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You searched for: Author/Creator Bonadona, Valérie

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1. A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screening. Issue 2 (16th December 2013)

2. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015)

3. Anti-müllerian hormone levels and antral follicle count in women with a BRCA1 or BRCA2 germline pathogenic variant: A retrospective cohort study. (October 2021)

4. Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease. (January 2023)

5. Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing. Issue 8 (13th November 2018)

6. First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants. Issue 12 (29th August 2022)

7. GENESIS: a French national resource to study the missing heritability of breast cancer. Issue 1 (December 2016)

8. Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility. Issue 8 (9th January 2021)

9. Mutational spectrum in a worldwide study of 29, 700 families with BRCA1 or BRCA2 mutations. Issue 5 (12th March 2018)

10. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study. Issue 7 (July 2021)