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- 2016
- Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
- Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
- Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
- Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
- Genetic and environmental influences on height from infancy to early adulthood : an individual-based pooled analysis of 45 twin cohorts
- Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
- ORMDL3 expression levels have no influence on the activity of serine palmitoyltransferase
- No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
- A comparative study of ethylene emanation upon nitrogen deficiency in natural accessions of Arabidopsis thaliana