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ThinkGenetic and Guardian Research Network Announce Partnership

July 28, 2022 Ruth O'Keefe 2 Comments

Guardian Research Network® and ThinkGenetic Announce Collaborative Partnership to Accelerate Diagnosis and Treatment Options for Patients with Genetic Diseases and Inherited Predisposition to Cancer Joint effort recognizes combined missions to support… CONTINUE

Filed Under: News, Partners, Press Tagged With: algorithm, announcement, Bruce Braughton, Dave Jacob, diagnostic odyssey, digital health, EHR, electronic health records, genetic condition, genetic disease, GRN, Guardian Research Network, healthcare, Mark Watson, partnership, press release, PTC Therapeutics, Rare Disease, ThinkGenetic

Do You Love Your Genetic Condition?

March 14, 2018 Morgan Simmons, MMSc, CGC Leave a Comment

ThinkGenetic Blog - Genetic Condition - Bottom Story - Morgan Simmons

Over the last few years, I’ve had the opportunity to work with patients at various stages in their diagnostic odyssey. I’ve seen people who have lived their whole lives knowing… CONTINUE

Filed Under: Education, News Tagged With: diagnosis, diagnostic odyssey, genes, genetic condition, genetic counseling, genetic diagnosis, genetic disease, Marfan syndrome, Morgan Simmons, Rare Disease Day

Fabry Disease Study Using ThinkGenetic Diagnostic Aid to be Showcased at WORLDSymposium

December 20, 2017 Ruth O'Keefe Leave a Comment

ThinkGenetic SymptomMatcherTM Diagnostic Aid Tested for Patients with Fabry Disease in Study by Emory University School of Medicine, Grady Memorial Hospital and University of Georgia College of Pharmacy ThinkGenetic today… CONTINUE

Filed Under: Events Tagged With: Carol Ogg, Dawn Jacob Laney, diagnostic odyssey, Emory University School of Medicine, Fabry disease, genetic disease, Grady Memorial Hospital, lysosomal diseases, Morgan Simmons, SymptomMatcher, Taylor Mitchell, ThinkGenetic SymptomMatcher, University of Georgia College of Pharmacy, WORLDSymposium

How Genetic Disease Families Push Through, Move Forward and Find Answers

May 5, 2017 Jennifer Sturges Shinn Leave a Comment

Such a sentiment is lived by the millions of individuals and families around the world who go through the genetic condition diagnostic odyssey. Search the news section on any rare… CONTINUE

Filed Under: News Tagged With: diagnosis, diagnostic odyssey, Gangliosidosis, genetic disease, Mowat-Wilson Symdrome, rare condition, Rare Disease

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