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Civil Society : Displaying 170-179 of 549


Why we Should Opt Out of the Government's New Patient Databaseby Edward HockingsThe GuardianJanuary 31st, 2014Medical records in England and Wales will soon be linked to whole-sequenced genomes. Choosing to "opt out" is also taking a stand on what kind of society we want in the future.
Is genius in the genes?by Steven RoseTESJanuary 24th, 2014The debate about genes and intelligence has resurfaced, and it’s more fervent than ever. Can achievement truly be inherited? Should education be tailored to individuals’ genetic potential?
CGS Letter to the FDA on Mitochondrial TransferThe Center for Genetics and Society's letter regarding the FDA's February 25-26 public meeting to discuss the advisability of a technique that would modify the human germline.
[UK] NHS patient data to be made available for sale to drug and insurance firmsby Randeep RameshThe GuardianJanuary 19th, 2014Drug and insurance companies will from later this year be able to buy information on patients – including mental health conditions and diseases such as cancer, as well as smoking and drinking habits – once a single English database of medical data has been created. Harvested from GP and hospital records, medical data covering the entire population will be uploaded to the repository controlled by a new arms-length NHS information centre, starting in March. Never before has the entire medical history of the nation been digitised and stored in one place.
A Short History of Biological Explanations for Povertyby Jessica CussinsBiopolitical TimesJanuary 2nd, 2014“The Biological Inferiority of the Undeserving Poor” sketches the history of biological explanations for social ills, and warns that we should pay close attention to their current resurgence.
The Biological Inferiority of the Undeserving Poorby Michael B. KatzSocial Work and Society International Online JournalDecember 24th, 2013The biological definition of poverty reinforces the idea of the undeserving poor, which is the oldest theme in post-Enlightenment poverty discourse.
Screening Newborns For Disease Can Leave Families In Limboby Nell GreenfieldboyceNPRDecember 23rd, 2013Patient advocacy groups have been pushing states to adopt mandatory newborn screening for more and more diseases, including ones that have no easy diagnosis or treatment.
Selling Tests, Selling Treatments: A Few Reflections on Medical Advertisingby George Estreich, Biopolitical Times guest contributorDecember 18th, 2013The questions raised by the recent New York Times article about aggressive selling of ADD drugs should also be posed to those marketing non-invasive prenatal gene tests.
‘Generation Cryo’: How A New Generation Is Redefining Familyby Marisa PeñalozaWBURDecember 17th, 2013Thousands of children are conceived using sperm and egg donors every year, a group large enough to entice MTV to air “Generation Cryo.”
Professor Plomin Goes to Parliamentby John GillottBioNewsDecember 16th, 2013The House of Commons Education Committee, currently investigating 'underachievement in education of white working class children,' heard about the genetics of children with learning disabilities.
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