The Office of Public Health Genomics (OPHG) provides updated and credible information on how genomic
information and family health history can improve health and influence policy and practice. We highlight
news and information on the use of genomic tests and other applications, including family health history,
in clinical and public health practice and programs, along with relevant data, policy, and legislation. We hope the update is informative to practitioners, policy makers, consumers, and researchers. Please send
your comments to: genetics@cdc.gov.
Public Health Sciences
- Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Wheeler E, Huang N, Bochukova E, et al. Nature Genetics 2013 Apr 7
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Bernt S, Gustafsson S, Maegi R, et al. Nature Genetics 2013 Apr 7 - Two genome-wide studies identify new links to obesity, PHG Foundation, Apr 15
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
- Long QT syndrome-associated mutations in intrauterine fetal death
Crotti L, et al. JAMA 2013 Apr;309(14):1473-82
- Long QT syndrome susceptibility mutations and pregnancy loss: another piece of a still unfinished puzzle?
Guttmacher AE, et al. JAMA 2013 Apr;309(14):1525-6
- Long QT syndrome susceptibility mutations and pregnancy loss: another piece of a still unfinished puzzle?
- Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E 4,and the risk of late-onset Alzheimer disease in African Americans
Reitz C, et al. JAMA 2013 Apr;309(14):1483-92
- Genome-wide association studies, Alzheimer disease, and understudied populations
Nussbaum RL JAMA 2013 Apr;309(14):1527-8
- Genome-wide association studies, Alzheimer disease, and understudied populations
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