Chris Amos
Impact in
-
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
- Neurology top 5%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
- Genetics 6
- Chronic Lymphocytic Leukemia Research 2
- BRCA gene mutations in cancer 2
- Diabetes and associated disorders 2
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- DNA Repair Mechanisms 2
- Co-authors
- Olga Zhuchenko (1 shared paper)William B. Dobyns (1 shared paper)Huda Y. Zoghbi (1 shared paper)Cheng Chi Lee (1 shared paper)S. H. Subramony (1 shared paper)Jennifer M. Bailey (1 shared paper)David W. Stockton (1 shared paper)Penelope E. Bonnen (1 shared paper)
- Journals
- Genetic Epidemiology (2 papers)Nature Genetics (1 paper)European Journal of Human Genetics (1 paper)Cancer (1 paper)Lara D. Veeken (1 paper)
- Partner nations
- United StatesTaiwanUnited Kingdom
In The Last Decade
Chris Amos
20 papers receiving 1.6k citations
Hit Papers
Peers
Comparison fields: 5 of 82
- Cellular and Molecular Neuroscience 1.1k
- Neurology 421
- Molecular Biology 1.1k
- Neurology 112
- Rheumatology 140
Countries citing papers authored by Chris Amos
This map shows the geographic impact of Chris Amos'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 Chris Amos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chris Amos more than expected).
Fields of papers citing papers by Chris Amos
This network shows the impact of papers produced by Chris Amos. 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 Chris Amos. The network helps show where Chris Amos may publish in the future.
Co-authors
The 25 scholars most cited alongside Chris Amos, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel Hit paper breakdown → | 1997 | 1240 |
| 2 | 1998 | 105 | |
| 3 | 1994 | 76 | |
| 4 | 2006 | 57 | |
| 5 | 1995 | 38 | |
| 6 | 2014 | 20 | |
| 7 | 2021 | 20 | |
| 8 | 1987 | 19 | |
| 9 | 2005 | 15 | |
| 10 | 2021 | 13 | |
| 11 | 2019 | 13 | |
| 12 | 1991 | 9 | |
| 13 | 2022 | 9 | |
| 14 | 2001 | 2 | |
| 15 | Fine mapping in over 14,000 rheumatoid arthritis cases and 18,500 controls refines associations to known loci, indicates multiple independent affects and reveals novel associations | 2012 | 1 |
| 16 | 2023 | 1 | |
| 17 | 2022 | 1 | |
| 18 | 2024 | 1 | |
| 19 | 2010 | 1 | |
| 20 | 2021 | 1 |
About Chris Amos
Chris Amos is a scholar working on Genetics, Molecular Biology, Genetics, Epidemiology and Rheumatology, having authored 20 papers that have together received 1.6k indexed citations. Recurring topics across this work include Hepatitis C virus research (3 papers), Chronic Lymphocytic Leukemia Research (2 papers), BRCA gene mutations in cancer (2 papers), Diabetes and associated disorders (2 papers), Cancer Genomics and Diagnostics (2 papers), Rheumatoid Arthritis Research and Therapies (2 papers), DNA Repair Mechanisms (2 papers) and Systemic Lupus Erythematosus Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (421 citations), Molecular Biology (1.1k citations), Neurology (112 citations) and Rheumatology (140 citations). Chris Amos has collaborated with scholars based in United States, Taiwan and United Kingdom. Frequent co-authors include Olga Zhuchenko, William B. Dobyns, Huda Y. Zoghbi, Cheng Chi Lee, S. H. Subramony, Jennifer M. Bailey, David W. Stockton, Penelope E. Bonnen, Tetsuo Ashizawa and Sherri J. Bale. Their work appears in journals such as Genetic Epidemiology, Nature Genetics, European Journal of Human Genetics, Cancer and Lara D. Veeken.
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.