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You searched for: Author/Creator Heutink, Peter

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1. A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family. (August 2016)

2. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. (18th October 2016)

3. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome‐wide meta‐analysis. Issue 1 (27th June 2014)

5. Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe. Issue 1 (December 2016)

6. CSIG-15. INHIBITION OF THE bHLH TRANSCRIPTIONAL NETWORKS BY A MUTATED E47 PROTEIN LEADS TO A STRONG ANTI-GLIOMA ACTIVITY IN VITRO AND IN VIVO. (11th November 2019)

7. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Issue 6 (May 2016)

8. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. Issue 10 (October 2015)

9. Differences in the Presentation and Progression of Parkinson's Disease by Sex. Issue 1 (1st October 2020)

10. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Issue 1 (December 2017)