Paul Grossfeld
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- Cardiomyopathy and Myosin Studies 6
- Epidemiology top 5%
- Congenital Heart Disease Studies 18
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 6
- Molecular Biology top 5%
- Congenital heart defects research 23
- RNA modifications and cancer 7
- RNA and protein synthesis mechanisms 6
- RNA regulation and disease 4
- Hematology top 5%
- Co-authors
- J. RansomVidu GargMarie K. SchlutermanDeepak SrivastavaR. Bowling BarnesIsabelle N. KingRémi FavierTeresa Mattina
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
Paul Grossfeld
52 papers receiving 2.8k citations
Hit Papers
Peers
Comparison fields: 5 of 97
- Cardiology and Cardiovascular Medicine 756
- Epidemiology 893
- Genetics 716
- Molecular Biology 1.7k
- Hematology 264
Countries citing papers authored by Paul Grossfeld
This map shows the geographic impact of Paul Grossfeld'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 Paul Grossfeld with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Grossfeld more than expected).
Fields of papers citing papers by Paul Grossfeld
This network shows the impact of papers produced by Paul Grossfeld. 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 Paul Grossfeld. The network helps show where Paul Grossfeld may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Paul Grossfeld, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2023 | 9 | |
| 3 | 2022 | 24 | |
| 4 | 2017 | 15 | |
| 5 | 2016 | 44 | |
| 6 | 2015 | 67 | |
| 7 | 2015 | 13 | |
| 8 | 2010 | 3 | |
| 9 | 2010 | 24 | |
| 10 | 2009 | 22 | |
| 11 | 2007 | 2 | |
| 12 | 2007 | 12 | |
| 13 | 2006 | 22 | |
| 14 | 2004 | 199 | |
| 15 | 2003 | 85 | |
| 16 | 2003 | 183 | |
| 17 | 2003 | 10 | |
| 18 | 2002 | 64 | |
| 19 | 2001 | 14 | |
| 20 | 1999 | 29 |
About Paul Grossfeld
Paul Grossfeld is a scholar working on Genetics, Epidemiology and Molecular Biology, having authored 53 papers that have together received 2.9k indexed citations. Recurring topics across this work include Congenital heart defects research (23 papers), Congenital Heart Disease Studies (18 papers), Genomic variations and chromosomal abnormalities (18 papers), RNA modifications and cancer (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cardiomyopathy and Myosin Studies (6 papers), RNA and protein synthesis mechanisms (6 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (756 citations), Epidemiology (893 citations) and Genetics (716 citations). Paul Grossfeld has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include J. Ransom, Vidu Garg, Marie K. Schluterman, Deepak Srivastava, R. Bowling Barnes, Isabelle N. King, Rémi Favier, Teresa Mattina, Christopher T. Jones and Concetta Simona Perrotta. Their work appears in journals such as Nature, Circulation and Nature Communications.
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.