Carlos E. Prada
Impact in
- Obstetrics and Gynecology top 2%
- Pregnancy and preeclampsia studies
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
Papers in
-
- Protein Tyrosine Phosphatases 7
- Congenital heart defects research 5
- Physiology 22
- Lysosomal Storage Disorders Research 20
- Co-authors
- Marcos López (2 shared papers)Lissette Sanchez-Aranguren (1 shared paper)Robert J. Hopkin (19 shared papers)Elizabeth K. Schorry (6 shared papers)Anne M. Lovell (3 shared papers)Thomas J. Kipps (8 shared papers)Januario E. Castro (7 shared papers)Howard M. Saal (4 shared papers)
- Journals
- Molecular Genetics and Metabolism (11 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (6 papers)Blood (5 papers)The Journal of Pediatrics (5 papers)European Journal of Medical Genetics (4 papers)
- Partner nations
- United StatesColombiaUnited Kingdom
In The Last Decade
Carlos E. Prada
81 papers receiving 1.7k citations
Carlos E. Prada's Hit Papers
Peers
Comparison fields: 5 of 100
- Obstetrics and Gynecology 275
- Neurology 303
- Genetics 182
- Clinical Biochemistry 89
- Pediatrics, Perinatology and Child Health 208
Countries citing papers authored by Carlos E. Prada
This map shows the geographic impact of Carlos E. Prada'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 Carlos E. Prada with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carlos E. Prada more than expected).
Fields of papers citing papers by Carlos E. Prada
This network shows the impact of papers produced by Carlos E. Prada. 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 Carlos E. Prada. The network helps show where Carlos E. Prada may publish in the future.
Co-authors
The 25 scholars most cited alongside Carlos E. Prada, 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 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Endothelial dysfunction and preeclampsia: role of oxidative stress Hit paper breakdown → | 2014 | 350 |
| 2 | 2011 | 129 | |
| 3 | 2012 | 112 | |
| 4 | 2005 | 106 | |
| 5 | 2015 | 76 | |
| 6 | 2005 | 66 | |
| 7 | 2012 | 64 | |
| 8 | 2014 | 61 | |
| 9 | 2022 | 57 | |
| 10 | 2010 | 41 | |
| 11 | 2006 | 41 | |
| 12 | 2011 | 36 | |
| 13 | 2022 | 35 | |
| 14 | 2006 | 33 | |
| 15 | 2012 | 31 | |
| 16 | 2012 | 25 | |
| 17 | 2018 | 25 | |
| 18 | 2019 | 25 | |
| 19 | 2020 | 24 | |
| 20 | 2019 | 23 |
About Carlos E. Prada
Carlos E. Prada is a scholar working on Molecular Biology, Physiology, Genetics, Cell Biology and Epidemiology, having authored 97 papers that have together received 1.7k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (20 papers), Cellular transport and secretion (10 papers), Metabolism and Genetic Disorders (9 papers), Neurofibromatosis and Schwannoma Cases (8 papers), Chronic Lymphocytic Leukemia Research (8 papers), Protein Tyrosine Phosphatases (7 papers), Genomics and Rare Diseases (6 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Obstetrics and Gynecology (275 citations), Neurology (303 citations), Genetics (182 citations), Clinical Biochemistry (89 citations) and Pediatrics, Perinatology and Child Health (208 citations). Carlos E. Prada has collaborated with scholars based in United States, Colombia and United Kingdom. Frequent co-authors include Marcos López, Lissette Sanchez-Aranguren, Robert J. Hopkin, Elizabeth K. Schorry, Anne M. Lovell, Thomas J. Kipps, Januario E. Castro, Howard M. Saal, Lisa J. Martin and Olivier Loria. Their work appears in journals such as Molecular Genetics and Metabolism, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Blood, The Journal of Pediatrics and European Journal of Medical Genetics.
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.