(Q33904720)

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A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

author name string

Lue Ping Zhao

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Shuying Sue Li

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Najma Khalid

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

0 references

publication date

16 April 2003

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

72

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Europe PubMed Central

PubMed publication ID

29 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1231-1250

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Generating samples under a Wright-Fisher neutral model of genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

The Sequence of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Association mapping in structured populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

A multilocus genotyping assay for candidate markers of cardiovascular disease risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

The future of genetic studies of complex human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

On the application of linear relative risk regression models.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

A deductive method of haplotype analysis in pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Allelic frequency of a p53 polymorphism in human lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

5 July 2018

Risk of breast cancer classified by joint estrogen receptor and progesterone receptor status among women 20-44 years of age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

29 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

29 October 2018

High-resolution haplotype structure in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

29 October 2018

Accessing genetic information with high-density DNA arrays.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

29 October 2018

Cladistic analysis of the apolipoprotein AI-CIII-AIV gene cluster using a healthy French Canadian sample. I. Haploid analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180275

29 October 2018

Population genetics--making sense out of sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/12704570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint linkage disequilibrium mapping with particular reference to the African-American population

1 reference

https://pubmed.ncbi.nlm.nih.gov/12704570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/12704570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

It's raining SNPs, hallelujah?

1 reference

https://pubmed.ncbi.nlm.nih.gov/12704570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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