SNP-based analysis of genetic substructure in the German population. - Wikidata - wikimedia - TriplyDB

SNP-based analysis of genetic substructure in the German population.

SNP-based analysis of genetic substructure in the German population.

http://www.wikidata.org/entity/Q45965746

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Systematic association mapping identifies NELL1 as a novel IBD disease gene Swedish population substructure revealed by genome-wide single nucleotide polymorphism data Genetic structure of Europeans: a view from the North-East Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis Discovery of sexual dimorphisms in metabolic and genetic biomarkers Association of FOXO3A variation with human longevity confirmed in German centenarians A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error Genome-wide association study of alcohol dependence Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor Genetic population structure analysis in New Hampshire reveals Eastern European ancestry SNPs and Hox gene mapping in Ciona intestinalis.Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years.Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 (MDM2) gene Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.Mutations in genes involved in nonsense mediated decay ameliorate the phenotype of sel-12 mutants with amber stop mutations in Caenorhabditis elegans NMR based metabonomics study on celiac disease in the blood serum.Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays Identifying modifier genes of monogenic disease: strategies and difficulties.Designing candidate gene and genome-wide case-control association studies.The genetic variation in monocarboxylic acid transporter 2 (MCT2) has functional and clinical relevance with male infertility Tobacco smoking leads to extensive genome-wide changes in DNA methylation.Genes and lifestyle factors in obesity: results from 12,462 subjects from MONICA/KORA.First investigation of two obesity-related loci (TMEM18, FTO) concerning their association with educational level as well as income: the MONICA/KORA study Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study.Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study Characterization of whole-genome autosomal differences of DNA methylation between men and women On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients.Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study.Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation The more the merrier? How a few SNPs predict pigmentation phenotypes in the Northern German population HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy.Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy.A genomewide comparison of population structure at STRPs and nearby SNPs in humans.Investigation of complement component C4 copy number variation in human longevity.

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P2860

SNP-based analysis of genetic substructure in the German population.

http://www.wikidata.org/entity/Q45965746

description

2006 nî lūn-bûn

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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2006年學術文章

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2006年學術文章

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name

SNP-based analysis of genetic substructure in the German population.

@en

SNP-based analysis of genetic substructure in the German population.

@nl

type

label

SNP-based analysis of genetic substructure in the German population.

@en

SNP-based analysis of genetic substructure in the German population.

@nl

prefLabel

SNP-based analysis of genetic substructure in the German population.

@en

SNP-based analysis of genetic substructure in the German population.

@nl

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SNP-based analysis of genetic substructure in the German population.

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Amalia Diaz Lacava

http://www.w3.org/2001/XMLSchema#string

Amke Caliebe

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Andreas Wolf

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Claudia Lamina

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Eun-Kyung Suk

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H-Erich Wichmann

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Jan Ludemann

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Karola Köhler

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Max P Baur

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Mohammad Reza Toliat

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P2860

The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data.

The effects of human population structure on large genetic association studies

Assessing the impact of population stratification on genetic association studies

Human population genetic structure and inference of group membership

An apportionment of human DNA diversity

Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms

Genomic control for association studies

The power of genomic control

Use of unlinked genetic markers to detect population stratification in association studies.

Unbiased methods for population-based association studies.

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20-29

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10.1159/000095850

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1

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62

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Thomas Meitinger

Andreas Ziegler

Michael Steffens

Michael Krawczak

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2006-09-21T00:00:00Z

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17003564

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