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MetroWest Daily News: Sudbury startup aids in diagnosing genetic conditions

March 7, 2019 Ruth O'Keefe Leave a Comment

ThinkGenetic Team Members

Original article: https://www.metrowestdailynews.com/news/20190307/sudbury-startup-aids-in-diagnosing-genetic-conditions By Zane Razzaq Daily News staff  SUDBURY – With the average patient struggling to find a diagnosis for a genetic condition for several years, a Sudbury family is… CONTINUE

Filed Under: Lafayette, News Tagged With: Cutis Laxa, Dave Jacob, Dawn Laney, Lafayette General Health System, MetroWest Daily News, Ruth O'Keefe, SymptomMatcher, ThinkGenetic

ThinkGenetic Signs First International Advocacy Partner

December 6, 2016 Ruth O'Keefe Leave a Comment

France based support group, Cutis Laxa Internationale, becomes first International ThinkGenetic Advocacy Partner Cutis Laxa Internationale became an official ThinkGenetic Advocacy Partner today, the first advocacy partner based outside the… CONTINUE

Filed Under: News, Partners Tagged With: advocacy, advocacy group, advocacy partner, Cutis Laxa, Cutis Laxa Internationale, Dave Jacob, Marie-Claude Boiteux, Partners, partnership, Ruth O'Keefe, support group, ThinkGenetic

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

Why My Kindred Spirit is a Rock Star

September 8, 2016 Dave Jacob Leave a Comment

CEO Post Austin Carlile

At first glance, it may not seem Austin Carlile, the front-man of the metal-core band Of Mice & Men and I have much in common. We grew up about 100… CONTINUE

Filed Under: News Tagged With: Austin Carlile, Cutis Laxa, Dave Jacob, Emory University, genetic disease, genetic disorder, IBM Watson, Marfan syndrome, Of Mice and Men

ThinkGenetic Father Hopes to Revolutionize Genetic Information on the Internet

July 6, 2016 thinkgenetic 3 Comments

Like many other people with a genetic disease, Dave Jacob did not learn that his childhood heart defect was related to an underlying genetic mutation until it was uncovered he… CONTINUE

Filed Under: News Tagged With: Cutis Laxa, Davalen, Dave Jacob, Dawn Laney, Ehler Danlos, Emory University, genetic diagnosis, genetic mutation, IBM, IBM Watson, kickstarter, Marfan syndrome, Massachusetts, medical mystery, News, press, Sudbury, ThinkGenetic, thinkgenetic.com, Watson

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