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- 2023
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Mark
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases
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- Contribution to journal › Article
- 2022
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Mark
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
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- Contribution to journal › Article
- 2020
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Mark
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
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- Contribution to journal › Article
- 2018
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Mark
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
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- Contribution to journal › Article
- 2017
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Mark
Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing
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- Contribution to journal › Article
- 2016
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Mark
Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
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- 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
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- Contribution to journal › Article
- 2014
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Mark
A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
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- Contribution to journal › Article
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Mark
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
(
- Contribution to journal › Article
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Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
(
- Contribution to journal › Article