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Wednesday, December 31, 2008 |
Volume
21 Number 25 |
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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.
Cancer |
In lung cancer, silencing one crucial gene disrupts normal functioning of genome, Medical News Today. December 31 |
Drinkers with the ADH1C gene at greater risk of colorectal cancer, News-Medical.Net, December 22 |
Prostate cancer screening has pros and cons, nj.com, December 30 |
Scientists find gene that is a powerful predictor of colon cancer metastasis, News-Medical.Net, December 22 |
Many studies needed to tie genes to cancer: study, Reuters Health, December 30 |
Baby girl free of breast cancer gene due to be born soon, Medical News Today, December 21 |
Targeted nanoparticles deliver therapeutic DNA to cancer cells, News-Medical.Net, December 29 |
Researchers identify gene linked to inherited form of fatal lung disease, News-Medical.Net, December 21 |
The Von Hippel-Lindau Gene: Turning discovery into therapy, Medical News Today, December 25 |
Researchers create 'suped up' gene that forces cancer cells to self destruct, News-Medical.Net, December 18 |
Breast cancer genome shows evolution, instability of cancer, Science Daily, December 24 |
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Other News |
Genome-wide association studies must account for ancestry, Medical News Today, December 31 |
Genetic diseases may be tougher to crack, new research suggests, CBCnews.ca, December 26 |
Facial expression of emotion is hardwired say scientists, Medical News Today, December 29 |
Various immune related diseases have a strong genetic overlap, Medical News Today, December 26 |
Gene expression and splicing vary widely from 1 tissue to the next, Medical News Today, December 29 |
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Cohort studies and the genetics of complex disease
Manolio TA
Nat Genet 2009 Jan;41(1):5-6
All we need is GWAS: Genome-Wide Association Studies in Type 2 Diabetes Mellitus presented on the 2008 EASD Meeting in Rome
Klupa T & Malecki MT
Rev Diabet Stud 2008 Fall;5(3):175-9
SNPHarvester: a filtering-based approach for detecting epistatic interactions in genome-wide association studies
Yang C, et al.
Bioinformatics 2008 Dec
Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all
Delgado-Escueta AV & Bourgeois BF
Epilepsia 2008 Dec;49 Suppl 9:13-24
Detecting shared pathogenesis from the shared genetics of immune-related diseases
Zhernakova A, et al.
Nat Rev Genet 2009 Jan;10(1):43-55
Breast cancer susceptibility: current knowledge and implications for genetic counseling
Ripperger T, et al.
Eur J Hum Genet 2008 Dec
Legal update: living with the Genetic Information Nondiscrimination Act
Erwin C
Genet Med 2008 Dec;10(12):869-73
Clinical practice and genetic counseling for cystic fibrosis and CFTR-related disorders
Moskowitz SM, et al.
Genet Med 2008 Dec;10(12):851-68
Pharmacogenetics in breast cancer therapy
Tan SH, et al.
Clin Cancer Res 2008 Dec;14(24):8027-41
Genetic susceptibility loci for breast cancer by estrogen receptor status
Garcia-Closas M & Chanock S
Clin Cancer Res 2008 Dec;14(24):8000-9
The genetic basis for type 1 diabetes
Mehers KL & Gillespie KM
Br Med Bull 2008;88(1):115-29
Asking the Right Questions: Views on Genetic Variation Research Among Black and White Research Participants
Bussey-Jones J, et al.
J Gen Intern Med 2008 Dec
Pharmacokinetics and pharmacogenomics in breast cancer chemotherapy
Marsh S & Liu G
Adv Drug Deliv Rev 2008 Dec
Pharmacogenetics in acute lymphoblastic leukemia
Cheok MH, et al.
Semin Hematol 2009 Jan;46(1):39-51
MedRefSNP: a database of medically investigated SNPs
Rhee H & Lee JS
Hum Mutat 2008 Dec
Prostate cancer genomics: towards a new understanding
Witte JS
Nat Rev Genet 2008 Dec
Oophorectomy for breast cancer prevention in women with BRCA1 or BRCA2 mutations
Metcalfe KA
Womens Health (Lond Engl) 2009 Jan;5(1):63-8
Clinical geneticists in birth defects surveillance and epidemiology research programs: Past, present and future roles
Lin AE, et al.
Birth Defects Res A Clin Mol Teratol 2008 Dec
Relation of familial patterns of coronary heart disease, stroke, and diabetes to subclinical atherosclerosis: the multi-ethnic study of atherosclerosis
Scheuner MT, et al.
Genet Med 2008 Dec;10(12):879-87
Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation
Metcalfe KA, et al.
Br J Cancer 2008 Dec
Patient interest in recording family histories of cancer via the Internet
Simon C, et al.
Genet Med 2008 Dec;10(12):895-902
Familial risks for amyotrophic lateral sclerosis and autoimmune diseases
Hemminki K, et al.
Neurogenetics 2008 Dec
Serum adiponectin is associated with family history of diabetes independently of obesity and insulin resistance in healthy Korean men and women
Sull JW, et al.
Eur J Endocrinol 2009 Jan;160(1):39-43
Selecting a BRCA risk assessment model for use in a familial cancer clinic
Panchal S, et al.
BMC Med Genet 2008 Dec;9(1):116
Clinical Utility of Genetic Tests for Inherited Hypertrophic and Dilated Cardiomyopathies
Colombo MG, et al.
Cardiovasc Ultrasound 2008 Dec;6(1):62
The influence of acculturation and breast cancer-specific distress on perceived barriers to genetic testing for breast cancer among women of African descent
Sussner KM, et al.
Psychooncology 2008 Dec
Genetic counselling and testing for inherited gene mutations in newly diagnosed patients with breast cancer: a review of the existing literature and a proposed research agenda
Meiser B, et al.
Breast Cancer Res 2008 Nov;10(6):216
The impact of direct-to-consumer marketing of cancer genetic testing on women according to their genetic risk
Lowery JT, et al.
Genet Med 2008 Dec;10(12):888-94
Molecular diagnosis of Fragile X syndrome
Sofocleous C, et al.
Expert Rev Mol Diagn 2009 Jan;9(1):23-30
Hereditary breast and ovarian cancer syndrome : the impact of race on uptake of genetic counseling and testing
Simon MS & Petrucelli N
Methods Mol Biol 2009;471:487-500
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
Muglia P, et al.
Mol Psychiatry 2008 Dec
New sequence variants associated with bone mineral density
Styrkarsdottir U, et al.
Nat Genet 2008 Dec
A Genome-wide Association Study Identifies Three Loci Associated with Mean Platelet Volume
Meisinger C, et al.
Am J Hum Genet 2008 Dec
Genome wide association for substance dependence: convergent results from epidemiologic and research volunteer samples
Johnson C, et al.
BMC Med Genet 2008 Dec;9(1):113
Distinct Genetic Loci Control Plasma HIV-RNA and Cellular HIV-DNA Levels in HIV-1 Infection: The ANRS Genome Wide Association 01 Study
Dalmasso C, et al.
PLoS ONE 2008;3(12):e3907
Cytochrome P-450 Polymorphisms and Response to Clopidogrel
Mega JL, et al.
N Engl J Med 2008 Dec
Genetic Determinants of Response to Clopidogrel and Cardiovascular Events
Simon T, et al.
N Engl J Med 2008 Dec
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