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- 2020
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Mark
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
(
- Contribution to journal › Article
- 2018
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Mark
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
(
- Contribution to journal › Article
- 2017
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Mark
Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing
(
- Contribution to journal › Article
- 2016
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Mark
Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
(
- Contribution to journal › Article
- 2015
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Mark
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
(
- Contribution to journal › Article
- 2014
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Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
(
- Contribution to journal › Article
- 2013
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Mark
Common variants associated with plasma triglycerides and risk for coronary artery disease
(
- Contribution to journal › Article
- 2012
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Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
(
- Contribution to journal › Article
- 2011
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Mark
Testing for an Unusual Distribution of Rare Variants
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- Contribution to journal › Article
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Mark
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction
(
- Contribution to journal › Article