Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
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Personal Name(s): | Hassanin, Emadeldin |
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Spier, Isabel / Bobbili, Dheeraj R. / Aldisi, Rana / Klinkhammer, Hannah / David, Friederike / Dueñas, Nuria / Hüneburg, Robert / Perne, Claudia / Brunet, Joan / Capella, Gabriel / Nöthen, Markus M. / Forstner, Andreas J. / Mayr, Andreas / Krawitz, Peter / May, Patrick / Aretz, Stefan (Corresponding author) / Maj, Carlo | |
Contributing Institute: |
Strukturelle und funktionelle Organisation des Gehirns; INM-1 |
Published in: | BMC medical genomics, 16 (2023) 1, S. 42 |
Imprint: |
London
BioMed Central
2023
|
DOI: |
10.34734/FZJ-2024-02034 |
DOI: |
10.1186/s12920-023-01469-z |
Document Type: |
Journal Article |
Research Program: |
Neuroscientific Data Analytics and AI |
Link: |
OpenAccess |
Publikationsportal JuSER |
Please use the identifier: http://dx.doi.org/10.1186/s12920-023-01469-z in citations.
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