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Author: Cornelis Blauwendraat

Rankings

  • All-time downloads: 21,799 (rank: 2,951 out of 428,675)
  • Categories:
    • genetics: 17,688 (rank: 647 (tie) out of 38,068)
    • genomics: 1,500 (rank: 13,189 (tie) out of 44,721)
    • neuroscience: 2,611 (rank: 6,556 (tie) out of 72,544)

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Preprints

Expanding Parkinson's disease genetics: novel risk loci, genomic context, causal insights and heritable risk.

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Parkinson disease age of onset GWAS: defining heritability, genetic loci and a-synuclein mechanisms

genetics more details view paper
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Genome-wide association study of Parkinson’s disease progression biomarkers in 12 longitudinal patients’ cohorts

genetics more details view paper
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A genome-wide genetic pleiotropy approach identified shared loci between multiple system atrophy and inflammatory bowel disease

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An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of a-synuclein

neuroscience more details view paper
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No genetic evidence for involvement of alcohol dehydrogenase genes in risk for Parkinson's disease

genetics more details view paper
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Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at Chr16q11.2 and on the MAPT H1 allele.

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Genetic modifiers of risk and age at onset in GBA associated Parkinson disease and Lewy body dementia

genetics more details view paper
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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease

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Parkinsons disease determinants, prediction and gene-environment interactions in the UK Biobank

genetics more details view paper
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The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

neuroscience more details view paper
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The Parkinson's Disease GWAS Locus Browser

genetics more details view paper
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Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk

genetics more details view paper
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The Parkinsons Disease Mendelian Randomization Research Portal

neuroscience more details view paper
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Penetrance of Parkinson’s disease in LRRK2 p.G2019S carriers is modified by a polygenic risk score

genetics more details view paper
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Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies

genetics more details view paper
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Genome-wide estimates of heritability and genetic correlations in Essential Tremor

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Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes

genomics more details view paper
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