(Q35946571)

11 August 2017

Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families (English)

1 reference

11 August 2017

2

David M Umbach

1 reference

11 August 2017

3

Clarice R Weinberg

1 reference

11 August 2017

Min Shi

1

1 reference

11 August 2017

language of work or name

English

0 references

publication date

15 May 2007

1 reference

American Journal of Human Genetics

11 August 2017

1 reference

11 August 2017

81

1 reference

11 August 2017

1

1 reference

11 August 2017

53-66

1 reference

Inference on haplotype/disease association using parent-affected-child data: the projection conditional on parental haplotypes method

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

High resolution T association tests of complex diseases based on family data

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Evaluating associations of haplotypes with traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Testing for candidate gene linkage disequilibrium using a dense array of single nucleotide polymorphisms in case-parents studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Genotype relative risks: methods for design and analysis of candidate-gene association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

A powerful strategy to account for multiple testing in the context of haplotype analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Implementing a unified approach to family-based tests of association.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

The APL test: extension to general nuclear families and haplotypes and examination of its robustness

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Invited commentary: making the most of genotype asymmetries.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Analysis of single-locus tests to detect gene/disease associations

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950926

Genetic association studies of adult-onset diseases using the case-spouse and case-offspring designs

14 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17564963

12 December 2020

inferred from PubMed ID database lookup

Distinguishing the Effects of Maternal and Offspring Genes through Studies of "Case-Parent Triads"

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17564963

12 December 2020

inferred from PubMed ID database lookup

Circumventing multiple testing: a multilocus Monte Carlo approach to testing for association

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17564963

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/518670

1 reference

release_6w4zta5yd5a6vnlb7i22a5xcvi

11 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6w4zta5yd5a6vnlb7i22a5xcvi

24 November 2022

mapped directly with Wikidata item

1 reference

11 August 2017

PubMed publication ID

17564963

1 reference