Sebastian Schönherr

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 12

Top Topics

Quality Control

Loop Mediated Isothermal Amplification

Top Venues

Nucleic acids research

Circulation. Genomic and precision medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Lukas Forer, Daniel Taliun, Jonathon LeFaive, Albert V Smith, Andrew P Boughton, Stefan Coassin, Claudia Lamina, Florian Kronenberg, Christian Fuchsberger, Sebastian Schönherr
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers. Nucleic acids research 52 (W1) (2024)
Lukas Forer, Daniel Taliun, Jonathon LeFaive, Albert V Smith, Andrew P Boughton, Stefan Coassin, Claudia Lamina, Florian Kronenberg, Christian Fuchsberger, Sebastian Schönherr
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers. Nucleic acids research (2024)
Hansi Weissensteiner, Lukas Forer, Florian Kronenberg, Sebastian Schönherr
mtDNA-Server 2: advancing mitochondrial DNA analysis through highly parallelized data processing and interactive analytics. Nucleic acids research 52 (W1) (2024)
Hansi Weissensteiner, Lukas Forer, Florian Kronenberg, Sebastian Schönherr
mtDNA-Server 2: advancing mitochondrial DNA analysis through highly parallelized data processing and interactive analytics. Nucleic acids research (2024)
Silvia Di Maio, Peter Zöscher, Hansi Weissensteiner, Lukas Forer, Johanna F Schachtl-Riess, Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Bernhard Paulweber, Florian Kronenberg, Stefan Coassin, Sebastian Schönherr
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model. Genome biology 25 (1) (2024)
Silvia Di Maio, Peter Zöscher, Hansi Weissensteiner, Lukas Forer, Johanna F Schachtl-Riess, Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Bernhard Paulweber, Florian Kronenberg, Stefan Coassin, Sebastian Schönherr
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model. Genome biology 25 (1) (2024)
Silvia Di Maio, Peter Zöscher, Hansi Weissensteiner, Lukas Forer, Johanna F Schachtl-Riess, Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Bernhard Paulweber, Florian Kronenberg, Stefan Coassin, Sebastian Schönherr
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model. Genome biology 25 (1) (2024)
Silvia Di Maio, Peter Zöscher, Hansi Weissensteiner, Lukas Forer, Johanna F Schachtl-Riess, Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Bernhard Paulweber, Florian Kronenberg, Stefan Coassin, Sebastian Schönherr
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model. Genome biology 25 (1) (2024)
Hansi Weissensteiner, Lukas Forer, Florian Kronenberg, Sebastian Schönherr
mtDNA-Server 2: advancing mitochondrial DNA analysis through highly parallelized data processing and interactive analytics. Nucleic acids research 52 (W1) (2024)
Lukas Forer, Daniel Taliun, Jonathon LeFaive, Albert V Smith, Andrew P Boughton, Stefan Coassin, Claudia Lamina, Florian Kronenberg, Christian Fuchsberger, Sebastian Schönherr
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers. Nucleic acids research 52 (W1) (2024)
Stefan Coassin, Kevin Chemello, Ilya Khantalin, Lukas Forer, Patricia Döttelmayer, Sebastian Schönherr, Rebecca Grüneis, Clément Chong-Hong-Fong, Brice Nativel, Stéphane Ramin-Mangata, Antonio Gallo, Mathias Roche, Beatrix E Mühlegger, Christian Gieger, Annette Peters, Johannes Zschocke, Catherine Marimoutou, Olivier Meilhac, Claudia Lamina, Florian Kronenberg, Valentin Blanchard, Gilles Lambert
Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk. Circulation. Genomic and precision medicine 15 (2) (2022)
Michelle Hämmerle, Lukas Forer, Sebastian Schönherr, Annette Peters, Harald Grallert, Florian Kronenberg, Christian Gieger, Claudia Lamina
A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study. Stroke 53 (7) (2022)