Timothy M. Olson

10.2k total citations
107 papers, 5.9k citations indexed

About

Timothy M. Olson is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Timothy M. Olson has authored 107 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Cardiology and Cardiovascular Medicine, 50 papers in Molecular Biology and 15 papers in Epidemiology. Recurrent topics in Timothy M. Olson's work include Cardiomyopathy and Myosin Studies (46 papers), Congenital heart defects research (20 papers) and Cardiovascular Effects of Exercise (17 papers). Timothy M. Olson is often cited by papers focused on Cardiomyopathy and Myosin Studies (46 papers), Congenital heart defects research (20 papers) and Cardiovascular Effects of Exercise (17 papers). Timothy M. Olson collaborates with scholars based in United States, Poland and Belarus. Timothy M. Olson's co-authors include Virginia V. Michels, Mark T. Keating, André Terzic, Leonid V. Zingman, Nina Kishimoto, Stephen N. Thibodeau, Frank G. Whitby, Yin-Shan Tai, Xiaoke Liu and Mariza de Andrade and has published in prestigious journals such as Science, New England Journal of Medicine and JAMA.

In The Last Decade

Timothy M. Olson

104 papers receiving 5.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Timothy M. Olson United States 38 4.2k 2.9k 531 429 402 107 5.9k
Sakthivel Sadayappan United States 41 3.9k 0.9× 3.2k 1.1× 562 1.1× 235 0.5× 174 0.4× 179 5.5k
Diane Fatkin Australia 49 4.8k 1.1× 4.3k 1.5× 432 0.8× 691 1.6× 72 0.2× 135 8.0k
Rupak Mukherjee United States 43 3.6k 0.8× 1.6k 0.5× 1.3k 2.4× 207 0.5× 413 1.0× 188 5.5k
David E. Gutstein United States 32 1.5k 0.3× 1.9k 0.6× 403 0.8× 115 0.3× 175 0.4× 80 3.3k
M. Benjamin Perryman United States 39 2.2k 0.5× 3.9k 1.3× 915 1.7× 353 0.8× 213 0.5× 83 6.9k
Frank Wiesmann Germany 34 2.8k 0.7× 1.1k 0.4× 536 1.0× 220 0.5× 100 0.2× 65 4.3k
William E. Louch Norway 38 2.9k 0.7× 2.6k 0.9× 413 0.8× 100 0.2× 236 0.6× 150 4.3k
Brian C. Jensen United States 31 1.4k 0.3× 1.5k 0.5× 339 0.6× 165 0.4× 161 0.4× 98 3.4k
Andrew A. Grace United Kingdom 43 4.0k 0.9× 3.2k 1.1× 457 0.9× 123 0.3× 235 0.6× 184 5.8k
Craig A. Lygate United Kingdom 36 1.8k 0.4× 1.1k 0.4× 294 0.6× 124 0.3× 410 1.0× 107 3.4k

Countries citing papers authored by Timothy M. Olson

Since Specialization
Citations

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

Fields of papers citing papers by Timothy M. Olson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Timothy M. Olson. 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 Timothy M. Olson. The network helps show where Timothy M. Olson may publish in the future.

Co-authorship network of co-authors of Timothy M. Olson

This figure shows the co-authorship network connecting the top 25 collaborators of Timothy M. Olson. A scholar is included among the top collaborators of Timothy M. Olson 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 Timothy M. Olson. Timothy M. Olson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Theis, Jeanne L., Jared M. Evans, Zachary C. Fogarty, et al.. (2023). Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways. Journal of Cardiovascular Development and Disease. 10(9). 393–393. 3 indexed citations
2.
Birker, Katja, Shuchao Ge, Jeanne L. Theis, et al.. (2023). Mitochondrial MICOS complex genes, implicated in hypoplastic left heart syndrome, maintain cardiac contractility and actomyosin integrity. eLife. 12. 9 indexed citations
3.
Theis, Jeanne L., Talha Niaz, Rhianna S. Sundsbak, et al.. (2022). CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circulation Genomic and Precision Medicine. 15(2). e003523–e003523. 13 indexed citations
4.
Niaz, Talha, Joseph T. Poterucha, Timothy M. Olson, et al.. (2017). Characteristic Morphologies of the Bicuspid Aortic Valve in Patients with Genetic Syndromes. Journal of the American Society of Echocardiography. 31(2). 194–200. 27 indexed citations
5.
Long, Pamela A., Michael T. Zimmermann, Maengjo Kim, et al.. (2016). De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy. Human Genetics. 135(8). 909–917. 24 indexed citations
6.
Brody, Matthew J., Adrian C. Grimes, Timothy A. Hacker, et al.. (2015). LRRC10 is required to maintain cardiac function in response to pressure overload. American Journal of Physiology-Heart and Circulatory Physiology. 310(2). H269–H278. 22 indexed citations
7.
Evans, Jared M., et al.. (2014). Characterizing Genetic Variation of Adrenergic Signalling Pathways in Takotsubo (Stress) Cardiomyopathy Exomes. European Journal of Heart Failure. 16(9). 942–949. 36 indexed citations
8.
Theis, Jeanne L., Michael T. Zimmermann, Brandon T. Larsen, et al.. (2014). TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy. Human Molecular Genetics. 23(21). 5793–5804. 33 indexed citations
9.
Cannone, Valentina, Guido Boerrigter, Alessandro Cataliotti, et al.. (2011). A Genetic Variant of the Atrial Natriuretic Peptide Gene Is Associated With Cardiometabolic Protection in the General Community. Journal of the American College of Cardiology. 58(6). 629–636. 78 indexed citations
10.
McKie, Paul M., Alessandro Cataliotti, Brenda K. Huntley, et al.. (2009). A Human Atrial Natriuretic Peptide Gene Mutation Reveals a Novel Peptide With Enhanced Blood Pressure-Lowering, Renal-Enhancing, and Aldosterone-Suppressing Actions. Journal of the American College of Cardiology. 54(11). 1024–1032. 46 indexed citations
11.
Reyes, Santiago, André Terzic, Douglas W. Mahoney, et al.. (2008). KATP channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study. Human Genetics. 123(6). 665–667. 29 indexed citations
12.
Olson, Timothy M., Alexey E. Alekseev, Christophe Moreau, et al.. (2007). KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation. Nature Clinical Practice Cardiovascular Medicine. 4(2). 110–116. 130 indexed citations
13.
Olson, Timothy M.. (2006). What makes the heart fail? New insights from defective genes. Acta Paediatrica. 95(S452). 17–21. 3 indexed citations
14.
Sutton, Thomas M., et al.. (2006). Congenital heart defects in siblings with partial aneuploidy of chromosome 2p. Cardiovascular Pathology. 15(1). 33–35. 1 indexed citations
15.
Chen, Lin Y., et al.. (2006). A Common Polymorphism in SCN5A is Associated with Lone Atrial Fibrillation. Clinical Pharmacology & Therapeutics. 81(1). 35–41. 105 indexed citations
16.
Olson, Timothy M.. (2005). Sodium Channel Mutations and Susceptibility to Heart Failure and Atrial Fibrillation. JAMA. 293(4). 447–447. 372 indexed citations
17.
Michels, Virginia V., Timothy M. Olson, Fletcher A. Miller, et al.. (2003). Frequency of development of idiopathic dilated cardiomyopathy among relatives of patients with idiopathic dilated cardiomyopathy. The American Journal of Cardiology. 91(11). 1389–1392. 21 indexed citations
18.
Darbar, Dawood, Arshad Jahangir, Bernard J. Gersh, et al.. (2003). Familial atrial fibrillation is a genetically heterogeneous disorder. Journal of the American College of Cardiology. 41(12). 2185–2192. 229 indexed citations
19.
Olson, Timothy M. & Mark T. Keating. (1996). Mapping a cardiomyopathy locus to chromosome 3p22-p25.. Journal of Clinical Investigation. 97(2). 528–532. 138 indexed citations
20.
Olson, Timothy M., Virginia V. Michels, Noralane M. Lindor, et al.. (1993). Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7. Human Molecular Genetics. 2(7). 869–873. 48 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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