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Human complex trait genetics: lifting the lid of the genomics toolbox - from pathways to prediction.
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Europe PubMed Central
PMC publication ID
3382276
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
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16 February 2020
title
Human complex trait genetics: lifting the lid of the genomics toolbox - from pathways to prediction
(English)
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stated in
Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
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16 February 2020
main subject
genomics
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complex trait
1 reference
based on heuristic
inferred from title
author
Suzanne J Rowe
series ordinal
1
1 reference
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Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 February 2020
author name string
Albert Tenesa
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2
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Europe PubMed Central
PMC publication ID
3382276
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16 February 2020
publication date
1 May 2012
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3382276
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16 February 2020
published in
Current Genomics
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3382276
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
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16 February 2020
volume
13
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Europe PubMed Central
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3382276
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16 February 2020
issue
3
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Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 February 2020
page(s)
213-224
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3382276
reference URL
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16 February 2020
cites work
Genome partitioning of genetic variation for complex traits using common SNPs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
SNP-based pathway enrichment analysis for genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genomic inflation factors under polygenic inheritance
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Initial impact of the sequencing of the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Synthetic associations created by rare variants do not explain most GWAS results
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Pathway-based analysis of GWAS datasets: effective but caution required
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Progress and promise of genome-wide association studies for human complex trait genetics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Rare variant association analysis methods for complex traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Predicting genetic predisposition in humans: the promise of whole-genome markers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Statistical methods for pathway analysis of genome-wide data for association with complex genetic traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
A map of human genome variation from population-scale sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
New copy number variations in schizophrenia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starch
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Hundreds of variants clustered in genomic loci and biological pathways affect human height
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Integrating common and rare genetic variation in diverse human populations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genotype imputation for genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Clinical assessment incorporating a personal genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Architecture of inherited susceptibility to common cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Integrating pathway analysis and genetics of gene expression for genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Accurate prediction of genetic values for complex traits by whole-genome resequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Performance of common genetic variants in breast-cancer risk models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
The genetic interpretation of area under the ROC curve in genomic profiling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genome-scale approaches to the epigenetics of common human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Finding the missing heritability of complex diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genotype imputation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Additive genetic variability and the Bayesian alphabet
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
New insights into the aetiology of colorectal cancer from genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Epigenetic inheritance and the missing heritability problem
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genotype score in addition to common risk factors for prediction of type 2 diabetes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Personal genomes: The case of the missing heritability
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Accuracy of predicting the genetic risk of disease using a genome-wide approach
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Extending genome-wide association studies to copy-number variation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Molecular signatures of cardiovascular disease risk: potential for test development and clinical application
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Pathway analysis of seven common diseases assessed by genome-wide association
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Prediction of individual genetic risk of complex disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Common and rare variants in multifactorial susceptibility to common diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Data and theory point to mainly additive genetic variance for complex traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Genetics of gene expression and its effect on disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Heritability in the genomics era — concepts and misconceptions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Pathway-based approaches for analysis of genomewide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Population genomics of human gene expression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Imputation-based analysis of association studies: candidate regions and quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Generalized genomic distance-based regression methodology for multilocus association analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Principal components analysis corrects for stratification in genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Mapping quantitative trait loci using linkage disequilibrium: marker- versus trait-based methods
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
The allelic architecture of human disease genes: common disease-common variant... or not?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
On the allelic spectrum of human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Are rare variants responsible for susceptibility to complex diseases?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Prediction of total genetic value using genome-wide dense marker maps
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Transmission-disequilibrium tests for quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
The TDT and other family-based tests for linkage disequilibrium and association
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
The future of genetic studies of complex human diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
2 October 2017
Multiple regions within 8q24 independently affect risk for prostate cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
11 July 2018
Bioinformatics for next generation sequencing.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
23 September 2018
Understanding human diversity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3382276
retrieved
5 December 2018
Evaluating diagnostic tests: The area under the ROC curve and the balance of errors
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23115523
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genomic selection: marker assisted selection on a genome wide scale
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23115523
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genomewide association studies--illuminating biologic pathways
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23115523
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The investigation of linkage between a quantitative trait and a marker locus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23115523
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Power of Linkage Disequilibrium Mapping to Detect a Quantitative Trait Locus (QTL) in Selected Samples of Unrelated Individuals
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23115523
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.2174/138920212800543101
1 reference
stated in
Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 February 2020
PMC publication ID
3382276
1 reference
stated in
Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 February 2020
PubMed publication ID
23115523
1 reference
stated in
Europe PubMed Central
PMC publication ID
3382276
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23115523%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 February 2020
ResearchGate publication ID
232746075
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