Author

Sailendra Pradhananga

Science for Life LaboratoryORCID 0000-0002-0834-3169Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Assay:Hi-C· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Pelin SahléniD· 2 shared Per Olof ErikssoniD· 2 shared Rapolas SpalinskasiD· 2 shared Anandashankar Anil· 1 shared Anders Franco‐CerecedaiD· 1 shared Andrey BuyaniD· 1 shared Artemy ZhiguleviD· 1 shared Doreen SchwochowiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Pelin SahlénORCID

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2 papers

Recent·Most cited

Rare gain-of-function regulatory mutations explain the missing heritability of bicuspid aortic valve

Artemy Zhigulev, Andrey Buyan, Enikő Lázár, Nikita Gryzunov, Karin Lång, Raphaël Mauron, Vladimir Nozdrin, Rapolas Spalinskas, Sailendra Pradhananga, Madeleine Petersson Sjögren, Doreen Schwochow, Anders Franco‐Cereceda, Joakim Lundeberg, Ivan V. Kulakovskiy, Per Eriksson, , Pelin Sahlén

The paper identifies rare gain-of-function regulatory mutations as significant contributors to the missing heritability of bicuspid aortic valve.

Nature Communications · Apr 18, 2026Peer-reviewedGenetic & Genomic Medicine

High-resolution regulatory maps connect cardiovascular risk variants to disease related pathways

Örjan Åkerborg, Rapolas Spalinskas, Sailendra Pradhananga, Anandashankar Anil, Pontus Höjer, Flore-Anne Poujade, Lasse Folkersen, Per Olof Eriksson, Pelin Sahlén

This study connects cardiovascular risk variants to disease-related pathways using high-resolution genomic interaction maps in relevant cell types.

bioRxiv · Jul 24, 2018 · PreprintGenomics