However, as Ioannidis and Khoury described in their article “Improving Validation PND-1186 research buy Practices in ‘Omics’ Research” (Ioannidis and Khoury 2011), there are numerous and challenging steps to be taken to translate “Omics” research into health care, i.e., to present solid scientific evidence to support recommendations and actions. We would like to thank our international expert guests for giving their time and care to make this special issue possible. We would also like to thank the peer reviewers for their valuable contributions. References Cornel M, El C, Borry P (2012) The challenge of implementing genetic tests with clinical utility while avoiding unsound applications. J Community Genet. doi:10.1007/s12687-012-0121-1
Darst BF, Madlensky L, Schork NJ et al (2013) Characteristics of genomic test consumers who spontaneously share results with their health care provider. Health Commun.
doi:10.1080/10410236.2012.717216 PubMed Ioannidis JP, Khoury MJ (2011) Improving validation practices in “Omics” research. Science 334(6060):1230–1232PubMedCrossRef Janssens S, Paepe A, Borry P (2012) Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature. J Community Genet. doi:10.1007/s12687-012-0131-z PubMed MK-8931 cost Kaphingst KA, McBride CM, Wade C et al (2012) Patients’ understanding of and responses to multiplex genetic susceptibility test results. Genet Med 14(7):681–687PubMedCentralPubMedCrossRef Nippert I, Julian-Reynier C, Harris H, Evans G, van Asperen CJ, Tibben A, Schmidtke J (2013) Cancer risk communication, CYTH4 BI 2536 cell line predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners’ and breast surgeons’ current practice and preferred practice responsibilities. J Community Genet. doi:10.1007/s12687-013-0173-x Nordgren A (2012) Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies. J Community Genet. doi:10.1007/s12687-012-0094-0 PubMed
Paul N, Banerjee M, Michl S (2013) Captious certainties: makings, meanings and misreadings of consumer-oriented genetic testing. J Community Genet. doi:10.1007/s12687-013-0172-y Petitti DB, Teutsch SM, Barton MB et al (2009) Update on the methods of the US Preventive Services Task Force: insufficient evidence. Ann Intern Med 150(3):199–205PubMedCrossRef Reid RJ, McBride CM, Alford SH et al (2012) Association between health-service use and multiplex genetic testing. Genet Med 14(10):852–859PubMedCentralPubMedCrossRef Schneider KI, Schmidtke J (2013) Patient compliance based on genetic medicine: a literature review. J Community Genet. doi:10.1007/s12687-013-0160-2 Zimmern RL (2012) Issues concerning the evaluation and regulation of predictive genetic testing. J Community Genet. doi:10.1007/s12687-012-0111-3 PubMed”
“Erratum to: J Community Genet DOI 10.