Markus Perola (Former)
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- 2021
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Mark
Genome-Wide Association Study of Peripheral Artery Disease
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- Contribution to journal › Article
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Mark
The genomics of heart failure : design and rationale of the HERMES consortium
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- Contribution to journal › Article
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Mark
A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study
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- Contribution to journal › Article
- 2020
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Mark
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
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- Contribution to journal › Article
- 2019
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Mark
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium
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- Contribution to journal › Article
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Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
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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
- 2016
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Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
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- Contribution to journal › Article
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Mark
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
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- Contribution to journal › Article
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Mark
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
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- Contribution to journal › Article
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Mark
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
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- Contribution to journal › Article
- 2015
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Mark
Gene×dietary pattern interactions in obesity: analysis of up to 68,317 adults of European ancestry.
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- Contribution to journal › Article
- 2014
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Mark
FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals.
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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.
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- Contribution to journal › Article
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Mark
Chromosome x-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation.
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- Contribution to journal › Article