The ThinkGenetic Foundation is very excited to announce the confirmed Speakers and Patient Panelists for the upcoming FREE Lunch and Learn:Closing the Genetics Gap: A Discussion on Increasing Education and… CONTINUE
About Ruth O'Keefe
MetroWest Daily News: Sudbury startup aids in diagnosing genetic conditions
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
Big News for ThinkGenetic Supporters – Angel Funding Round is Closed
In a very exciting announcement from the news desk, ThinkGenetic announced the closure of its $1.5M Angel Funding round. (See the full announcement here.) When asked about the incredible accomplishment,… CONTINUE
Introducing Michael Mgbemena – ThinkGenetic’s 2019 Intern Class
ThinkGenetic is honored to work with incredible interns eager to help ThinkGenetic achieve its mission of reaching and empowering those living with and at risk for genetic conditions. With each… CONTINUE
Introducing Pauline Kitolo – ThinkGenetic’s 2019 Intern Class
Each year, ThinkGenetic is honored to work with incredible interns eager to help ThinkGenetic achieve its mission of reaching and empowering those living with and at risk for genetic conditions…. CONTINUE
Primary Distal Renal Tubular Acidosis (dRTA) Added to ThinkGenetic Knowledge Base
Never heard of Primary distal renal tubular acidosis (primary dRTA)? You’re not alone! This rare genetic condition results in problems with kidney function, bone formation, hearing, and managing potassium, calcium,… CONTINUE
Taking a Closer Look at Advocacy: Accelerating The Cures of Tomorrow
More than just an organization, advocacy partner, the Rare Genomics Institute (RG), is a community dedicated to helping rare disease patients find hope for a cure. Sharing a mission of… CONTINUE
Endless Hope for Klippel-Feil Syndrome
Editor’s Note: It has been such an honor working with Sharon Rose to represent the Klippel-Feil syndrome (KFS) community. Sharon Rose shared her strong desire to work with ThinkGenetic to… CONTINUE
Taking a Closer Look at Advocacy: Creating Hope with a Support Network for the Rare Disease Community
ThinkGenetic is honored to partner with many incredible organizations, each with their own stories, struggles and triumphs. This month, we are taking a moment to highlight the incredible work of… CONTINUE
NGLY1 Added to ThinkGenetic Genetic Condition Knowledge Base
Co-founded by a patient advocate and a genetic counselor, ThinkGenetic helps individuals harness their personal power of advocacy by offering trustworthy information to guide them to the help they need,… CONTINUE
Informative Videos on ThinkGenetic
Interested in learning more about ThinkGenetic and our mission and services? We know sometimes seeing is more helpful then reading. We encourage you to take a look at some of… CONTINUE
From Friend to Intern to Advocate: A Reflection on My Experience with Duchenne Muscular Dystrophy
Editor’s Note: Today I am excited to release this article, written by an incredible young woman I’ve grown to know and respect as our Digital Marketing Intern. Courtney Burt’s time… CONTINUE
ThinkGenetic Partners with Genome Medical
New Partnership Strengthens ThinkGenetic’s Continued Effort to Reduce Time to Diagnosis In an influential move for the genetics community, ThinkGenetic (ThinkGenetic.com) and Genome Medical (GenomeMedical.com), a nationwide specialty medical practice… CONTINUE
ThinkGenetic Named Finalist in Largest Veteran Business Competition in the United States
In a recent press release, The Veterans in Business Association (VIBA) at Rice University announced that ThinkGenetic has been accepted as a finalist into the 2018 Veterans Business Battle out… CONTINUE
ThinkGenetic Supports Homocystinuria Patients Through Partnership with HCU Network Australia
ThinkGenetic welcomes HCU Network Australia to the ThinkGenetic Advocacy Partner Program. Through this partnership, people impacted by the genetic condition homocystinuria in Australia and beyond will have a wider array of… CONTINUE
ThinkGenetic Provided $100,000 Credit from Amazon Web Services as Part of MassChallenge
ThinkGenetic is excited to announce that Amazon Web Services, Inc. (AWS), a subsidiary of Amazon.com, Inc., has approved ThinkGenetic into it’s AWS Activate program. Amazon Web Services provides startups with… CONTINUE
Partnering to Bring Meaningful Progress Toward Treatments and Cures for Fatal Neurodegenerative Disorder
Beyond Batten Disease Foundation Partners with ThinkGenetic in Support of Mission Spearheading a unique, cohesive strategy, Beyond Batten Disease Foundation has added ThinkGenetic to its collaborators by joining the ThinkGenetic… CONTINUE
Advocacy Partnership Raises Awareness of Stomach Cancer as a Global Issue
Advocacy Partnership with No Stomach for Cancer Raises Profile of Valuable Stomach Cancer and Hereditary Diffuse Gastric Cancer Resources No Stomach For Cancer (NSFC), a worldwide organization known for helping… CONTINUE
ThinkGenetic Supports Rare Disease Day – Show Your Rare
ThinkGenetic is proud to support Rare Disease Day. Why? Because we’re a part of your community! We live and breathe the struggles and triumphs firsthand. Do you know the ThinkGenetic… CONTINUE
Kids with Pfeiffer Syndrome Get More Support with ThinkGenetic / BORN A HERO Partnership
BORN A HERO has joined the ThinkGenetic Advocacy Partner Program to help educate the world about children and others with the genetic condition Pfeiffer syndrome. Through this partnership, more people… CONTINUE
ThinkGenetic Streamlines Access to Patient Resources in India with New Cooperative Agreement with Mapmygenome
Today ThinkGenetic has announced a partnership with Mapmygenome™, a leading personal genomics company based in India specializing in clinical genomics and molecular diagnostics focused on preventive healthcare. Through this partnership,… CONTINUE
ThinkGenetic Declared a PULSE@MassChallenge Top Digital Health Startup
In a recent press release, PULSE@MassChallenge announced that ThinkGenetic was accepted into the Boston-based 2018 startup class out of 500 worldwide applicants. Previous startups that have participated in PULSE@MassChallenge have… CONTINUE
Stealth BioTherapeutics Supports Addition of Mitochondrial Genetic Diseases in ThinkGenetic Knowledge Base
In a public press release this week, ThinkGenetic announced that Stealth BioTherapeutics (Stealth) has funded content design, content creation, and clinical trials advertising for mitochondrial diseases. As a first step… CONTINUE
Bringing Light to Rare Neuromuscular Disease with New ThinkGenetic Advocacy Partnership
Neuromuscular Disease Foundation Partners with ThinkGenetic to Boost Awareness In a move that will broaden the reach of valuable resources available to those living with GNE Myopathy (or HIBM), the… CONTINUE
Fabry Disease Study Using ThinkGenetic Diagnostic Aid to be Showcased at WORLDSymposium
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
ThinkGenetic Supports Pregnant Women with New Advocacy Partner, National CMV Foundation
In a move to help educate pregnant women and those of childbearing age learn about congenital cytomegalovirus (CMV), ThinkGenetic and the National CMV Foundation have entered into an Advocacy Partner… CONTINUE
ThinkGenetic Integrates with FDNA’s Face2Gene to Help Undiagnosed Patients Find Answers
In a public press release today, ThinkGenetic announced a collaboration with FDNA to help patients with undiagnosed genetic diseases. FDNA uses AI to detect physiological patterns that reveal genes affecting… CONTINUE
“Rare is Everywhere” Author Partners with ThinkGenetic
Deborah Katz, health practitioner, author, illustrator, and founder of Rare is Everywhere Global Productions, has officially partnered with ThinkGenetic to support those living with rare genetic disorders. In November 2016,… CONTINUE
Introducing Courtney Burt, Part Three of ThinkGenetic’s 2017 Intern Class
In our third and final part of our ThinkGenetic intern introductions, we are highlighting our intern from Saint Michael’s College, Courtney Burt. Each of our three interns is eager to… CONTINUE
Canadian Fabry Association Partners with ThinkGenetic To Broaden Support for Patients with Fabry Disease
The Canadian Fabry Association (CFA), a non-profit organization raising awareness and educating the public about Fabry disease, has joined ThinkGenetic’s Advocacy Partner program. The CFA is committed to improving the… CONTINUE