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Disability : Displaying 11-20 of 169


Community Concerns Regarding the Google-Autism Speaks Ten Thousand Genomes Program (AUT10K)ASANJune 12th, 2014In response to the recent announcement of the new Google-Autism Speaks collaboration to produce, expand and analyze the world’s largest private collection of DNA samples of autistic children and adults.
A Medical Student’s Call for Action Against Research Misconductby Eden AlmasudeThe Hastings CenterJune 3rd, 2014Is research misconduct and abuse the norm in the University of Minnesota’s Department of Psychiatry? A recent investigative report suggests that the answer may well be yes.
Loophole in Genetic Testing Lawby Rachel GlaserWHAM TVMay 23rd, 2014People who undergo increasingly popular genetic testing could be penalized, forced to pay higher premiums or denied coverage for certain policies.
On Dialogue: Disability Studies and Science & Technology Studiesby Laura MauldinSomatosphereMay 19th, 2014The intersection of disability studies with science and technology studies can illuminate how we understand, act upon, cope with, and expect others to cope with human bodies.
Advancing the Disability Rights Perspective on Bioethics Issuesby Diane ColemanNot Dead YetMay 2nd, 2014The first ever Disability Rights Leadership Institute on Bioethics drew more than 60 participants.
NIPS SPINby Robert RestaThe DNA ExchangeApril 21st, 2014Every few years a new screening technology comes zooming down the prenatal pike, sometimes arriving more quickly than we might like. The latest iteration – Non-Invasive Prenatal Screening – stands head and shoulders above the rest.
Genetic Inheritance: How Much do you Want to Know?by Stuart JeffriesThe GuardianApril 4th, 2014Scientist Sharon Moalem says we will soon be able to alter our children's lives with genetic manipulation – would you do it if you could?
A Disturbing Trend: Conscience Clauses Threaten Genetic Counselingby Alex SternHuffington PostApril 2nd, 2014Conscience clauses place genetic counselors in an untenable predicament: State laws and hospital directives are in conflict with professional ethics and best practices.
Adrienne Asch: A Career at the Intersection of Bioethics and Disability Studiesby Sara BergstresserVoices in BioethicsMarch 12th, 2014Recognizing Adrienne Asch's pioneering work: Remembrances by three people who knew her both professionally and personally.
When Science Doesn't Have all the Answersby Louise KinrossBloomMarch 6th, 2014My son’s rare genetic deletion is on the list of disorders identified by microarray analysis of a fetus’s DNA. It makes me sad to think that the lives of children like my son are being targeted for termination. Is this a step forward?
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