Marc Cruts
- Neurology top 0.1%
- Amyotrophic Lateral Sclerosis Research 38
- Parkinson's Disease Mechanisms and Treatments 27
- Neurological diseases and metabolism 17
- Physiology top 0.1%
- Alzheimer's disease research and treatments 74
- Neurology top 0.2%
- Amyotrophic Lateral Sclerosis Research 38
- Parkinson's Disease Mechanisms and Treatments 27
- Neurological diseases and metabolism 17
- Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 14
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- Dementia and Cognitive Impairment Research 18
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- Cholinesterase and Neurodegenerative Diseases 12
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- Amyloidosis: Diagnosis, Treatment, Outcomes 11
- Co-authors
- Christine Van BroeckhovenWouter De CosterSvenn D’HertDarrin T. SchultzCornelia M. van DuijnJessie TheunsIlse GijselinckKristel Sleegers
- Cited by
- NeurologyPhysiologyGenetics
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Marc Cruts
147 papers receiving 13.0k citations
Hit Papers
Peers
Comparison fields: 5 of 159
- Neurology 4.4k
- Physiology 5.8k
- Neurology 1.8k
- Genetics 1.5k
- Cellular and Molecular Neuroscience 1.7k
Countries citing papers authored by Marc Cruts
This map shows the geographic impact of Marc Cruts'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 Marc Cruts with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc Cruts more than expected).
Fields of papers citing papers by Marc Cruts
This network shows the impact of papers produced by Marc Cruts. 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 Marc Cruts. The network helps show where Marc Cruts may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Marc Cruts, 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 | NanoPack: visualizing and processing long-read sequencing databreakdown → | 2018 | 1729 |
| 2 | Unraveling the genetic role of SORT1 in the Belgian frontotemporal dementia population | 2016 | 1 |
| 3 | 2015 | 46 | |
| 4 | 2015 | 12 | |
| 5 | 2015 | 11 | |
| 6 | C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia | 2015 | 12 |
| 7 | 2013 | 148 | |
| 8 | 2013 | 35 | |
| 9 | 2011 | 94 | |
| 10 | Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS | 2007 | 3 |
| 11 | Parietal cortex activation predicts longitudinal memory decline in APOE ε4 carriers. | 2006 | 2 |
| 12 | The molecular genetics of early-onset Alzheimer's disease | 2004 | 2 |
| 13 | 2004 | 147 | |
| 14 | Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample | 2002 | 1 |
| 15 | Novel German APP V715A mutation associated with presenile Alzheimer's disease | 2002 | 5 |
| 16 | In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing | 2002 | 1 |
| 17 | Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cm interval | 2002 | 17 |
| 18 | Amyloid beta-secretase gene (BACE) is neither mutated nor associated with early-onset Alzheimers disease | 2001 | 1 |
| 19 | Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion | 1999 | 10 |
| 20 | 1998 | 60 |
About Marc Cruts
Marc Cruts is a scholar working on Neurology, Physiology, Neurology, Genetics and Psychiatry and Mental health, having authored 148 papers that have together received 13.2k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (74 papers), Amyotrophic Lateral Sclerosis Research (38 papers), Parkinson's Disease Mechanisms and Treatments (27 papers), Dementia and Cognitive Impairment Research (18 papers), Neurological diseases and metabolism (17 papers), Neurogenetic and Muscular Disorders Research (14 papers), Cholinesterase and Neurodegenerative Diseases (12 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (11 papers). The work is most often cited by research in Neurology (4.4k citations), Physiology (5.8k citations), Neurology (1.8k citations), Genetics (1.5k citations) and Cellular and Molecular Neuroscience (1.7k citations). Marc Cruts has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Christine Van Broeckhoven, Wouter De Coster, Svenn D’Hert, Darrin T. Schultz, Cornelia M. van Duijn, Jessie Theuns, Ilse Gijselinck, Kristel Sleegers, Julie van der Zee and Rosa Rademakers. Their work appears in journals such as Neurobiology of Aging, Human Mutation, Neurology, Human Molecular Genetics and The American Journal of 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.