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Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

The American Journal of Human Genetics · 2003 · Vol. 72(5) · pp. 1117–1130
Antonis C. AntoniouPaul D.P. PharoahSteven A. NarodHarvey A. RischJ.E. EyfjördJohn L. HopperNiklas LomanHåkan OlssonOskar T. JohannssonÅke BorgBarbara PasiniPaolo RadiceSiranoush ManoukianDiana EcclesNelson L.S. TangEdith OláhHoda Anton‐CulverEllen WarnerJan LubińskiJacek GronwaldBohdan GórskiHrafn TuliniusSteinunn ThorlaciusHannaleena EerolaHeli NevanlinnaKirsi SyrjäkoskiOlli KallioniemiDeborah J. ThompsonChris EvansJulian PetoFiona LallooD. Gareth EvansDouglas F. Easton
BRCA gene mutations in cancerCancer Genomics and DiagnosticsOvarian cancer diagnosis and treatmentBreast cancerOvarian cancerFamily historyMedicineGermline mutationOncologyCancerContext (archaeology)Relative riskInternal medicine

MeSH terms

AdultAgedBreast NeoplasmsFamilyFemaleGenetic TestingHeterozygoteHumansMaleMiddle AgedMutationOvarian NeoplasmsPedigreeRiskGlobal Health
Citations
3,661
FWCI
63.41
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References
57
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