Peter Heutink
Impact in
- Neurology top 0.05%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
- Neurological disorders and treatments
- Cellular and Molecular Neuroscience top 0.2%
- Nuclear Receptors and Signaling
- Genetic Neurodegenerative Diseases
Papers in
- Neurology 81
- Parkinson's Disease Mechanisms and Treatments 53
- Neurological diseases and metabolism 30
- Amyotrophic Lateral Sclerosis Research 26
- Co-authors
- John C. van SwietenBen A. OostraCornelia M. van DuijnGuido J. BreedveldVincenzo BonifatiMarijke JoossePatrizia RizzuAlexis Brice
- Journals
- European Journal of Human Genetics (15 papers)Annals of Neurology (13 papers)The American Journal of Human Genetics (11 papers)Movement Disorders (10 papers)Neurology (10 papers)
- Partner nations
- NetherlandsGermanyUnited States
In The Last Decade
Peter Heutink
228 papers receiving 16.0k citations
Hit Papers
Peers
Comparison fields: 5 of 160
- Neurology 6.2k
- Neurology 2.4k
- Cellular and Molecular Neuroscience 3.6k
- Developmental Biology 356
- Genetics 1.5k
Countries citing papers authored by Peter Heutink
This map shows the geographic impact of Peter Heutink'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 Peter Heutink with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Heutink more than expected).
Fields of papers citing papers by Peter Heutink
This network shows the impact of papers produced by Peter Heutink. 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 Peter Heutink. The network helps show where Peter Heutink may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Heutink, 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 | 2025 | 0 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 0 | |
| 4 | 2023 | 30 | |
| 5 | 2023 | 6 | |
| 6 | 2021 | 27 | |
| 7 | 2021 | 11 | |
| 8 | 2020 | 2 | |
| 9 | 2020 | 129 | |
| 10 | 2017 | 4 | |
| 11 | 2011 | 7 | |
| 12 | 2009 | 42 | |
| 13 | Family-based association approach provides further evidence for a role of the CHRM2 gene in cognition. | 2006 | 0 |
| 14 | 2006 | 155 | |
| 15 | 2005 | 366 | |
| 16 | 2001 | 8 | |
| 17 | A study of ADHD in a genetic isolate | 2000 | 1 |
| 18 | A Mutation in Codon-142 in Central Areolar Choroidal Dystrophy | 1995 | 5 |
| 19 | Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome | 1991 | 21 |
| 20 | A Collaborative Linkage Study on Gilles-De-La-Tourette Syndrome | 1991 | 1 |
About Peter Heutink
Peter Heutink is a scholar working on Developmental Biology, Neurology, Neurology, Genetics and Cellular and Molecular Neuroscience, having authored 235 papers that have together received 16.3k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (53 papers), Alzheimer's disease research and treatments (38 papers), Neurological diseases and metabolism (30 papers), Amyotrophic Lateral Sclerosis Research (26 papers), Genetic Associations and Epidemiology (23 papers), Genetics and Neurodevelopmental Disorders (15 papers), Nuclear Receptors and Signaling (14 papers) and Autism Spectrum Disorder Research (14 papers). The work is most often cited by research in Neurology (6.2k citations), Neurology (2.4k citations), Cellular and Molecular Neuroscience (3.6k citations), Developmental Biology (356 citations) and Genetics (1.5k citations). Peter Heutink has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include John C. van Swieten, Ben A. Oostra, Cornelia M. van Duijn, Guido J. Breedveld, Vincenzo Bonifati, Marijke Joosse, Patrizia Rizzu, Alexis Brice, Ferdinando Squitieri and Elmar Krieger. Their work appears in journals such as European Journal of Human Genetics, Annals of Neurology, The American Journal of Human Genetics, Movement Disorders and 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.