensation in Females with X-Linked Metabolic Disorders
Patrycja Juchniewicz, Ewa Piotrowska, Anna Kłoska, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4514-4514
Open Access | Times Cited: 11
Adrenoleukodystrophy
Marc Engelen, Stephan Kemp, Florian Eichler
Handbook of clinical neurology (2024), pp. 133-138
Closed Access | Times Cited: 1
Targeted metabolomics revealed changes in phospholipids during the development of neuroinflammation in Abcd1tm1Kds mice and X‐linked adrenoleukodystrophy patients
Matthias Kettwig, Henry Gerd Klemp, Stefan Nessler, et al.
Journal of Inherited Metabolic Disease (2021) Vol. 44, Iss. 5, pp. 1174-1185
Open Access | Times Cited: 10
Fatty Acid Metabolism in Peroxisomes and Related Disorders
Katsuya Morito, Hanif Ali, Shigenobu Kishino, et al.
Advances in experimental medicine and biology (2024), pp. 31-55
Closed Access | Times Cited: 1
Evolution of adrenoleukodystrophy model systems
Roberto Montoro, Vivi M. Heine, Stephan Kemp, et al.
Journal of Inherited Metabolic Disease (2020) Vol. 44, Iss. 3, pp. 544-553
Open Access | Times Cited: 9
Detection of Characteristic Phosphatidylcholine Containing Very Long Chain Fatty Acids in Cerebrospinal Fluid from Patients with X-Linked Adrenoleukodystrophy
Naoki Fujitani, Masayoshi Saito, Tomoya Akashi, et al.
Biological and Pharmaceutical Bulletin (2022) Vol. 45, Iss. 11, pp. 1725-1727
Open Access | Times Cited: 3
The variability conundrum in neurometabolic degenerative diseases
Clara van Karnebeek, Phillip A. Richmond, Frans van der Kloet, et al.
Molecular Genetics and Metabolism (2020) Vol. 131, Iss. 4, pp. 367-369
Closed Access | Times Cited: 3
Bone marrow transplantation into Abcd1‐deficient mice: Distribution of donor derived‐cells and biological characterization of the brain of the recipient mice
Masashi Morita, Taro Kaizawa, Taiki Yoda, et al.
Journal of Inherited Metabolic Disease (2020) Vol. 44, Iss. 3, pp. 718-727
Closed Access | Times Cited: 1
Defective neuritogenesis inAbcd1/2deficient rat neurons due to intrinsic and astrocyte-dependent mechanisms
Arantxa Golbano, Luis Pardo, Carmen Menacho, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Establishing parameters for the characterization of rare neurometabolic and neurodegenerative diseases using mass-spectrometry based Metabolomics
Henry Gerd Klemp
(2021)
Open Access
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