Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

• Published in: European journal of clinical investigation 2011-09, Vol.41 (9), p.1004-1009
• Main Authors: Janssens, A. Cecile J. W., Ioannidis, John P. A., van Duijn, Cornelia M., Little, Julian, Khoury, Muin J.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; General aspects; Genetic Predisposition to Disease - genetics; Genetic Research; Genome, Human - genetics; Genome-Wide Association Study - methods; Genome-Wide Association Study - standards; Genomics - methods; Guidelines as Topic; Humans; Medical sciences; Models, Genetic; Publishing - standards; Risk Assessment
• ISSN: 0014-2972; 1365-2362
• DOI: 10.1111/j.1365-2362.2011.02494.x

Eur J Clin Invest 2011; 41 (9): 1004–1009 Summary Points •  The rapid and continuing progress in gene discovery for complex diseases is fuelling interest in the potential application of genetic risk models for clinical and public health practice. •  The number of studies assessing the predictive ability is steadily increasing, but the quality and completeness of reporting vary. •  A multidisciplinary workshop sponsored by the Human Genome Epidemiology Network developed a checklist of 25 items recommended for strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS), building on the principles established by prior reporting guidelines. •  These recommendations aim to enhance the transparency of study reporting and thereby to improve the synthesis and application of information from multiple studies that might differ in design, conduct or analysis. •  A detailed Explanation and Elaboration document is published as an accompanying article [1].