To a future of genetic medicine.

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

37 citing papers in PubMed.

1. In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in HumanGenes · 2022
   Article
2. Glucocorticoid Receptor Polymorphisms in Children Undergoing Congenital Heart Surgery with Cardiopulmonary Bypass.Journal of pediatric intensive care · 2020
   Article
3. An application of competitive reporter monitored amplification (CMA) for rapid detection of single nucleotide polymorphisms (SNPs).PloS one · 2017
   Article
4. Multivariate models from RNA-Seq SNVs yield candidate molecular targets for biomarker discovery: SNV-DA.BMC genomics · 2016
   Article
5. DBDiaSNP: An Open-Source Knowledgebase of Genetic Polymorphisms and Resistance Genes Related to Diarrheal Pathogens.Omics : a journal of integrative biology · 2015
   Article
6. Functional and Structural Consequences of Damaging Single Nucleotide Polymorphisms in Human Prostate Cancer Predisposition Gene RNASEL.BioMed research international · 2015
   Article
7. Single nucleotide variations: biological impact and theoretical interpretation.Protein science : a publication of the Protein Society · 2014
   Review
8. Amplified single base-pair mismatch detection via aggregation of exonuclease-sheared gold nanoparticles.Analytical chemistry · 2014
   Article
9. Distilling pathophysiology from complex disease genetics.Cell · 2013
   Article
10. The epilepsy phenome/genome project.Clinical trials (London, England) · 2013
    Article
11. Chapter 15: disease gene prioritization.PLoS computational biology · 2013
    Article
12. Is type I alpha 2 collagen gene responsible for intracranial aneurysm in Northeast China?Neural regeneration research · 2013
    Article
13. Ovarian cancer and DNA repair: DNA ligase IV as a potential key.World journal of clinical oncology · 2013
    Article
14. Paying for personalized care: cancer biomarkers and comparative effectiveness.Molecular oncology · 2012
    Article
15. Management of retinal vascular diseases: a patient-centric approach.Eye (London, England) · 2012
    Review
16. SNP calling using genotype model selection on high-throughput sequencing data.Bioinformatics (Oxford, England) · 2012
    Article
17. Evaluation of High Resolution Melting analysis as an alternate tool to screen for risk alleles associated with small kidneys in Indian newborns.BMC nephrology · 2011
    Article
18. Endothelial nitric oxide synthase (eNOS) variants in cardiovascular disease: pharmacogenomic implications.The Indian journal of medical research · 2011
    Article
19. Genome-wide prediction of splice-modifying SNPs in human genes using a new analysis pipeline called AASsites.BMC bioinformatics · 2011
    Article
20. Physiology, structure, and regulation of the cloned organic anion transporters.Xenobiotica; the fate of foreign compounds in biological systems · 2008
    Review

Corrections and comments

• Comment on
  Initial sequencing and analysis of the human genome.2001
• Comment on
  A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.2001

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as