Author

Burcu Atasu

German Center for Neurodegenerative DiseasesORCID 0000-0002-7662-5803Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Javier Simón‐SáncheziD· 2 shared Alan Michael PittmaniD· 1 shared André FischeriD· 1 shared Apostolos PapandreouiD· 1 shared Arianna TucciiD· 1 shared Ashutosh DhingraiD· 1 shared Audrey Ker Shin SooiD· 1 shared Barbara BorroniiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersNeuroscience

Javier Simón‐SánchezORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

NeuroscienceScientific DataPeer-reviewedDec 1, 2023

A multi-omics dataset for the analysis Frontotemporal Dementia genetic subtypes

Kevin Menden, Margherita Francescatto, Tenzin Nyima…·Peter Heutink

The paper presents a multi-omics dataset for genetic subtypes of frontotemporal dementia to identify molecular mechanisms disrupted in the disease.

24 citations

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsJournal of Clinical InvestigationPeer-reviewedFeb 4, 2021

Bi-allelic variants in TSPOAP1, encoding the active zone protein RIMBP1, cause autosomal recessive dystonia

Niccolò Emanuele Mencacci, Marisa M. Brockmann, Jinye Dai…·Claudio Acuna

The paper identifies bi-allelic variants in TSPOAP1 as a cause of autosomal recessive dystonia, showing different clinical presentations based on variant type.

37 citations

𝕏 PostBluesky