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- 2017
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Mark
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
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- Contribution to journal › Article
- 2016
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Mark
Evidence of Inbreeding in Hodgkin Lymphoma
(
- Contribution to journal › Article
- 2015
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Mark
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
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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.
(
- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
- 2014
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Mark
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
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- Contribution to journal › Article
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Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
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- Contribution to journal › Article
- 2013
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Mark
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma
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- Contribution to journal › Article
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Mark
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
(
- Contribution to journal › Article
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article