Ida Höijer (Ida Hoijer)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Venues

Human mutation

Genome research

Genome biology

Nature communications

Uppsala University

Uppsala University (PHD)

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

Affiliation History

Uppsala University Oct 01 2011 - Jul 01 2017

Sweden

Research Engineer :: National Genomics Infrastructure

Education History

Uppsala University Jul 01 2017

Sweden

PHD :: Immunology, Genetics and Pathology

Uppsala University Sep 01 2005 - Jun 01 2011

Sweden

MSC

Publications

Wouter De Coster, Ida Höijer, Inge Bruggeman, Svenn D'Hert, Malin Melin, Adam Ameur, Rosa Rademakers
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR. Genome research (2024)
Ida Höijer, Anastasia Emmanouilidou, Rebecka Östlund, Robin van Schendel, Selma Bozorgpana, Marcel Tijsterman, Lars Feuk, Ulf Gyllensten, Marcel den Hoed, Adam Ameur
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations. Nature communications 13 (1) (2022)
Esben B Madsen, Ida Höijer, Thomas Kvist, Adam Ameur, Marie J Mikkelsen
Xdrop: Targeted sequencing of long DNA molecules from low input samples using droplet sorting. Human mutation 41 (9) (2020)
Ida Höijer, Josefin Johansson, Sanna Gudmundsson, Chen-Shan Chin, Ignas Bunikis, Susana Häggqvist, Anastasia Emmanouilidou, Maria Wilbe, Marcel den Hoed, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity. Genome biology 21 (1) (2020)
Ida Höijer, Yu-Chih Tsai, Tyson A Clark, Paul Kotturi, Niklas Dahl, Eva-Lena Stattin, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur
Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing. Human mutation 39 (9) (2018)
Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall Olason, Lars Feuk, Ulf Gyllensten
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data. Genes 9 (10) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ida Höijer (Ida Hoijer)