A response to "Personalised medicine and population health: breast and ovarian cancer". Read more about A response to "Personalised medicine and population health: breast and ovarian cancer".
Importance of complete phenotyping in prenatal whole exome sequencing. Read more about Importance of complete phenotyping in prenatal whole exome sequencing.
Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Read more about Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases. Read more about Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.
No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population. Read more about No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.
Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Read more about Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus. Read more about Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus.
Genome-wide association study of glioma and meta-analysis. Read more about Genome-wide association study of glioma and meta-analysis.
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma. Read more about Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma.
Sex differences in disease risk from reported genome-wide association study findings. Read more about Sex differences in disease risk from reported genome-wide association study findings.
