Ryan Pfeiffer

3.7k total citations
23 papers, 698 citations indexed

About

Ryan Pfeiffer is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ryan Pfeiffer has authored 23 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cardiology and Cardiovascular Medicine, 16 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ryan Pfeiffer's work include Cardiac electrophysiology and arrhythmias (21 papers), Ion channel regulation and function (16 papers) and Cardiac Arrhythmias and Treatments (4 papers). Ryan Pfeiffer is often cited by papers focused on Cardiac electrophysiology and arrhythmias (21 papers), Ion channel regulation and function (16 papers) and Cardiac Arrhythmias and Treatments (4 papers). Ryan Pfeiffer collaborates with scholars based in United States, Germany and Denmark. Ryan Pfeiffer's co-authors include Charles Antzelevitch, Elena Burashnikov, Héctor Barajas-Martínez, Jonathan M. Cordeiro, Dan Hu, Yuesheng Wu, Guido D. Pollevick, Alejandra Guerchicoff, Michael Springer and András Varró and has published in prestigious journals such as Circulation, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Ryan Pfeiffer

22 papers receiving 684 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ryan Pfeiffer United States	11	644	564	105	19	14	23	698
J SMITS Netherlands	9	1.1k 1.7×	880 1.6×	113 1.1×	15 0.8×	26 1.9×	14	1.2k
Sung Yon Um United States	9	302 0.5×	270 0.5×	122 1.2×	28 1.5×	15 1.1×	13	397
Althea Goosen South Africa	14	669 1.0×	390 0.7×	47 0.4×	29 1.5×	7 0.5×	21	750
Dina Myers Stroud United States	11	411 0.6×	390 0.7×	124 1.2×	12 0.6×	3 0.2×	12	544
Stéphanie C.M. Choisy United Kingdom	10	396 0.6×	228 0.4×	69 0.7×	8 0.4×	4 0.3×	24	482
Jan G. Zegers Netherlands	10	433 0.7×	354 0.6×	186 1.8×	6 0.3×	3 0.2×	15	530
Po Wei Kang United States	11	182 0.3×	246 0.4×	101 1.0×	16 0.8×	5 0.4×	15	308
Jon Arne Kro Birkeland Norway	10	223 0.3×	209 0.4×	69 0.7×	10 0.5×	9 0.6×	18	334
Pedro Iturralde-Torres Mexico	7	446 0.7×	329 0.6×	68 0.6×	5 0.3×	7 0.5×	33	508
Judith M.B. Pinto United States	12	415 0.6×	295 0.5×	116 1.1×	3 0.2×	19 1.4×	25	525

Countries citing papers authored by Ryan Pfeiffer

Since Specialization

Citations

This map shows the geographic impact of Ryan Pfeiffer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ryan Pfeiffer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan Pfeiffer more than expected).

Fields of papers citing papers by Ryan Pfeiffer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan Pfeiffer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ryan Pfeiffer. The network helps show where Ryan Pfeiffer may publish in the future.

Co-authorship network of co-authors of Ryan Pfeiffer

This figure shows the co-authorship network connecting the top 25 collaborators of Ryan Pfeiffer. A scholar is included among the top collaborators of Ryan Pfeiffer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ryan Pfeiffer. Ryan Pfeiffer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Treat, Jacqueline A., Ryan Pfeiffer, Robert J. Goodrow, et al.. (2024). Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome. PLoS ONE. 19(1). e0287206–e0287206.

Amancherla, Kaushik, Juan Qin, Ryan Pfeiffer, et al.. (2022). Single-Nuclear RNA-Sequencing Identifies Cell-Specific Transcriptional Programs in Cardiac Allograft Vasculopathy. The Journal of Heart and Lung Transplantation. 41(4). S150–S150. 1 indexed citations

Treat, Jacqueline A., Ryan Pfeiffer, Héctor Barajas-Martínez, et al.. (2021). Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. International Journal of Molecular Sciences. 22(13). 7108–7108. 5 indexed citations

Barajas-Martínez, Héctor, Dan Hu, Robert J. Goodrow, et al.. (2020). Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes. Stem Cells International. 2020. 1–16. 14 indexed citations

Shi, Shaobo, Tao Liu, Héctor Barajas-Martínez, et al.. (2017). Atrial fibrillation associated with Wolff-Parkinson-White syndrome in a patient with concomitant Brugada syndrome. HeartRhythm Case Reports. 3(1). 13–17. 2 indexed citations

Veltmann, Christian, Héctor Barajas-Martínez, Christian Wolpert, et al.. (2016). Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Journal of the American Heart Association. 5(7). 39 indexed citations

Hasdemir, Can, Serdar Payzın, Mehmet Aydın, et al.. (2015). High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia. Heart Rhythm. 12(7). 1584–1594. 55 indexed citations

Hennessey, Jessica A., Nicole J. Boczek, William L. Patrick, et al.. (2014). A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis. PLoS ONE. 9(9). e106982–e106982. 40 indexed citations

Kanter, Ronald J., Ryan Pfeiffer, Dan Hu, et al.. (2011). Brugada-Like Syndrome in Infancy Presenting With Rapid Ventricular Tachycardia and Intraventricular Conduction Delay. Circulation. 125(1). 14–22. 40 indexed citations

10.

Calløe, Kirstine, Nicole Schmitt, Søren Grubb, et al.. (2011). Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A. Canadian Journal of Physiology and Pharmacology. 89(10). 723–736. 9 indexed citations

11.

Hu, Dan, Héctor Barajas-Martínez, Argelia Medeiros‐Domingo, et al.. (2011). A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents. Heart Rhythm. 9(5). 760–769. 84 indexed citations

12.

Barajas-Martínez, Héctor, Dan Hu, Elena Burashnikov, et al.. (2010). Abstract 15855: A Novel Mutation (D538E) in CACNB2b Associated with Infant Brugada Syndrome. Circulation. 122. 1 indexed citations

13.

Hu, Dan, et al.. (2010). Abstract 18124: The Role of SCN5A Mutations in J Wave Syndromes. Circulation. 122(5). 629–43. 2 indexed citations

14.

Schmitt, Nicole, Kirstine Calløe, Christian Veltmann, et al.. (2010). Mutation in Nav1.5 Associated with Brugada Syndrome - a Mutational Hotspot?. Biophysical Journal. 98(3). 311a–311a. 1 indexed citations

15.

Burashnikov, Elena, Ryan Pfeiffer, Martin Borggrefe, et al.. (2009). Abstract 1929: Mutations in the Cardiac L-Type Calcium Channel Associated With Four Sudden Cardiac Death Syndromes. Circulation. 120. 172858–172858. 5 indexed citations

16.

Cordeiro, Jonathan M., Mark Marieb, Ryan Pfeiffer, et al.. (2009). Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome. Journal of Molecular and Cellular Cardiology. 46(5). 695–703. 83 indexed citations

17.

Hu, Dan, Héctor Barajas-Martínez, Vladislav V. Nesterenko, et al.. (2009). Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome. Pacing and Clinical Electrophysiology. 33(3). 274–285. 28 indexed citations

18.

Hu, Dan, Héctor Barajas-Martínez, Elena Burashnikov, et al.. (2009). A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype. Circulation Cardiovascular Genetics. 2(3). 270–278. 190 indexed citations

19.

Cordeiro, Jonathan M., Mark Marieb, Ryan Pfeiffer, et al.. (2008). Abstract 4413: Accelerated Inactivation of the L-type Calcium due to a Mutation in CACNB2b Underlies the Development of a Brugada ECG Phenotype. Circulation. 118(suppl_18). 1 indexed citations

20.

Cordeiro, Jonathan M., Héctor Barajas-Martínez, Kui Hong, et al.. (2006). Compound Heterozygous Mutations P336L and I1660V in the Human Cardiac Sodium Channel Associated With the Brugada Syndrome. Circulation. 114(19). 2026–2033. 83 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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