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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 Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction
Birgit Stallmeyer, Johanna Kuß, S. Kotthoff, et al.
Circulation Research (2017) Vol. 120, Iss. 10
Open Access | Times Cited: 47

Showing 26-50 of 47 citing articles:

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
Deep learning on resting electrocardiogram to identify impaired heart rate recovery
Nathaniel Diamant, Paolo Di Achille, Lu‐Chen Weng, et al.
Cardiovascular Digital Health Journal (2022) Vol. 3, Iss. 4, pp. 161-170
Open Access | Times Cited: 7
Relevance of KCNJ5 in Pathologies of Heart Disease
Karisa M. Meyer, Nipun Malhotra, Jung seo Kwak, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 10849-10849
Open Access | Times Cited: 4
Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)
Anne Kayser, Sven Dittmann, Jassin Hamidi, et al.
Stem Cell Research (2024) Vol. 78, pp. 103446-103446
Open Access | Times Cited: 1
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank
Celine A. Manigbas, Bharati Jadhav, Paras Garg, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
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
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
Matrix metalloproteinase 1 1 G/2 G gene polymorphism is associated with acquired atrioventricular block via linking a higher serum protein level
Jan‐Yow Chen, Kuan‐Cheng Chang, Ying‐Ming Liou
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 5
Cardiogenetics in Germany— a view and review
Eric Schulze‐Bahr
Herzschrittmachertherapie + Elektrophysiologie (2024) Vol. 35, Iss. S1, pp. 127-137
Open Access
TMPRSS6 cleaves KCNE1 and causes arrhythmias in iron overload disease
Stefan Peischard, Philipp Kastl, Gunnar Goerges, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
Mitochondrial dysfunction is a key link involved in the pathogenesis of sick sinus syndrome: a review
Xinxin Shi, Liming He, Yucheng Wang, et al.
Frontiers in Cardiovascular Medicine (2024) Vol. 11
Open Access
Molecular Remodeling of Cardiac Sinus Node Associated with Acute Chagas Disease Myocarditis
Héctor O. Rodríguez‐Angulo, Diana Colombet-Naranjo, María del Carmen Lapo Maza, et al.
Microorganisms (2021) Vol. 9, Iss. 11, pp. 2208-2208
Open Access | Times Cited: 3
Preliminary Analysis of the Risk Factor Identification Embedding Model for Cardiovascular Disease
Ji-Hye Moon, Hugo F. Posada–Quintero, In-Soo Kim, et al.
2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC) (2021), pp. 1946-1949
Closed Access | Times Cited: 3
Pacing Discovery
Elisabeth M. Lodder, Arie O. Verkerk, Connie R. Bezzina
Circulation Research (2017) Vol. 120, Iss. 10, pp. 1524-1526
Open Access | Times Cited: 1
Circulation Research “In This Issue” Anthology
Ruth Williams
Circulation Research (2018) Vol. 122, Iss. 12
Open Access | Times Cited: 1
Reevaluating the Mutation Classification in Genetic Studies of Bradycardia Using ACMG/AMP Variant Classification Framework
Liting Cheng, Xiaoyan Li, Lin Zhao, et al.
International Journal of Genomics (2020) Vol. 2020, pp. 1-12
Open Access | Times Cited: 1
Second patient with GNB2-related neurodevelopmental disease: Further evidence for a gene-disease association
Lisa A. Lansdon, Emily Fleming, Florencia Del Viso, et al.
European Journal of Medical Genetics (2021) Vol. 64, Iss. 7, pp. 104243-104243
Closed Access | Times Cited: 1
Characterization of VU0468554, a New Selective Inhibitor of Cardiac G Protein–Gated Inwardly Rectifying K+ Channels
Allison Anderson, Baovi N. Vo, Ezequiel Marrón Fernández de Velasco, et al.
Molecular Pharmacology (2021) Vol. 100, Iss. 6, pp. 540-547
Open Access | Times Cited: 1
Identification Of Platelet-related Biomarkers And Construction of Transcriptional Regulatory Network in Patients with Proliferative Diabetic Retinopathy
Mingzhi Lu, Jiao Feng, Xiulan Lu, et al.
Research Square (Research Square) (2023)
Open Access
Unique Features of the Human Sinoatrial Node Structure, Function, and Arrhythmias: Mechanistic Insights from Integrated 3D Mapping Approaches
Anuradha Kalyanasundaram, Ning Li, Vadim V. Fedorov
Springer eBooks (2023), pp. 109-129
Closed Access
Sinus Node Disease and Cardiac Conduction Disease
Patrick A. Schweizer
Cardiac and vascular biology (2018), pp. 215-229
Closed Access
Molecular therapies for bradyarrhythmias
Anna M. D. Végh, Harsha D. Devalla, Dirk Geerts, et al.
Elsevier eBooks (2020), pp. 811-840
Closed Access
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