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Author Details

Peter Heutink
German Center for Neurodegenerative Diseases (DZNE).
1988
312
86
PMIDPaper TitleJournal TitlePublished Year
36343661Mitochondrial haplogroups and cognitive progression in Parkinson's disease.Brain2023
37704671Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37790572Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesia.medRxiv2023
37508584Epigenetic Age Acceleration in Frontotemporal Lobar Degeneration: A Comprehensive Analysis in the Blood and Brain.Cells2023
38040703A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes.Sci Data2023
36950378The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.Cell Genom2023
37149835Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes.Acta Neuropathol2023
37369645Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37198259Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.Mol Psychiatry2023
34871736Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing.Neurobiol Dis2022
35675776Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G<sub>4</sub>C<sub>2</sub>)<sub>n</sub> expression in C9orf72 ALS/FTD.Cell Rep2022
35799292Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia.Acta Neuropathol Commun2022
36338986Transcription start site signal profiling improves transposable element RNA expression analysis at locus-level.Front Genet2022
36385530Medin co-aggregates with vascular amyloid-β in Alzheimer's disease.Nature2022
34942606A multimodal 3D neuro-microphysiological system with neurite-trapping microelectrodes.Biofabrication2022
33002231Differences in the Presentation and Progression of Parkinson's Disease by Sex.Mov Disord2021
33619157Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosis.Life Sci Alliance2021
34705895Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interference.PLoS Pathog2021
34693284Evidence for <i>GRN</i> connecting multiple neurodegenerative diseases.Brain Commun2021
34532319iPS Cell-Based Model for <i>MAPT</i> Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression.Front Cell Dev Biol2021
33958783Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease.Nat Genet2021
34083785Non-invasive and high-throughput interrogation of exon-specific isoform expression.Nat Cell Biol2021
33200446From iPS Cells to Rodents and Nonhuman Primates: Filling Gaps in Modeling Parkinson's Disease.Mov Disord2021
33433880A Multi-omics Data Resource for Frontotemporal Dementia Research.Adv Exp Med Biol2021
33446877Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening.Sci Rep2021
32814053Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.Cell Rep2020
31755958Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.Brain2020
31955222Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.Acta Neuropathol2020
33134924Experimental glioma with high bHLH expression harbor increased replicative stress and are sensitive toward ATR inhibition.Neurooncol Adv2020
32832661Deep learning-based cell composition analysis from tissue expression profiles.Sci Adv2020
32831313Automated Production of Human Induced Pluripotent Stem Cell-Derived Cortical and Dopaminergic Neurons with Integrated Live-Cell Monitoring.J Vis Exp2020
30610612Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.Mol Neurobiol2019
31404238Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts.Neurol Genet2019
31505070Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts.Mov Disord2019
30739198Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.Acta Neuropathol2019
30957308Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.Mov Disord2019
30482917Publisher Correction: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease.Nat Neurosci2019
28749476The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects.Genet Med2018
29886022No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.Neurobiol Aging2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30145809HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.Mov Disord2018
30224808Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease.Nat Neurosci2018
30538238Author Correction: Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system.Sci Data2018
29724592Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.Lancet Neurol2018
29494619Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease.PLoS Comput Biol2018
27760429Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia.Neurodegener Dis2017
28387812Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia.Brain2017
28137300Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.Genome Biol2017
28241135An atlas of human long non-coding RNAs with accurate 5' ends.Nature2017
29087374Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system.Sci Data2017
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Co-authored papers 67
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Co-authored papers 46
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Co-authored papers 35
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Danielle Posthuma
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University of Antwerp
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Piero Carninci
RIKEN Center for Integrative Medical Sciences
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Alistair R R Forrest
RIKEN Center for Integrative Medical Sciences
Co-authored papers 10
Valentina Escott-Price
Co-authored papers 9
Yoshihide Hayashizaki
Center for Integrative Medical Sciences
Co-authored papers 9
Margherita Francescatto
German Center for Neurodegenerative Diseases
Co-authored papers 9
Albert Hofman
Harvard T.H. Chan School of Public Health
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Brenda W J H Penninx
Co-authored papers 9
Bradley F Boeve
Mayo Clinic Rochester
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Carsten O Daub
International Institute of Molecular and Cell Biology in Warsaw
Co-authored papers 8
Carlos N Pato
Co-authored papers 8
Tinca J C Polderman
Co-authored papers 8
Roger A Barker
John Van Geest Center for Brain Repair, University of Cambridge
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