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 Thursday, September 13, 2007 Volume 19   Number 11
Weekly Update banner Family History Population Research Genomics in Practice General Public Family History Population Research Genomics in Practice General Public
  This weekly update provides information about the impact of human genetic research on disease prevention & public health. open mailbox for email deliveryGet email updates
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When is BRCA Genetic Testing for Breast and Ovarian Cancer Appropriate?
The U.S. Preventive Services Task Force (USPSTF) recommends against routine referral for BRCA testing if a woman’s

family history does not suggest an increased risk for harmful BRCA mutations. The USPSTF recommends that women with a family history associated with an increased risk for BRCA mutations be referred to suitably trained health care providers.

> Read the USPSTF recommendations and clinical considerations.


 > View Current Update
blue dotAnnouncements
blue dotGenomics In The News
blue dotScientific Literature
blue dotHuGE Articles
blue dotBack Issues

 

 

 

 

 

Genomics Announcements
   
CDC-sponsored event

New HuGE Review
A Meta-Analysis of the Association of N-Acetyltransferase 2 Gene (NAT2) Variants with Breast Cancer PDF only(164kb)
Heather M. Ochs-Balcom, et al.
Am J Epidemiol 2007;166:246–254

   
CDC-sponsored event

September public health genomics seminar presented by CDC
“How do we monitor the impact of genomics on population health?"
Sep 20, 2007, Rockville, MD (ENVISION – Atlanta, GA)

   


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.

Cancer

New insight into breast cancer development in high-risk women, non-gov warning icon
News-Medical.Net, September 12

Gene mutation helps predict thyroid cancer treatment, non-gov warning icon Medical News Today, September 10

Altered expression of ultraconserved noncoding RNAs linked to human leukemias and carcinomas, non-gov warning icon EurekAlert, September 10

Microarray provides three genomic guides to breast cancer treatment decisions, non-gov warning icon Medical News Today, September 7

Diabetes

Ethical, Legal, and Social Issues (ELSI)

Mutations in the insulin gene can cause permanent neonatal diabetes, non-gov warning icon News-Medical.Net, September 11

Personal genomics and the end of insurance, non-gov warning icon VentureBeat, September 11

line

Family History

Genetic Testing

Family history has strong effect on cardiac risk, non-gov warning icon Washington Post, September 7

A genetic test that very few need, marketed to the masses, non-gov warning icon The New York Times, September 11

 

DNA helps pave the way for a specific cure for each individual, non-gov warning icon San Francisco Chronicle, September 9

line

Other News

Gene in HIV makes hiv-2 susceptible to immune system response, researchers say, non-gov warning icon Medical News Today, September 13

Caught on camera: 3D images give early warning of genetic disorders in children, non-gov warning icon Guardian Unlimited, September 10

Gene-drug interactions that lower blood
pressure
, non-gov warning icon News-Medical.Net, September 13

Scientists demonstate link between genetic variant and effectiveness of smoking cessation meds, non-gov warning icon EurekAlert, September 10

Genetic map researchers at show, non-gov warning icon BBC News, September 12

Study finds evidence of genetic response to
diet
, non-gov warning icon The New York Times, September 10

Northwest Genome Engineering Consortium receives NIH grant to study gene repair, non-gov warning icon Medical News Today, September 12

Genetics forum in Dubai, non-gov warning icon AME Info, September 9

Coding and noncoding genes are involved in and cooperate in human tumorigenesis, non-gov warning icon News-Medical.Net, September 11

South Africa: Mbeki to open a science research centre, non-gov warning icon all Africa.com, September 9

Two girls, one genetic 'blip' and a story of hope and courage, non-gov warning icon Daily Mail, September 11

Alnylam, Isis form venture to develop gene technology, non-gov warning icon Bloomberg, September 7

$7.8 million award for autism genetics research, non-gov warning icon Medical News Today, September 10  
line
Genomics in Scientific Literature
Featured Item

Studies in 3,523 Norwegians (HUNT2) and Meta-Analysis in 11,571 Subjects Indicate that Variants in the HNF4A P2 Region are Associated with Type 2 Diabetes in Scandinavians
Johansson S, et al.
Diabetes 2007 Sep

 General Articles

Prediction of individual genetic risk to disease from genome-wide association studies
Wray NR, et al.
Genome Res 2007 Sep

Simulating association studies: a data-based resampling method for candidate regions or whole genome scans
Wright FA, et al.
Bioinformatics 2007 Sep

The role of genetics in stroke
Francis J, et al.
Postgrad Med J 2007 Sep;83(983):590-5

Simultaneously correcting for population stratification and for genotyping error  in case-control association studies
Cheng KF & Lin WJ
Am J Hum Genet 2007 Oct;81(4):726-43

Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies
Kohler JR & Cutler DJ
Am J Hum Genet 2007 Oct;81(4):684-99

Studying Genetic Predisposition Among Small-for-Gestational-Age Newborns
Infante-Rivard C
Semin Perinatol 2007 Aug;31(4):213-8

The Genetic Basis of Thyroid Autoimmunity
Jacobson EM & Tomer Y
Thyroid 2007 Sep

Asthma Genetics: From Linear to Multifactorial Approaches
Guerra S & Martinez FD
Annu Rev Med 2007 Sep

 

 Genetic Testing

The impact of clinical and genetic screenings on the management of the multiple endocrine neoplasia type 1
Lourenco-Jr DM, et al.
Clinics 2007;62(4):465-70

Epidermal Growth Factor Receptor Mutation Testing in Lung Cancer: Searching for the Ideal Method
Pao W & Ladanyi M
Clin Cancer Res 2007 Sep;13(17):4954-5

The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test
Schneider SA, et al.
Nat Clin Pract Neurol 2007 Sep;3(9):517-25

 

 Family History

An LRP8 Variant Is Associated with Familial and Premature Coronary Artery Disease and Myocardial Infarction
Shen GQ, et al.
Am J Hum Genet 2007 Oct;81(4):780-91

How common is familial cancer?
Hemminki K, et al.
Ann Oncol 2007 Sep

Evidence of shared risk for Alzheimer's disease and Parkinson's disease using family history
Rosen AR, et al.
Neurogenetics 2007 Sep

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HuGE Published Literature [ back to top ]

Articles that report on population prevalence of genotypes, gene-disease associations, gene-environment and gene-gene interactions and evaluation of genetic tests. For more information on HuGE, please visit the HuGENet™ home page

For the week ending September 12, 2007, there are HuGE articles in the following areas:

Gene Variant Frequency
Infectious and Parasitic Diseases
Neoplasms
Endocrine, Nutritional and Metabolic Diseases
Mental Disorders
Diseases of the Nervous System and Sense Organs
Diseases of the Circulatory System
Diseases of the Respiratory System
Diseases of the Digestive System
Diseases of the Genitourinary System
Complications of Pregnancy, Childbirth, and the Puerperium
Diseases of the Skin and Subcutaneous Tissue
Diseases of the Musculoskeletal System and Connective Tissue

For more information on HuGE, please visit the HuGENet™ home page

 

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The CDC National Office of Public Health Genomics makes available the above information as a public service only. Providing
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 Provides link to non-governmental sites and does not necessarily represent the views of the Centers  for Disease Control and Prevention.
Page last reviewed: September 13, 2005 (archived document)
Content Source: National Office of Public Health Genomics