about
Fulfilling the promise of personalized medicine? Systematic review and field synopsis of pharmacogenetic studiesHuman genetics and genomics a decade after the release of the draft sequence of the human genomeDifferent differences: the use of 'genetic ancestry' versus race in biomedical human genetic researchThe PhenX Toolkit: get the most from your measuresGenome-wide association studies in neurological disordersSomatic mutations in aging, cancer and neurodegenerationPEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing dataGenotyping panel for assessing response to cancer chemotherapy.Fetal inflammatory response in women with proteomic biomarkers characteristic of intra-amniotic inflammation and preterm birth.Community-based dialogue: engaging communities of color in the United states' genetics policy conversationThe roadmap to personalized medicineElectronic signatures of all four DNA nucleosides in a tunneling gap.Gene by social context interactions for number of sexual partners among white male youths: genetics-informed sociologySocial and ethical implications of genomics, race, ethnicity, and health inequities.Alta-Cyclic: a self-optimizing base caller for next-generation sequencing.Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common strokePhysicians' attitudes toward race, genetics, and clinical medicineThe current excitement about copy-number variation: how it relates to gene duplications and protein families.Genome-wide association study of metabolic syndrome in koreans.Compartmentalization of acute phase reactants Interleukin-6, C-Reactive Protein and Procalcitonin as biomarkers of intra-amniotic infection and chorioamnionitisHidden copy number variation in the HapMap population.The cycle of genome-directed medicineAncestry-related differences in gene expression: findings may enhance understanding of health disparities between populations.Personalized medicine: a transformative approach is needed.Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders.Clinical utility of microarrays: current status, existing challenges and future outlook.Brain tumor susceptibility: the role of genetic factors and uses of mouse models to unravel risk.Association between lymphotoxin-alpha (tumor necrosis factor-beta) intron polymorphism and predisposition to severe sepsis is modified by gender and age.Genetics of chronic obstructive pulmonary disease: a succinct review, future avenues and prospective clinical applications.Progress in the detection of human genome structural variations.Don't throw the baby out with the bathwater: enabling a bottom-up approach in genome-wide association studies.Recent advances in association studies of osteoarthritis susceptibility genes.A short history of the genome-wide association study: where we were and where we are going.Understanding human diseases with high-throughput quantitative measurement and analysis of molecular signatures.International Consensus Statement on Allergy and Rhinology: Rhinosinusitis.Building a biomedical cyberinfrastructure for collaborative research.Genetics and genome-wide association studies: surgery-guided algorithm and promise for future breast cancer personalized surgery.Randomized controlled studies and the treatment of middle-ear effusions and tonsillar pharyngitis: how random are the studies and what are their limitations?Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental DelayExperimental therapeutics: a paradigm for personalized medicine.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
name
Breakthrough of the year. Human genetic variation
@ast
Breakthrough of the year. Human genetic variation
@en
Breakthrough of the year. Human genetic variation
@nl
type
label
Breakthrough of the year. Human genetic variation
@ast
Breakthrough of the year. Human genetic variation
@en
Breakthrough of the year. Human genetic variation
@nl
prefLabel
Breakthrough of the year. Human genetic variation
@ast
Breakthrough of the year. Human genetic variation
@en
Breakthrough of the year. Human genetic variation
@nl
P1433
P1476
Breakthrough of the year. Human genetic variation
@en
P304
P356
10.1126/SCIENCE.318.5858.1842
P407
P577
2007-12-21T00:00:00Z