Genomics|Update|Non Communicable Diseases: Genomics in Practice

Genomics|Update|Non Communicable Diseases

Volume 35  Number 4  July 23-30, 2015

Genomics in Practice

Achieving high-sensitivity for clinical applications using augmented exome sequencing
Patwardhan A, et al. Genome Medicine 2015, 7:71 Jul 16

Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases. 
Genome Biol. 2015 16(1) 134

Genetic testing: Low-cost clinical testing for Mendelian diseases. 
Waldron D et al. Nat. Rev. Genet. 2015 Jul 17. 16(8) 439

Making personalized health care even more personalized: Insights from activities of the IOM Genomics Roundtable. 
David SP et al. Ann Fam Med 2015 Jul 13(4) 373-80

Optimal screening for genetic diseases. 
Nævdal E et al. Econ Hum Biol 2014 Dec 15129-39

Prevention, use of health services, and genes: Implications of genetics for policy formation. 
Wehby GL et al. J Policy Anal Manage 2015 34(3) 519-36

Secondary findings and carrier test frequencies in a large multiethnic sample. 
Gambin T et al. Genome Med 2015 7(1) 54

The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing. 
Sukenik-HR et al. Genet. Med. 2015 Jul 16.

[Implementation of Italian guidelines on public health genomics in Italy: a challenging policy of the NHS]. 
Boccia S et al. Epidemiol Prev 38(6 Suppl 2) 29-34 

High-risk world of rare genetic diseases: Research efforts improving, by Andrew Porterfield, Genetic Literacy Project, Jul 19