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Replication in Genome-Wide Association StudiesEvaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's diseaseThe role of LTA4H and ALOX5AP genes in the risk for asthma in LatinosHigh-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older menGenes, cognition, and communication: insights from neurodevelopmental disordersFolate and one-carbon metabolism gene polymorphisms and their associations with oral facial cleftsGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease lociComprehensive testing of positionally cloned asthma genes in two populationsEthnic differences in gastric cancer genetic susceptibility: allele flips of interleukin geneFrom pharmacogenetics to pharmacogenomics: the way toward the personalization of antidepressant treatmentOpposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.UGMDR: a unified conceptual framework for detection of multifactor interactions underlying complex traits.Genetics of Common Antipsychotic-Induced Adverse EffectsFurther evidence of association between two NET single-nucleotide polymorphisms with ADHDAssociation and heterogeneity at the GAPDH locus in Alzheimer's diseaseAffect-modulated startle: interactive influence of catechol-O-methyltransferase Val158Met genotype and childhood trauma.Dietary factors impact on the association between CTSS variants and obesity related traitsLarge scale association analysis identifies three susceptibility loci for coronary artery diseaseLINGO1 variants in the French-Canadian populationIntermediate phenotypes identify divergent pathways to Alzheimer's diseaseAn ImmunoChip study of multiple sclerosis risk in African Americans.Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense.Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice.Genes involved in sex pheromone discrimination in Drosophila melanogaster and their background-dependent effect.Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures.New statistical approaches exploit the polygenic architecture of schizophrenia--implications for the underlying neurobiology.On the analysis of genome-wide association studies in family-based designs: a universal, robust analysis approach and an application to four genome-wide association studiesTransferability and fine-mapping of genome-wide associated loci for adult height across human populations.Combining information on multiple instrumental variables in Mendelian randomization: comparison of allele score and summarized data methods.Analysis of heterogeneity and epistasis in physiological mixed populations by combined structural equation modelling and latent class analysis.Strong signature of natural selection within an FHIT intron implicated in prostate cancer risk.Assessing the reproducibility of asthma candidate gene associations, using genome-wide data.A common variant associated with dyslexia reduces expression of the KIAA0319 geneGenetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis.Discovery properties of genome-wide association signals from cumulatively combined data sets.A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS).Polymorphisms in MMP9 and SIPA1 are associated with increased risk of nodal metastases in early-stage cervical cancer.Association of Parkinson disease risk loci with mild parkinsonian signs in older persons.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
No gene is an island: the flip-flop phenomenon
@ast
No gene is an island: the flip-flop phenomenon
@en
type
label
No gene is an island: the flip-flop phenomenon
@ast
No gene is an island: the flip-flop phenomenon
@en
prefLabel
No gene is an island: the flip-flop phenomenon
@ast
No gene is an island: the flip-flop phenomenon
@en
P2860
P50
P356
P1476
No gene is an island: the flip-flop phenomenon
@en
P2093
Eden R Martin
P2860
P304
P356
10.1086/512133
P407
P577
2007-01-22T00:00:00Z