Stuart J. Newfeld
Impact in
- Aging top 10%
- Molecular Biology top 10%
- TGF-β signaling in diseases
- Developmental Biology and Gene Regulation
- Ubiquitin and proteasome pathways
- Cancer-related gene regulation
- Wnt/β-catenin signaling in development and cancer
- Kruppel-like factors research
Papers in
-
- TGF-β signaling in diseases 19
- Developmental Biology and Gene Regulation 18
- Cancer-related gene regulation 10
- Ubiquitin and proteasome pathways 5
- Kruppel-like factors research 4
- Congenital heart defects research 3
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- Hippo pathway signaling and YAP/TAZ 7
- Co-authors
- Michael J Stinchfield (12 shared papers)Norma T. Takaesu (13 shared papers)Michael B. O’Connor (8 shared papers)Sirio Dupont (3 shared papers)Masafumi Inui (2 shared papers)William M Gelbart (2 shared papers)Vern Twombly (1 shared paper)Jeffrey L. Wrana (1 shared paper)
- Journals
- Genetics (11 papers)G3 Genes Genomes Genetics (7 papers)Development (4 papers)PLoS ONE (3 papers)Molecular Biology and Evolution (2 papers)
- Partner nations
- United StatesFinlandItaly
In The Last Decade
Stuart J. Newfeld
39 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 73
- Aging 32
- Molecular Biology 1.0k
- Cell Biology 190
- Oncology 166
- Cellular and Molecular Neuroscience 110
Countries citing papers authored by Stuart J. Newfeld
This map shows the geographic impact of Stuart J. Newfeld'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 Stuart J. Newfeld with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stuart J. Newfeld more than expected).
Fields of papers citing papers by Stuart J. Newfeld
This network shows the impact of papers produced by Stuart J. Newfeld. 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 Stuart J. Newfeld. The network helps show where Stuart J. Newfeld may publish in the future.
Co-authors
The 25 scholars most cited alongside Stuart J. Newfeld, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 417 | |
| 2 | 1994 | 279 | |
| 3 | 2001 | 42 | |
| 4 | 2003 | 36 | |
| 5 | 2012 | 35 | |
| 6 | 2006 | 34 | |
| 7 | 2008 | 26 | |
| 8 | 2005 | 24 | |
| 9 | 2007 | 23 | |
| 10 | 2009 | 22 | |
| 11 | 2013 | 22 | |
| 12 | 2012 | 21 | |
| 13 | 1999 | 16 | |
| 14 | 2013 | 16 | |
| 15 | 1997 | 16 | |
| 16 | 2011 | 15 | |
| 17 | 2002 | 14 | |
| 18 | 2008 | 14 | |
| 19 | 2012 | 12 | |
| 20 | 2002 | 12 |
About Stuart J. Newfeld
Stuart J. Newfeld is a scholar working on Molecular Biology, Cell Biology, Cellular and Molecular Neuroscience, Oncology and Plant Science, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include TGF-β signaling in diseases (19 papers), Developmental Biology and Gene Regulation (18 papers), Cancer-related gene regulation (10 papers), Hippo pathway signaling and YAP/TAZ (7 papers), Ubiquitin and proteasome pathways (5 papers), Kruppel-like factors research (4 papers), Chromosomal and Genetic Variations (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Aging (32 citations), Molecular Biology (1.0k citations), Cell Biology (190 citations), Oncology (166 citations) and Cellular and Molecular Neuroscience (110 citations). Stuart J. Newfeld has collaborated with scholars based in United States, Finland and Italy. Frequent co-authors include Michael J Stinchfield, Norma T. Takaesu, Michael B. O’Connor, Sirio Dupont, Masafumi Inui, William M Gelbart, Vern Twombly, Jeffrey L. Wrana, Joan Massagué and Guillermo Marqués. Their work appears in journals such as Genetics, G3 Genes Genomes Genetics, Development, PLoS ONE and Molecular Biology and Evolution.
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.