Thomas Rosenberg
4PUBLICATIONS
47CO-AUTHORS
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Publications (4)
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|Jun 27, 2022
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.Bernd Wissinger, Britta Baumann, Elena Buena-Atienza
|Mar 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.Maria Solaki, Britta Baumann, Peggy Reuter
|Feb 06, 2019
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.Cathrine Jespersgaard, Mingyan Fang, Mette Bertelsen
|Jan 26, 2019
A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1.Karen Grønskov, Cathrine Jespersgaard, Gitte Hoffmann Bruun
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Frequent Collaborators
2 joint publications
Karen Grønskov
2 joint publications
Susanne Kohl
2 joint publications
Loreto Martorell-Sampol
2 joint publications
Isabelle Audo
2 joint publications
Birgit Lorenz
2 joint publications
Bernd Wissinger
2 joint publications
Ulrich Kellner
2 joint publications
Jaume Català-Mora
1 joint publications
Brage S Andresen
1 joint publications
Peggy Reuter
