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| Thursday, February 19, 2009 |
Volume
22 Number 7 |
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| This weekly update provides information about the impact of human genomic research on disease prevention & population health. |
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| There are no announcements this week. |

- 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.
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Other News |
Adding genetics to a patient's clinical profile might lead to more accurate blood-thinner dosing, insciences.org, February 18 |
Picture emerging on genetic risks of IVF, New York Times, February 16 |
HMC lecture spotlights role of genetics in
medicines, LDNews, February 18 |
Pharmacogenetic-based prescribing slow to take hold, Genome Web, February 16 |
For some counselors, it's in the genes, The Wall Street Journal, February 17 |
Genomics: The convoluted promise of our generation, The Crimson White, February 15 |
Guidelines for genetic-association studies
published, GenomeWeb, February 17 |
Statistical analysis could yield new drug target for multiple sclerosis, News-Medical.Net, February 15 |
Star Trek-style device may check patients' genetic suitability to different medicines, newKerala.com, February 17 |
The secrets in Lincoln’s DNA, Newsweek, February 14 |
Gene Logic announces launch of Illumina SNP genotyping services, Gene Logic, February 16 |
Scientists unravel genetic codes and family trees of common cold viruses, Medical News Today, February 13 |
Insights into human genetic makeup provided by mixed population, Medical News Today, February 16 |
Next gen sequencing technology pinpoint 'on-off switches' in genomes, EurekAlert, February 12 |
Jumping genes play significant role in gene regulatory networks, News-Medical.Net, February 16 |
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Polymorphisms of pro-inflammatory genes and prostate cancer risk: a pharmacogenomic approach
Caruso C, et al.
Cancer Immunol Immunother 2009 Feb
Genotype-Phenotype Relationships of Presenilin-1 Mutations in Alzheimer's Disease: An Update
Larner AJ & Doran M
J Alzheimers Dis 2009 Feb
Experiences and Decisions that Motivate Women at Increased Risk of Breast Cancer to Participate in an Experimental Screening Program
Proulx M, et al.
J Genet Couns 2009 Feb
Strengthening the reporting of genetic association studies (STREGA)-an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement
Little J, et al.
J Clin Epidemiol 2009 Feb
Session 2: Personalised nutrition Genetic variation and disease risk: new advances
Scott J
Proc Nutr Soc 2009 Feb:1-9
Family-based genome-wide association studies
Benyamin B, et al.
Pharmacogenomics 2009 Feb;10(2):181-90
The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA
Plomin R & Davis OS
J Child Psychol Psychiatry 2009 Jan;50(1-2):63-71
GWA studies: rewriting the story of IBD
Budarf ML, et al.
Trends Genet 2009 Feb
NKX2.5 mutations and congenital heart disease: Is it a marker of cardiac anomalies?
Balci MM & Akdemir R
Int J Cardiol 2009 Feb
Likelihood ratio tests for maternal and fetal genetic effects on obstetric complications
Chen J, et al.
Genet Epidemiol 2009 Feb
Extracting a needle from a haystack: reanalysis of whole genome data reveals a readily translatable finding
Keers R, et al.
Psychol Med 2009 Feb:1-5
Distress among women receiving uninformative BRCA1/2 results: 12-month outcomes
O'Neill SC, et al.
Psychooncology 2009 Feb
Cancer Genetic Counselees' Self-Reported Psychological Distress, Changes in Life, and Adherence to Recommended Surveillance Programs 3-7 Years Post Counseling
Hayat Roshanai A, et al.
J Genet Couns 2009 Feb
Predictors of decision making in families at risk for inherited breast/ovarian cancer
Mellon S, et al.
Health Psychol 2009 Jan;28(1):38-47
Methods for analysis in pharmacogenomics: lessons from the Pharmacogenetics Research Network Analysis Group
Srinivasan BS, et al.
Pharmacogenomics 2009 Feb;10(2):243-51
Genome-wide association studies of coronary artery disease and heart failure: where are we going?
Dorn GW & Cresci S
Pharmacogenomics 2009 Feb;10(2):213-23
Genetic assessment of breast cancer risk in primary care practice
Burke W, et al.
Am J Med Genet A 2009 Feb
Family history of suicide: A clinical marker for major depression in primary care practice?
Torzsa P, et al.
J Affect Disord 2009 Feb
Family letters are an effective way to inform relatives about inherited cardiac disease
van der Roest WP, et al.
Am J Med Genet A 2009 Feb
The relationship between knowledge of family history and cancer characteristics at diagnosis in women newly-diagnosed with invasive breast cancer
Lijovic M, et al.
Fam Cancer 2009 Feb
Diagnosis of Hepatic Iron Overload: A Family Study Illustrating Pitfalls in Diagnosing Hemochromatosis
Schranz M, et al.
Diagn Mol Pathol 2009 Feb
Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction
Schwartz MD, et al.
Health Psychol 2009 Jan;28(1):11-9
Genetic association studies to detect adverse drug reactions: abacavir hypersensitivity as an example
Hughes AR, et al.
Pharmacogenomics 2009 Feb;10(2):225-33
Histopathological criteria and selection algorithms for BRCA1 genetic testing
Gadzicki D, et al.
Cancer Genet Cytogenet 2009 Mar;189(2):105-11
Genome-wide association study of acute post-surgical pain in humans
Kim H, et al.
Pharmacogenomics 2009 Feb;10(2):171-9
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
Zheng W, et al.
Nat Genet 2009 Feb
Metaanalysis of Methylenetetrahydrofolate Reductase (MTHFR) Polymorphisms Affecting Methotrexate Toxicity
Fisher MC & Cronstein BN
J Rheumatol 2009 Feb
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