SNPassoc: an R package to perform whole genome association studies
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North African influences and potential bias in case-control association studies in the Spanish populationMeta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame sizeCX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosisConfirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitisInvestigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal diseaseGenotyping by sequencing approaches to characterise crop genomes: choosing the right tool for the right applicationGenetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritisAssociation of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disordersAssociation of common variants of CYP4A11 and CYP4F2 with stroke in the Han Chinese populationA novel sex-determining QTL in Nile tilapia (Oreochromis niloticus)The expression of VEGF-A is down regulated in peripheral blood mononuclear cells of patients with secondary progressive multiple sclerosisIntegrating Genetic, Neuropsychological and Neuroimaging Data to Model Early-Onset Obsessive Compulsive Disorder SeverityGenomic insights on the ethno-history of the Maya and the ‘Ladinos’ from GuatemalaHow the folding rates of two- and multistate proteins depend on the amino acid properties.Reduced alphabet for protein folding prediction.Genomic data and disease forecasting: application to type 2 diabetes (T2D).Analysis of baseline, average, and longitudinally measured blood pressure data using linear mixed modelsInference of Ancestry in Forensic Analysis II: Analysis of Genetic Data.-Omic and Electronic Health Record Big Data Analytics for Precision Medicine.Inter-population variability of DEFA3 gene absence: correlation with haplotype structure and population variability.Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibilityImpact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant riskPolymorphisms in SLCO1B3 and NR1I2 as genetic determinants of hematotoxicity of carboplatin and paclitaxel combination.Two-stage case-control association study of dopamine-related genes and migraineIdentification of copy number variants defining genomic differences among major human groupsA variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.SNP_tools: A compact tool package for analysis and conversion of genotype data for MS-ExcelNucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism.Exploring epistatic relationships of NO biosynthesis pathway genes in susceptibility to CHD.Traffic-related air pollution, oxidative stress genes, and asthma (ECHRS)Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-studyMAVEN: a tool for visualization and functional analysis of genome-wide association results.FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databasesThe CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease.Genome-wide association studies--data generation, storage, interpretation, and bioinformatics.Neuropeptide S receptor induces neuropeptide expression and associates with intermediate phenotypes of functional gastrointestinal disordersTransforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children.Are genes encoding proteoglycans really associated with the risk of anterior cruciate ligament rupture?Common variants of TLR1 associate with organ dysfunction and sustained pro-inflammatory responses during sepsis.Haplotype-based interaction of the PPARGC1A and UCP1 genes is associated with impaired fasting glucose or type 2 diabetes mellitus.
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SNPassoc: an R package to perform whole genome association studies
description
im Januar 2007 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 31 January 2007
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2007
@uk
name
SNPassoc: an R package to perform whole genome association studies
@en
SNPassoc: an R package to perform whole genome association studies
@nl
type
label
SNPassoc: an R package to perform whole genome association studies
@en
SNPassoc: an R package to perform whole genome association studies
@nl
prefLabel
SNPassoc: an R package to perform whole genome association studies
@en
SNPassoc: an R package to perform whole genome association studies
@nl
P50
P356
P1433
P1476
SNPassoc: an R package to perform whole genome association studies
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P2093
Lluís Armengol
P2860
P304
P356
10.1093/BIOINFORMATICS/BTM025
P407
P50
P577
2007-01-31T00:00:00Z