D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 88 Citations 41,755 260 World Ranking 689 National Ranking 37

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

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 most cited work include:

  • A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (2859 citations)
  • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 (2839 citations)
  • Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism (2167 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (70.61%)
  • Gene (22.81%)
  • Disease (24.12%)

What were the highlights of his more recent work (between 2017-2021)?

  • Disease (24.12%)
  • Genetics (70.61%)
  • Genome-wide association study (24.34%)

In recent papers he was focusing on the following fields of study:

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.

Between 2017 and 2021, his most popular works were:

  • Analysis of shared heritability in common disorders of the brain (726 citations)
  • Analysis of shared heritability in common disorders of the brain (726 citations)
  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies (353 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Genetics

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

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.
Nature (1998)

3532 Citations

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.
Neuron (2011)

3265 Citations

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap.
Science (2003)

2801 Citations

An atlas of active enhancers across human cell types and tissues

Robin Andersson;Claudia Gebhard;Irene Miguel-Escalada;Ilka Hoof.
Nature (2014)

1829 Citations

A promoter-level mammalian expression atlas

Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Nature (2014)

1134 Citations

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)

1006 Citations

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)

867 Citations

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

Brais B;Bouchard Jp;Xie Yg;Rochefort Dl.
Nature Genetics (1998)

854 Citations

Somatic retrotransposition alters the genetic landscape of the human brain

J. Kenneth Baillie;Mark W. Barnett;Kyle R. Upton;Daniel J. Gerhardt.
Nature (2011)

685 Citations

An atlas of human long non-coding RNAs with accurate 5′ ends

Chung Chau Hon;Jordan A. Ramilowski;Jayson Harshbarger;Nicolas Bertin;Nicolas Bertin.
Nature (2017)

622 Citations

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