14 results on '"Ovarian cancer -- Research -- Genetic aspects -- Risk factors"'
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2. Researcher at Fudan University Shanghai Cancer Center Has Published New Study Findings on Ovarian Cancer (Risk-reducing salpingo-oophorectomy for hereditary ovarian cancer)
3. The origins of ovarian cancer
4. Rare gene mutations ‘increase cancer risk’; Researchers in the city identify the two new types in a study involving 4,900 breast and ovarian tumour patients and their family members
5. Findings from Charite University Hospital and School of Medicine Yields New Data on Ovarian Cancer (Interdisciplinary Risk Counseling for Hereditary Breast and Ovarian Cancer: Real-world Data From a Specialized Center)
6. Radboud University Nijmegen Reports Findings in Atherosclerosis (No Signs of Subclinical Atherosclerosis After Risk-reducing Salpingo-oophorectomy In Brca1/2 Mutation Carriers)
7. Ovarian cancer and the microbiome: a complex relationship
8. Shengjing Hospital of China Medical University Researcher Broadens Understanding of Ovarian Cancer (Strong Cumulative Evidence of Associations of 6 Single Nucleotide Polymorphisms with Ovarian Cancer Risk: An Umbrella Review)
9. Women with genes for endometriosis have higher risk of ovarian cancer; Researchers find odds of having ovarian cancer up to 2.6 times higher for women carrying genetic risk factors for endometriosis
10. University of Campania 'Luigi Vanvitelli' Researchers Describe Findings in Ovarian Cancer (Increased Risk of Hereditary Prostate Cancer in Italian Families with Hereditary Breast and Ovarian Cancer Syndrome Harboring Mutations in * * BRCA* *
11. New Ovarian Cancer Research from University of Basel Described (The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband-Provider and Proband-Family Communication in Hereditary Breast and Ovarian Cancer)
12. Study shows how genetic mutation puts women at risk for ovarian cancer
13. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
14. High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series
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