Most published research findings are false-but a little replication goes a long wayGenome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseasesStrengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaborationGenome-wide association scan for five major dimensions of personalityBiological, clinical and population relevance of 95 loci for blood lipidsThree genome-wide association studies and a linkage analysis identify HERC2 as a human iris color geneDoes genetic testing really improve the prediction of future type 2 diabetes?Research Conducted Using Data Obtained through Online Communities: Ethical Implications of Methodological LimitationsUsefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemiaComparison of participant information and informed consent forms of five European studies in genetic isolated populationsPredicting Polygenic Obesity Using Genetic Information.Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies.Constructing Hypothetical Risk Data from the Area under the ROC Curve: Modelling Distributions of Polygenic Risk.Genetic factors influence the clustering of depression among individuals with lower socioeconomic status.Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence.Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement.Personal genome testing: test characteristics to clarify the discourse on ethical, legal and societal issuesInsulin-resistance and metabolic syndrome are related to executive function in women in a large family-based study.HFE gene mutations increase the risk of coronary heart disease in women.Perspectives on the use of multiple sclerosis risk genes for predictionThe Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.The role of disease characteristics in the ethical debate on personal genome testing.Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.Longevity candidate genes and their association with personality traits in the elderly.Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.Predicting human height by Victorian and genomic methods.How can polygenic inheritance be used in population screening for common diseases?Genome-wide analysis of genetic loci associated with Alzheimer disease.B-type natriuretic peptide and C-reactive protein in the prediction of atrial fibrillation risk: the CHARGE-AF Consortium of community-based cohort studies.The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association dataEthnic differences and parental beliefs are important for overweight prevention and management in children: a cross-sectional study in the NetherlandsDiscriminative accuracy of genomic profiling comparing multiplicative and additive risk models.Self reported stressful life events and exacerbations in multiple sclerosis: prospective study.CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease.Genome-based prediction of common diseases: advances and prospects.Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
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