Peter Heutink mainly investigates Genetics, Genome-wide association study, Frontotemporal dementia, Single-nucleotide polymorphism and Genetic association. His Genetics research focuses on Gene, Locus, Mutation, Haplotype and Exon. His Genome-wide association study research is multidisciplinary, incorporating elements of Linkage disequilibrium, Meta-analysis, Quantitative trait locus, Heritability and Major depressive disorder.
His Frontotemporal dementia research is multidisciplinary, relying on both Tau protein and Neuroscience. Peter Heutink combines subjects such as Neuropathology and Genetic variation with his study of Single-nucleotide polymorphism. As a member of one scientific family, Peter Heutink mostly works in the field of Genetic association, focusing on Genotyping and, on occasion, GPNMB, Multiple alleles, Glucocerebrosidase and Anxiety.
His primary areas of study are Genetics, Gene, Disease, Genome-wide association study and Parkinson's disease. His study in Locus, Single-nucleotide polymorphism, Genetic association, Haplotype and Allele is carried out as part of his Genetics studies. His study focuses on the intersection of Locus and fields such as Chromosome with connections in the field of Genetic linkage.
His Disease study combines topics in areas such as Odds ratio, Oncology and Bioinformatics. His studies deal with areas such as Linkage disequilibrium, Age of onset, Heritability, Genetic variation and Genetic architecture as well as Genome-wide association study. His Frontotemporal dementia research includes themes of Progressive supranuclear palsy, Tau protein and Missense mutation.
His main research concerns Disease, Genetics, Genome-wide association study, Parkinson's disease and Gene. His Disease research incorporates elements of Expression quantitative trait loci and Genetic architecture. While working on this project, Peter Heutink studies both Genetics and Context.
His biological study spans a wide range of topics, including Allele, Genetic association and Age of onset. His research in Parkinson's disease intersects with topics in Progressive supranuclear palsy and Dementia. As a part of the same scientific study, Peter Heutink usually deals with the Gene, concentrating on Computational biology and frequently concerns with Gene expression, Functional annotation and Neurodegeneration.
Peter Heutink mainly focuses on Disease, Genetics, Genome-wide association study, Parkinson's disease and Context. His Disease study incorporates themes from Odds ratio, Single-nucleotide polymorphism, Gene and Oncology. Peter Heutink works in the field of Genetics, namely C9orf72.
The Genome-wide association study study combines topics in areas such as Genetic association and Age of onset. His Genetic association research includes elements of Comorbidity and Heritability. His study in Parkinson's disease is interdisciplinary in nature, drawing from both Alzheimer's disease, Dementia with Lewy bodies, Progressive supranuclear palsy and Missense mutation.
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Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
M. Hutton;C. L. Lendon;P. Rizzu;M. Baker.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap.
An atlas of active enhancers across human cell types and tissues
Robin Andersson;Claudia Gebhard;Irene Miguel-Escalada;Ilka Hoof.
A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper.
Lancet Neurology (2012)
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Michael A. Nalls;Vincent Plagnol;Dena G. Hernandez;Dena G. Hernandez;Manu Sharma;Manu Sharma.
The Lancet (2011)
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
Brais B;Bouchard Jp;Xie Yg;Rochefort Dl.
Nature Genetics (1998)
Somatic retrotransposition alters the genetic landscape of the human brain
J. Kenneth Baillie;Mark W. Barnett;Kyle R. Upton;Daniel J. Gerhardt.
An atlas of human long non-coding RNAs with accurate 5′ ends
Chung Chau Hon;Jordan A. Ramilowski;Jayson Harshbarger;Nicolas Bertin;Nicolas Bertin.
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