Mark W. Russell

9.7k total citations · 1 hit paper
113 papers, 4.0k citations indexed

About

Mark W. Russell is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Mark W. Russell has authored 113 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Cardiology and Cardiovascular Medicine, 50 papers in Molecular Biology and 22 papers in Epidemiology. Recurrent topics in Mark W. Russell's work include Cardiomyopathy and Myosin Studies (31 papers), Congenital Heart Disease Studies (17 papers) and Congenital heart defects research (16 papers). Mark W. Russell is often cited by papers focused on Cardiomyopathy and Myosin Studies (31 papers), Congenital Heart Disease Studies (17 papers) and Congenital heart defects research (16 papers). Mark W. Russell collaborates with scholars based in United States, Australia and Germany. Mark W. Russell's co-authors include Maide Ö. Raeker, Andrei B. Borisov, Aikaterini Kontrogianni‐Konstantopoulos, Wendy K. Chung, Margaret V. Westfall, Robert J. Bloch, David S. Milstone, Christine Y. Ivashchenko, Sheng Zhong Duan and Richard M. Mortensen and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Mark W. Russell

110 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

2018 370 citations Vidu Garg, Seema Mital et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark W. Russell United States	38	1.9k	1.6k	901	510	436	113	4.0k
Wolfgang Rottbauer Germany	39	2.4k 1.2×	2.9k 1.8×	1.0k 1.1×	821 1.6×	614 1.4×	251	5.7k
Sek Won Kong United States	36	3.6k 1.9×	836 0.5×	966 1.1×	380 0.7×	229 0.5×	84	5.7k
Yan Huang China	34	2.7k 1.4×	532 0.3×	354 0.4×	394 0.8×	445 1.0×	104	5.3k
James Scott United Kingdom	31	3.3k 1.7×	544 0.3×	529 0.6×	949 1.9×	473 1.1×	51	5.6k
Simon Walker United Kingdom	34	1.9k 1.0×	654 0.4×	2.0k 2.2×	422 0.8×	1.2k 2.9×	83	5.1k
Carolyn Y. Ho United States	50	2.1k 1.1×	5.9k 3.7×	1.0k 1.2×	544 1.1×	109 0.3×	135	7.1k
Deborah Hunter United States	31	1.9k 1.0×	334 0.2×	955 1.1×	507 1.0×	189 0.4×	54	5.1k
Jenny C. Taylor United Kingdom	29	1.7k 0.9×	716 0.5×	244 0.3×	214 0.4×	156 0.4×	96	4.0k
Siu Yuen Chan Hong Kong	32	1.4k 0.7×	409 0.3×	216 0.2×	292 0.6×	213 0.5×	99	3.5k
Christine Fischer Germany	32	1.8k 0.9×	794 0.5×	248 0.3×	180 0.4×	231 0.5×	112	4.4k

Countries citing papers authored by Mark W. Russell

Since Specialization

Citations

This map shows the geographic impact of Mark W. Russell'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 Mark W. Russell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark W. Russell more than expected).

Fields of papers citing papers by Mark W. Russell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark W. Russell. 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 Mark W. Russell. The network helps show where Mark W. Russell may publish in the future.

Co-authorship network of co-authors of Mark W. Russell

This figure shows the co-authorship network connecting the top 25 collaborators of Mark W. Russell. A scholar is included among the top collaborators of Mark W. Russell 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 Mark W. Russell. Mark W. Russell 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

Kaski, Juan Pablo, Paul F. Kantor, Stephanie J. Nakano, et al.. (2025). Efficacy and Safety of Aficamten in Children and Adolescents With Obstructive Hypertrophic Cardiomyopathy: Study Design and Rationale of CEDAR-HCM. Circulation Heart Failure. 19(2). e013418–e013418.

Repetti, Giuliana G., Yuri Kim, Alexandre C. Pereira, et al.. (2021). Discordant clinical features of identical hypertrophic cardiomyopathy twins. Proceedings of the National Academy of Sciences. 118(10). 27 indexed citations

Vigneault, Davis M., Eunice Yang, Michael Tee, et al.. (2018). Left Ventricular Strain Is Abnormal in Preclinical and Overt Hypertrophic Cardiomyopathy: Cardiac MR Feature Tracking. Radiology. 290(3). 640–648. 62 indexed citations

Mital, Seema, Kiran Musunuru, Vidu Garg, et al.. (2016). Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Circulation Cardiovascular Genetics. 9(5). 448–467. 57 indexed citations

White, Michelle J., Eméfah Loccoh, Monica Martin Goble, et al.. (2016). Availability of Automated External Defibrillators in Public High Schools. The Journal of Pediatrics. 172. 142–146.e1. 15 indexed citations

Stillwell, Terri, Matthew Greenhawt, Kathleen A. Stringer, et al.. (2015). Immune Abnormalities in Fontan Protein-Losing Enteropathy: A Case-Control Study. The Journal of Pediatrics. 167(2). 331–337. 38 indexed citations

Russell, Mark W., Maide Ö. Raeker, Sarah Geisler, et al.. (2014). Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. Human Molecular Genetics. 23(16). 4272–4284. 48 indexed citations

Dorfman, Adam L., Sunkyung Yu, Mark W. Russell, et al.. (2014). Clinical Significance of Late Gadolinium Enhancement in Patients <20 Years of Age With Hypertrophic Cardiomyopathy. The American Journal of Cardiology. 113(7). 1234–1239. 45 indexed citations

Kamp, Anna, Nicholas H. Von Bergen, Charles A. Henrikson, et al.. (2013). Implanted Defibrillators in Young Hypertrophic Cardiomyopathy Patients: A Multicenter Study. Pediatric Cardiology. 34(7). 1620–1627. 31 indexed citations

10.

Racz, Jennifer, Michael Ford, Lindsay Schmidt, et al.. (2013). Immunophenotyping and Protein Profiling of Fontan-associated Plastic Bronchitis Airway Casts. Annals of the American Thoracic Society. 10(2). 98–107. 18 indexed citations

11.

LaPage, Martin J., Mark W. Russell, David J. Bradley, & Macdonald Dick. (2012). Novel Ryanodine Receptor 2 Mutation Associated with a Severe Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia. The Journal of Pediatrics. 161(2). 362–364. 6 indexed citations

12.

Fu, Xueyao, Takae Kiyama, Renzhong Li, et al.. (2009). Epitope‐tagging Math5 and Pou4f2: New tools to study retinal ganglion cell development in the mouse. Developmental Dynamics. 238(9). 2309–2317. 22 indexed citations

13.

Raeker, Maide Ö., et al.. (2009). Targeted deletion of the zebrafish obscurin A RhoGEF domain affects heart, skeletal muscle and brain development. Developmental Biology. 337(2). 432–443. 25 indexed citations

14.

Tokusumi, Tsuyoshi, Richard Paul Sorrentino, Mark W. Russell, et al.. (2009). Characterization of a Lamellocyte Transcriptional Enhancer Located within the misshapen Gene of Drosophila melanogaster. PLoS ONE. 4(7). e6429–e6429. 54 indexed citations

15.

Russell, Mark W., et al.. (2008). Cardiac involvement in the dystrophinopathies. Journal of Pediatric Rehabilitation Medicine. 1(3). 211–223. 2 indexed citations

16.

Borisov, Andrei B., et al.. (2007). Intracardiac lipid accumulation, lipoatrophy of muscle cells and expansion of myocardial infarction in type 2 diabetic patients. Micron. 39(7). 944–951. 21 indexed citations

17.

Tokusumi, Tsuyoshi, Mark W. Russell, Kathleen Gajewski, Nancy Fossett, & Robert A. Schulz. (2006). U-shaped protein domains required for repression of cardiac gene expression in Drosophila. Differentiation. 75(2). 166–174. 8 indexed citations

18.

Samai, Cyrus, Carlen A. Gomez, Mark W. Russell, David Parra, & Achi Ludomirsky. (2003). The fetus with hypoplastic left heart syndrome: Risk factors and outcomes. Journal of the American College of Cardiology. 41(6). 483–483. 3 indexed citations

19.

Russell, Mark W., et al.. (2002). Identification, tissue expression and chromosomal localization of human Obscurin-MLCK, a member of the titin and Dbl families of myosin light chain kinases. Gene. 282(1-2). 237–246. 88 indexed citations

20.

Russell, Mark W., Paul R. Kemp, Lihong Wang, Lawrence C. Brody, & Seigo Izumo. (1998). Molecular cloning of the human HAND2 gene. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1443(3). 393–399. 18 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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