Author

Isa Amalie Olofsson

Copenhagen University HospitalORCID 0000-0002-7500-8045Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jes OleseniD· 1 shared Karina BanasikiD· 1 shared Lisette J. A. KogelmaniD· 1 shared Mette NyegaardiD· 1 shared Mona Ameri ChalmeriD· 1 shared Peter Loof MølleriD· 1 shared Tanya Ramdal TechloiD· 1 shared Thomas Folkmann HanseniD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Jes OlesenORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 20, 2021

Rare risk variants associate with epigenetic dysregulation in migraine

Tanya Ramdal Techlo, Mona Ameri Chalmer, Peter Loof Møller…·Thomas Folkmann Hansen

The paper identifies rare variants in the ASTN2 locus associated with migraine, independent of GWAS findings, and proposes a role for Polycomb Response Elements in migraine etiology.

DOI 10.1101/2021.12.20.21268001

humanwhole-genome sequencing

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