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PLINK: a tool set for whole-genome association and population-based linkage analyses

PLINK: a tool set for whole-genome association and population-based linkage analyses

http://www.wikidata.org/entity/Q24677407

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Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture OTX2 duplication is implicated in hemifacial microsomia A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs.Swedish population substructure revealed by genome-wide single nucleotide polymorphism data Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee Web-based, participant-driven studies yield novel genetic associations for common traits High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size A flexible and accurate genotype imputation method for the next generation of genome-wide association studies Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers Genomics assisted ancestry deconvolution in grape Afghan Hindu Kush: where Eurasian sub-continent gene flows converge Fast association tests for genes with FAST Non-cholesterol sterol levels predict hyperglycemia and conversion to type 2 diabetes in Finnish men Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease Heterogeneity in genetic admixture across different regions of Argentina Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study The genetic structure of the Swedish population Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data Data integration workflow for search of disease driving genes and genetic variants Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey A conserved role for syndecan family members in the regulation of whole-body energy metabolism A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies Genetic structure of Europeans: a view from the North-East Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs Early back-to-Africa migration into the Horn of Africa Relationship estimation from whole-genome sequence data Genome-wide diversity in the levant reveals recent structuring by culture Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

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PLINK: a tool set for whole-genome association and population-based linkage analyses

http://www.wikidata.org/entity/Q24677407

description

2007 nî lūn-bûn

@nan

2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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American Journal of Human Genetics

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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Benjamin Neale

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David Bender

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Kathe Todd-Brown

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Lori Thomas

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Manuel A R Ferreira

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Pak C Sham

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Pamela Sklar

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Paul I W de Bakker

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A comprehensive review of genetic association studies

Are rare variants responsible for susceptibility to complex diseases?

Assessing the impact of population stratification on genetic association studies

A note on exact tests of Hardy-Weinberg equilibrium

Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

Inference of population structure using multilocus genotype data

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

The transmission/disequilibrium test: history, subdivision, and admixture

Haploview: analysis and visualization of LD and haplotype maps

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10.1086/519795

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Mark Joseph Daly

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6137675

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17701901

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1950838

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