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:

Identification of cerebral spinal fluid protein biomarkers in Niemann-Pick disease, type C1
Kiersten Campbell, Niamh X. Cawley, Rachel Luke, et al.
Biomarker Research (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 16

Showing 16 citing articles:

The Niemann-Pick type diseases – A synopsis of inborn errors in sphingolipid and cholesterol metabolism
Frank W. Pfrieger
Progress in Lipid Research (2023) Vol. 90, pp. 101225-101225
Open Access | Times Cited: 28

Addressing inter individual variability in CSF levels of brain derived proteins across neurodegenerative diseases
Sára Mravinacová, Sofia Bergström, Jennie Olofsson, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1

Olink® Explore for High-Throughput Protein Biomarker Discovery in Cerebrospinal Fluid
Mireia Boluda-Navarro
Methods in molecular biology (2025), pp. 141-163
Closed Access

Characterizing circulating biomarkers for childhood dementia disorders: A scoping review of clinical trials
Arlene D’Silva, James Barnes, Jason V. Djafar, et al.
Neurotherapeutics (2025), pp. e00546-e00546
Open Access

Emerging Trends: Neurofilament Biomarkers in Precision Neurology
Priti Sharma, Aditi Giri, Prabhash Nath Tripathi
Neurochemical Research (2024)
Closed Access | Times Cited: 3

Elevated cerebrospinal fluid ubiquitin C-terminal hydrolase-L1 levels correlate with phenotypic severity and therapeutic response in Niemann-Pick disease, type C1
Niamh X. Cawley, Spencer Giddens, Nicole M. Farhat, et al.
Molecular Genetics and Metabolism (2023) Vol. 140, Iss. 3, pp. 107656-107656
Open Access | Times Cited: 5

Differently increased volumes of multiple brain areas in Npc1 mutant mice following various drug treatments
Veronica Antipova, Diana Heimes, Katharina Seidel, et al.
Frontiers in Neuroanatomy (2024) Vol. 18
Open Access | Times Cited: 1

Advancing Frontiers in Colorectal Cancer: Exploring Novel Insights and Emerging Trends in Research and Therapy
Amer Al Ali
Advancements in Life Sciences (2024) Vol. 11, Iss. 4, pp. 714-714
Open Access | Times Cited: 1

Cerebrospinal Fluid Protein Biomarker Discovery in CLN3
An Dang, David E. Sleat, Kiersten Campbell, et al.
Journal of Proteome Research (2023) Vol. 22, Iss. 7, pp. 2493-2508
Open Access | Times Cited: 3

Addressing inter-individual variability in CSF levels of brain-derived proteins across neurodegenerative diseases
Sára Mravinacová, Sofia Bergström, Jennie Olofsson, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Evaluation of the landscape of pharmacodynamic biomarkers in Niemann-Pick Disease Type C (NPC)
Sydney Stern, Karryn Crisamore, Robert N. Schuck, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access

Neimann-Pick Diseases: Beyond Lipid Accumulation – Genetic, Diagnostics, and Therapeutic Strategies
Hind M. Naffadi
Advancements in Life Sciences (2024) Vol. 11, Iss. 4, pp. 703-703
Open Access

Associations between plasma caspase-1 levels and cardiovascular disease, and the mediating role of metabolic syndrome: Findings from the UK Biobank
Yajuan Zhang, Yumei Huang, Shaobo Hu, et al.
Atherosclerosis (2024) Vol. 401, pp. 119090-119090
Closed Access

Implications of the choroid plexus in Niemann-Pick disease Type C neuropathogenesis
Raquel van Gool, Mariesa Cay, Boyu Ren, et al.
Brain Behavior and Immunity (2024) Vol. 124, pp. 376-384
Closed Access

Cerebrospinal Fluid and Serum Neuron‐Specific Enolase in Niemann‐Pick Disease Type C1
Cameron Padilla, Derek Alexander, Desiree A. Labor, et al.
American Journal of Medical Genetics Part A (2024)
Open Access

Npc1 gene mutation abnormally activates the classical Wnt signalling pathway in mouse kidneys and promotes renal fibrosis
Lihong Guan, Zisen Jia, Keli Xu, et al.
Animal Genetics (2023) Vol. 55, Iss. 1, pp. 99-109
Closed Access | Times Cited: 1

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