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| Thursday, May 14, 2009 |
Volume
22 Number 19 |
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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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- 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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Cancer |
Gene in breast cancer pathway identified, Medical News Today, May 13 |
UNC study identifies genetic cause of most common form of breast cancer, EurekAlert, May 11 |
New biomarker for aggressive prostate cancer, study, Medical News Today, May 13 |
New technique may help detect potential breast cancer spread, Science Daily, May 9 |
Genetic research work opens up new horizons to the design of customized medicines against breast cancer, Science Daily, May 12 |
Breast cancer conference highlights, Medical News Today, May 8 |
Genome wide analysis and clinical correlation of chromosomal and transcriptional mutations in cancers of the biliary tract, 7th Space, May 12 |
New universal breast cancer marker predicts recurrence and clinical outcome, Science Daily, May 7 |
475,000 faulty cancer tests sent out, ABC News Australia, May 11 |
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Flu |
Landmark study reveals significant genetic variation between Mexico's population and world's other known genetic subgroups, Science Daily, May 12 |
British scientists produce first genetic fingerprint of Swine Flu virus infecting humans in Europe, Medical News Today, May 9 |
H1N1 flu hits Norway, global death toll 53: WHO, Reuters Health, May 11 |
Testing for the flu, from swab to finish, PE.com, May 8 |



Other News |
$3.3 million awarded to university of Liverpool, UK, for genomics hub, Medical News Today, May 14 |
Muscular dystrophy diagnosis delayed almost 2.5 years in boys, EurekAlert, May 11 |
Gene responsible for rare form of congenital anemia discovered, Science Daily, May 14 |
Novel genetic risk factors for kidney disease revealed by study, Medical News Today, May 11 |
Consumer genetics conference: Top thought leaders in health and genetics weigh in, Yahoo Finance, May 13 |
Vision loss in genetic diseases explained by protein-protein interaction, Medical News Today, May 11 |
What is Progeria, Medical News Today, May 13 |
TAU investigates MicroRNA and its role in human disease, Medical News Today, May 9 |
Geneticists streamline gene searches, The Money Times, May 12 |
Researchers uncovering variants in 1000 genomes pilot data, GenomeWeb, May 8 [by free subscription only] |
Google, Microsoft may help usher in personalized medicine wave, says George Church, Xconomy Boston, May 12 |
Genetic factors for common traits in Asians, hum-molgen.org, May 7 |
Personalized Medicine Coalition publishes The Case for Personalized Medicine, Business Wire, May 12 |
In gene identification, random picks better than complicated process, Medical News Today, May 7 |
American College of Medical Genetics affirms importance of newborn screening dried blood spots, EurekAlert, May 11 |
“The future of genetic studies of complex human diseases”: Drs. Merikangas..., hum-molgen.org, May 7 |
Do-it-yourself genetic sleuthing, Boston.com, May 11 |
UAE GDA urges general public to get screened for genetic diseases, Zawya, May 7 |
Genetic make-up influences biased economic decision-making, study shows, Science Daily, May 11 |
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The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism
Depaolo J, et al.
Mov Disord 2009 May
Genetically based impairment in CYP2C8- and CYP2C9-dependent NSAID metabolism as a risk factor for gastrointestinal bleeding: Is a combination of pharmacogenomics and metabolomics required to improve personalized medicine?
Agundez JA, et al.
Expert Opin Drug Metab Toxicol 2009 May
Fcgamma receptors: structure, function and role as genetic risk factors in SLE
Li X, et al.
Genes Immun 2009 May
Genetic and environmental pathways to complex diseases
Gohlke JM, et al.
BMC Syst Biol 2009 May;3(1):46
Pharmacogenetics in chemotherapy of colorectal cancer
Henriette Tanja L, et al.
Best Pract Res Clin Gastroenterol 2009;23(2):257-73
Hereditary pancreatic cancer: a clinical perspective
Greer JB, et al.
Best Pract Res Clin Gastroenterol 2009;23(2):159-70
Hereditary gastric cancer
Oliveira C, et al.
Best Pract Res Clin Gastroenterol 2009;23(2):147-57
Introduction to molecular and clinical genetics of colorectal cancer syndromes
Tops CM, et al.
Best Pract Res Clin Gastroenterol 2009;23(2):127-46
The genetics of Parkinson's syndromes: a critical review
Hardy J, et al.
Curr Opin Genet Dev 2009 May
Shrinkage estimation for robust and efficient screening of single-SNP association from case-control genome-wide association studies
Luo S, et al.
Genet Epidemiol 2009 May
Case-only genome-wide interaction study of disease risk, prognosis and treatment
Pierce BL & Ahsan H
Genet Epidemiol 2009 May
Avoiding the high Bonferroni penalty in genome-wide association studies
Gao X, et al.
Genet Epidemiol 2009 May
Genome-wide association studies: Detecting gene-gene interactions that underlie human diseases
Cordell HJ
Nat Rev Genet 2009 May
Genomics and the efficacy of aspirin in the treatment of cerebrovascular disease
Cavallari LH & Momary KM
Curr Treat Options Cardiovasc Med 2009 Jun;11(3):191-200
A Robust Genome-Wide Scan Statistic of the Wellcome Trust Case-Control Consortium
Joo J, et al.
Biometrics 2009 May
A Robust Test for Two-Stage Design in Genome-Wide Association Studies
Kwak M, et al.
Biometrics 2009 May
Relationship between a family history of malignancy and the incidence of laryngeal carcinoma in the Liaoning province of China
Li XY, et al.
Clin Otolaryngol 2009 Apr;34(2):127-31
Familial Recurrence of Midline Birth Defects--A Nationwide Danish Cohort Study
Oyen N, et al.
Am J Epidemiol 2009 May
Family cancer history affecting risk of colorectal cancer in a prospective cohort of Chinese women
Murphy G, et al.
Cancer Causes Control 2009 May
Genetic testing in gastroenterology: Lynch syndrome
Grover S & Syngal S
Best Pract Res Clin Gastroenterol 2009;23(2):185-96
Genetic testing in other GI diseases
Hodgson S & Ioannides AS
Best Pract Res Clin Gastroenterol 2009;23(2):245-56
Genetic counselling and genetic testing in hereditary gastrointestinal cancer syndromes
Raymond VM & Everett JN
Best Pract Res Clin Gastroenterol 2009;23(2):275-83
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Barrett JC, et al.
Nat Genet 2009 May
Genome-wide Association Analysis Identifies PDE4D as an Asthma-Susceptibility Gene
Himes BE, et al.
Am J Hum Genet 2009 May
Genome-wide association study of blood pressure and hypertension
Levy D, et al.
Nat Genet 2009 May
Multiple loci associated with indices of renal function and chronic kidney disease
Kottgen A, et al.
Nat Genet 2009 May
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C, et al.
Nat Genet 2009 May
A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS)
Rich SS, et al.
Diabetologia 2009 May
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
Scott LJ, et al.
Proc Natl Acad Sci U S A 2009 May;106(18):7501-6
Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan
Yang HC, et al.
PLoS ONE 2009;4(5):e5459
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The CDC 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.
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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. |
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