Author

Sandy Lösecke

TUM Klinikum

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

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aïcha BoughalemiD· 1 shared Alexander HoischeniD· 1 shared Bart P. G. H. van der SandeniD· 1 shared Detlef Trost· 1 shared Elisa RahikkalaiD· 1 shared Elisabeth GrafiD· 1 shared Eva Maria Christina SchwaiboldiD· 1 shared Eveline J. KampingiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aïcha BoughalemORCID

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1 paper

Recent·Most cited

Systematic assessment of rare and de novo structural variants in 57 patient-parent trios using optical genome mapping

Bart P. G. H. van der Sanden, Sandra Vorimo, Theresa Brunet, Aïcha Boughalem, Maureen Jacob, Ronald van Beek, Eveline J. Kamping, Elisa Rahikkala, Outi Kuismin, Jukka Moilanen, Katri Pylkäs, Elisabeth Graf, Sandy Lösecke, Melanie Brügger, Kevork Derderian, , Alexander Hoischen

This study uses optical genome mapping to identify de novo and rare inherited structural variants in 57 patient-parent trios, finding 13 de novo SVs and 11 rare inherited SVs, some of which are pathogenic or candidate disease-causing.

medRxiv · Jan 21, 2026 · PreprintGenetic & Genomic Medicine