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3. Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma

6. A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1

12. Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk

22. The C/C_ 13910 mismatch repairgenotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population

23. Exon 3 betacatenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome

29. Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neck

37. STK11 status and intussusception risk in Peutz-Jeghers syndrome

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