ArticleBioinformatics and biology insights2008
The HapMap Resource is Providing New Insights into Ourselves and its Application to Pharmacogenomics.
Article in Bioinformatics and biology insights, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 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
30 citing papers in PubMed, 53 citations in OpenAlex.
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- MicroRNAs Implicated in Dysregulation of Gene Expression Following Human Lung Transplantation.Translational respiratory medicine · 2013Article
- Pharmacogenomic technologies: a necessary "luxury" for better global public health?Globalization and health · 2011Article
- Integrating microRNAs into a system biology approach to acute lung injury.Translational research : the journal of laboratory and clinical medicine · 2011Review
- Connecting the Human Variome Project to nutrigenomics.Genes & nutrition · 2010Article
- Genetic determinants of osteoporosis: common bases to cardiovascular diseases?International journal of hypertension · 2010Article
- Modeling expression quantitative trait loci in data combining ethnic populations.BMC bioinformatics · 2010Article
- Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset.PloS one · 2010Article
- Impact of the 1000 genomes project on the next wave of pharmacogenomic discovery.Pharmacogenomics · 2010Review
- SCAN: SNP and copy number annotation.Bioinformatics (Oxford, England) · 2010Article
- Pharmacogenomic discovery using cell-based models.Pharmacological reviews · 2009Review
- A pharmacogene database enhanced by the 1000 Genomes Project.Pharmacogenetics and genomics · 2009Article
- A survey of the population genetic variation in the human kinome.Journal of human genetics · 2009Article
- The case for personalized medicine.Journal of diabetes science and technology · 2009Review
- Exploring the relationship between polymorphic (TG/CA)n repeats in intron 1 regions and gene expression.Human genomics · 2009Article
- SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.Bioinformatics (Oxford, England) · 2009Article
- Identification of common genetic variants that account for transcript isoform variation between human populations.Human genetics · 2009Article
- Improved Statistical Methods are Needed to Advance Personalized Medicine.The open translational medicine journal · 2009Article
- Use of cell lines in the investigation of pharmacogenetic loci.Current pharmaceutical design · 2009Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 1 institution in 2 countries.
Funding
Abstract
The exploration of quantitative variation in complex traits such as gene expression and drug response in human populations has become one of the major priorities for medical genetics. The International HapMap Project provides a key resource of genotypic data on human lymphoblastoid cell lines derived from four major world populations of European, African, Chinese and Japanese ancestry for researchers to associate with various phenotypic data to find genes affecting health, disease and response to drugs. Recent progress in dissecting genetic contribution to natural variation in gene expression within and among human populations and variation in drug response are two examples in which researchers have utilized the HapMap resource. The HapMap Project provides new insights into the human genome and has applicability to pharmacogenomics studies leading to personalized medicine.
Indexed as
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What OpenQuestion holds
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.