(Q40415853)

20 September 2017

Trimming, weighting, and grouping SNPs in human case-control association studies (English)

1 reference

20 September 2017

J Hoh

1

1 reference

PMCID

311222

20 September 2017

A Wille

series ordinal

2

1 reference

PMCID

311222

20 September 2017

J Ott

series ordinal

3

1 reference

20 September 2017

1 December 2001

1 reference

20 September 2017

1 reference

20 September 2017

11

1 reference

20 September 2017

2115-2119

1 reference

20 September 2017

12

1 reference

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

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

A confidence-set approach for finding tightly linked genomic regions

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Selecting SNPs in two-stage analysis of disease association data: a model-free approach

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Variance component methods for detecting complex trait loci

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Scan statistics to scan markers for susceptibility genes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

The power of genomic control

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Multilocus linkage tests based on affected relative pairs.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Use of unlinked genetic markers to detect population stratification in association studies.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

A DNA polymorphism discovery resource for research on human genetic variation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

The future of genetic studies of complex human diseases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Statistical methods for linkage analysis of complex traits from high-resolution maps of identity by descent.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Extension of the Haseman-Elston method to multiple alleles and multiple loci: theory and practice for candidate genes.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311222

17 June 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/11731502

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Tightening the clinical trial

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11731502

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1101/GR.204001

1 reference

20 September 2017

1 reference

20 September 2017

1 reference

PMCID

311222