A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents. (Q28768577)

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

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15162128 AND SRC:MED&resulttype=core&format=json

28 December 2019

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

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15162128 AND SRC:MED&resulttype=core&format=json

28 December 2019

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Anne M. Bowcock

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28 December 2019

Shailendra B. Patel

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28 December 2019

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Derek Gordon

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28 December 2019

Chad Haynes

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28 December 2019

Christopher Johnnidis

3

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28 December 2019

Jürg Ott

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28 December 2019

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1 September 2004

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28 December 2019

European Journal of Human Genetics

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28 December 2019

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28 December 2019

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28 December 2019

752-761

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28 December 2019

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

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Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively

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Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities

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Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption

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16 March 2017

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

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16 March 2017

The TDT and other family-based tests for linkage disequilibrium and association

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16 March 2017

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

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7 April 2017

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

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7 April 2017

AN INVESTIGATION OF THE EFFECT OF MISCLASSIFICATION ON THE PROPERTIES OF CHI-2-TESTS IN THE ANALYSIS OF CATEGORICAL DATA.

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3 June 2018

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

1 reference

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3 June 2018

Sitosterolemia.

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3 June 2018

Detection and integration of genotyping errors in statistical genetics

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3 June 2018

Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

A general test of association for quantitative traits in nuclear families

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

Allowing for missing parents in genetic studies of case-parent triads

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

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3 June 2018

Tests for linkage and association in nuclear families

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

A note on the application of the transmission disequilibrium test when a parent is missing.

1 reference

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3 June 2018

A General Model for the Genetic Analysis of Pedigree Data

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1356564

3 June 2018

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

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3 June 2018

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

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https://api.crossref.org/works/10.1038/SJ.EJHG.5201219

21 January 2018

Bayesian trio models for association in the presence of genotyping errors.

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https://api.crossref.org/works/10.1038/SJ.EJHG.5201219

21 January 2018

Testing for association with a case-parents design in the presence of genotyping errors

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https://api.crossref.org/works/10.1038/SJ.EJHG.5201219

21 January 2018

Pedigree tests of transmission disequilibrium

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https://api.crossref.org/works/10.1038/SJ.EJHG.5201219

21 January 2018

Transmission/disequilibrium test when neither parent is available in some families: a non-iterative approach.

1 reference

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27 November 2018

Computer programs for multilocus haplotyping of general pedigrees.

1 reference

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27 November 2018

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15162128

12 December 2020

based on heuristic

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Statistical properties of the haplotype relative risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/15162128

12 December 2020

based on heuristic

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Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15162128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confidence Limits for an Unknown Distribution Function

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201219

7 January 2021

based on heuristic

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10.1038/SJ.EJHG.5201219

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28 December 2019

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28 December 2019

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28 December 2019

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