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National Office of Public Health Genomics
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 Thursday, June 5, 2008 Volume 20   Number 23
Family History Population Research Genomics in Practice General Public
This weekly update provides information about the impact of human genomic research on disease prevention & population health. open mailbox for email deliveryGet email updates
Spotlight
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Skin Cancer Awareness
Skin cancer is the most common form of cancer in the United States. People who have a close relative (parent, sibling, or child) with a specific type of skin cancer called melanoma may be at greater risk of developing the disease than the general population
Read more.

EGAPP Initiative announces five new EGAPP Working Group Members
The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) initiative announces the selection of five new members who will join the EGAPP Working Group. Two current members complete their terms this year. More about the EGAPP initiative.
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blue dotAnnouncements
blue dotGenomics In The News
blue dotScientific Literature
blue dotHuGE Articles
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 Upcoming Events

Community Centered Family Health History Program Award
Recipients
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2008 Clinical and Translational Science Awards, NIH non-gov warning icon

New Michael F. Price Center for Genetic and Translational Medicine, Albert Einstein College of Medicine non-gov warning icon

Genomics Announcements
 

CDCD sponsored material
Final applications are due June 6, 2008 for CDC's National Office of Public Health Genomics funding opportunity for genomics translation in education, surveillance, and policy interventions.


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

Malignant Melanoma Classification Given Additional Genetic Component, non-gov warning icon Medical News Today, June 5 Researchers find gene signature profile for metastasis, non-gov warning icon News-Medical.Net, June 2

Colon Cancer Survival Has Family Link, non-gov warning icon CBS News, June 3

Abnormalities found in gene for melanoma, non-gov warning icon Medical New Today, May 30

Erbitux effective for advanced colorectal cancer patients with normal gene, non-gov warning icon Medical News Today, June 2

4 your health - Skin and colon cancer, non-gov warning icon My Fox, May 30

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Cardiovascular Disease

Diabetes

Ischemic heart disease not associated with low HDL levels from gene variation, non-gov warning icon Medical News Today, June 3

Discovery of genes that regulate glucose levels, non-gov warning icon News-Medical.Net, June 3

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Ethical, Legal, and Social Issues (ELSI)

IEEE-USA-supported genetic Information Nondiscrimination Act signed into law, non-gov warning icon Medical News Today, May 2

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Family History

Surviving colon cancer is tied to family history of it, non-gov warning icon New York Times, June 4

Family tree is important to personal health, non-gov warning icon BDN Connection, June 2

Genetic Alliance announces 'family health history' grant award recipients,non-gov warning icon Ascribe, June 3

 

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Genetic Testing

Baby born free of hereditary gene peril thanks to controversial screening, non-gov warning icon Mail Online, June 4

Prenatal biochemical screening only detects half of chromosomal abnormalities, non-gov warning icon News-Medical.Net, June 1

Expert cautions against rushing into genetic testing, non-gov warning icon News-Medical.Net, June 1

 

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Mental Health

Genetic cause for a type of childhood epilepsy identified by UCLA/VA scientists, non-gov warning icon Medical New Today, May 30

Spontaneous mutations rife in non-familial schizophrenia, non-gov warning icon NIH News, May 30

NARSAD researchers identify specific genes and family traits linked to schizophrenia, bipolar disorder and depression, non-gov warning icon chron.com, May 30

NIH researchers find that Rett syndrome gene is full of surprises, non-gov warning icon NIH News, May 29

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Pharmacogenomics

Studies advance emerging field of "Personalized Medicine", non-gov warning icon Medical News Today, June 3

Personal genomes may lead to personalized vitamin supplements, non-gov warning icon News-Medical.Net, June 2

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Other News

6 Nobel Prize winners at international congress of genetics, non-gov warning icon Medical News Today, June 4

New genetic mutations involved in inflammatory intestinal disorders discovered, non-gov warning icon News-Medical.Net, June 2

Guidelines for standard descriptions and terminology in genomics and regenerative
medicine
, non-gov warning icon PHG Foundation, June 4

Gene discovery could help answer basic questions of upright walking, non-gov warning icon News-Medical.Net, June 1

New open-access journal: Human genomics and proteomics, non-gov warning icon Medical News Today, June 4

Genetic patients across Europe feeling real benefits claims EuroGentest NoE at ESHG, non-gov warning icon News-Medical.Net, June 1

DNA 11's DNA art portraits now offer more insight into your genes, non-gov warning icon Yahoo Finance, June 3

New insight into the genetics of Lou Gehrig's
disease
, non-gov warning icon News-Medical.Net, June 1

Clusters of genetic variants linked to distinct treatment responses for smoking cessation, non-gov warning icon NIH News, June 2

3 distinct and devastating human diseases caused by defects in 1 gene, non-gov warning icon Medical New Today, May 30

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Genomics in Scientific Literature
Featured Item

Genetic susceptibility to cancer: the role of polymorphisms in candidate genes
Dong LM, et al.
JAMA 2008 May;299(20):2423-36


 General Articles

Has enhanced folate status during pregnancy altered natural selection and possibly Autism prevalence? A closer look at a possible link
Rogers EJ
Med Hypotheses 2008 May

Age related mitochondrial degenerative disorders in humans
Reeve AK, et al.
Biotechnol J 2008 Jun

Pharmacogenetics of Immunosuppressants: Progress, Pitfalls and Promises
Cattaneo D, et al.
Am J Transplant 2008 May

Common and rare variants in multifactorial susceptibility to common diseases
Bodmer W & Bonilla C
Nat Genet 2008 Jun;40(6):695-701

Ethical Issues Related To BRCA Gene Testing in Orthodox Jewish Women
Mor P & Oberle K
Nurs Ethics 2008 Jul;15(4):512-22

The impact of inherited thrombophilia on surgery: A factor to consider before transplantation?
Kfoury E, et al.
Mol Biol Rep 2008 May

Pharmacogenetics of bone treatments: the VDR and ERalpha gene story
Massart F, et al.
Pharmacogenomics 2008 Jun;9(6):733-46

Pharmacogenetics of Gilbert's syndrome
Strassburg CP
Pharmacogenomics 2008 Jun;9(6):703-15

Genetic susceptibility to the respiratory effects of air pollution
Yang IA, et al.


 Family History

Family history of diabetes impacts on interactions between minimal model estimates of insulin sensitivity and glucose effectiveness
Lopez X, et al.
Diabetes Obes Metab 2008 Jun

Family history of suicidal behavior predicts impulsive-aggressive behavior levels in psychiatric outpatients
Diaconu G & Turecki G
J Affect Disord 2008 May

 

 Genetic Testing

BRCA1 germline mutations and tumor characteristics in Chinese women with familial or early-onset breast cancer
Chen W, et al.
Breast Cancer Res Treat 2008 May

Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms
Monsuur AJ, et al.
PLoS ONE 2008;3(5):e2270

Can complement factors 5 and 8 and transthyretin be used as biomarkers for MODY 1 (HNF4A-MODY) and MODY 3 (HNF1A-MODY)?
Karlsson E, et al.
Diabet Med 2008 May

Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer burden in the family
Evans DG, et al.
BMC Cancer 2008 May;8(1):155

 

 Genome-Wide Association Studies

Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study
Lavedan C, et al.
Mol Psychiatry 2008 Jun

Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia
Volpi S, et al.
Mol Psychiatry 2008 Jun

Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels
Chen WM, et al.
J Clin Invest 2008 Jun

Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays
Wang L, et al.
Haematologica 2008 May

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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 June 4, 2008, 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
Diseases of the Skin and Subcutaneous Tissue
Symptoms, Signs, and Ill-defined Conditions

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

 

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Page last updated: June 5, 2008 (archived document)
Content Source: National Office of Public Health Genomics