Mark Consugar
Impact in
- Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Nephrology top 5%
Papers in
- Genetics 13
- Genetic and Kidney Cyst Diseases 12
- Genetic Syndromes and Imprinting 4
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- Renal and related cancers 7
- Mitochondrial Function and Pathology 2
- Co-authors
- Peter C. Harris (13 shared papers)Sandro Rossetti (11 shared papers)Vicente E. Torres (10 shared papers)Vickie Kubly (6 shared papers)Eric A. Pierce (7 shared papers)Paul A. Thompson (2 shared papers)William M. Bennett (2 shared papers)Kyongtae T. Bae (2 shared papers)
- Journals
- Journal of the American Society of Nephrology (3 papers)Kidney International (3 papers)American Journal of Kidney Diseases (2 papers)Genetics in Medicine (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomBelgium
In The Last Decade
Mark Consugar
26 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 82
- Genetics 1.5k
- Nephrology 151
- Molecular Biology 1.4k
- Pathology and Forensic Medicine 243
- Ophthalmology 119
Countries citing papers authored by Mark Consugar
This map shows the geographic impact of Mark Consugar'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 Mark Consugar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Consugar more than expected).
Fields of papers citing papers by Mark Consugar
This network shows the impact of papers produced by Mark Consugar. 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 Mark Consugar. The network helps show where Mark Consugar may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Consugar, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 345 | |
| 2 | 2009 | 244 | |
| 3 | 2006 | 214 | |
| 4 | 2006 | 195 | |
| 5 | 2014 | 194 | |
| 6 | 2006 | 161 | |
| 7 | 2001 | 148 | |
| 8 | 2013 | 123 | |
| 9 | 2003 | 102 | |
| 10 | 2011 | 62 | |
| 11 | 2005 | 60 | |
| 12 | 2007 | 60 | |
| 13 | 2016 | 46 | |
| 14 | Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome. | 2012 | 45 |
| 15 | 2016 | 44 | |
| 16 | 2005 | 35 | |
| 17 | 2017 | 34 | |
| 18 | 2013 | 33 | |
| 19 | 2002 | 31 | |
| 20 | 1996 | 31 |
About Mark Consugar
Mark Consugar is a scholar working on Genetics, Molecular Biology, Surgery, Ophthalmology and Oncology, having authored 26 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Renal and related cancers (7 papers), Genetic Syndromes and Imprinting (4 papers), Metabolism and Genetic Disorders (2 papers), Retinal Diseases and Treatments (2 papers), Mitochondrial Function and Pathology (2 papers), Sarcoma Diagnosis and Treatment (1 paper) and Biomedical Research and Pathophysiology (1 paper). The work is most often cited by research in Genetics (1.5k citations), Nephrology (151 citations), Molecular Biology (1.4k citations), Pathology and Forensic Medicine (243 citations) and Ophthalmology (119 citations). Mark Consugar has collaborated with scholars based in United States, United Kingdom and Belgium. Frequent co-authors include Peter C. Harris, Sandro Rossetti, Vicente E. Torres, Vickie Kubly, Eric A. Pierce, Paul A. Thompson, William M. Bennett, Kyongtae T. Bae, J. Philip Miller and Jared J. Grantham. Their work appears in journals such as Journal of the American Society of Nephrology, Kidney International, American Journal of Kidney Diseases, Genetics in Medicine and Human Molecular 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.