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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:

A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient
Natascia Malerba, Shelley Towner, Katherine E. Keating, et al.
Frontiers in Genetics (2018) Vol. 9
Open Access | Times Cited: 11

Showing 11 citing articles:

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
Autism Spectrum Disorder: Genetic Mechanisms and Inheritance Patterns
Ilaria La Monica, Maria Rosaria Di Iorio, Antonello Sica, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 478-478
Open Access
The epileptology of GNB5 encephalopathy
Gemma Poke, Chontelle King, Alison M. Muir, et al.
Epilepsia (2019) Vol. 60, Iss. 11
Open Access | Times Cited: 15
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
Severe Phenotype in a Patient With Homozygous 15q21.2 Microdeletion Involving BCL2L10, GNB5, and MYO5C Genes, Resembling Infantile Developmental Disorder With Cardiac Arrhythmias (IDDCA)
Francesca L. Sciacca, Claudia Ciaccio, Federica Fontana, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 9
The genetic basis of sudden death in young people – Cardiac and non-cardiac
Fan Li, Ping Yin, Zuojun Xu
Gene (2021) Vol. 810, pp. 146067-146067
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
Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome
Shahram Yazdani, Anish Badjatiya, Naghmeh Dorrani, et al.
Molecular Genetics and Metabolism Reports (2020) Vol. 23, pp. 100582-100582
Open Access | Times Cited: 5
IDDCA syndrome in a Chinese infant due to GNB5 biallelic mutations
Mingxing Tang, Yajian Wang, Yuanyuan Xu, et al.
Journal of Human Genetics (2020) Vol. 65, Iss. 7, pp. 627-631
Closed Access | Times Cited: 4
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
GNB5-Related Neurodevelopmental Disorder
Gemma Poke, Lynette G. Sadleir, Giuseppe Merla, et al.
(2021)
Closed Access
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