Ronen Schweitzer

9.4k total citations · 3 hit papers
51 papers, 7.4k citations indexed

About

Ronen Schweitzer is a scholar working on Orthopedics and Sports Medicine, Molecular Biology and Surgery. According to data from OpenAlex, Ronen Schweitzer has authored 51 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Orthopedics and Sports Medicine, 22 papers in Molecular Biology and 18 papers in Surgery. Recurrent topics in Ronen Schweitzer's work include Tendon Structure and Treatment (24 papers), Congenital limb and hand anomalies (13 papers) and Developmental Biology and Gene Regulation (13 papers). Ronen Schweitzer is often cited by papers focused on Tendon Structure and Treatment (24 papers), Congenital limb and hand anomalies (13 papers) and Developmental Biology and Gene Regulation (13 papers). Ronen Schweitzer collaborates with scholars based in United States, Israel and United Kingdom. Ronen Schweitzer's co-authors include Clifford J. Tabin, Ava E. Brent, Ben‐Zion Shilo, Brian A. Pryce, Cliff Tabin, Roderick T. Bronson, Daniel Caput, Annie Yang, Deqin Sun and Christopher P. Crum and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Ronen Schweitzer

51 papers receiving 7.3k citations

Hit Papers

p63 is essential for regenerative proliferation in limb, ... 1999 2026 2008 2017 1999 2001 2007 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ronen Schweitzer United States 33 3.8k 2.6k 2.0k 1.2k 1.2k 51 7.4k
Elazar Zelzer Israel 39 3.6k 0.9× 1.0k 0.4× 1.2k 0.6× 677 0.6× 729 0.6× 73 8.4k
Matthias Chiquet Switzerland 51 3.1k 0.8× 746 0.3× 1.0k 0.5× 519 0.4× 3.4k 2.9× 101 8.7k
L. Charles Murtaugh United States 29 3.1k 0.8× 525 0.2× 2.3k 1.1× 986 0.8× 468 0.4× 40 5.3k
Delphine Duprez France 43 3.6k 1.0× 1.5k 0.6× 1.4k 0.7× 120 0.1× 719 0.6× 82 5.7k
Ivo Kalajzić United States 40 2.7k 0.7× 724 0.3× 637 0.3× 1.1k 0.9× 330 0.3× 110 5.0k
Attila Aszódi Germany 46 2.9k 0.8× 422 0.2× 836 0.4× 511 0.4× 2.1k 1.8× 131 7.2k
Vicki Rosen United States 56 10.1k 2.7× 2.1k 0.8× 4.6k 2.3× 2.0k 1.6× 747 0.6× 133 19.7k
Karen M. Lyons United States 66 11.2k 2.9× 408 0.2× 1.6k 0.8× 1.0k 0.8× 1.0k 0.9× 157 15.3k
Kathryn S.E. Cheah Hong Kong 50 5.3k 1.4× 422 0.2× 1.4k 0.7× 944 0.8× 964 0.8× 153 10.6k
Petra Knaus Germany 50 4.6k 1.2× 237 0.1× 741 0.4× 749 0.6× 1.1k 0.9× 132 7.4k

Countries citing papers authored by Ronen Schweitzer

Since Specialization
Citations

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

Fields of papers citing papers by Ronen Schweitzer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ronen Schweitzer

This figure shows the co-authorship network connecting the top 25 collaborators of Ronen Schweitzer. A scholar is included among the top collaborators of Ronen Schweitzer 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 Ronen Schweitzer. Ronen Schweitzer 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.
Lim, Joohyun, Caressa Lietman, Matthew W. Grol, et al.. (2021). Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta. Proceedings of the National Academy of Sciences. 118(25). 7 indexed citations
2.
Riester, Scott M., Bashar Hasan, Sara F. Tufa, et al.. (2021). Ezh2 Is Essential for Patterning of Multiple Musculoskeletal Tissues but Dispensable for Tendon Differentiation. Stem Cells and Development. 30(11). 601–609. 5 indexed citations
3.
Comai, Glenda, Markéta Tesařová, Valérie Dupé, et al.. (2020). Local retinoic acid signaling directs emergence of the extraocular muscle functional unit. PLoS Biology. 18(11). e3000902–e3000902. 22 indexed citations
4.
Pryce, Brian A., et al.. (2020). Loss of Smad4 in the scleraxis cell lineage results in postnatal joint contracture. Developmental Biology. 470. 108–120. 10 indexed citations
5.
Tuzon, Creighton T., et al.. (2019). FGF signaling patterns cell fate at the interface between tendon and bone. Development. 146(15). 27 indexed citations
6.
Scott, R. Wilder, Martin Arostegui, Ronen Schweitzer, Fábio Rossi, & T. Michael Underhill. (2019). Hic1 Defines Quiescent Mesenchymal Progenitor Subpopulations with Distinct Functions and Fates in Skeletal Muscle Regeneration. Cell stem cell. 25(6). 797–813.e9. 151 indexed citations
7.
Sakabe, Tomoya, Keiko Sakai, Toru Maeda, et al.. (2018). Transcription factor scleraxis vitally contributes to progenitor lineage direction in wound healing of adult tendon in mice. Journal of Biological Chemistry. 293(16). 5766–5780. 90 indexed citations
8.
Lim, Joohyun, Elda Munivez, Ming‐Ming Jiang, et al.. (2017). mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development. Scientific Reports. 7(1). 17175–17175. 21 indexed citations
9.
Huang, Alice H., Helen H. Lu, & Ronen Schweitzer. (2015). Molecular regulation of tendon cell fate during development. Journal of Orthopaedic Research®. 33(6). 800–812. 87 indexed citations
10.
Huang, Alice H., Timothy J. Riordan, Brian A. Pryce, et al.. (2015). Musculoskeletal integration at the wrist underlies modular development of limb tendons. Development. 142(14). 2431–41. 79 indexed citations
11.
Huang, Alice H., Timothy J. Riordan, Lingyan Wang, et al.. (2013). Repositioning Forelimb Superficialis Muscles: Tendon Attachment and Muscle Activity Enable Active Relocation of Functional Myofibers. Developmental Cell. 26(5). 544–551. 39 indexed citations
12.
Blitz, Einat, Sergey Viukov, Amnon Sharir, et al.. (2009). Bone Ridge Patterning during Musculoskeletal Assembly Is Mediated through SCX Regulation of Bmp4 at the Tendon-Skeleton Junction. Developmental Cell. 17(6). 861–873. 225 indexed citations
13.
Riordan, Timothy J., et al.. (2009). Tendons and muscles of the mouse forelimb during embryonic development. Developmental Dynamics. 238(3). 693–700. 26 indexed citations
14.
Staverosky, Julia A., Brian A. Pryce, Spencer S. Watson, & Ronen Schweitzer. (2009). Tubulin polymerization‐promoting protein family member 3, Tppp3, is a specific marker of the differentiating tendon sheath and synovial joints. Developmental Dynamics. 238(3). 685–692. 44 indexed citations
15.
Conner, David A., et al.. (2007). Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons. Development. 134(14). 2697–2708. 449 indexed citations breakdown →
16.
DeLaurier, April, Ronen Schweitzer, & Malcolm Logan. (2006). Pitx1 determines the morphology of muscle, tendon, and bones of the hindlimb. Developmental Biology. 299(1). 22–34. 111 indexed citations
17.
Smith, Devyn M., Lisa A. Collins‐Racie, Valeria Marigo, et al.. (2001). Cloning and expression of a novel cysteine-rich secreted protein family member expressed in thyroid and pancreatic mesoderm within the chicken embryo. Mechanisms of Development. 102(1-2). 223–226. 16 indexed citations
18.
Schweitzer, Ronen, Kyle Vogan, & Clifford J. Tabin. (2000). Similar expression and regulation of Gli2 and Gli3 in the chick limb bud. Mechanisms of Development. 98(1-2). 171–174. 31 indexed citations
19.
Yang, Annie, Ronen Schweitzer, Deqin Sun, et al.. (1999). p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature. 398(6729). 714–718. 1836 indexed citations breakdown →
20.
Donaldson, T., et al.. (1998). EGF domain swap converts a Drosophila EGF receptor activator into an inhibitor. Genes & Development. 12(7). 908–913. 53 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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