Author

Simon Frueh

University of Bern

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· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alain VerloèsiD· 1 shared Almuth CaliebeiD· 1 shared Annette SchenckiD· 1 shared Bernt PoppiD· 1 shared Christiane ZweieriD· 1 shared Fabian HummeliD· 1 shared Hilde Van EschiD· 1 shared Melek Firat AltayiD· 1 shared

Activity by Year

2026-2026 · 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

1 shared paperGenetics

Alain VerloèsORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

SysNDD: A Systematic Database for Neurodevelopmental Disorders

Bernt Popp, Simon Frueh, Melek Firat Altay, Hilde Van Esch, Almuth Caliebe, Nuria C. Bramswig, Fabian Hummel, Sopio Gverdtsiteli, Tjitske Kleefstra, Annette Schenck, Zeynep Tümer, Alain Verloès, Christiane Zweier

SysNDD is a curated database of gene-disease associations for neurodevelopmental disorders, providing standardized evidence and annotations for 4,275 entities from 4,932 publications.

bioRxiv · Oct 1, 2026 · PreprintGenetics