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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:

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 3, pp. 704-710
Open Access | Times Cited: 66

Showing 1-25 of 66 citing articles:

MUSCLEMOTION
Luca Sala, Berend J. van Meer, Leon G.J. Tertoolen, et al.
Circulation Research (2017) Vol. 122, Iss. 3
Open Access | Times Cited: 295
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
Lessons learned from additional research analyses of unsolved clinical exome cases
Mohammad K. Eldomery, Zeynep Coban‐Akdemir, Tamar Harel, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 219
Zebrafish as a tractable model of human cardiovascular disease
George Bowley, Elisabeth Kugler, Robert N. Wilkinson, et al.
British Journal of Pharmacology (2021) Vol. 179, Iss. 5, pp. 900-917
Open Access | Times Cited: 106
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
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
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders
Lydie Bürglen, Evelien Van Hoeymissen, Leila Qebibo, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 22
On the Evolution of the Cardiac Pacemaker
Silja Burkhard, Vincent van Eif, Laurence Garric, et al.
Journal of Cardiovascular Development and Disease (2017) Vol. 4, Iss. 2, pp. 4-4
Open Access | Times Cited: 53
Spatially resolved RNA-sequencing of the embryonic heart identifies a role for Wnt/β-catenin signaling in autonomic control of heart rate
Silja Burkhard, Jeroen Bakkers
eLife (2018) Vol. 7
Open Access | Times Cited: 52
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
The association of GNB5 with Alzheimer disease revealed by genomic analysis restricted to variants impacting gene function
Jianhua Zhang, Mritunjay Pandey, Adam M. Awe, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 3, pp. 473-486
Open Access | Times Cited: 5
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
Intramolecular domain dynamics regulate synaptic MAGUK protein interactions
Nils Rademacher, Benno Kuropka, Stella‐Amrei Kunde, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 39
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
SUDEP risk and autonomic dysfunction in genetic epilepsies
Ahmed N. Sahly, Michael Shevell, Lynette G. Sadleir, et al.
Autonomic Neuroscience (2021) Vol. 237, pp. 102907-102907
Closed Access | Times Cited: 24
Zebrafish as a Model of Cardiac Pathology and Toxicity: Spotlight on Uremic Toxins
Annapaola Coppola, Patrizia Lombari, Elvira Mazzella, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 6, pp. 5656-5656
Open Access | Times Cited: 11
Identification of GBN5 as a molecular biomarker of pan-cancer species by integrated multi-omics analysis
Qian Guo, Xin-Xin Zhong, Zihan Dang, et al.
Discover Oncology (2025) Vol. 16, Iss. 1
Open Access
Toddler Cavotricuspid Valve Isthmus Ablation for Typical Atrial Flutter with Cryoablation
Ebrahim Mohammad A, Muhammad A. Hasan, Abdelnaby Mohamed A, et al.
Journal of Cardiology and Cardiovascular Medicine (2025) Vol. 10, Iss. 3, pp. 057-061
Closed Access
Cardiac Ca2+ signalling in zebrafish: Translation of findings to man
Chantal J.M. van Opbergen, Stephanie M. van der Voorn, Marc A. Vos, et al.
Progress in Biophysics and Molecular Biology (2018) Vol. 138, pp. 45-58
Closed Access | Times Cited: 29
Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy
Francisco del Caño‐Ochoa, Bobby G. Ng, Malak Abedalthagafi, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 10, pp. 1598-1605
Open Access | Times Cited: 24
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
Gene mutations in comorbidity of epilepsy and arrhythmia
Cheng Yu, Xuejun Deng, Da Xu
Journal of Neurology (2022) Vol. 270, Iss. 3, pp. 1229-1248
Closed Access | Times Cited: 13
Differentially expressed gene (DEG) based protein-protein interaction (PPI) network identifies a spectrum of gene interactome, transcriptome and correlated miRNA in nondisjunction Down syndrome
Sriroopreddy Ramireddy, Rakshanda Sajeed, P. Raghuraman, et al.
International Journal of Biological Macromolecules (2018) Vol. 122, pp. 1080-1089
Closed Access | Times Cited: 22
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