Brain and Spine (Jan 2022)
Population-based whole-genome sequencing with constrained gene analysis identifies predisposing germline variants in children with central nervous system tumors
- J. Foss-Skiftesvik,
- U. Stoltze,
- T. van Overeem Hansen,
- A. Byrjalsen,
- A. Sehested,
- D. Scheie,
- T. Stamm Mikkelsen,
- S. Rasmussen,
- M. Bak,
- H. Okkels,
- M.T. Callesen,
- J. Skjøth-Rasmussen,
- A.-M. Gerdes,
- K. Schmiegelow,
- R. Mathiasen,
- K. Wadt
Affiliations
- J. Foss-Skiftesvik
- Rigshospitalet University Hospital, Department of Neurosurgery, Copenhagen, Denmark
- U. Stoltze
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- T. van Overeem Hansen
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- A. Byrjalsen
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- A. Sehested
- Rigshospitalet University Hospital, Dept. of Adolescent and Pediatric Medicine, Copenhagen, Denmark
- D. Scheie
- Rigshospitalet University Hospital, Dept. of Neuro-Pathology, Copenhagen, Denmark
- T. Stamm Mikkelsen
- Aarhus University Hospital, Dept. of Adolescent and Pediatric Medicine, Aarhus, Denmark
- S. Rasmussen
- Copenhagen University, Novo Nordisk Foundation Center for Protein Research, Copenhagen, Denmark
- M. Bak
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- H. Okkels
- Aalborg University Hospital, Dept. of Molecular Diagnostics, Aalborg, Denmark
- M.T. Callesen
- Odense University Hospital, Dept. of Adolescent and Pediatric Medicine, Odense, Denmark
- J. Skjøth-Rasmussen
- Rigshospitalet University Hospital, Dept. of Neurosurgery, Copenhagen, Denmark
- A.-M. Gerdes
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- K. Schmiegelow
- Rigshospitalet University Hospital, Dept. of Adolescent and Pediatric Medicine, Copenhagen, Denmark
- R. Mathiasen
- Rigshospitalet University Hospital, Dept. of Adolescent and Pediatric Medicine, Copenhagen, Denmark
- K. Wadt
- Rigshospitalet University Hospital, Dept. of Medical Genetics, Copenhagen, Denmark
- Journal volume & issue
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Vol. 2
p. 101279