|
|
Thursday, October 25, 2007 |
Volume
19 Number 17 |
|
|
This weekly update provides information about the impact of human genetic research on disease prevention & public health. |
Get email updates |
|
|
|
|
- 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.
|
Other News |
GABRA2 genotype may moderate alcohol-psychotherapy outcomes, EurekAlert, October 24 |
Stem cells to treat damaged eyes and a rare skin disorder, News-Medical.Net, October 22 |
Hate those greens?....Could be in your genes, News-Medical.Net, October 24 |
Gene mutation could shape children's eating,
(last accessed 2/2008) USA Today, October 21 |
Genetic code could hold key to medical fate, ABC News, October 23 |
Genetic factor in AIDS progression is higher than thought: study,
(last accessed 2/2008) Yahoo News, October 21 |
Scientist plotting genetic revolution, BBC, October 23 |
Massive reanalysis of genome data solves case of the lethal genes, News-Medical.Net, October 21 |
Diet choices 'written in genes', BBC News, October 22 |
New links in the cystic fibrosis chain uncover potential therapeutics, News-Medical.Net, October 21 |
Discovery of 2 genes related to disabling form of arthritis, Medical News Today, October 22 |
Oral medication restores missing protein in boys with muscular dystrophy, News-Medical.Net, October 21 |
Genes that make drinking riskier identified, Ketalanext.com, October 22 |
Discovery of binocular vision gene, News-Medical.Net, October 19 |
New links in the cystic fibrosis chain uncover potential therapeutics, Science Daily, October 22 |
|
|
|
|
|
|
Bad Nature, Bad Nurture, and Testimony Regarding MAOA and SLC6A4 Genotyping at Murder Trials
Bernet W, et al.
J Forensic Sci 2007 Oct
Silent polymorphisms speak: how they affect pharmacogenomics and the treatment of cancer
Sauna ZE, et al.
Cancer Res 2007 Oct;67(20):9609-12
Genetic Factors in Diabetic Nephropathy
Freedman BI, et al.
Clin J Am Soc Nephrol 2007 Oct
Combining Association Tests across Multiple Genetic Markers in Case-Control Studies
Zhou H, et al.
Hum Hered 2007 Oct;65(3):166-74
Designing candidate gene and genome-wide case-control association studies
Zondervan KT & Cardon LR
Nat Protoc 2007;2(10):2492-501
Experiencing the genetic body: parents' encounters with pediatric clinical genetics
Raspberry K & Skinner D
Med Anthropol 2007 Oct-2007 Dec;26(4):355-91
Genetic counseling and clinical management of newly diagnosed breast cancer patients at genetic risk for BRCA germline mutations: perspective of a surgical oncologist
Silva E
Fam Cancer 2007 Oct
The Predominant Role of Surgery in the Prevention and New Trends in the Surgical Treatment of Women With BRCA1/2 Mutations
Fatouros M, et al.
Ann Surg Oncol 2007 Oct
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Estivill X & Armengol L
PLoS Genet 2007 Oct;3(10):e190
Society of gynecologic oncologists education committee statement on risk assessment for inherited gynecologic cancer predispositions
Lancaster JM, et al.
Gynecol Oncol 2007 Nov;107(2):159-62
The effect of the plasminogen activator inhibitor-1 4G/5G polymorphism on the thrombotic risk
Tsantes AE, et al.
Thromb Res 2007 Oct
Development and pilot evaluation of novel genetic educational materials designed for an underserved patient population
Lubitz RJ, et al.
Genet Test 2007 Fall;11(3):276-90
Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease
Penziner E, et al.
Am J Med Genet B Neuropsychiatr Genet 2007 Oct
Information Needs of Mothers Regarding Communicating BRCA1/2 Cancer Genetic Test Results to Their Children
Tercyak KP, et al.
Genet Test 2007 Fall;11(3):249-55
Attitudes of Families Affected by Adrenoleukodystrophy toward Prenatal Diagnosis, Presymptomatic and Carrier Testing, and Newborn Screening
Schaller J, et al.
Genet Test 2007 Fall;11(3):296-302
Should Individuals Be Informed about Their Salt Sensitivity Status? First Indications of the Value of Testing for Genetic Predisposition to Low-Risk Conditions
Smerecnik CM, et al.
Genet Test 2007 Fall;11(3):307-14
Neonatal screening for sickle cell disease in Central Africa: a study of 1825 newborns with a new enzyme-linked immunosorbent assay test
Mutesa L, et al.
J Med Screen 2007;14(3):113-6
Genetic counseling for inherited thrombophilias
Varga EA
J Thromb Thrombolysis 2007 Oct
Ethnic Differences in Parental Perceptions of Genetic Testing for Deaf Infants
Palmer CG, et al.
J Genet Couns 2007 Oct
Living at Risk: Concealing Risk and Preserving Hope in Huntington Disease
Quaid KA, et al.
J Genet Couns 2007 Oct
Can we identify the high-risk patients to be screened? A genetic approach
Gammon A, et al.
Digestion 2007;76(1):7-19
A genetic history questionnaire-based system in primary prenatal care to screen for selected fetal disorders
Bradley LA, et al.
Genet Test 2007 Fall;11(3):291-5
Data reduction for prediction: A case study on robust coding of age and family history for the risk of having a genetic mutation
Steyerberg EW, et al.
Stat Med 2007 Oct 19
|
|
Send websites that you would like to see included in a future update to genetics@cdc.gov
To receive notification of this update by e-mail, please send the following message:
To: listserv@listserv.cdc.gov
Subject: (leave blank)
Message: subscribe genetics
(to unsubscribe, replace Message text with "unsubscribe genetics")
The CDC National Office of Public Health Genomics makes available the above information as a public service only. Providing
this information does not constitute endorsement by the CDC. Note that some links may become invalid over time. |
|
|
|
Provides link to non-governmental sites and does not necessarily represent the views of the Centers for Disease Control and Prevention. |
|
|
|