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Connecting, Collaborating, and Activating at the Vibrant 2017 RARE Patient Advocacy Summit

September 28, 2017 Dawn Laney, MS, CGC, CCRC | ThinkGenetic Co-Founder Leave a Comment

Connecting, Collaborating, and Activating at the Vibrant 2017 RARE Patient Advocacy Summit

While many of our ThinkGenetic teammates helped others “harness their inner power” at the National Society of Genetic Counselors Annual Conference in Columbus, Ohio, ThinkGenetic CEO, Dave Jacob and I… CONTINUE

Filed Under: Events Tagged With: advocacy, Dave Jacob, Dawn Laney, Deborah Katz, Dekel Gelbman, Face2Gene, FDNA, genetic counselor, genetic disease, Global Genes, Rare Disease, summit, SymptomMatcher

ThinkGenetic to Engage with Rare Disease Community at Global Genes’ 6th Annual RARE Patient Advocacy Summit

August 10, 2017 thinkgenetic Leave a Comment

ThinkGenetic to Engage with Rare Disease Community at Global Genes’ 6th Annual RARE Patient Advocacy Summit

ThinkGenetic, Inc. is delighted to be participating in the 6th Annual RARE Patient Advocacy Summit and Partnering and Investor Forum to further its mission of empowering the rare disease community… CONTINUE

Filed Under: Events Tagged With: artificial intelligence, Dave Jacob, Dawn Laney, Dekel Glebman, diagnosis, FDNA, Global Genes, rare patient advocacy summit

Partnership in the FDNA Year of Discovery

May 15, 2017 Carol Ogg, BS Pharm 2 Comments

Partnership in the FDNA Year of Discovery

   Not too long ago it was taught in medical school that rare diseases were just that- rare and you probably wouldn’t see a patient with a rare disease in… CONTINUE

Filed Under: Education, Partners Tagged With: Carol Ogg, Fabry, Fabry disease, Face2Gene, Facial Phenotypes, FDNA, Homocystinuria, IEM, inborn errors of metabolism, inherited metablic disorder, LSD, lysosomal storage diseases, metabolic conditions, MPS Diseases, Mucopolysaccharidosis, Rare Disease, Year of Discovery

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