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PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 7, p. e1004494
Exome sequencing studies in complex diseases are challenged by the allelic heterogeneity, large number and modest effect sizes of associated variants on... 
PROFILE | GENE | MUTATION | DISEASE | GENETICS & HEREDITY | LEVEL | ASSOCIATION | CARDIOVASCULAR RISK | Physiological aspects | Genetic research | Genome-wide association studies | Research | Lipoprotein A | Heart attacks | Disease | Genomics | Genes | Biomarkers | Medical records | Population | Grants
Journal Article
ISSN 1553-7390, 2014
Author Summary We explored the coding regions of 3,000 Finnish individuals with 3,000 non-Finnish Europeans (NFEs) using whole-exome sequence data, in order to... 
Genetics, Population | Genetic Drift | Genome-Wide Association Study | Humans | Gene Frequency | Genetic Diseases, Inborn | European Continental Ancestry Group | Male | Genetic Variation | Exome | Founder Effect | Phenotype | Finland | Female | Sequencing Initiative Suomi (SISu) Project
Journal Article
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