Susan E. Ide
Impact in
- Neurology top 0.1%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Neurological diseases and metabolism
- Cellular and Molecular Neuroscience top 0.5%
- Nuclear Receptors and Signaling
- Genetic Neurodegenerative Diseases
- Nerve injury and regeneration
Papers in
-
- Acute Myeloid Leukemia Research 3
- Chronic Myeloid Leukemia Treatments 3
-
- Parkinson's Disease Mechanisms and Treatments 3
- Co-authors
- Mihael H. Polymeropoulos (12 shared papers)Edward S. Stenroos (2 shared papers)William G. Johnson (2 shared papers)Roger C. Duvoisin (2 shared papers)Giuseppe Di Iorio (2 shared papers)Robert L. Nussbaum (2 shared papers)Alice M. Lazzarini (2 shared papers)Lawrence I. Golbe (2 shared papers)
- Journals
- Blood (3 papers)Science (3 papers)Genomics (3 papers)Nature Genetics (2 papers)Human Genetics (1 paper)
- Partner nations
- United StatesSwitzerlandItaly
In The Last Decade
Susan E. Ide
24 papers receiving 8.8k citations
Susan E. Ide's Hit Papers
Peers
Comparison fields: 5 of 139
- Neurology 6.0k
- Neurology 1.5k
- Cellular and Molecular Neuroscience 3.4k
- Physiology 2.0k
- Aging 100
Countries citing papers authored by Susan E. Ide
This map shows the geographic impact of Susan E. Ide'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 Susan E. Ide with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susan E. Ide more than expected).
Fields of papers citing papers by Susan E. Ide
This network shows the impact of papers produced by Susan E. Ide. 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 Susan E. Ide. The network helps show where Susan E. Ide may publish in the future.
Co-authors
The 25 scholars most cited alongside Susan E. Ide, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease Hit paper breakdown → | 1997 | 6997 |
| 2 | 1996 | 626 | |
| 3 | 1996 | 600 | |
| 4 | 2000 | 253 | |
| 5 | 2003 | 94 | |
| 6 | 1996 | 91 | |
| 7 | 2005 | 77 | |
| 8 | 2017 | 63 | |
| 9 | 2013 | 59 | |
| 10 | 1996 | 45 | |
| 11 | 1995 | 38 | |
| 12 | 2015 | 33 | |
| 13 | 1995 | 22 | |
| 14 | 2009 | 18 | |
| 15 | 1996 | 15 | |
| 16 | 2008 | 15 | |
| 17 | 2001 | 14 | |
| 18 | 2014 | 13 | |
| 19 | 1996 | 10 | |
| 20 | 1997 | 9 |
About Susan E. Ide
Susan E. Ide is a scholar working on Hematology, Neurology, Genetics, Cellular and Molecular Neuroscience and Molecular Biology, having authored 24 papers that have together received 9.1k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (3 papers), Mitochondrial Function and Pathology (3 papers), Genomics and Chromatin Dynamics (3 papers), Nuclear Receptors and Signaling (3 papers), Acute Myeloid Leukemia Research (3 papers), Chronic Myeloid Leukemia Treatments (3 papers), Genetic Syndromes and Imprinting (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Neurology (6.0k citations), Neurology (1.5k citations), Cellular and Molecular Neuroscience (3.4k citations), Physiology (2.0k citations) and Aging (100 citations). Susan E. Ide has collaborated with scholars based in United States, Switzerland and Italy. Frequent co-authors include Mihael H. Polymeropoulos, Edward S. Stenroos, William G. Johnson, Roger C. Duvoisin, Giuseppe Di Iorio, Robert L. Nussbaum, Alice M. Lazzarini, Lawrence I. Golbe, Christian N. Lavedan and Elisabeth Leroy. Their work appears in journals such as Blood, Science, Genomics, Nature Genetics and Human 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.