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You searched for: Author/Creator Damiola, Francesca

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1. Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants. Issue 11 (31st August 2021)

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. Contribution of ATM and FOXE1 (TTF2) to risk of papillary thyroid carcinoma in Belarusian children exposed to radiation. Issue 7 (15th October 2013)

4. 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)

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

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

7. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Issue 1 (December 2016)

8. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Issue 5 (26th February 2016)