(Q29615822)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

genome-wide association study

30 April 2017

main subject

0 references

1 reference

2

Daly MJ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

author name string

Hirschhorn JN

series ordinal

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

February 2005

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

published in

Nature Reviews Genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

volume

6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

issue

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

30 April 2017

page(s)

95-108

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

Initial sequencing and analysis of the human genome

30 April 2017

cites work

1 reference

The Sequence of the Human Genome

1 May 2017

1 reference

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 May 2017

1 reference

The International HapMap Project

1 May 2017

1 reference

How many diseases does it take to map a gene with SNPs?

1 May 2017

1 reference

Methods for high-density admixture mapping of disease genes

1 May 2017

1 reference

Design and analysis of admixture mapping studies

1 May 2017

1 reference

Are rare variants responsible for susceptibility to complex diseases?

1 May 2017

1 reference

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 May 2017

1 reference

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 May 2017

1 reference

Genetic variation in DLG5 is associated with inflammatory bowel disease

1 May 2017

1 reference

Neuregulin 1 and susceptibility to schizophrenia

1 May 2017

1 reference

Genomewide scans of complex human diseases: true linkage is hard to find

1 May 2017

1 reference

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

1 May 2017

1 reference

Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

1 May 2017

1 reference

Searching for genetic determinants in the new millennium

1 May 2017

1 reference

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 May 2017

1 reference

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

1 May 2017

1 reference

Replication validity of genetic association studies

1 May 2017

1 reference

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 May 2017

1 reference

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

1 May 2017

1 reference

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 May 2017

1 reference

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 May 2017

1 reference

A comprehensive review of genetic association studies

1 May 2017

1 reference

Accessing genetic variation: genotyping single nucleotide polymorphisms

1 May 2017

1 reference

The structure of haplotype blocks in the human genome

1 May 2017

1 reference

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 May 2017

1 reference

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 May 2017

1 reference

Advanced sequencing technologies: methods and goals

1 May 2017

1 reference

Initial sequencing and comparative analysis of the mouse genome

1 May 2017

1 reference

Identification of a Coordinate Regulator of Interleukins 4, 13, and 5 by Cross-Species Sequence Comparisons

1 May 2017

1 reference

Comparative analyses of multi-species sequences from targeted genomic regions

1 May 2017

1 reference

Scanning Human Gene Deserts for Long-Range Enhancers

1 May 2017

1 reference

Statistical significance for genomewide studies

1 May 2017

1 reference

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 May 2017

1 reference

Genomic control for association studies

1 May 2017

1 reference

Assessing the impact of population stratification on genetic association studies

1 May 2017

1 reference

Tests and estimates of allelic association in complex inheritance

1 May 2017

1 reference

Population stratification and spurious allelic association

1 May 2017

1 reference

The effects of human population structure on large genetic association studies

1 May 2017

1 reference

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

1 May 2017

1 reference

A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.

1 May 2017

1 reference

Effects of stratification in the analysis of affected-sib-pair data: benefits and costs

1 May 2017

1 reference

Localization and identification of human quantitative trait loci: king harvest has surely come

1 May 2017

1 reference

Mapping genes that underlie ethnic differences in disease risk: methods for detecting linkage in admixed populations, by conditioning on parental admixture

21 January 2018

1 reference

Linkage analysis of a complex disease through use of admixed populations.

21 January 2018

1 reference

On the allelic spectrum of human disease

21 January 2018

1 reference

Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

21 January 2018

1 reference

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

21 January 2018

1 reference

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

21 January 2018

1 reference

Association study designs for complex diseases

21 January 2018

1 reference

Candidate-gene approaches for studying complex genetic traits: practical considerations

21 January 2018

1 reference

Genome-wide association studies: theoretical and practical concerns

21 January 2018

1 reference

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

21 January 2018

1 reference

Association study of neuregulin 1 gene with schizophrenia.

21 January 2018

1 reference

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease

21 January 2018

1 reference

IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis

21 January 2018

1 reference

The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits

21 January 2018

1 reference

Once and Again—Issues Surrounding Replication in Genetic Association Studies

21 January 2018

1 reference

Mapping complex disease loci in whole-genome association studies

21 January 2018

1 reference

Linkage disequilibrium and the search for complex disease genes

21 January 2018

1 reference

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

1 reference

A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

1 reference

Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations

21 January 2018

1 reference

A dynamic programming algorithm for haplotype block partitioning

21 January 2018

1 reference

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

21 January 2018

1 reference

Efficient selective screening of haplotype tag SNPs

21 January 2018

1 reference

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

21 January 2018

1 reference

Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies

21 January 2018

1 reference

Sequence diversity in 36 candidate genes for cardiovascular disorders

21 January 2018

1 reference

Genomic strategies to identify mammalian regulatory sequences

21 January 2018

1 reference

Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional

21 January 2018

1 reference

Comparative genomics at the vertebrate extremes

21 January 2018

1 reference

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

21 January 2018

1 reference

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

21 January 2018

1 reference

False discoveries and models for gene discovery

21 January 2018

1 reference

Cost-effective analysis of candidate genes using htSNPs: a staged approach

21 January 2018

1 reference

Controlling the false discovery rate in behavior genetics research

21 January 2018

1 reference

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

21 January 2018

1 reference

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

21 January 2018

1 reference

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

21 January 2018

1 reference

DNA Pooling: a tool for large-scale association studies

21 January 2018

1 reference

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

21 January 2018

1 reference

Combined linkage and association sib-pair analysis for quantitative traits

21 January 2018

1 reference

Pedigree tests of transmission disequilibrium

21 January 2018

1 reference

A general test of association for quantitative traits in nuclear families

21 January 2018

1 reference

Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals.

21 January 2018

1 reference

Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals

21 January 2018

1 reference

Association mapping in structured populations

21 January 2018

1 reference

Testing for population subdivision and association in four case-control studies

21 January 2018

1 reference

Informativeness of genetic markers for inference of ancestry.

21 January 2018

1 reference

A discordant-sibship test for disequilibrium and linkage: no need for parental data

21 January 2018

1 reference

Genetic association mapping based on discordant sib pairs: the discordant-alleles test

21 January 2018

1 reference

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

21 January 2018

1 reference

Allele sharing and allelic association I: sib pair tests with increased power

21 January 2018

1 reference

Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test

21 January 2018

1 reference

Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans

21 January 2018

1 reference

Multilocus linkage tests based on affected relative pairs.

21 January 2018

1 reference

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

21 January 2018

1 reference

Mathematical multi-locus approaches to localizing complex human trait genes

21 January 2018

1 reference

Genetic dissection of complex traits with chromosome substitution strains of mice.

21 January 2018

1 reference

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

21 January 2018

1 reference

Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi

21 January 2018

1 reference

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.

21 January 2018

1 reference

CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure

21 January 2018

1 reference

Genetic isolates: separate but equal?

21 January 2018

1 reference

Linkage disequilibrium patterns of the human genome across populations

21 January 2018

1 reference

Extensive linkage disequilibrium in small human populations in Eurasia

21 January 2018

1 reference

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

1 reference

The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

21 January 2018

1 reference

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

21 January 2018

1 reference

21 January 2018

1 reference

Haplotype tagging for the identification of common disease genes

21 January 2018

1 reference

New approaches to gene hunting in IBD.

21 January 2018

1 reference

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

31 March 2020

1 reference

The future of genetic studies of complex human diseases

31 March 2020

1 reference

Population genetics--making sense out of sequence

31 March 2020

1 reference

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

31 March 2020

1 reference

Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region

31 March 2020

1 reference

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

31 March 2020

1 reference

Variation is the spice of life

31 March 2020

1 reference

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

31 March 2020

1 reference

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

31 March 2020

1 reference

A transmission disequilibrium test for quantitative trait loci

31 March 2020

1 reference

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.

31 March 2020

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

31 March 2020

Identifiers

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1022754728

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15716906

PubMed publication ID

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017