Alfredo Ramı́rez
Impact in
- Neurology top 0.5%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
-
- RNA Research and Splicing 4
- Physiology 19
- Alzheimer's disease research and treatments 13
- Co-authors
- Christian Kubisch (10 shared papers)Christine Klein (18 shared papers)Axel M. Hillmer (2 shared papers)María Isabel Behrens (8 shared papers)L. Pablo Cid (2 shared papers)Ingrid Goebel (3 shared papers)Jan Gründemann (1 shared paper)Barbara Stiller (2 shared papers)
- Journals
- Alzheimer s & Dementia (10 papers)Movement Disorders (5 papers)Nature Genetics (4 papers)Proceedings of the National Academy of Sciences (3 papers)Nutrients (3 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Alfredo Ramı́rez
115 papers receiving 4.7k citations
Alfredo Ramı́rez's Hit Papers
Peers
Comparison fields: 5 of 164
- Neurology 1.4k
- Neurology 703
- Sensory Systems 324
- Cellular and Molecular Neuroscience 823
- Cell Biology 716
Countries citing papers authored by Alfredo Ramı́rez
This map shows the geographic impact of Alfredo Ramı́rez'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 Alfredo Ramı́rez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alfredo Ramı́rez more than expected).
Fields of papers citing papers by Alfredo Ramı́rez
This network shows the impact of papers produced by Alfredo Ramı́rez. 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 Alfredo Ramı́rez. The network helps show where Alfredo Ramı́rez may publish in the future.
Co-authors
The 25 scholars most cited alongside Alfredo Ramı́rez, 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 126 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase Hit paper breakdown → | 2006 | 896 |
| 2 | 2001 | 394 | |
| 3 | 2008 | 297 | |
| 4 | 2012 | 295 | |
| 5 | 2007 | 285 | |
| 6 | 2001 | 144 | |
| 7 | 2020 | 131 | |
| 8 | 2010 | 123 | |
| 9 | 2012 | 114 | |
| 10 | 2010 | 104 | |
| 11 | 2008 | 89 | |
| 12 | 2020 | 88 | |
| 13 | 2012 | 73 | |
| 14 | 2001 | 69 | |
| 15 | 2010 | 68 | |
| 16 | 2012 | 67 | |
| 17 | 2007 | 62 | |
| 18 | 2005 | 61 | |
| 19 | 2007 | 61 | |
| 20 | 2015 | 58 |
About Alfredo Ramı́rez
Alfredo Ramı́rez is a scholar working on Molecular Biology, Physiology, Cellular and Molecular Neuroscience, Genetics and Neurology, having authored 126 papers that have together received 4.8k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (13 papers), Parkinson's Disease Mechanisms and Treatments (11 papers), Genetic Associations and Epidemiology (9 papers), Dementia and Cognitive Impairment Research (8 papers), Nuclear Receptors and Signaling (6 papers), Neuroinflammation and Neurodegeneration Mechanisms (5 papers), Tryptophan and brain disorders (5 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Neurology (1.4k citations), Neurology (703 citations), Sensory Systems (324 citations), Cellular and Molecular Neuroscience (823 citations) and Cell Biology (716 citations). Alfredo Ramı́rez has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Christian Kubisch, Christine Klein, Axel M. Hillmer, María Isabel Behrens, L. Pablo Cid, Ingrid Goebel, Jan Gründemann, Barbara Stiller, C. Geoffrey Woods and Jochen Roeper. Their work appears in journals such as Alzheimer s & Dementia, Movement Disorders, Nature Genetics, Proceedings of the National Academy of Sciences and Nutrients.
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.