Genetic links between ovarian ageing, cancer risk and de novo mutation rates
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Genetic links between ovarian ageing, cancer risk and de novo mutation rates ; volume:633 ; number:8030 ; day:11 ; month:9 ; year:2024 ; pages:608-614 ; date:9.2024
Nature; 633, Heft 8030 (11.9.2024), 608-614, 9.2024
- Urheber
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Stankovic, Stasa
Shekari, Saleh
Huang, Qin Qin
Gardner, Eugene J.
Ivarsdottir, Erna V.
Owens, Nick D. L.
Mavaddat, Nasim
Azad, Ajuna
Hawkes, Gareth
Kentistou, Katherine A.
Beaumont, Robin N.
Day, Felix R.
Zhao, Yajie
Jonsson, Hakon
Rafnar, Thorunn
Tragante, Vinicius
Sveinbjornsson, Gardar
Oddsson, Asmundur
Styrkarsdottir, Unnur
Gudmundsson, Julius
Stacey, Simon N.
Gudbjartsson, Daniel F.
Kennedy, Kitale
Wood, Andrew R.
Weedon, Michael N.
Ong, Ken K.
Wright, Caroline F.
Hoffmann, Eva R.
Sulem, Patrick
Hurles, Matthew E.
Ruth, Katherine S.
Martin, Hilary C.
Stefansson, Kari
Perry, John R. B.
Murray, Anna
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41586-024-07931-x
- URN
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urn:nbn:de:101:1-2501252123557.676148087466
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:35 MESZ
Datenpartner
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Beteiligte
- Stankovic, Stasa
- Shekari, Saleh
- Huang, Qin Qin
- Gardner, Eugene J.
- Ivarsdottir, Erna V.
- Owens, Nick D. L.
- Mavaddat, Nasim
- Azad, Ajuna
- Hawkes, Gareth
- Kentistou, Katherine A.
- Beaumont, Robin N.
- Day, Felix R.
- Zhao, Yajie
- Jonsson, Hakon
- Rafnar, Thorunn
- Tragante, Vinicius
- Sveinbjornsson, Gardar
- Oddsson, Asmundur
- Styrkarsdottir, Unnur
- Gudmundsson, Julius
- Stacey, Simon N.
- Gudbjartsson, Daniel F.
- Kennedy, Kitale
- Wood, Andrew R.
- Weedon, Michael N.
- Ong, Ken K.
- Wright, Caroline F.
- Hoffmann, Eva R.
- Sulem, Patrick
- Hurles, Matthew E.
- Ruth, Katherine S.
- Martin, Hilary C.
- Stefansson, Kari
- Perry, John R. B.
- Murray, Anna
- SpringerLink (Online service)
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FMCGP: frameshift mutation cartesian genetic programming
CHEK2 1100delC mutation in Russian ovarian cancer patients
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
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CHEK2 1100delC mutation in Russian ovarian cancer patients
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