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pro vyhledávání: '"Hillemanns, Peter"'
Autor:
Dicks, Ed, Song, Honglin, Ramus, Susan J., Van Oudenhove, Elke, Tyrer, Jonathan P., Intermaggio, Maria P., Kar, Siddhartha, Harrington, Patricia, Bowtell, David D., Study Group, Aocs, Cicek, Mine S., Cunningham, Julie M., Fridley, Brooke L., Alsop, Jennifer, Jimenez-Linan, Mercedes, Piskorz, Anna, Goranova, Teodora, Kent, Emma, Siddiqui, Nadeem, Paul, James, Crawford, Robin, Poblete, Samantha, Lele, Shashi, Sucheston-Campbell, Lara, Moysich, Kirsten B., Sieh, Weiva, McGuire, Valerie, Lester, Jenny, Odunsi, Kunle, Whittemore, Alice S., Bogdanova, Natalia, Dürst, Matthias, Hillemanns, Peter, Karlan, Beth Y., Gentry-Maharaj, Aleksandra, Menon, Usha, Tischkowitz, Marc, Levine, Douglas, Brenton, James D., Dörk, Thilo, Goode, Ellen L., Gayther, Simon A., Pharoah, Paul D.P.
Publikováno v:
Dicks, E; Song, H; Ramus, SJ; Oudenhove, EV; Tyrer, JP; Intermaggio, MP; et al.(2017). Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene.. Oncotarget, 8(31), 50930-50940. doi: 10.18632/oncotarget.15871. UCLA: Retrieved from: http://www.escholarship.org/uc/item/2n08c81b
Oncotarget, vol 8, iss 31
Oncotarget, vol 5, iss 0
Dicks, E; Song, H; Ramus, SJ; Van Oudenhove, E; Tyrer, JP; Intermaggio, MP; et al.(2017). Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene. ONCOTARGET, 8(31), 50930-50940. doi: 10.18632/oncotarget.15871. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3902d64z
ONCOTARGET
Oncotarget, vol 8, iss 31
Oncotarget, vol 5, iss 0
Dicks, E; Song, H; Ramus, SJ; Van Oudenhove, E; Tyrer, JP; Intermaggio, MP; et al.(2017). Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene. ONCOTARGET, 8(31), 50930-50940. doi: 10.18632/oncotarget.15871. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3902d64z
ONCOTARGET
We analyzed whole exome sequencing data in germline DNA from 412 high grade serous ovarian cancer (HGSOC) cases from The Cancer Genome Atlas Project and identified 5,517 genes harboring a predicted deleterious germline coding mutation in at least one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f6ffdf4889aff1796479ce9d2678d4c
https://www.repository.cam.ac.uk/handle/1810/280221
https://www.repository.cam.ac.uk/handle/1810/280221