Pages that link to "Q36924486"
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The following pages link to Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO). (Q36924486):
Displaying 13 items.
- Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation. (Q31159863) (← links)
- Reproductive risk factors and breast cancer subtypes: a review of the literature (Q33632008) (← links)
- Modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: systematic review and meta-analysis (Q33845209) (← links)
- Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population (Q35163365) (← links)
- The impact of reproductive life on breast cancer risk in women with family history or BRCA mutation (Q37705926) (← links)
- Impact of BRCA1/2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort). (Q39065794) (← links)
- Young age at first pregnancy does protect against early onset breast cancer in BRCA1 and BRCA2 mutation carriers. (Q47586232) (← links)
- Genetic testing in women with breast cancer: implications for treatment (Q47884776) (← links)
- GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in and Pathogenic Variant Carriers (Q59138109) (← links)
- Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population (Q60912589) (← links)
- Diagnostic mRNA splicing assay for variants in and identified two novel pathogenic splicing aberrations (Q64279762) (← links)
- Study on mouse model of triple-negative breast cancer: association between higher parity and triple-negative breast cancer (Q87950010) (← links)
- Non-BRCA1/2 Variants Detected in a High-Risk Chilean Cohort With a History of Breast and/or Ovarian Cancer (Q92269326) (← links)