Robert Marion
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Cleft Lip and Palate Research
- Genetics and Neurodevelopmental Disorders
-
- Congenital heart defects research
Papers in
-
- Congenital heart defects research 6
- Surgery 8
- Congenital Anomalies and Fetal Surgery 4
- Tissue Engineering and Regenerative Medicine 2
- Co-authors
- Rosalie Goldberg (2 shared papers)Peter Scambler (1 shared paper)Paul Saenger (1 shared paper)Robert J. Shprintzen (1 shared paper)Elaine M. Pereira (4 shared papers)K.H. Ramesh (2 shared papers)Alan Shanske (3 shared papers)Thomas V. McDonald (5 shared papers)
- Journals
- Cardiovascular Pathology (1 paper)The Journal of Pediatrics (1 paper)International Journal of Pharmaceutics (1 paper)Journal of Pediatric Hematology/Oncology (1 paper)Molecular Cytogenetics (1 paper)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Robert Marion
23 papers receiving 574 citations
Peers
Comparison fields: 5 of 73
- Genetics 245
- Genetics 86
- Molecular Biology 385
- Pulmonary and Respiratory Medicine 183
- Epidemiology 173
Countries citing papers authored by Robert Marion
This map shows the geographic impact of Robert Marion'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 Robert Marion with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Marion more than expected).
Fields of papers citing papers by Robert Marion
This network shows the impact of papers produced by Robert Marion. 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 Robert Marion. The network helps show where Robert Marion may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Marion, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 321 | |
| 2 | 1993 | 76 | |
| 3 | 1994 | 60 | |
| 4 | Communicating with parents of culturally diverse exceptional children. | 1980 | 39 |
| 5 | 2014 | 21 | |
| 6 | 2012 | 19 | |
| 7 | 1993 | 13 | |
| 8 | 2005 | 9 | |
| 9 | 2022 | 8 | |
| 10 | 1979 | 8 | |
| 11 | 2018 | 7 | |
| 12 | 2015 | 6 | |
| 13 | 2006 | 4 | |
| 14 | 2016 | 4 | |
| 15 | 2015 | 3 | |
| 16 | 1998 | 3 | |
| 17 | 2012 | 2 | |
| 18 | 2012 | 2 | |
| 19 | 2015 | 2 | |
| 20 | 2015 | 1 |
About Robert Marion
Robert Marion is a scholar working on Molecular Biology, Surgery, Cardiology and Cardiovascular Medicine, Genetics and Cellular and Molecular Neuroscience, having authored 25 papers that have together received 611 indexed citations. Recurring topics across this work include Congenital heart defects research (6 papers), Congenital Anomalies and Fetal Surgery (4 papers), Prenatal Screening and Diagnostics (3 papers), Cardiac electrophysiology and arrhythmias (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Moyamoya disease diagnosis and treatment (2 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Family and Disability Support Research (2 papers). The work is most often cited by research in Genetics (245 citations), Genetics (86 citations), Molecular Biology (385 citations), Pulmonary and Respiratory Medicine (183 citations) and Epidemiology (173 citations). Robert Marion has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Rosalie Goldberg, Peter Scambler, Paul Saenger, Robert J. Shprintzen, Elaine M. Pereira, K.H. Ramesh, Alan Shanske, Thomas V. McDonald, Constance M. Barone and Jane S. Kim. Their work appears in journals such as Cardiovascular Pathology, The Journal of Pediatrics, International Journal of Pharmaceutics, Journal of Pediatric Hematology/Oncology and Molecular Cytogenetics.
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.