Kari Hemminki
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- 2015
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Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
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- Contribution to journal › Article
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Mark
Frequent DPH3 promoter mutations in skin cancers.
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- Contribution to journal › Article
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Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
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- Contribution to journal › Article
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Mark
TERT promoter mutations and telomere length in adult malignant gliomas and recurrences.
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- Contribution to journal › Article
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Mark
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
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- Contribution to journal › Article
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Mark
Population Landscape of Familial Cancer.
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- Contribution to journal › Article
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Mark
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
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- Contribution to journal › Article
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Mark
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A.
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- Contribution to journal › Article
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Mark
Joint occurrence of Merkel cell carcinoma and non-Hodgkin lymphomas in four Nordic countries
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- Contribution to journal › Article
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Mark
Cancer risk in patients with type 2 diabetes mellitus and their relatives.
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- Contribution to journal › Article