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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:

Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response
Danique Beijer, Thomas Agnew, J.G.M. Rack, et al.
Life Science Alliance (2021) Vol. 4, Iss. 11, pp. e202101057-e202101057
Open Access | Times Cited: 17

Showing 17 citing articles:

Modular antibodies reveal DNA damage-induced mono-ADP-ribosylation as a second wave of PARP1 signaling
Edoardo José Longarini, Helen Dauben, Carolina Locatelli, et al.
Molecular Cell (2023) Vol. 83, Iss. 10, pp. 1743-1760.e11
Open Access | Times Cited: 38
Serine ADP-ribosylation in Drosophila provides insights into the evolution of reversible ADP-ribosylation signalling
Pietro Fontana, Sara C. Buch-Larsen, Osamu Suyari, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19
ADP-ribosylation, a multifaceted modification: Functions and mechanisms in aging and aging-related diseases
Wu Hao, Zhao Jialong, Yuan Jiuzhi, et al.
Ageing Research Reviews (2024) Vol. 98, pp. 102347-102347
Open Access | Times Cited: 3
The function and regulation of ADP-ribosylation in the DNA damage response
Lena Duma, Ivan Ahel
Biochemical Society Transactions (2023) Vol. 51, Iss. 3, pp. 995-1008
Open Access | Times Cited: 8
The Making and Breaking of Serine-ADP-Ribosylation in the DNA Damage Response
Kira Schützenhofer, J.G.M. Rack, Ivan Ahel
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 18
Expanding the Spectrum of Stress-Induced Childhood-Onset Neurodegeneration with Variable Ataxia and Seizures (CONDSIAS)
Filippa Orlien Lindskov, William Kristian Karlsson, Sara Lyngby Skovbølling, et al.
The Cerebellum (2023) Vol. 23, Iss. 2, pp. 861-871
Closed Access | Times Cited: 7
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia
Amokelani C. Mahungu, Elizabeth Steyn, Niki Floudiotis, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 6
Mono-ADP-ribosylation, a MARylationmultifaced modification of protein, DNA and RNA: characterizations, functions and mechanisms
Hao Wu, Anqi Lu, Jiuzhi Yuan, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 2
Delineation of ADPRHL2 Variants: Report of Two New Patients with Review of the Literature
Sibel Öz Yıldız, Dilek Yalnızoğlu, Pelin Özlem Şimşek‐Kiper, et al.
Neuropediatrics (2024) Vol. 55, Iss. 03, pp. 156-165
Open Access | Times Cited: 1
ADP-ribose hydrolases: biological functions and potential therapeutic targets
Jingpeng Wang, Zhao‐Qi Wang, Wen Zong
Expert Reviews in Molecular Medicine (2024) Vol. 26
Closed Access | Times Cited: 1
ARH Family of ADP-Ribose-Acceptor Hydrolases
Hiroko Ishiwata-Endo, Jiro Kato, Sachiko Yamashita, et al.
Cells (2022) Vol. 11, Iss. 23, pp. 3853-3853
Open Access | Times Cited: 6
Research Progress on Mono-ADP-Ribosyltransferases in Human Cell Biology
Yujie Gan, Huanhuan Sha, Renrui Zou, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 4
Hereditary Motor Neuropathy
Jonathan De Winter, Jonathan Baets
Elsevier eBooks (2024)
Closed Access
A novel variant inADPRSdisrupts ARH3 stability and subcellular localization in children with neurodegeneration and respiratory failure
Maxwell Bannister, Sarah J. Bray, Anjali Aggarwal, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Clinical, Genetic, and Pathological Studies in Two Brothers with Stress-Induced Childhood-Onset Neurodegeneration with Variable Ataxia and Seizures: A Case Report
Márton Tompa, Balázs Tolvaj, Árpád Vadvári, et al.
Case Reports in Neurology (2024) Vol. 16, Iss. 1, pp. 188-195
Open Access
An ADPRS variant disrupts ARH3 stability and subcellular localization in children with neurodegeneration and respiratory failure
Maxwell Bannister, Sarah J. Bray, Anjali Aggarwal, et al.
Human Genetics and Genomics Advances (2024) Vol. 6, Iss. 1, pp. 100386-100386
Open Access
A PARP inhibitor, rucaparib, improves cardiac dysfunction inADP-ribose-acceptor hydrolase 3(Arh3) deficiency
Sachiko Yamashita, Xiangning Bu, Hiroko Ishiwata-Endo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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