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:

Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic Paraplegia
Patricia Morejón‐García, Boris Keren, Íñigo Marcos‐Alcalde, et al.
Neurology Genetics (2021) Vol. 7, Iss. 5
Open Access | Times Cited: 7

Showing 7 citing articles:

The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation
Metin Mercan, Serhat Seyhan, Vildan Yayla
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (2025), pp. 1-18
Closed Access

VRK1 variants at the cross road of Cajal body neuropathogenic mechanisms in distal neuropathies and motor neuron diseases
Pedro A. Lazo, Patricia Morejón‐García
Neurobiology of Disease (2023) Vol. 183, pp. 106172-106172
Open Access | Times Cited: 10

The VRK1 chromatin kinase regulates the acetyltransferase activity of Tip60/KAT5 by sequential phosphorylations in response to DNA damage
Raúl García-González, Eva Monte-Serrano, Patricia Morejón‐García, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2022) Vol. 1865, Iss. 8, pp. 194887-194887
Open Access | Times Cited: 9

Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathy
Aurora Campos-Díaz, Patricia Morejón‐García, Eva Monte-Serrano, et al.
Journal of Molecular Medicine (2024) Vol. 102, Iss. 6, pp. 801-817
Open Access | Times Cited: 1

Nuclear functions regulated by the VRK1 kinase
Pedro A. Lazo
Nucleus (2024) Vol. 15, Iss. 1
Open Access

CMT2 and distal hereditary motor neuropathy associated with VRK1 variants: case series
Sasha Živković, Richard J. Nowak, Daniel DiCapua
Neuromuscular Disorders (2024) Vol. 47, pp. 105254-105254
Closed Access

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