Author

Sebastian Schoenherr

Innsbruck Medical University

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

Biology Disciplines

Click to filter author papers

Genetics· 2 Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 4 Assay:whole-genome sequencing· 4 Organism:human· 3 Research Focus:variant effect prediction· 2 Research Focus:database / resource· 1 Research Focus:GWAS / association mapping· 1 Research Focus:imputation· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Christian FuchsbergeriD· 4 shared Lukas ForeriD· 4 shared Carlo SidoreiD· 2 shared Chad M. BrummettiD· 2 shared Charles L KooperbergiD· 2 shared David SchlessingeriD· 2 shared Francesco CuccaiD· 2 shared Gonçalo R. AbecasisiD· 2 shared

Activity by Year

2016-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

4 shared papersGenomics

Christian FuchsbergerORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

South Asian patient population genetics reveal strong founder effects and high rates of homozygosity - new resources for precision medicine

Jeffrey D. Wall, J. Fah Sathirapongsasuti, Ravi Kr Gupta, Anamitra Barik, Rajesh Kumar, Asif Rasheed, Venkatesan Radha, Saurabh Belsare, Ramesh Menon, Sameer Phalke, Anuradha Mittal, John Z. Fang, Deepak Tanneeru, Manjari Deshmukh, Akshi Bassi, , Andrew S. Peterson

The paper characterizes the genetic structure of South Asian populations, identifies founder effects and high homozygosity, and develops a custom SNP array for genetic studies in the region.

bioRxiv · Oct 2, 2020 · PreprintGenomics

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

Jonas Bille Nielsen, Oren Rom, Ida L. Surakka, Sarah E. Graham, Wei Zhou, Lars G. Fritsche, Sarah A. Gagliano Taliun, Carlo Sidore, Yuhao Liu, Maiken Elvestad Gabrielsen, Anne Heidi Skogholt, Brooke N. Wolford, William Overton, Whitney Hornsby, Akua Acheampong, , Y. Eugene Chen

The paper identifies loss-of-function variants affecting liver-related blood traits that reduce CVD risk without increasing metabolic disease risk, highlighting potential therapeutic targets.

bioRxiv · Apr 2, 2019 · PreprintGenomics

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

Luke M. Evans, Rasool Tahmasbi, Matthew Jones, Scott I. Vrieze, Gonçalo R. Abecasis, Sayantan Das, Douglas W. Bjelland, Teresa R de Candia, David Altshuler, Carl A. Anderson, Andrea Angius, Jeffrey C. Barrett, Sonja I. Berndt, Michael Boehnke, Dorrett Boomsma, , George Davey Smith

This paper estimates narrow-sense heritability using identity-by-descent information in unrelated individuals and finds that IBD-based methods can capture rare variant contributions but are affected by stratification.

Heredity · Mar 28, 2018Peer-reviewedGenetics

Reference-based phasing using the Haplotype Reference Consortium panel

Po-Ru Loh, Petr Danecek, Pier Francesco Palamara, Christian Fuchsberger, Yakir A Reshef, Hilary K Finucane, Sebastian Schoenherr, Lukas Forer, Shane McCarthy, Goncalo R Abecasis, Richard Durbin, Alkes L Price

This paper introduces Eagle2, a reference-based phasing algorithm that improves accuracy and speed compared to SHAPEIT2 using the Haplotype Reference Consortium panel.

bioRxiv · Jul 7, 2016Genetics