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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 1-25 of 47 citing articles:

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
EP Europace (2022) Vol. 24, Iss. 8, pp. 1307-1367
Open Access | Times Cited: 259
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Heart Rhythm (2022) Vol. 19, Iss. 7, pp. e1-e60
Open Access | Times Cited: 160
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
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Journal of Arrhythmia (2022) Vol. 38, Iss. 4, pp. 491-553
Open Access | Times Cited: 41
From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies
Lia Crotti, Pedro Brugada, Hugh Calkins, et al.
EP Europace (2023) Vol. 25, Iss. 8
Open Access | Times Cited: 24
Genetic insight into sick sinus syndrome
Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Hildur M. Aegisdottir, et al.
European Heart Journal (2021) Vol. 42, Iss. 20, pp. 1959-1971
Open Access | Times Cited: 46
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
Sinus node dysfunction: current understanding and future directions
Pavan Manoj, Jitae A. Kim, Stephanie Kim, et al.
AJP Heart and Circulatory Physiology (2022) Vol. 324, Iss. 3, pp. H259-H278
Open Access | Times Cited: 23
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.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Cardiac Arrhythmias Related to Sodium Channel Dysfunction
Eleonora Savio‐Galimberti, Mariana Argenziano, Charles Antzelevitch
Handbook of experimental pharmacology (2017), pp. 331-354
Closed Access | Times Cited: 46
Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells
Maike Marczenke, Ilaria Piccini, Isabella Mengarelli, et al.
Frontiers in Physiology (2017) Vol. 8
Open Access | Times Cited: 44
Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K + Channel) Channel Function
Johanna Kuß, Birgit Stallmeyer, Matthias Goldstein, et al.
Circulation Genomic and Precision Medicine (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 43
Pharmacologic Approach to Sinoatrial Node Dysfunction
Pietro Mesirca, Vadim V. Fedorov, Thomas J. Hund, et al.
The Annual Review of Pharmacology and Toxicology (2020) Vol. 61, Iss. 1, pp. 757-778
Open Access | Times Cited: 38
Genetic Complexity of Sinoatrial Node Dysfunction
Michael B. Wallace, Mona El Refaey, Pietro Mesirca, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 32
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
Atrial GIRK Channels Mediate the Effects of Vagus Nerve Stimulation on Heart Rate Dynamics and Arrhythmogenesis
Steven W. Lee, Allison Anderson, Pilar Guzmán, et al.
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 32
Direct Effects of Antipsychotics on Potassium Channels
Wenwen Zhuang, Seo‐Yeong Mun, Won Sun Park
Biochemical and Biophysical Research Communications (2025) Vol. 749, pp. 151344-151344
Closed Access
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
Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
Jing Ma, Shiyu Chen, Lili Hao, et al.
Journal of Cellular and Molecular Medicine (2020) Vol. 24, Iss. 11, pp. 6472-6484
Open Access | Times Cited: 21
Genetics of sinoatrial node function and heart rate disorders
Lieve E. van der Maarel, Alex V. Postma, Vincent M. Christoffels
Disease Models & Mechanisms (2023) Vol. 16, Iss. 5
Open Access | Times Cited: 7
Exome reports A de novo GNB2 variant associated with global developmental delay, intellectual disability, and dysmorphic features
Tokiko Fukuda, Takuya Hiraide, Kaori Yamoto, et al.
European Journal of Medical Genetics (2019) Vol. 63, Iss. 4, pp. 103804-103804
Open Access | Times Cited: 17
Inhibition of G protein-gated K+ channels by tertiapin-Q rescues sinus node dysfunction and atrioventricular conduction in mouse models of primary bradycardia
Isabelle Bidaud, Antony Chung You Chong, Agnès Carcouët, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 16
Rare variants in drug target genes contributing to complex diseases, phenome-wide
Shefali S. Verma, Navya Shilpa Josyula, Anurag Verma, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 15
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
Susanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 14215-14215
Open Access | Times Cited: 9
Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2
Jing Ma, Shiyu Chen, Lili Hao, et al.
Frontiers of Medicine (2020) Vol. 15, Iss. 1, pp. 91-100
Closed Access | Times Cited: 12
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