Image Rotator

Nearly 5 percent of U.S. children may be affected by FASD, according to a new study co-authored by Sanford Research’s Gene Hoyme, MD, and Amy Elliott, PhD.
Sanford Study Reveals FASD Prevalence
Nearly 5 percent of U.S. children may be affected by FASD, according to a new study co-authored by Sanford Research’s Gene Hoyme, MD, and Amy Elliott, PhD.
 

Children's Health Research

The Sanford Children’s Health Research Center is leading the way in translational pediatric research, including cancer and rare diseases.

Learn More

 

The Sanford Project

The Sanford Project is focused on restoring a patients’ own pancreatic insulin production by reviving their insulin-producing pancreatic islet beta cells.

Learn More

 

Clinical Research at Sanford

Sanford Health offers a robust clinical research platform where bench and translational research can be combined seamlessly with medical care delivery.

Learn More

  • Sanford Discoveries e-Publication: Subscribe Today!

    Keep in touch with all of the innovation happening in Sanford Research and Development. Subscribe to the Sanford Discoveries e-Publication for quarterly updates.

    Learn More

  • Exploring American Indian Infant Mortality

    Amy Elliott, PhD, and Jyoti Angal have a secured more than $1.7 million in NIH funding.

    Learn More

  • Baack Receives NIH Grant

    Research will focus on preventing cardiovascular disease in the offspring of diabetic mothers.

    Learn More

  • Study Replicates Genetic Mutations

    David Pearce, PhD, has developed a mouse model replicating the genetic mutations in Batten disease.

    Learn More

Twitter Updates on Sanford Research
  • @DrMLBooze
    @SanfordPROMISE community lecture series tying into #RareDiseaseDay2015 @AlphaFriend @SanfordCoRDS

  • @Kegottsleben
    Looking forward to attending @SanfordCoRDS' 5th Annual Sanford Rare Disease Symposium tomorrow! #SanfordRDD #WRDD2015 #CareAboutRare #MPS

  • @SanfordCoRDS
    Happy Global Rare Disease Day! CoRDS is celebrating at 5th Annual Sanford Rare Disease Symposium! #SanfordRDD #WRDD2015 #CareAboutRare

  • @KFS_Freedom
    RT @Rose_of_Sharon8: Your child defies Rare Disease! SATURDAY is Rare Disease Day ! #WRDD2015 @KFS_Freedom @RareDiseases @SanfordCoRDS htt…

  • @Rose_of_Sharon8
    Your child defies Rare Disease! SATURDAY is Rare Disease Day ! #WRDD2015 @KFS_Freedom @RareDiseases @SanfordCoRDS http://t.co/v2d1oe7R7a

  • @pedrolesteban
    RT @KFS_Freedom: We R pumped that Dr Giampietro 2 speak @SanfordCoRDS Rare Disease Day about rare skeletal Klippel-Feil Syndrome! A huge m…

  • @theonlybernster
    RT @KFS_Freedom: We R pumped that Dr Giampietro 2 speak @SanfordCoRDS Rare Disease Day about rare skeletal Klippel-Feil Syndrome! A huge m…

  • @spineday
    RT @KFS_Freedom: We R pumped that Dr Giampietro 2 speak @SanfordCoRDS Rare Disease Day about rare skeletal Klippel-Feil Syndrome! A huge m…

  • @Rose_of_Sharon8
    RT @KFS_Freedom: We R pumped that Dr Giampietro 2 speak @SanfordCoRDS Rare Disease Day about rare skeletal Klippel-Feil Syndrome! A huge m…

  • @KFS_Freedom
    We R pumped that Dr Giampietro 2 speak @SanfordCoRDS Rare Disease Day about rare skeletal Klippel-Feil Syndrome! A huge milestone! Thanks

  • @tealakerda
    RT @CheckOrphan: Read about the great working being done by @SanfordCoRDS in developing patient registries for #RareDiseases http://t.co/2H…

  • @SanfordCoRDS
    Take a few minutes to read this article which features CoRDS and our Director, Catie Oslon! http://t.co/Kl8vH7k0K9 Thanks to @CheckOrphan

  • @CheckOrphan
    Read about the great working being done by @SanfordCoRDS in developing patient registries for #RareDiseases http://t.co/2HY2IR9jqJ

  • @SanfordCoRDS
    RT @NIH: Join the #NIHchat tomorrow, 2/25 at 2:30 ET in honor of Rare Disease Day! http://t.co/tc6ZvCpHYn

  • @NPallone
    RT @SanfordCoRDS: Join us and help kick off #WRDD2015 #CareAboutRare There's still time to register! http://t.co/VfCtT6o8NV http://t.co/gE…