( en | de | ru )

 

Disambiguierung von "Goldgar, David"

Autor der Publikation

KopierenLöschenDiese Publikation zur Ablage hinzufügen
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , und . Human molecular genetics, 20 (23): 4732–4747 (2011)

Bitte wählen Sie eine Person um die Publikation zuzuordnen

Um zwischen Personen mit demselben Namen zu unterscheiden, wird der akademische Grad und der Titel einer wichtigen Publikation angezeigt. Zudem lassen sich über den Button neben dem Namen einige der Person bereits zugeordnete Publikationen anzeigen.

Bodo David

Erich David

Ernst David

Baruch Davidoff

Frida David

 

Weitere Publikationen von Autoren mit dem selben Namen

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2, , , , , , , , , und 172 andere Autor(en). Breast cancer research : BCR, 13 (6): R110 (2011)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers, , , , , , , , , und 99 andere Autor(en). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers, , , , , , , , , und 169 andere Autor(en). Human molecular genetics, 20 (16): 3304–3321 (2011)Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), , , , , , , , , und 123 andere Autor(en). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (1): 134–147 (2012)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers, , , , , , , , , und 127 andere Autor(en). Human molecular genetics, 18 (22): 4442–4456 (2009)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers, , , , , , , , , und 171 andere Autor(en). Breast cancer research : BCR, 14 (1): R33 (2012)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers, , , , , , , , , und 176 andere Autor(en). Human mutation, 33 (4): 690–702 (2012)Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction, , , , , , , , , und 168 andere Autor(en). Cancer research, 70 (23): 9742–9754 (2010)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk, , , , , , , , , und 252 andere Autor(en). PLoS genetics, 9 (3): e1003212 (2013)A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity, , , , , , , , , und 5 andere Autor(en). Cancer research, 73 (1): 265–275 (2013)