PHG Foundation | April 2009

  PHG Foundation genomics and policy news
    15 April 2009
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A new initiative linked to the famous Framingham Heart Study has been announced to look for novel biomarkers for cardiovascular disease risk (21 March), whilst in the scientific literature results from large-scale trials of prostate cancer screening have reignited debate (25 March). Genome wide association studies have identified some common genetic variants associated with increased risk of sudden cardiac death (9 April). In the US, there has been further discussion in the area of open access publishing of scientific research (31 March).

Biobanks and databases: research and regulation
Issues surrounding access to information held in databases have been in the UK news, with concerns about privacy and discussion of public attitudes (16 March) and a new report looking at government databases, including those holding health information (8 April). Another UK report discusses the appropriate regulation of biomedical research (1 April).

New initiatives to create biobanks and databases for research purposes have been announced, including plans for a study to identify genetic factors involved in Parkinson’s disease hosted by genetic testing company 23andMe (18 March), for a large-scale TwinBank to facilitate research into the genetic and environmental factors involved in common diseases, and for a Baby BioBank for work on genetic contributions to complications of pregnancy (11 April). However, there has been controversy in the UK over policies in different NHS hospitals towards collection and storage of umbilical cord blood for deposition in public or private stem cell banks (27 March).

Genetic tests and gene patenting
In Australia, a new survey and report has found that access to genetic tests across the country is inequitable (6 April), whilst in Europe the results of a large survey of patients with rare diseases (many of them inherited) have been published by the European Organisation for Rare Diseases (24 March).
In the US, a government advisory committee has released a draft report on the impact of gene patents on patient access to genetic tests (17 March), and proposals for the implementation of a compulsory web-based registry of genetic tests have been developed (13 April).

New reviews and commentaries
Our selection of recent articles of interest (2 April)

Other recent news and research
New type of stem cell holds promise for multiple sclerosis
Scientists discover gene that controls blood-cell formation
NIAID Funding Malaria Genomics, Field Studies
Mutation 'sparks most melanoma'

Killing faulty stem cells holds promise for treating bowel cancer

Gene defect clue to male pill
DeCODE faces financial crisis
Stem cell 'deafness cure' closer

Scientists map copy number variations of whites, blacks in genome

Scientists find genes linked to various cancers
3 genes determine right warfarin dose
Gene technique treats dogs with fatal muscle disease
Scientists to use stem cells to produce synthetic blood
FTO obesity gene associated with susceptibility to polycystic ovary syndrome
Gene plays role in converting carbohydrates to fat
Children of cousins 'have greater risk of catching infectious disease'
Gene shows promise for Type 1 diabetes in animal study
Study tests technique to prevent spread of hepatitis C virus
Test accurate in spotting early-stage Alzheimer's
Fishing for microdeletions that predispose an embryo to develop cancer syndromes
Personalized cancer therapy gets closer
NIH Working on DTC Genomics Public Resource

See also the Genomics & Health Weekly Update from the CDC Office of Public Health Genomics and the GenInfo Monthly Newsletter from HumGen.

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Created: 15 May 2009