Genomics & Health Weekly Update
This weekly update provides information about the impact of human genomic research on disease prevention & population health. Learn more about the Genomics & Health Weekly Update.
Thursday, October 1, 2009 Volume 23 Number 14
Spotlight
Breast and Ovarian Cancer Awareness in September and October
Breast cancer is the most common form of cancer in women. During an average lifetime, a woman’s risk to develop breast cancer is about 1 of 8 or 12%. Ovarian cancer is less common; affecting about 1 out of every 70 women (less than 2%) during their lifetime. Learn more about topics related to breast and ovarian cancer: the role of family health history and risk categories, genetic testing information and guidelines, and genetic counseling.
Announcements
- New Web pages for the CDC-funded genomics translation project entitled Oregon Genomics Surveillance Program: Translation of Genomics Applications into Health Practice at the Oregon Department of Human Services. Visit the Web pages. Learn more about other CDC-funded translation genomics.
- Obtain free access to the August 2009 issue of Genetics in Medicine, focusing on personal genomics.
Genomics In The News
- The following are headlines from on-line news articles published during the past week.
- The headlines and lead sentence are exactly as they appear in the popular press & do not necessarily reflect the opinions or recommendations of CDC.
- Free registration required for some articles.
Autoimmune Diseases
Scientists identify genetic cause of previously undefined primary immune deficiency disease, EurekAlert, September 24
Symposium on genetics of psoriasis and psoriatic arthritis to be held, News-Medical.Net, September 24
Cancer
Lung cancer risk increases with expression of specific genes, EurekAlert, October 1
Bowel cancer gene discovery, Yahoo News, September 30
NCI and NHGRI collaborate to characterize genetic and genomic changes that occur in cancers, News-Medical.Net, September 30
UCSD takes lead in landmark study of breast cancer, Sign on San Diego, September 30
Genetic testing helps sisters in fight against cancer, The News-Gazette.com, September 29
New genetic variants for prostate cancer susceptibility, PHG Foundation, September 28
New cancer drug test promises safer and more effective clinical trials, Science Daily, September 24
Ethical, Legal, and Social Issues (ELSI)
Sharing genetic data may lead to better treatments, Deseret News, October 1
Stakes rise in gene-patenting lawsuit: Hearing today pits AMA, other heavyweights, against the U., Myriad Genetics and the patents office, Trading Markets, September 30
Doctors told to warn patients of their genetic risks, Medical News Today, September 29
Guidance on patient confidentiality and genetic diseases, PHG Foundation, September 29
How to deliver the news? New advice for doctors diagnosing prenatal Down syndrome, EurekAlert, September 28
Family History
Your family's medical history could affect your care, lifestyle, Star-Telegram, September 25
Genetic Testing
Gene tests rate sudden cardiac death risk, CBS News, September 30
Don't skip newborn screening, The Baltimore Sun, September 29
Ohio State joins huge genetic screening study, The Columbus Dispatch, September 29
New DNA test predicts risk of severe scoliosis, Health News Digest, September 24
Influenza
CDC again cautions against using rapid flu tests for H1N1 detection, Genome Web, September 25
Mental Health
Study of genes, toxic metals in children with autism spectrum disorders launched by UT Houston, Jamaica researchers, Medical News Today, October 1
Wayne State University to lead first ever combined imaging and genetics study in childhood OCD, Medical News Today, September 29
Improving the accuracy of predicting violent behaviour may alleviate negative effects of violence, News-Medical.Net, September 28
Schizophrenia gene linked with abnormal neurogenesis in adult and postnatal brain, Science Daily, September 24
Other News
$16.8 million NIH grant received by Johns Hopkins Epigenetic center, Medical News Today, September 30
UNC awarded Cancer Genome Atlas grant, EurekAlert, September 30
NIH funds Brown University's Samoan genotyping project, News-Medical.Net, September 28
NIH funds four centers of excellence in genomic science, NIH News, September 28
C. difficile hypervirulence genes identified, Medical News Today, September 26
Haussler and Kent honored by American Society of Human Genetics, UCSC News, September 25
Genome Standards Consortium evolves and expands to keep pace with rapid advances in the field, Genome Web, September 24 [by free subscription only]
Genomics in Scientific Literature
Topics in Scientific Literature
Family History
The Family Atherosclerosis Monitoring In earLY life (FAMILY) study: rationale, design, and baseline data of a study examining the early determinants of atherosclerosis
Morrison KM, et al.
Am Heart J 2009 Oct;158(4):533-9
Family history of myocardial infarction predicts incident coronary heart disease in postmenopausal women with diabetes: the Women's Health Initiative Observational Study
Li R, et al.
Diabetes Metab Res Rev 2009 Sep
Genotype to Phenotype: Analyzing the Effects of Inherited Mutations in Colorectal Cancer Families
Heinen CD
Mutat Res 2009 Sep
Genetic Testing
Cancer risk assessment by rural and Appalachian family medicine physicians
Kelly KM, et al.
J Rural Health 2009 Fall;25(4):372-7
Development and Characterization of Reference Materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 Genetic Testing
Barker SD, et al.
J Mol Diagn 2009 Sep
Genome Wide
Genomewide Association Study for Onset Age in Parkinson Disease
Latourelle JC, et al.
BMC Med Genet 2009 Sep;10(1):98
A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1
Nakanishi H, et al.
PLoS Genet 2009 Sep;5(9):e1000660
Pharmacogenomics
UGT1A1 genotyping: a predictor of irinotecan-associated side effects and drug efficacy?
Schulz C, et al.
Anticancer Drugs 2009 Sep
Pharmacogenomic variations in treatment protocols for childhood acute lymphoblastic leukemia
Yang YL, et al.
Pediatr Blood Cancer 2009 Sep
General Articles
Endothelial nitric oxide synthase gene polymorphisms and diabetic nephropathy: A HuGE review and meta-analysis
Zintzaras E et al.
Genet Med 2009 Sep
Genetic basis of neural tube defects
Bassuk AG & Kibar Z
Semin Pediatr Neurol 2009 Sep;16(3):101-10
The potential for automated question answering in the context of genomic medicine: an assessment of existing resources and properties of answers
Overby CL, et al.
BMC Bioinformatics 2009;10 Suppl 9:S8
FADS Gene Cluster Polymorphisms: Important Modulators of Fatty Acid Levels and Their Impact on Atopic Diseases
Lattka E, et al.
J Nutrigenet Nutrigenomics 2009 Sep;2(3):119-28
Views on Personalized Medicine: Do the Attitudes of African American and White Prescription Drug Consumers Differ?
De Marco M
Public Health Genomics 2009 Sep
China: Public Health Genomics
Zheng S, et al.
Public Health Genomics 2009 Sep
Rheumatoid arthritis genetics: 2009 update
Plenge RM
Curr Rheumatol Rep 2009 Oct;11(5):351-6
Are essential genes really essential?
D'Elia MA, et al.
Trends Microbiol 2009 Sep
Musings on genome medicine: the Obama effect redux
Nathan DG & Orkin SH
Genome Med 2009 Sep;1(9):86
Developments in Genomics to Improve Understanding, Diagnosis and Management of Aneurysms and Peripheral Artery Disease
Tromp G & Kuivaniemi H
Eur J Vasc Endovasc Surg 2009 Sep
Perceptions of the Concept of Mutation among Family Members of Patients Receiving Outpatient Genetic Services and University Students
Ando N, et al.
J Genet Couns 2009 Sep
Recent studies on the genetic basis of ankylosing spondylitis
Reveille JD
Curr Rheumatol Rep 2009 Oct;11(5):340-8
HuGE
For this week's human genome epidemiology articles, please visit the HuGE Navigator.
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