Leslie Smoot

4.9k total citations · 1 hit paper
45 papers, 3.0k citations indexed

About

Leslie Smoot is a scholar working on Molecular Biology, Surgery and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Leslie Smoot has authored 45 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 13 papers in Surgery and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Leslie Smoot's work include Transplantation: Methods and Outcomes (10 papers), Williams Syndrome Research (7 papers) and Congenital heart defects research (6 papers). Leslie Smoot is often cited by papers focused on Transplantation: Methods and Outcomes (10 papers), Williams Syndrome Research (7 papers) and Congenital heart defects research (6 papers). Leslie Smoot collaborates with scholars based in United States, United Kingdom and Canada. Leslie Smoot's co-authors include Vijak Mahdavi, Roger E. Breitbart, Yi‐Tao Yu, B Nadal-Ginard, Christine E. Seidman, Mary P. Mullen, Barbara McDonough, John A. Jarcho, Sapna Sharma and J G Seidman and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Leslie Smoot

44 papers receiving 2.9k citations

Hit Papers

Mutations in Sarcomere Protein Genes as a Cause of Dilate... 2000 2026 2008 2017 2000 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leslie Smoot United States 23 1.9k 890 437 384 347 45 3.0k
Naohito Yamasaki Japan 26 963 0.5× 1.3k 1.5× 170 0.4× 362 0.9× 346 1.0× 100 2.2k
Gregory F. Egnaczyk United States 14 1.1k 0.5× 545 0.6× 99 0.2× 252 0.7× 530 1.5× 36 1.7k
Mitsuhiro Kamisago Japan 16 1.4k 0.7× 1.1k 1.2× 240 0.5× 335 0.9× 349 1.0× 36 2.2k
Kristy Red-Horse United States 18 1.2k 0.6× 301 0.3× 121 0.3× 185 0.5× 309 0.9× 25 2.9k
Nolan L. Boyd United States 22 1.0k 0.5× 304 0.3× 123 0.3× 128 0.3× 680 2.0× 33 2.3k
Atsushi Ikeda Japan 25 1.3k 0.7× 148 0.2× 134 0.3× 110 0.3× 586 1.7× 94 2.6k
Piotr Religa Sweden 24 1.1k 0.6× 301 0.3× 86 0.2× 383 1.0× 519 1.5× 65 2.9k
Laurent Metzinger France 27 2.0k 1.0× 287 0.3× 284 0.6× 87 0.2× 180 0.5× 51 2.6k
Ingrid Struman Belgium 35 2.3k 1.2× 900 1.0× 211 0.5× 109 0.3× 738 2.1× 64 4.0k
Siddharth K. Prakash United States 25 554 0.3× 1.1k 1.2× 670 1.5× 477 1.2× 250 0.7× 85 2.2k

Countries citing papers authored by Leslie Smoot

Since Specialization
Citations

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

Fields of papers citing papers by Leslie Smoot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leslie Smoot. 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 Leslie Smoot. The network helps show where Leslie Smoot may publish in the future.

Co-authorship network of co-authors of Leslie Smoot

This figure shows the co-authorship network connecting the top 25 collaborators of Leslie Smoot. A scholar is included among the top collaborators of Leslie Smoot 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 Leslie Smoot. Leslie Smoot 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.
Smoot, Leslie, et al.. (2023). Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases. Molecular Genetics and Metabolism. 139(3). 107626–107626. 10 indexed citations
2.
Stein, Deborah R., Michael A. Ferguson, Diego Porras, et al.. (2020). Surgical management of pediatric renovascular hypertension and midaortic syndrome at a single-center multidisciplinary program. Journal of Vascular Surgery. 74(1). 79–89.e2. 9 indexed citations
3.
Peng, David M., Yulin Zhang, David N. Rosenthal, et al.. (2017). Impact of Heart Transplantation on the Functional Status of US Children With End-Stage Heart Failure. Circulation. 135(10). 939–950. 12 indexed citations
4.
Kowalczyk, Monika S., Jim R. Hughes, Christian Babbs, et al.. (2012). Nprl3 is required for normal development of the cardiovascular system. Mammalian Genome. 23(7-8). 404–415. 34 indexed citations
5.
Morell, Emily, Joanne Wolfe, Mark A. Scheurer, et al.. (2012). Patterns of Care at End of Life in Children With Advanced Heart Disease. Archives of Pediatrics and Adolescent Medicine. 166(8). 745–8. 63 indexed citations
6.
Saleeb, Susan F., Renée Margossian, Carolyn T. Spencer, et al.. (2011). Reproducibility of Echocardiographic Diagnosis of Left Ventricular Noncompaction. Journal of the American Society of Echocardiography. 25(2). 194–202. 46 indexed citations
7.
Almond, Christopher S., Kimberlee Gauvreau, Gary Piercey, et al.. (2011). Association of graft ischemic time with survival after heart transplant among children in the United States. The Journal of Heart and Lung Transplantation. 30(11). 1244–1249. 26 indexed citations
8.
Wu, Bai‐Lin, Va Lip, Elicia Estrella, et al.. (2010). Familial Dilated Cardiomyopathy Secondary to Dystrophin Splice Site Mutation. Journal of Cardiac Failure. 16(3). 194–199. 13 indexed citations
9.
Silva, Jennifer N. Avari, Charles E. Canter, Tajinder P. Singh, et al.. (2010). Outcomes of heart transplantation using donor hearts from infants with sudden infant death syndrome. The Journal of Heart and Lung Transplantation. 29(11). 1226–1230. 1 indexed citations
10.
Singh, Tajinder P., Elizabeth D. Blume, Sarah Worley, et al.. (2010). Safety and early outcomes using a corticosteroid-avoidance immunosuppression protocol in pediatric heart transplant recipients. The Journal of Heart and Lung Transplantation. 29(5). 517–522. 48 indexed citations
11.
Smoot, Leslie, et al.. (2009). Clinical features of pulmonary arterial hypertension in young people with an ALK1 mutation and hereditary haemorrhagic telangiectasia. Archives of Disease in Childhood. 94(7). 506–511. 18 indexed citations
12.
Sol‐Church, Katia, Deborah L. Stabley, Laurie Demmer, et al.. (2009). Male‐to‐male transmission of Costello syndrome: G12S HRAS germline mutation inherited from a father with somatic mosaicism. American Journal of Medical Genetics Part A. 149A(3). 315–321. 42 indexed citations
13.
Juraszek, Amy L., et al.. (2008). Double outlet right ventricle: aetiologies and associations. Journal of Medical Genetics. 45(8). 481–497. 68 indexed citations
14.
Rajagopal, Satish, Qing Ma, Jie Shen, et al.. (2007). Spectrum of heart disease associated with murine and human GATA4 mutation. Journal of Molecular and Cellular Cardiology. 43(6). 677–685. 189 indexed citations
15.
Tubman, Venée N., Leslie Smoot, & Matthew M. Heeney. (2006). Acquired immune cytopenias post‐cardiac transplantation respond to rituximab. Pediatric Blood & Cancer. 48(3). 339–344. 22 indexed citations
16.
Urbán, Zsolt, Sheila Riazi, Thomas L. Seidl, et al.. (2002). Connection between Elastin Haploinsufficiency and Increased Cell Proliferation in Patients with Supravalvular Aortic Stenosis and Williams-Beuren Syndrome. The American Journal of Human Genetics. 71(1). 30–44. 138 indexed citations
17.
Lin, Angela E., Paul Grossfeld, Robert M. Hamilton, et al.. (2002). Further delineation of cardiac abnormalities in Costello syndrome. American Journal of Medical Genetics. 111(2). 115–129. 78 indexed citations
18.
Metcalfe, Kay, Leslie Smoot, Pascal McKeown, et al.. (2000). Elastin: mutational spectrum in supravalvular aortic stenosis. European Journal of Human Genetics. 8(12). 955–963. 110 indexed citations
19.
Kamisago, Mitsuhiro, Sapna Sharma, Steven R. DePalma, et al.. (2000). Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy. New England Journal of Medicine. 343(23). 1688–1696. 527 indexed citations breakdown →
20.
Smoot, Leslie. (1995). Elastin gene deletions in Williams syndrome. The Journal of Pediatrics. 7(6). 698–701. 2 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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