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Sanford Research is a non-profit research organization that is a part of Sanford Health, the largest rural, not-for-profit health care system in the nation. Transformational gifts by Denny Sanford have propelled Sanford Research in its goal of becoming a world class research institution. Sanford Research has sought to establish a core of scientists that are studying disease at a fundamental level with the expectation that these current efforts will pay off in the future by advancing disease therapy and prevention.
With a team of over 200 researchers, Sanford Research is comprised of eight groups that bridge bench, translational and clinical research including: Cancer Biology and Immunotherapies, Pediatrics and Rare Diseases, Diabetes, Cellular Therapies and Stem Cell Biology, Enabling Technology, Environmental Influences on Health and Disease, Genetics and Genomics, and Population Health. |
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Twitter Updates on Sanford Research
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#Genetic test for prediction of #Cancer reoccurrence https://t.co/MfJMklisHZ #PrecisionMedicine -
Progress!!!! https://t.co/ofouUceBkV -
The 'flesh-eating' #genes of streptococcus reported https://t.co/tAVVmwbudF #genetics -
Possible #GeneTherapy for #Usher syndrome being developed https://t.co/yGA3VS25YW #RareDiseases -
Possible #GeneTherapy being developed for #MultipleSclerosis #MS https://t.co/Tmws6JoO2C #Neuroscience -
@SanfordCoRDS @N0oLo So this is one of the two main medical providers near me ... gotta check this research area out! -
RT @_mai_ran: Thank you @SanfordCoRDS for speaking with @ASGCGP 2nd years. A great resource for our patients! -
Thank you @SanfordCoRDS for speaking with @ASGCGP 2nd years. A great resource for our patients! -
Thanks @ORDR 4 supporting first hand patient med experience w Rare Disease @KFS_Freedom @SanfordCoRDS @RareDiseases… https://t.co/0vhjPrDDRJ -
@KFS_Freedom @SanfordCoRDS @GlobalGenes Love you guys! 💜🎶 -
RT @LittleLobbyists: This is a must watch. Thank you, @jimmykimmel. Thank you thank you thank you for speaking up to protect our kids. http… -
RT @SanfordCoRDS: CoRDS is the advocacy group for all #raredisease #patients & those without a support group, because rare is common for 30… -
Missed #2017GGsummit but we're unstoppable 4 #RareDisease #research #data #patients #patients c our pinned post… https://t.co/2AGaAhG80x -
RT @JFCConsultants: @JFCConsultants @PPALSorg was happy to share an exhibit table with @SanfordCoRDS at @GlobalGenes Patient Summit! Wonder… -
@JFCConsultants @PPALSorg was happy to share an exhibit table with @SanfordCoRDS at @GlobalGenes Patient Summit! Wonderful collaboration!!