Browse by Author "Caldés, T."

Now showing items 1-6 of 6

Comprehensive annotation of splice junctions supports pervasive alternative splicing at the BRCA1 locus: a report from the ENIGMA consortium

2014- Colombo, M.; Blok, M. J.; Whiley, P.; Santamariña Pena, Marta; Gutiérrez-Enríquez, S.; [et al.]
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

2019- Figlioli, G.; Bogliolo, M.; Catucci, I.; Caleca, L.; Lasheras, S. V.; [et al.]
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

2019- Ferreira, M. A.; Gamazon, E. R.; Al-Ejeh, F.; Aittomäki, K.; Andrulis, I. L.; [et al.]
Genome-wide association study of germline variants and breast cancer-specific mortality

2019- Escala-Garcia, M.; Guo, Q.; Dörk, T.; Canisius, S.; Keeman, R.; [et al.]
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

2019- Parsons, M. T.; Tudini, E.; Li, H.; Hahnen, E.; Wappenschmidt, B.; [et al.]
Shared heritability and functional enrichment across six solid cancers

2019- Jiang, X.; Finucane, H. K.; Schumacher, F. R.; Schmit, S. L.; Tyrer, J. P.; [et al.]