James A. Trofatter
Impact in
- Neurology top 0.5%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Neurological diseases and metabolism
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Papers in
-
- Glycosylation and Glycoproteins Research 4
- RNA modifications and cancer 4
- Ubiquitin and proteasome pathways 3
-
- Hereditary Neurological Disorders 11
- Nuclear Receptors and Signaling 3
- Co-authors
- James F. Gusella (14 shared papers)Jonathan L. Haines (14 shared papers)Jill R. Murrell (4 shared papers)Vijaya Ramesh (5 shared papers)Bernd R. Seizinger (2 shared papers)P. Michael Conneally (3 shared papers)Guy A. Rouleau (3 shared papers)Alan Buckler (4 shared papers)
- Journals
- Genomics (8 papers)Human Molecular Genetics (3 papers)Nature Genetics (3 papers)Nucleic Acids Research (2 papers)Genome Research (2 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
James A. Trofatter
52 papers receiving 3.6k citations
James A. Trofatter's Hit Papers
Peers
Comparison fields: 5 of 101
- Neurology 1.7k
- Cellular and Molecular Neuroscience 846
- Neurology 260
- Cell Biology 504
- Epidemiology 729
Countries citing papers authored by James A. Trofatter
This map shows the geographic impact of James A. Trofatter'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 James A. Trofatter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James A. Trofatter more than expected).
Fields of papers citing papers by James A. Trofatter
This network shows the impact of papers produced by James A. Trofatter. 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 James A. Trofatter. The network helps show where James A. Trofatter may publish in the future.
Co-authors
The 25 scholars most cited alongside James A. Trofatter, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor Hit paper breakdown → | 1993 | 1099 |
| 2 | 1987 | 350 | |
| 3 | 1990 | 239 | |
| 4 | 1994 | 225 | |
| 5 | 1994 | 183 | |
| 6 | 1994 | 160 | |
| 7 | 1999 | 128 | |
| 8 | 1993 | 104 | |
| 9 | 1989 | 93 | |
| 10 | Mutational analysis of patients with neurofibromatosis 2. | 1994 | 91 |
| 11 | 1990 | 88 | |
| 12 | 1988 | 85 | |
| 13 | 1989 | 83 | |
| 14 | 1990 | 83 | |
| 15 | 1993 | 67 | |
| 16 | Linkage localization of X-linked Charcot-Marie-Tooth disease. | 1993 | 67 |
| 17 | 1994 | 61 | |
| 18 | 1994 | 57 | |
| 19 | Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy. | 1991 | 51 |
| 20 | 1991 | 36 |
About James A. Trofatter
James A. Trofatter is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Neurology, having authored 53 papers that have together received 3.7k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (11 papers), Neurofibromatosis and Schwannoma Cases (8 papers), Neurological diseases and metabolism (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Glycosylation and Glycoproteins Research (4 papers), RNA modifications and cancer (4 papers), Ubiquitin and proteasome pathways (3 papers) and Nuclear Receptors and Signaling (3 papers). The work is most often cited by research in Neurology (1.7k citations), Cellular and Molecular Neuroscience (846 citations), Neurology (260 citations), Cell Biology (504 citations) and Epidemiology (729 citations). James A. Trofatter has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include James F. Gusella, Jonathan L. Haines, Jill R. Murrell, Vijaya Ramesh, Bernd R. Seizinger, P. Michael Conneally, Guy A. Rouleau, Alan Buckler, Christy Stotler and M. E. Hodes. Their work appears in journals such as Genomics, Human Molecular Genetics, Nature Genetics, Nucleic Acids Research and Genome Research.
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.