The use of inferred haplotypes in downstream analyses.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

24 citing papers in PubMed.

1. Association of CCL5 rs2107538, and CCL2 rs3760396 Gene Polymorphisms with the Risk of Cardiovascular Disease.Iranian journal of public health · 2021
   Article
2. Genome-wide haplotype association analysis of primary biliary cholangitis risk in Japanese.Scientific reports · 2018
   Article
3. Critical Issues in the Inclusion of Genetic and Epigenetic Information in Prevention and Intervention Trials.Prevention science : the official journal of the Society for Prevention Research · 2018
   Article
4. Comparison of haplotype-based statistical tests for disease association with rare and common variants.Briefings in bioinformatics · 2016
   Article
5. A penalized likelihood approach for investigating gene-drug interactions in pharmacogenetic studies.Biometrics · 2015
   Article
6. Genome-wide estimation of linkage disequilibrium from population-level high-throughput sequencing data.Genetics · 2014
   Article
7. Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Genetic epidemiology · 2013
   Article
8. A genome-wide scan for breast cancer risk haplotypes among African American women.PloS one · 2013
   Article
9. Gene genealogies for genetic association mapping, with application to Crohn's disease.Frontiers in genetics · 2013
   Article
10. Haplotype-based methods for detecting uncommon causal variants with common SNPs.Genetic epidemiology · 2012
    Article
11. Dynamic modeling of genes controlling cancer stem cell proliferation.Frontiers in genetics · 2012
    Article
12. The use of imputed values in the meta-analysis of genome-wide association studies.Genetic epidemiology · 2011
    Article
13. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee.PLoS genetics · 2011
    Article
14. A Monte Carlo test of linkage disequilibrium for single nucleotide polymorphisms.BMC research notes · 2011
    Article
15. Meta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literature.BMC genetics · 2011
    Article
16. Evidence for more than one Parkinson's disease-associated variant within the HLA region.PloS one · 2011
    Article
17. Association between CST3 rs2424577 polymorphism and corpulence related phenotypes during lifetime in populations of European ancestry.Obesity facts · 2011
    Article
18. Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?Genetic epidemiology · 2010
    Article
19. A general framework for studying genetic effects and gene-environment interactions with missing data.Biostatistics (Oxford, England) · 2010
    Article
20. Improved IBD detection using incomplete haplotype information.BMC genetics · 2010
    Article

Corrections and comments

• Commented on by
  Re: the use of inferred haplotypes in downstream analysis.2007
• Comment on
  A comparison of phasing algorithms for trios and unrelated individuals.2006

Authors and funding

2 authors.

Funding

Abstract

PubMed holds no abstract for this paper.

Indexed as