Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Rescue of protein expression defects may not be enough to abolish the pro‐arrhythmic phenotype of long QT type 2 mutations
Matthew D. Perry, Chai‐Ann Ng, Kevin Phan, et al.
The Journal of Physiology (2016) Vol. 594, Iss. 14, pp. 4031-4049
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Murine Electrophysiological Models of Cardiac Arrhythmogenesis
Christopher Huang
Physiological Reviews (2016) Vol. 97, Iss. 1, pp. 283-409
Open Access | Times Cited: 102
Phenanthrene impacts zebrafish cardiomyocyte excitability by inhibiting IKr and shortening action potential duration
Shiva N. Kompella, Fabien Brette, Jules C. Hancox, et al.
The Journal of General Physiology (2021) Vol. 153, Iss. 2
Open Access | Times Cited: 33
A massively parallel assay accurately discriminates between functionally normal and abnormal variants in a hotspot domain of KCNH2
Chai‐Ann Ng, Rizwan Ullah, Jessica Farr, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 7, pp. 1208-1216
Open Access | Times Cited: 21
Fatty acid analogue N-arachidonoyl taurine restores function of IKs channels with diverse long QT mutations
Sara I. Liin, Johan Larsson, René Barro-Soria, et al.
eLife (2016) Vol. 5
Open Access | Times Cited: 36
Pharmacological activation of IKr in models of long QT Type 2 risks overcorrection of repolarization
Matthew D. Perry, Chai‐Ann Ng, Melissa Mangala, et al.
Cardiovascular Research (2019) Vol. 116, Iss. 8, pp. 1434-1445
Open Access | Times Cited: 32
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias
Karina O. Brandão, Lettine van den Brink, Duncan C. Miller, et al.
Stem Cell Reports (2020) Vol. 15, Iss. 5, pp. 1127-1139
Open Access | Times Cited: 31
Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes
Bailey J. O’Hare, C.S. John Kim, Samantha K. Hamrick, et al.
Circulation Genomic and Precision Medicine (2020) Vol. 13, Iss. 5, pp. 466-475
Open Access | Times Cited: 30
Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations
Jinyuan Vero Li, Chai‐Ann Ng, Delfine Cheng, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 23
Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families
Maria‐Christina Kotta, Margherita Torchio, Pauline Bayliss, et al.
Journal of the American Heart Association (2023) Vol. 12, Iss. 17
Open Access | Times Cited: 9
Development of a High-Throughput Flow Cytometry Assay to Monitor Defective Trafficking and Rescue of Long QT2 Mutant hERG Channels
Scott A. Kanner, Ananya Jain, Henry M. Colecraft
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 27
KCNE1 tunes the sensitivity of KV7.1 to polyunsaturated fatty acids by moving turret residues close to the binding site
Johan Larsson, H. Peter Larsson, Sara I. Liin
eLife (2018) Vol. 7
Open Access | Times Cited: 25
The hERG channel activator, RPR260243, enhances protective IKr current early in the refractory period reducing arrhythmogenicity in zebrafish hearts
Yu Shi, ZhaoKai Pang, Ravichandra Venkateshappa, et al.
AJP Heart and Circulatory Physiology (2020) Vol. 319, Iss. 2, pp. H251-H261
Open Access | Times Cited: 21
Electrophysiological characterization of the hERG R56Q LQTS variant and targeted rescue by the activator RPR260243
Jacob Kemp, David J. Whittaker, Ravichandra Venkateshappa, et al.
The Journal of General Physiology (2021) Vol. 153, Iss. 10
Open Access | Times Cited: 17
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology
Chai‐Ann Ng, Jessica Farr, Paul Young, et al.
Biology Methods and Protocols (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 15
Pharmacological Chaperones: Beyond Conformational Disorders
Nancy J. Leidenheimer
Handbook of experimental pharmacology (2017), pp. 135-153
Closed Access | Times Cited: 15
Prediction of Kv11.1 potassium channel PAS-domain variants trafficking via machine learning
Kalyan Immadisetty, Xuan Fang, G. San Ramon, et al.
Journal of Molecular and Cellular Cardiology (2023) Vol. 180, pp. 69-83
Closed Access | Times Cited: 4
The S1 helix critically regulates the finely tuned gating of Kv11.1 channels
Kevin Phan, Chai‐Ann Ng, Erikka David, et al.
Journal of Biological Chemistry (2017) Vol. 292, Iss. 18, pp. 7688-7705
Open Access | Times Cited: 11
Development of automated patch clamp assays to overcome the burden of variants of uncertain significance in inheritable arrhythmia syndromes
G. Joanne, Jamie I. Vandenberg, Chai‐Ann Ng
Frontiers in Physiology (2023) Vol. 14
Open Access | Times Cited: 3
A High-Throughput Screening Assay to Identify Drugs that Can Treat Long QT Syndrome Caused by Trafficking-Deficient KV11.1 (hERG) Variants
Christian Egly, Daniel J. Blackwell, Jeffrey Schmeckpeper, et al.
Molecular Pharmacology (2022) Vol. 101, Iss. 4, pp. 236-245
Open Access | Times Cited: 5
Recent advances in understanding and prevention of sudden cardiac death
Jamie I. Vandenberg, Matthew D. Perry, Adam P. Hill
F1000Research (2017) Vol. 6, pp. 1614-1614
Open Access | Times Cited: 6
Deciphering HERG mutation in long QT syndrome type 2 using antisense oligonucleotide–mediated techniques: Lessons from cystic fibrosis
Zequn Zheng, Yongfei Song, Xuerui Tan
Heart Rhythm (2023) Vol. 20, Iss. 8, pp. 1169-1177
Closed Access | Times Cited: 2
Tyrosine Residues from the S4-S5 Linker of Kv11.1 Channels Are Critical for Slow Deactivation
Chai‐Ann Ng, Andrée E. Gravel, Matthew D. Perry, et al.
Journal of Biological Chemistry (2016) Vol. 291, Iss. 33, pp. 17293-17302
Open Access | Times Cited: 2
Functional characterization of a novel hERG variant in a family with recurrent sudden infant death syndrome: Retracting a genetic diagnosis
Valentine Sergeev, Frances Perry, Thomas M. Roston, et al.
Forensic Science International (2017) Vol. 284, pp. 39-45
Closed Access | Times Cited: 2
hERG long QT syndrome type 2 mutants need more than a chaperone to dance
David Fedida, Logan C. Macdonald
The Journal of Physiology (2016) Vol. 594, Iss. 15, pp. 4095-4096
Open Access | Times Cited: 1
Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations
Jinyuan Vero Li, Chai‐Ann Ng, Delfine Cheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 1
Page 1 - Next Page

Scroll to top