Association of rare haplotypes on

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

11 citing papers in PubMed, 14 citations in OpenAlex.

1. Genetic architecture of cardiac dynamic flow volumes.Nature genetics · 2024
   Article
2. Bivariate quantitative Bayesian LASSO for detecting association of rare haplotypes with two correlated continuous phenotypes.Frontiers in genetics · 2023
   Article
3. Whole-Genome Sequencing of 100 Genomes Identifies a Distinctive Genetic Susceptibility Profile of Qatari Patients with Hypertension.Journal of personalized medicine · 2022
   Article
4. Comparison of haplotype-based tests for detecting gene-environment interactions with rare variants.Briefings in bioinformatics · 2020
   Review
5. Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes.Genetic epidemiology · 2019
   Article
6. Advances in the Genetics of Hypertension: The Effect of Rare Variants.International journal of molecular sciences · 2018
   Review
7. A Family-Based Rare Haplotype Association Method for Quantitative Traits.Human heredity · 2018
   Article
8. Logistic Bayesian LASSO for genetic association analysis of data from complex sampling designs.Journal of human genetics · 2017
   Article
9. Detecting rare and common haplotype-environment interaction under uncertainty of gene-environment independence assumption.Biometrics · 2017
   Article
10. Comparison of haplotype-based statistical tests for disease association with rare and common variants.Briefings in bioinformatics · 2016
    Article
11. Above and beyond state-of-the-art approaches to investigate sequence data: summary of methods and results from the population-based association group at the Genetic Analysis Workshop 19.BMC genetics · 2016
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

4 authors at 1 institution in 1 country.

Funding

Abstract