Reed E. Pyeritz
Impact in
- Genetics top 0.02%
- Connective tissue disorders research
- Mesenchymal stem cell research
-
- Cardiac Valve Diseases and Treatments
- Cardiovascular Issues in Pregnancy
Papers in
- Genetics 125
- Connective tissue disorders research 89
- Vascular Anomalies and Treatments 21
- BRCA gene mutations in cancer 19
-
- Aortic Disease and Treatment Approaches 75
- Aortic aneurysm repair treatments 21
- Co-authors
- Harry C. Dietz (23 shared papers)Victor A. McKusick (5 shared papers)Richard B. Devereux (15 shared papers)Clair A. Francomano (21 shared papers)Edmond A. Murphy (10 shared papers)Lynn Y. Sakai (5 shared papers)Raoul C. M. Hennekam (2 shared papers)Anne De Paepe (1 shared paper)
- Journals
- Genetics in Medicine (19 papers)Journal of the American College of Cardiology (17 papers)Circulation (11 papers)The American Journal of Cardiology (10 papers)New England Journal of Medicine (8 papers)
- Partner nations
- United StatesItalyGermany
In The Last Decade
Reed E. Pyeritz
260 papers receiving 19.5k citations
Reed E. Pyeritz's Hit Papers
Peers
Comparison fields: 5 of 178
- Genetics 9.0k
- Genetics 2.4k
- Cardiology and Cardiovascular Medicine 4.7k
- Pulmonary and Respiratory Medicine 6.8k
- Rheumatology 1.6k
Countries citing papers authored by Reed E. Pyeritz
This map shows the geographic impact of Reed E. Pyeritz'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 Reed E. Pyeritz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reed E. Pyeritz more than expected).
Fields of papers citing papers by Reed E. Pyeritz
This network shows the impact of papers produced by Reed E. Pyeritz. 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 Reed E. Pyeritz. The network helps show where Reed E. Pyeritz may publish in the future.
Co-authors
The 25 scholars most cited alongside Reed E. Pyeritz, 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 266 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene Hit paper breakdown → | 1991 | 1475 |
| 2 | Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta Hit paper breakdown → | 1999 | 1448 |
| 3 | The revised Ghent nosology for the Marfan syndrome: Table 1 Hit paper breakdown → | 2010 | 1376 |
| 4 | Revised diagnostic criteria for the Marfan syndrome Hit paper breakdown → | 1996 | 1138 |
| 5 | The natural history of homocystinuria due to cystathionine beta-synthase deficiency. Hit paper breakdown → | 1985 | 957 |
| 6 | Progression of Aortic Dilatation and the Benefit of Long-Term β-Adrenergic Blockade in Marfan's Syndrome Hit paper breakdown → | 1994 | 680 |
| 7 | The Marfan Syndrome: Diagnosis and Management Hit paper breakdown → | 1979 | 637 |
| 8 | 2001 | 426 | |
| 9 | 1993 | 373 | |
| 10 | 2000 | 367 | |
| 11 | 1990 | 302 | |
| 12 | 2002 | 275 | |
| 13 | 2011 | 248 | |
| 14 | 1993 | 241 | |
| 15 | 2008 | 236 | |
| 16 | 1992 | 205 | |
| 17 | 2013 | 198 | |
| 18 | 1995 | 189 | |
| 19 | 2012 | 188 | |
| 20 | Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic amplicons. | 1995 | 187 |
About Reed E. Pyeritz
Reed E. Pyeritz is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Cardiology and Cardiovascular Medicine, Surgery and Molecular Biology, having authored 266 papers that have together received 20.3k indexed citations. Recurring topics across this work include Connective tissue disorders research (89 papers), Aortic Disease and Treatment Approaches (75 papers), Cardiac Valve Diseases and Treatments (36 papers), Vascular Anomalies and Treatments (21 papers), Aortic aneurysm repair treatments (21 papers), BRCA gene mutations in cancer (19 papers), Congenital Heart Disease Studies (19 papers) and Cardiac Structural Anomalies and Repair (15 papers). The work is most often cited by research in Genetics (9.0k citations), Genetics (2.4k citations), Cardiology and Cardiovascular Medicine (4.7k citations), Pulmonary and Respiratory Medicine (6.8k citations) and Rheumatology (1.6k citations). Reed E. Pyeritz has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Harry C. Dietz, Victor A. McKusick, Richard B. Devereux, Clair A. Francomano, Edmond A. Murphy, Lynn Y. Sakai, Raoul C. M. Hennekam, Anne De Paepe, Barbara A. Bernhardt and Paul D. Sponseller. Their work appears in journals such as Genetics in Medicine, Journal of the American College of Cardiology, Circulation, The American Journal of Cardiology and New England Journal of Medicine.
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.