Henry M. Sucov

12.1k total citations · 4 hit papers
88 papers, 9.4k citations indexed

About

Henry M. Sucov is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Henry M. Sucov has authored 88 papers receiving a total of 9.4k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 22 papers in Genetics and 18 papers in Surgery. Recurrent topics in Henry M. Sucov's work include Congenital heart defects research (49 papers), Retinoids in leukemia and cellular processes (15 papers) and Congenital Heart Disease Studies (13 papers). Henry M. Sucov is often cited by papers focused on Congenital heart defects research (49 papers), Retinoids in leukemia and cellular processes (15 papers) and Congenital Heart Disease Studies (13 papers). Henry M. Sucov collaborates with scholars based in United States, Canada and Japan. Henry M. Sucov's co-authors include Ronald M. Evans, Xiaobing Jiang, Andrew P. McMahon, David H. Rowitch, Philippe Soriano, Robert E. Maxson, Kenneth R. Chien, Yang Chai, Jun Han and Yoshihiro Ito and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Henry M. Sucov

88 papers receiving 9.2k citations

Hit Papers

Fate of the mammalian cra... 1994 2026 2004 2015 2000 2000 2002 1994 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Henry M. Sucov United States 50 7.4k 2.4k 1.3k 1.0k 949 88 9.4k
Brian L. Black United States 49 8.5k 1.1× 1.7k 0.7× 938 0.7× 581 0.6× 1.3k 1.3× 103 10.0k
Andreas Kispert Germany 62 13.4k 1.8× 4.0k 1.6× 1.9k 1.5× 1.5k 1.5× 874 0.9× 178 16.4k
Miguel Torres Spain 48 6.1k 0.8× 1.7k 0.7× 1.2k 0.9× 564 0.5× 526 0.6× 125 8.6k
Yumiko Saga Japan 60 9.6k 1.3× 3.1k 1.3× 1.3k 1.0× 412 0.4× 461 0.5× 181 13.1k
Andreas Schedl France 52 9.6k 1.3× 4.3k 1.8× 1.3k 1.0× 1.1k 1.1× 507 0.5× 116 13.4k
Antonio Baldini United States 50 8.5k 1.2× 3.4k 1.4× 1.0k 0.8× 1.2k 1.1× 1.9k 2.0× 191 10.8k
Ángel Raya Spain 44 8.6k 1.2× 1.1k 0.4× 1.5k 1.2× 602 0.6× 1.1k 1.1× 124 11.3k
David Sassoon United States 57 8.8k 1.2× 1.9k 0.8× 1.1k 0.9× 351 0.3× 277 0.3× 110 11.0k
Hiromi Yanagisawa United States 43 3.3k 0.4× 2.2k 0.9× 1.1k 0.8× 1.3k 1.2× 336 0.4× 112 7.0k
Elisabeth Tournier‐Lasserve France 67 4.2k 0.6× 924 0.4× 637 0.5× 1.1k 1.1× 745 0.8× 230 16.6k

Countries citing papers authored by Henry M. Sucov

Since Specialization
Citations

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

Fields of papers citing papers by Henry M. Sucov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henry M. Sucov

This figure shows the co-authorship network connecting the top 25 collaborators of Henry M. Sucov. A scholar is included among the top collaborators of Henry M. Sucov 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 Henry M. Sucov. Henry M. Sucov 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.
Li, Shuang, Patrick Roddy, Chun Liu, et al.. (2024). Cardiomyocyte-fibroblast interaction regulates ferroptosis and fibrosis after myocardial injury. iScience. 27(3). 109219–109219. 16 indexed citations
2.
3.
Li, Shuang, Patrick Roddy, Kristine Y. DeLeon‐Pennell, et al.. (2024). Anti-Ferroptotic Treatment Deteriorates Myocardial Infarction by Inhibiting Angiogenesis and Altering Immune Response. Antioxidants. 13(7). 769–769. 1 indexed citations
4.
Watanabe, Hirofumi, Ge Tao, Peiheng Gan, et al.. (2023). Purkinje Cardiomyocytes of the Adult Ventricular Conduction System Are Highly Diploid but Not Uniquely Regenerative. Journal of Cardiovascular Development and Disease. 10(4). 161–161. 1 indexed citations
5.
Dhakal, Pramod, Khursheed Iqbal, Lindsey N. Kent, et al.. (2023). CITED2 is a conserved regulator of the uterine–placental interface. Proceedings of the National Academy of Sciences. 120(3). e2213622120–e2213622120. 17 indexed citations
6.
Toubat, Omar, Jongkyu Choi, Anne Moon, et al.. (2020). Delta-like ligand-4 mediated Notch signaling controls proliferation of second heart field progenitor cells by regulating Fgf8 expression. Development. 147(17). 14 indexed citations
7.
Gan, Peiheng, Michaela Patterson, Di Tian, et al.. (2019). Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency. PLoS Genetics. 15(10). e1008354–e1008354. 26 indexed citations
8.
Patterson, Michaela, Lindsey Barske, Ben Van Handel, et al.. (2017). Frequency of mononuclear diploid cardiomyocytes underlies natural variation in heart regeneration. Nature Genetics. 49(9). 1346–1353. 241 indexed citations
9.
Li, Peng, Hua Shen, Kristine D. Estrada, et al.. (2015). Dysregulated endocardial TGFβ signaling and mesenchymal transformation result in heart outflow tract septation failure. Developmental Biology. 409(1). 272–276. 7 indexed citations
10.
Cavallero, Susana, Hua Shen, Christopher E. Yi, et al.. (2015). CXCL12 Signaling Is Essential for Maturation of the Ventricular Coronary Endothelial Plexus and Establishment of Functional Coronary Circulation. Developmental Cell. 33(4). 469–477. 80 indexed citations
11.
Li, Peng, Mohammad Pashmforoush, & Henry M. Sucov. (2011). Mesodermal retinoic acid signaling regulates endothelial cell coalescence in caudal pharyngeal arch artery vasculogenesis. Developmental Biology. 361(1). 116–124. 25 indexed citations
12.
Li, Peng, Mohammad Pashmforoush, & Henry M. Sucov. (2010). Retinoic Acid Regulates Differentiation of the Secondary Heart Field and TGFβ-Mediated Outflow Tract Septation. Developmental Cell. 18(3). 480–485. 71 indexed citations
13.
Chen, Yi-Hui, Mamoru Ishii, Henry M. Sucov, & Robert E. Maxson. (2008). Msx1 and Msx2are required for endothelial-mesenchymal transformation of the atrioventricular cushions and patterning of the atrioventricular myocardium. BMC Developmental Biology. 8(1). 75–75. 72 indexed citations
14.
Chen, Yihui, Mamoru Ishii, Jingjing Sun, Henry M. Sucov, & Robert E. Maxson. (2007). Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract. Developmental Biology. 308(2). 421–437. 75 indexed citations
15.
Kang, Ji‐One, Bibha Choudhary, Takako Makita, et al.. (2002). Epicardial Induction of Fetal Cardiomyocyte Proliferation via a Retinoic Acid-Inducible Trophic Factor. Developmental Biology. 250(1). 198–207. 179 indexed citations
16.
Jiang, Xiaobing, Sachiko Iseki, Robert E. Maxson, Henry M. Sucov, & Gillian Morriss‐Kay. (2002). Tissue Origins and Interactions in the Mammalian Skull Vault. Developmental Biology. 241(1). 106–116. 585 indexed citations breakdown →
17.
Sucov, Henry M., et al.. (1998). The RXRα gene functions in a non-cell-autonomous manner during mouse cardiac morphogenesis. Development. 125(10). 1951–1956. 57 indexed citations
18.
Giguère, Vincent, et al.. (1996). Genetic Analysis of the Retinoid Signala. Annals of the New York Academy of Sciences. 785(1). 12–22. 4 indexed citations
19.
Gruber, Peter J., S. Kubalak, Tomáš Pexieder, et al.. (1996). RXR alpha deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice.. Journal of Clinical Investigation. 98(6). 1332–1343. 157 indexed citations
20.
Sucov, Henry M., Jian-Shu Lou, Peter J. Gruber, et al.. (1996). The molecular genetics of retinoic acid receptors: cardiovascular and limb development.. PubMed. 62. 143–56. 7 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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