ArticleNucleic acids research2002
Single nucleotide polymorphism seeking long term association with complex disease.
Article in Nucleic acids research, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.
What it found
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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
31 citing papers in PubMed.
- LnCeVar 2.0: an updated resource and web tools for genomic variations disrupting ceRNA networks from single-cell/spatial transcriptomics data.Nucleic acids research · 2026Article
- Genetic insights into 5-LOX-activating protein: a narrative review of disease associations.Human genomics · 2025Review
- Nanoparticles for Thrombus Diagnosis and Therapy: Emerging Trends in Thrombus-theranostics.Nanotheranostics · 2024Review
- Effect of MALAT1 Polymorphisms on Papillary Thyroid Cancer in a Chinese Population.Journal of Cancer · 2019Article
- A universal probe design for colorimetric detection of single-nucleotide variation with visible readout and high specificity.Scientific reports · 2016Article
- Correlation between SNP genotypes and periodontitis in Japanese type II diabetic patients: a preliminary study.Odontology · 2015Article
- Genetic risk of lung cancer associated with a single nucleotide polymorphism from EXO1: a meta analysis.International journal of clinical and experimental medicine · 2015Article
- Rapid Genotyping of MSTN Gene Polymorphism Using High-resolution Melting for Association Study in Rabbits.Asian-Australasian journal of animal sciences · 2013Article
- The significance of Exonuclease 1 K589E polymorphism on hepatocellular carcinoma susceptibility in the Turkish population: a case-control study.Molecular biology reports · 2012Article
- Towards in vitro molecular diagnostics using nanostructures.Cellular and molecular life sciences : CMLS · 2012Review
- Susceptibility of XPD and RAD51 genetic variants to carcinoma of urinary bladder in North Indian population.DNA and cell biology · 2012Article
- Polymorphism in exon 4 of TP53 gene associated to HPV 16 and 18 in Mexican women with cervical cancer.Medical oncology (Northwood, London, England) · 2011Article
- Development and evaluation of single-nucleotide polymorphism markers in allotetraploid rapeseed (Brassica napus L.).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2009Article
- Specific mutation screening of TP53 gene by low-density DNA microarray.Nanotechnology, science and applications · 2009Article
- Single-nucleotide polymorphism (SNP) genotyping using cationic conjugated polymers in homogeneous solution.Nature protocols · 2009Article
- Nanoparticle diffraction gratings for DNA detection on photopatterned glass substrates.Biointerphases · 2008Article
- Real-Time PCR: Revolutionizing Detection and Expression Analysis of Genes.Current genomics · 2007Article
- Single-nucleotide polymorphism genotyping by nanoparticle-enhanced surface plasmon resonance imaging measurements of surface ligation reactions.Analytical chemistry · 2006Article
- Homogeneous point mutation detection by quantum dot-mediated two-color fluorescence coincidence analysis.Nucleic acids research · 2006Article
- Loss of heterozygosity analyzed by single nucleotide polymorphism array in cancer.World journal of gastroenterology · 2005Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Successful investigation of common diseases requires advances in our understanding of the organization of the genome. Linkage disequilibrium provides a theoretical basis for performing candidate gene or whole-genome association studies to analyze complex disease. However, to constructively interrogate SNPs for these studies, technologies with sufficient throughput and sensitivity are required. A plethora of suitable and reliable methods have been developed, each of which has its own unique advantage. The characteristics of the most promising genotyping and polymorphism scanning technologies are presented. These technologies are examined both in the context of complex disease investigation and in their capacity to face the unique physical and molecular challenges (allele amplification, loss of heterozygosity and stromal contamination) of solid tumor research.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.