about
Promise of personalized omics to precision medicineInsights into the genetic basis of type 2 diabetesPeriodontal disease immunology: 'double indemnity' in protecting the hostA comparison of genomic profiles of complex diseases under different models.Epidemiology of environmental exposures and human autoimmune diseases: findings from a National Institute of Environmental Health Sciences Expert Panel WorkshopRegularized Machine Learning in the Genetic Prediction of Complex TraitsFinding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data.The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort.Incorporation of personal single nucleotide polymorphism (SNP) data into a national level electronic health record for disease risk assessment, part 1: an overview of requirements.Predicting disease risk using bootstrap ranking and classification algorithms.Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study.Familial Risk and Heritability of Cancer Among Twins in Nordic Countries.Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--MultiBLUP: improved SNP-based prediction for complex traits.Genomics and perinatal carePooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population.Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X.Commentary on a GWAS: HDAC9 and the risk for ischaemic stroke.Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.Common low-penetrance risk variants associated with breast cancer in Polish women.Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruptionA weighted genetic risk score using all known susceptibility variants to estimate rheumatoid arthritis risk.Jumping on the Train of Personalized Medicine: A Primer for Non- Geneticist Clinicians: Part 3. Clinical Applications in the Personalized Medicine Area.Metagenomic predictions: from microbiome to complex health and environmental phenotypes in humans and cattleUsing genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments.A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.Resolving the variable genome and epigenome in human disease.Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease.Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome.Sparse Modeling Reveals miRNA Signatures for Diagnostics of Inflammatory Bowel Disease.Improving accuracy of genomic prediction by genetic architecture based priors in a Bayesian modelContemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach.A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.Sibling method increases risk assessment estimates for type 1 diabetes.Assessing Heavy Metal and PCB Exposure from Tap Water by Measuring Levels in Plasma from Sporadic Breast Cancer Patients, a Pilot Study.Personalized medicine and access to health care: potential for inequitable access?Multi-locus genetic risk score predicts risk for Crohn's disease in Slovenian populationAnnotation of genes having candidate somatic mutations in acute myeloid leukemia with whole-exome sequencing using concept lattice analysis.Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence.Interpreting noncoding genetic variation in complex traits and human disease.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
name
Genetic risk prediction in complex disease
@ast
Genetic risk prediction in complex disease
@en
Genetic risk prediction in complex disease
@nl
type
label
Genetic risk prediction in complex disease
@ast
Genetic risk prediction in complex disease
@en
Genetic risk prediction in complex disease
@nl
prefLabel
Genetic risk prediction in complex disease
@ast
Genetic risk prediction in complex disease
@en
Genetic risk prediction in complex disease
@nl
P2860
P356
P1476
Genetic risk prediction in complex disease
@en
P2093
Luke Jostins
P2860
P304
P356
10.1093/HMG/DDR378
P407
P577
2011-08-25T00:00:00Z