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Search Results to Tomi Pastinen

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Pastinen, Tomi

Item TypeName
Concept Genetics, Population
Concept Rural Population
Academic Article Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population.
Academic Article Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population.
Academic Article Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.
Academic Article Dissecting a population genome for targeted screening of disease mutations.
Academic Article Folate intake, plasma folate and homocysteine status in a random Finnish population.
Academic Article No evidence for an association between common nonsynonymous polymorphisms in delta and bristle number variation in natural and laboratory populations of Drosophila melanogaster.
Academic Article The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster.
Academic Article Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro.
Academic Article Population genomics in a disease targeted primary cell model.
Academic Article Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.
Academic Article Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits.
Academic Article Introducing the Endotype Concept to Address the Challenge of Disease Heterogeneity in Type 1 Diabetes.
Academic Article Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations.

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