Author

Sven Hauns

University of FreiburgORCID 0000-0002-5492-1871Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:machine learning (classical)· 1 Approach:statistical model· 1

Frequent Co-Authors

Rolf BackofeniD· 3 shared Omer S. AlkhnbashiiD· 2 shared Ahmad N. Abou TayouniD· 1 shared Ahmed Abou Tayoun· 1 shared Costerwell KhyriemiD· 1 shared Giulia CardamoneiD· 1 shared Irina I. BodeiD· 1 shared Melanie FlohriD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersMolecular Biology

Rolf BackofenORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Molecular BiologyPLoS ONEPeer-reviewedJun 25, 2026

Enhanced IGFL1 translation in response to IL-1β is controlled by distinct 3UTR elements

Giulia Cardamone, Melanie Flohr, Rebecca Raue…·Tobias Schmid

The paper shows IL-1β enhances IGFL1 translation through a G-rich 3UTR element in MCF7 cells.

DOI 10.1371/journal.pone.0342288

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 18, 2026

Structural variation landscape of Middle Eastern and North African individuals from long-read nanopore sequencing reveals medically relevant variants

Talal Al‐Yazeedi, Sophie Tandonnet, Sven Hauns…·Omer S. Alkhnbashi

The paper identifies structural variants in MENA individuals using long-read sequencing, revealing previously unreported variants and population-specific disease-related variants.

DOI 10.64898/2026.02.20.26346743

humanlong-read sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintAug 24, 2025

VDB: The Arab Variation and Disease Burden Database

Omer S. Alkhnbashi, Ruchi Jain, Sathishkumar Ramaswamy…·Ahmad N. Abou Tayoun

The paper introduces AVDB, a database of genetic variants from Arab populations, providing pathogenicity classifications and disease burden metrics to improve genomic screening and diagnostics.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky