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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:

The Emerging Role of Gβ Subunits in Human Genetic Diseases
Natascia Malerba, Pasquelena De Nittis, Giuseppe Merla
Cells (2019) Vol. 8, Iss. 12, pp. 1567-1567
Open Access | Times Cited: 12

Showing 12 citing articles:

Diversity of the Gβγ complexes defines spatial and temporal bias of GPCR signaling
Ikuo Masuho, Nickolas K. Skamangas, Brian S. Muntean, et al.
Cell Systems (2021) Vol. 12, Iss. 4, pp. 324-337.e5
Open Access | Times Cited: 65
Subtype-dependent regulation of Gβγ signalling
Mithila Tennakoon, Kanishka Senarath, Dinesh Kankanamge, et al.
Cellular Signalling (2021) Vol. 82, pp. 109947-109947
Open Access | Times Cited: 43
A detailed multi-omics analysis of GNB2 gene in human cancers
L. Zhang, Aamina Murad Sahar, Chongfei Li, et al.
Brazilian Journal of Biology (2022) Vol. 84
Open Access | Times Cited: 22
Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor
Sophie Colombo, Haritha P. Reddy, Sabrina Petri, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 11
Genetic variation in GNB5 causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (IK,ACh)
Christiaan C. Veerman, Isabella Mengarelli, Charlotte D. Koopman, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 7
Open Access | Times Cited: 23
Antimigraine activity of Asarinin by OPRM1 pathway with multifaceted impacts through network analysis
Rapuru Rushendran, Vellapandian Chitra
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability
Natalie B. Tan, Alistair T. Pagnamenta, Matteo P. Ferla, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 5, pp. 511-516
Open Access | Times Cited: 8
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome
Pasquelena De Nittis, Stéphanie Efthymiou, Alexandre Sarre, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 12, pp. 815-831
Open Access | Times Cited: 6
High G protein subunit beta 4 protein level is correlated to poor prognosis of urothelial carcinoma
Tzu‐Ju Chen, Seyedeh Zahra Dehghanian, Ti‐Chun Chan, et al.
Medical Molecular Morphology (2021) Vol. 54, Iss. 4, pp. 356-367
Closed Access | Times Cited: 5
Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing Overlapping Phenotypes
Zhuo Shao, Ikuo Masuho, Anupreet Tumber, et al.
Genes (2021) Vol. 12, Iss. 9, pp. 1352-1352
Open Access | Times Cited: 4
The severity of endothelial dysfunction, oxidative stress, lipid metabolism disorders, decreased elastic properties and tone of peripheral vessels in patients with different POAG course variants, depending on the polymorphism of the genes of the biological clock
Yu E Filippova, Т. N. Malishevskaya, С. Н. Коломейчук, et al.
Russian Ophthalmological Journal (2022) Vol. 15, Iss. 1, pp. 78-88
Open Access | Times Cited: 1
Neurotransmitters, neuromodulators, synapses
Moyra Smith
Elsevier eBooks (2021), pp. 21-48
Closed Access
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