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Nature Reviews. Genetics|July 18, 2015
Start me up: ways to encourage sharing of genomic information with research participantsMisha AngristMolecular Diagnosis & Therapy|April 3, 2010
Only connect: personal genomics and the future of American medicineMisha AngristTrends in Biotechnology|January 5, 2005
Breast cancer: integrating the patient with her genomeMisha AngristPlos One|March 21, 2014
Open window: when easily identifiable genomes and traits are in the public domainMisha AngristPersonalized Medicine|December 27, 2011
You never call, you never write: why return of 'omic' results to research participants is both a good idea and a moral imperativeMisha AngristPersonalized Medicine|February 14, 2012
Eyes wide open: the personal genome project, citizen science and veracity in informed consentMisha AngristPersonalized Medicine|May 26, 2018
The future may be closer than you think: a response from the Personalized Medicine Coalition to the Royal Society's report on personalized medicineGeoffrey S Ginsburg, Misha AngristPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 13, 2005
Genomic medicine: genetic variation and its impact on the future of health careHuntington F Willard, Misha Angrist, Geoffrey S GinsburgLife Sciences, Society and Policy|October 12, 2020
Good problems to have? Policy and societal implications of a disease-modifying therapy for presymptomatic late-onset Alzheimer's diseaseMisha Angrist, Anna Yang, Boris Kantor, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2010
Impact of gene patents and licensing practices on access to genetic testing for long QT syndromeMisha Angrist, Subhashini Chandrasekharan, Christopher Heaney, et al.Pageof 4