LAFAYETTE, La., April 20, 2021 (Newswire.com) – Today ThinkGenetic, Inc. (thinkgenetic.com) announces the official acceptance of a $500,000 investment from the Ochsner Lafayette General Healthcare Innovation Fund. “After years of working… CONTINUE
April Book Spotlight: “Can I Play if I Have Fabry?” by Dawn Laney
by Jessica Dronen, MS, CGC, Genetic Diseases Research and Information Specialist, ThinkGenetic Welcome to ThinkGenetic’s first genetic book spotlight! Starting this month we will be pairing a review of one… CONTINUE
Job Posting: Genetic Diseases Research and Information Specialist in Lafayette
No longer accepting applications Posted March 5, 2021 As a Genetic Diseases Research and Information Specialist, you will be responsible for working with ThinkGenetic data scientists, senior genetic counselors and… CONTINUE
Job Posting: Full Stack Java Developer in Lafayette Louisiana
No longer accepting applications Posted February 4, 2021 Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by deploying our disease screening… CONTINUE
ThinkGenetic Announces Integration of Innovative Diagnostic Aid in Takeda Pilot Awareness Initiative
Pilot program brings genetic tools and education to patients searching for answers tied to their chronic medical conditions in Taiwan, Mexico, Argentina, Brazil, Turkey, and Russia BOSTON, December 15, 2020… CONTINUE
Job Posting: Full Stack Java Developer in Lafayette Louisiana
No longer accepting applications Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by deploying our disease screening algorithms on patient facing… CONTINUE
Job Posting: Senior Data Engineer in Lafayette Louisiana
No longer accepting applications Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by applying our disease screening algorithms to de-identified patient… CONTINUE
Unraveling Usher Syndrome through Community
EDITOR’S NOTE: It has been such an honor working with Lanya McKittrick, Krista Vasi, Dan and Annie Arabie, and other members of the vibrant Usher syndrome community. ThinkGenetic is delighted… CONTINUE
Are new shows like “Chasing the Cure”, changing lives?
by Lacie Mehr Editor’s Note: I am excited to present the following blog that brings up several important points about the new TNT/TBS show “Chasing the Cure” and similar shows… CONTINUE
Is all cancer genetic? Understanding hereditary risk
Editor’s Note: I am so thrilled that my colleague and friend, Jennifer Propst, is able to share her genetic cancer expertise with all of us through this piece. It can… CONTINUE
Speakers Announced – Lafayette Lunch and Learn
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
Ruth O’Keefe Promoted to ThinkGenetic Vice President, Marketing and Patient Advocacy
BOSTON, Ma., April 2, 2019 (Newswire.com) – ThinkGenetic, Inc. (www.ThinkGenetic.com), is excited to announce the promotion of Ruth O’Keefe to Vice President, Marketing and Patient Advocacy. ThinkGenetic, the creators of… CONTINUE
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
Holiday History Hunt Down – Getting to Know Your Family’s Health Background
With the holidays fast approaching, lots of comfort food, fall sports, and time with family come to mind. What might not come to mind is genetics, however, the holidays, and… CONTINUE
Good Golly Miss Molly – The Birth of a Mascot for Pompe Disease
Molly bobs around the clinic room, her strawberry blonde hair bouncing with every move. She has spread out her array of toys – stickers, books, a baby doll named Jack… 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
Could a Biological Trojan Horse Help Us Cure Genetic Diseases?
Most medical treatments fall into four broad categories based on their goal: Preventive/prophylactic – avoiding the disease altogether Disease management – taking steps to ensure a long and healthy life… 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
How Being Your Own Best Advocate Can Lead to Better Care for Genetic Conditions
by Deon Durst, Guest Contributor, Patient Advocate Living with Cat Eye Syndrome Editor’s Note: I am overjoyed to share this informative piece written by a gentleman who first contacted us… 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
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