Author

Henrikki Almusa

Institute for Molecular Medicine Finland

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

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aashish SrivastavaiD· 1 shared Anders JemtiD· 1 shared Anil Kumar GiriiD· 1 shared Ashish Kumar SinghiD· 1 shared D. T. AndreaseniD· 1 shared Edda María Elvarsdóttir· 1 shared Eevi KaasineniD· 1 shared Eiríkur BriemiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperBioinformatics

Aashish SrivastavaORCID

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2 papers

Recent·Most cited

BioinformaticsGenome MedicinePeer-reviewedOct 17, 2025

Recommendations for Bioinformatics in Clinical Practice

Ksenia Lavrichenko, Emilie Sofie Engdal, Rasmus L. Marvig…·Frederik Otzen Bagger

This paper provides consensus recommendations for standardizing bioinformatics practices in clinical whole genome sequencing to ensure accuracy, reproducibility, and comparability of results.

21 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineBMC Medical GenomicsPeer-reviewedApr 4, 2025

Exome-wide association study reveals 7 functional variants associated with ex-vivo drug response in acute myeloid leukaemia patients

Anil Kumar Giri, Jake Lin, Konstantinos Kyriakidis…·Henrikki Almusa

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky