Author

Amos D. Korczyn

Tel Aviv UniversityORCID 0000-0001-5721-0437Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Assay:whole-exome sequencing· 2 Research Focus:cell-cell communication· 1 Research Focus:GWAS / association mapping· 1 Assay:imaging· 1

Frequent Co-Authors

Alexandra MacDonaldiD· 2 shared Andrea Byrnes· 2 shared Annika Rademacher· 2 shared Anthony Guy MarsoniD· 2 shared Brigid M. ReganiD· 2 shared Caitlin A. BennettiD· 2 shared Catharine Freyer· 2 shared Chantal DepondtiD· 2 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Alexandra MacDonaldORCID

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3 papers

Recent·Most cited

NeuroscienceHuman Brain MappingPeer-reviewedMar 1, 2024

Lost in space(s): multimodal neuroimaging of disorientation along the Alzheimer's disease continuum

Gregory Peters‐Founshtein, Lidor Gazit, Tahel Naveh…·Shahar Arzy

The paper investigates disorientation across spatial, temporal, and social domains in Alzheimer's disease using fMRI and identifies distinct brain network and metabolic patterns associated with different stages of the disease.

11 citations

humanimaging

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GenomicsEBioMedicinePeer-reviewedSep 24, 2021

Ultra-rare constrained missense variants in the epilepsies: Shared and specific enrichment patterns in neuronal gene-sets

Mahmoud Koko, Roland Krause, Thomas Sander…·Christian Hengsbach

The paper analyzes ultra-rare variants in epilepsy patients to identify gene-set enrichment patterns and differential impacts in neuronal gene categories.

18 citations

humanwhole-exome sequencing

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GeneticsThe American Journal of Human GeneticsPeer-reviewedJul 18, 2019

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam E. Abbott…·Ingo Borggräfe

This study identifies ultra-rare genetic variants associated with different epilepsy types using whole-exome sequencing in 17,634 individuals.

297 citationstop 1%

humanwhole-exome sequencing

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