Astrid Lunkes
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 2%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- Genetic Neurodegenerative Diseases 15
- Hereditary Neurological Disorders 3
-
- Mitochondrial Function and Pathology 11
- DNA Repair Mechanisms 2
- Muscle Physiology and Disorders 2
- Co-authors
- Jean‐Louis Mandel (5 shared papers)Georg Auburger (6 shared papers)Suzana Gispert (4 shared papers)Guy A. Rouleau (2 shared papers)Stefan-M. Pulst (1 shared paper)Julie R. Korenberg (1 shared paper)Susan Pearlman (1 shared paper)Xiao–Ning Chen (1 shared paper)
- Journals
- Genomics (3 papers)Molecular Cell (1 paper)Human Genetics (1 paper)The EMBO Journal (1 paper)Experimental Neurology (1 paper)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Astrid Lunkes
18 papers receiving 1.7k citations
Astrid Lunkes's Hit Papers
Peers
Comparison fields: 5 of 71
- Cellular and Molecular Neuroscience 1.5k
- Neurology 568
- Molecular Biology 1.3k
- Neurology 88
- Clinical Biochemistry 63
Countries citing papers authored by Astrid Lunkes
This map shows the geographic impact of Astrid Lunkes'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 Astrid Lunkes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Astrid Lunkes more than expected).
Fields of papers citing papers by Astrid Lunkes
This network shows the impact of papers produced by Astrid Lunkes. 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 Astrid Lunkes. The network helps show where Astrid Lunkes may publish in the future.
Co-authors
The 25 scholars most cited alongside Astrid Lunkes, 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 | Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 Hit paper breakdown → | 1996 | 905 |
| 2 | 2002 | 317 | |
| 3 | 1998 | 163 | |
| 4 | 1996 | 98 | |
| 5 | 1996 | 72 | |
| 6 | 1993 | 48 | |
| 7 | 1997 | 45 | |
| 8 | 1995 | 33 | |
| 9 | 1998 | 32 | |
| 10 | 1999 | 19 | |
| 11 | 1996 | 14 | |
| 12 | 1994 | 12 | |
| 13 | 2009 | 8 | |
| 14 | 2020 | 7 | |
| 15 | 2001 | 3 | |
| 16 | Mutation analysis of spinocerebellar ataxia type 1 (SCA1) in a large Iakut kinship of Eastern Siberia | 1994 | 2 |
| 17 | 1993 | 2 | |
| 18 | 1993 | 2 |
About Astrid Lunkes
Astrid Lunkes is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Clinical Biochemistry and Neurology, having authored 18 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (11 papers), Neurological disorders and treatments (4 papers), Hereditary Neurological Disorders (3 papers), DNA Repair Mechanisms (2 papers), Muscle Physiology and Disorders (2 papers), Metabolism and Genetic Disorders (2 papers) and Neurological diseases and metabolism (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.5k citations), Neurology (568 citations), Molecular Biology (1.3k citations), Neurology (88 citations) and Clinical Biochemistry (63 citations). Astrid Lunkes has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Jean‐Louis Mandel, Georg Auburger, Suzana Gispert, Guy A. Rouleau, Stefan-M. Pulst, Julie R. Korenberg, Susan Pearlman, Xiao–Ning Chen, Sidney Starkman and Alex Nechiporuk. Their work appears in journals such as Genomics, Molecular Cell, Human Genetics, The EMBO Journal and Experimental Neurology.
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.