ThinkGenetic Blog

News from ThinkGenetic

  • Home
  • FindEHR
  • Disease Knowledge Base
  • News
  • About Us
  • Contact Us
Browse Diseases

The FDA Adds Gene Therapy to the Menu

January 24, 2018 Morgan Simmons, MMSc, CGC 1 Comment

Sometimes (read: most of the time), I think we as a society are pretty spoiled. Unlike our ancestors, we live in an age where many medical conditions and ailments can… CONTINUE

Filed Under: Education, News Tagged With: blindness, FDA, gene therapy, genetic condition, genetic disease, inherited disease, Jesse Gelsinger, Leber congenital amaurosis, Luxturna, Morgan Simmons, rare diseases, Retinitis pigmentosa, RPE65 gene

VUS Detectives: Recognizing the Individuals Who Seek to Understand Genomic Variants

October 22, 2017 Dawn Laney, MS, CGC, CCRC | ThinkGenetic Co-Founder 1 Comment

“Thanks for the genetic testing results, but what do they MEAN?!!” could be the unifying cry of thousands of patients and family members after receiving genetic test results that show… CONTINUE

Filed Under: Education Tagged With: ClinVar, Dawn Laney, Emory University, Find My Variant, Free the Data, InformedDNA, Karmen Trzupek, Morgan Simmons, PROMPT, Retinitis pigmentosa, Simons VIP, University of Washington, variant, variant of uncertain significance, VOUS, VUS

Weekly Site Update for 11/15/2016

November 11, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: adrenal cortex, Alzheimer, Alzheimer disease, ARSA, arylsulfatase A, atrophy, Beckwith-wiedemann syndrome, Bilateral renal agenesis, biotin, biotinidase, Biotinidase deficiency, birth defects, CARASIL, Choroideremia, congenital, Congenital Adrenal Hyperplasia, Cutis Laxa, dementia, DMD, Duchenne muscular dystrophy, dystroglycanopathies, EIEE2, Epileptic encephalopathy, fetal varicella syndrome, genetic disorder, GM2, HD, Hirschsprung disease, Holocarboxylase synthetase deficiency, Huntington's disease, lactase, Lactase deficiency, metabolic condition, Metachromatic leukodystrophy, MLD, Mowat-Wilson syndrome, Mucolipidosis iii alpha, Mucolipidosis iii beta, muscle disorder, muscular dystrophy, neurologic disorder, polydystrophy, Retinitis pigmentosa, Rubinstein-Taybi syndrome, seizures, strokes, Tay-sachs disease, vision, Walker-Warburg syndrome, WWS, Xeroderma pigmentosum, XP

Search the News & Press

Connect with Us

     
  • Home
  • News
  • About Us
  • Contact Us
  • Sponsor / Advertise
  • Disclaimers
  • Terms and Conditions
  • Privacy Policy
©2022 ThinkGenetic. All Rights Reserved.ThinkGenetic does not provide medical advice, diagnosis or treatment. Click here for more information.

Copyright © 2022 · Genesis Framework · WordPress · Log in