# Peter Heutink

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/peter-heutink/

## Facts

| Field | Value |
| --- | --- |
| Citations | 58,780 |
| Field | Parkinson's Disease Mechanisms and Treatments |
| h-index | 109 |
| i10-index | 326 |
| Last Known Institution | German Center for Neurodegenerative Diseases |
| OpenAlex ID | https://openalex.org/A5057989264 |
| ORCID iD | https://orcid.org/0000-0001-5218-1737 |
| Works | 716 |

## Researcher papers

Showing 12 of 17.

- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism](https://scholariq.org/papers/mutations-in-the-i-dj-1-i-gene-associated-with-autosomal-recessive-early-onset/)
- [Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease](https://scholariq.org/papers/large-scale-meta-analysis-of-genome-wide-association-data-identifies-six-new/)
- [Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1](https://scholariq.org/papers/endoglin-a-tgf-binding-protein-of-endothelial-cells-is-the-gene-for-hereditary/)
- [Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study](https://scholariq.org/papers/frequency-of-the-c9orf72-hexanucleotide-repeat-expansion-in-patients-with/)
- [Somatic retrotransposition alters the genetic landscape of the human brain](https://scholariq.org/papers/somatic-retrotransposition-alters-the-genetic-landscape-of-the-human-brain/)
- [Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions](https://scholariq.org/papers/common-variants-at-7p21-are-associated-with-frontotemporal-lobar-degeneration/)
- [Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke](https://scholariq.org/papers/role-of-col4a1-in-small-vessel-disease-and-hemorrhagic-stroke/)
- [Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database](https://scholariq.org/papers/comprehensive-research-synopsis-and-systematic-meta-analyses-in-parkinson-s/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy](https://scholariq.org/papers/loss-of-vps13c-function-in-autosomal-recessive-parkinsonism-causes-mitochondrial/)
- [β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson’s disease](https://scholariq.org/papers/2-adrenoreceptor-is-a-regulator-of-the-synuclein-gene-driving-risk-of-parkinson/)

## Researcher topics

- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)

## Researcher university

- [German Center for Neurodegenerative Diseases](https://scholariq.org/institutions/german-center-for-neurodegenerative-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.