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:

Longitudinal Brain Atrophy Rates in Presymptomatic Carriers of Genetic Frontotemporal Dementia
Jackie M. Poos, Leonie D. M. Grandpierre, Emma L. van der Ende, et al.
Neurology (2022) Vol. 99, Iss. 24
Open Access | Times Cited: 10

Showing 10 citing articles:

Biomarker-guided decision making in clinical drug development for neurodegenerative disorders
Jeffrey L. Cummings, Charlotte E. Teunissen, Brian Fiske, et al.
Nature Reviews Drug Discovery (2025)
Closed Access | Times Cited: 3

Clinical Value of Longitudinal Serum Neurofilament Light Chain in Prodromal Genetic Frontotemporal Dementia
Lucia Giannini, Harro Seelaar, Emma L. van der Ende, et al.
Neurology (2023) Vol. 101, Iss. 10
Open Access | Times Cited: 13

Thalamus as a neural marker of cognitive reserve in bilinguals with frontotemporal dementia
Nithin Thanissery, Faheem Arshad, Sunil Kumar Khokhar, et al.
Bilingualism Language and Cognition (2025), pp. 1-10
Closed Access

AI-based staging, causal hypothesis and progression of subjects at risk of Alzheimer’s disease: a multicenter study
Simona Aresta, Raffaello Nemni, Moreno Zanardo, et al.
Frontiers in Neurology (2025) Vol. 16
Open Access

Genetic evidence for the causal relationships between migraine, dementia, and longitudinal brain atrophy
Lei Zhao, Yilan Tang, Yiheng Tu, et al.
The Journal of Headache and Pain (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 3

Sex differences in the executive and behavioral reserve of autosomal dominant frontotemporal dementia
J. García Castro, Sara Rubio‐Guerra, Kaitlin B. Casaletto, et al.
Alzheimer s & Dementia (2025) Vol. 21, Iss. 4
Open Access

A mutation in the PRKAR1B gene drives pathological mechanisms of neurodegeneration across species
Tal Benjamin-Zukerman, Gilat Shimon, Marie E. Gaine, et al.
Brain (2024) Vol. 147, Iss. 11, pp. 3890-3905
Open Access | Times Cited: 1

Cortical thickness modeling and variability in Alzheimer’s disease and frontotemporal dementia
Agnès Pérez‐Millan, Sergi Borrego‐Écija, Neus Falgàs, et al.
Journal of Neurology (2023) Vol. 271, Iss. 3, pp. 1428-1438
Open Access | Times Cited: 3

Presymptomatic and early pathological features of MAPT-associated frontotemporal lobar degeneration
Lucia Giannini, Merel O. Mol, Ana Rajicic, et al.
Acta Neuropathologica Communications (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 2

Clinical and neuroimaging characterization of the first frontotemporal dementia family carrying the MAPT p.K298E mutation
Federico Emanuele Pozzi, Vittoria Aprea, Ginevra Giovannelli, et al.
Neurogenetics (2024) Vol. 25, Iss. 3, pp. 215-223
Open Access

Foreseeing Before Disease Onset
Federica Agosta, Edoardo Gioele Spinelli, Massimo Filippi
Neurology (2022) Vol. 99, Iss. 24, pp. 1077-1078
Closed Access

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