Author

Javier Simón-Sánchez

German Center for Neurodegenerative Diseases

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

Signature Assays, Organisms & Methods

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Assay:clinical cohort / trial· 1 Assay:DNA methylation· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Research Focus:polygenic risk· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Akbota M. AitkulovaiD· 1 shared Alastair John NoyceiD· 1 shared Alexis BriceiD· 1 shared Ana CámaraiD· 1 shared Andrew SingletoniD· 1 shared Angli XueiD· 1 shared Ari SiitoneniD· 1 shared Astrid Daniela Adarmes-GómeziD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Akbota M. AitkulovaORCID

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1 paper

Recent·Most cited

GeneticsThe Lancet NeurologyPeer-reviewedNov 6, 2019

✦ In-depth digest

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

Mike A. Nalls, Cornelis Blauwendraat, Costanza Ludovica Vallerga…·Ciara García

Across 37,688 Parkinson's cases, 18,618 proxy-cases and 1.4M controls, 90 risk signals map to 78 loci (37 new); an 1805-variant polygenic score explains 26-36% of heritability.

2,451 citationstop 1%

humanGWAS summary statistics

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