Author

Asgeir Orn Arnthorsson

Humboldt-Universität zu BerlinORCID 0000-0002-0087-2525Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:clustering· 1

Frequent Co-Authors

Amal Abu RayyaniD· 1 shared Amihood Singer· 1 shared Amir PelegiD· 1 shared Anna Margret Jonsdottir· 1 shared Ásgeir SigurðssoniD· 1 shared Bella DavidoviD· 1 shared Bergrún ÁsbjörnsdóttiriD· 1 shared Chana VinkleriD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Amal Abu RayyanORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Endometriosis lesions are oligoclonal structures derived from the normal endometrium

Sigurgeir Ólafsson, Asgeir Orn Arnthorsson, Kirsten Kübler, Ásgeir Sigurðsson, Helga Sigrun Gunnarsdottir, Hákon Jónsson, Bergrún Ásbjörnsdóttir, Louise le Roux, Jona Saemundsdottir, Valgerður Steinthórsdóttir, Gudmundur Logi Norddahl, Ingileif Jónsdóttir, Jon Gunnlaugur Jonasson, Droplaug N. Magnúsdóttir, Ólafur Þ. Magnússon, , Kāri Stefánsson

This study shows endometriosis lesions originate from the normal endometrium through clonal expansion, with distinct clones at different body sites.

bioRxiv · Feb 26, 2026 · PreprintGenetics

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Zippora Brownstein, Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov, Ming K. Lee, Mor Bordeynik‐Cohen, Maria Birkan, Weise Chang, Silvia Casadei, Nada Danial‐Farran, Amal Abu Rayyan, Ryan J. Carlson, Lara Kamal, , Karen B. Avraham

The paper identifies genetic causes of inherited hearing loss in the Israeli Jewish population, finding a novel deafness gene ATOH1 and demonstrating the effectiveness of targeted genomic sequencing.

Clinical Genetics · Jul 20, 2020Peer-reviewedGenetics