Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe - Wikidata - awgldk - TriplyDB

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

http://www.wikidata.org/entity/Q27438161

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A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe Swedish population substructure revealed by genome-wide single nucleotide polymorphism data Genetic structure of Europeans: a view from the North-East Genome-wide insights into the patterns and determinants of fine-scale population structure in humans High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis An integrated map of genetic variation from 1,092 human genomes Genetic markers and population history: Finland revisited Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia Genome-wide association study of intracranial aneurysm identifies three new risk loci The Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics Approach Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe Gene flow between the Korean peninsula and its neighboring countries The genome-wide patterns of variation expose significant substructure in a founder population Genome-wide analysis of blood pressure variability and ischemic stroke.NordicDB: a Nordic pool and portal for genome-wide control data.International trends in the incidence of testicular cancer, 1973-2002 Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance Family origin and mortality: prospective Finnish cohort study.Application of genetic/genomic approaches to allergic disorders.Genomic landscape of positive natural selection in Northern European populations.Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies Genetic variation in RNASEL and risk for prostate cancer in a population-based case-control study GIMAP GTPase family genes: potential modifiers in autoimmune diabetes, asthma, and allergy.Worldwide variation in human drug-metabolism enzyme genes CYP2B6 and UGT2B7: implications for HIV/AIDS treatment.Overcoming the dichotomy between open and isolated populations using genomic data from a large European dataset.Anisotropic isolation by distance: the main orientations of human genetic differentiation.Increased Female MS Incidence and Differences in Gender-Specific Risk in Medium- and High-Risk Regions in Finland from 1981-2010.Genomic dissection of population substructure of Han Chinese and its implication in association studies.Genetic variants in association studies--review of strengths and weaknesses in study design and current knowledge of impact on cancer risk.Next-generation sequencing for mitochondrial disorders Infant mortality and ethnicity in an indigenous European population: novel evidence from the Finnish population register.Identification and analysis of mtDNA genomes attributed to Finns reveal long-stagnant demographic trends obscured in the total diversity.Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.Discrepancy in prevalence of Huntington's disease in two Swedish regions.Familial risk of non-Hodgkin lymphoma by sex, relationship, age at diagnosis and histology: a joint study from five Nordic countries.Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.Fine-Scale Genetic Structure in Finland Assessment of Population Structure and Its Effects on Genome-Wide Association Studies.Post-mortem ABCB1 genotyping reveals an elevated toxicity for female digoxin users.

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Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

http://www.wikidata.org/entity/Q27438161

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P2860

European population substructure: clustering of northern and southern populations

Isolated populations and complex disease gene identification

Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs

The effects of human population structure on large genetic association studies

Assessing the impact of population stratification on genetic association studies

Dual origins of Finns revealed by Y chromosome haplotype variation

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Genes mirror geography within Europe

A second generation human haplotype map of over 3.1 million SNPs

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA

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