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Finding Patients At Risk for Rare Disease

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About Ruth O'Keefe

Ruth maintains strong engagement with patients, partners, healthcare providers, and other communities to further the ThinkGenetic mission effectively and successfully. When not advocating for ThinkGenetic and its community, Ruth enjoys spending time outdoors with her three boys and helping businesses create and maintain a productive footprint online.

ThinkGenetic to Present Research Findings at 2023 NSGC Annual Meeting

August 1, 2023 by Ruth O'Keefe

ThinkGenetic announces its participation at the 2023 National Society of Genetic Counselors (NSGC) Annual Meeting in Chicago, IL this October through the presentation of two poster sessions.

News Dawn Laney, events, genetic counseling, genetic counselors, Jessica Dronen, NSGC

ThinkGenetic to Attend ACMG/SIMD Joint Meeting

March 10, 2023 by Ruth O'Keefe

ThinkGenetic announces its participation at the 2023 ACMG Annual Clinical Genetics Meeting which is being held in conjunction with the Society for Inherited Metabolic Disorders Meeting for the first time in Salt Lake City, Utah, this March.

News @SIMDtweets, #ACMGMtg23, #SIMD2023, ACMG, Annual Clinical Genetics Meeting, Dawn Laney, Jessica Dronen, medical genetics, metabolics, SIMD, Society for Inherited Metabolic Disorders

ThinkGenetic Announces Participation at 19th Annual WORLDSymposium™ 2023

February 8, 2023 by Ruth O'Keefe

ThinkGenetic announces that Chief Genetic Officer, Dawn Laney, MS, CGC, CCRC, will be participating in a 19th Annual WORLDSymposium™ Satellite Symposia entitled “Understanding Phenotypic Variability in Lysosomal Diseases – Gaining a Foothold in Precision Medicine” sponsored by Takeda Pharmaceutical Company Limited.

News Dawn Laney, lysosomal diseases, Takeda, Takeda Pharmaceutical Company Limited, WORLDSymposium

[Press Release] ThinkGenetic Announces Cian Robinson as Chief Revenue Officer to Focus on Growth and Partnership Opportunities

February 7, 2023 by Ruth O'Keefe

ThinkGenetic, Inc. (thinkgenetic.com) today announces the onboarding of entrepreneurial leader, Cian Robinson, MS, EdD-ABD as Chief Revenue Officer. Mr. Robinson is responsible for collaborating with potential ThinkGenetic clients to uncover opportunities for growth and partnership within ThinkGenetic.

Investor News, News, Press Releases Chief Revenue Officer, Cian Robinson, FindEHR, FindSM, investment, staff, Team, WORLDSymposium

[Audio Interview] ThinkGenetic Leadership Team Interview with RV Radio Part 2

December 16, 2022 by Ruth O'Keefe

In this second part, RV Radio continues the conversation with four members of the ThinkGenetic Leadership Team to focus the conversation on the day-to-day business and finding investment funding.

Investor News Cian Robinson, Dave Jacob, Dawn Laney, FindEHR, investment, Len Barker, podcast, Robinson Ventures, Ruth O'Keefe, RV Radio, startup, SymptomMatcher, ThinkGenetic

[Audio Interview] ThinkGenetic Leadership Team Interview with RV Radio Part 1

November 22, 2022 by Ruth O'Keefe

The ThinkGenetic leadership team was recently interviewed for the RV Radio podcast with Cian Robinson, discussing the origin of ThinkGenetic while giving insight into what it’s like to be diagnosed with a genetic condition later in life when doctors are stumped and existing tools to diagnose are limited.

Investor News AccelerateSouth, Cian Robinson, Dave Jacob, Dawn Laney, Lafayette, Len Barker, MassChallenge, Robinson Ventures, Ruth O'Keefe, RV Radio, Shire, startup, Takeda, ThinkGenetic, Tucker Robinson

[Press Release] Guardian Research Network and ThinkGenetic Announce Collaborative Partnership to Accelerate Diagnosis and Treatment Options for Patients with Genetic Diseases and Inherited Predisposition to Cancer

July 28, 2022 by Ruth O'Keefe

 Guardian Research Network, Inc.® (GRN) and ThinkGenetic, Inc. announce a strategic collaboration to accelerate the diagnosis and support the development of treatment options for patients with rare and genetic diseases.

News, Partners, Press Releases 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

New Research to be Presented at AAAAI 2022 on Hereditary Angioedema

January 8, 2022 by Ruth O'Keefe

ThinkGenetic is proud to announce a recent collaborative research project will be presented at the 2022 American Academy of Allergy, Asthma & Immunology (AAAAI) annual meeting this February 25-29th in […]

News AAAI, algorithm, Amanda Logue, American Academy of Allergy, Ami Rosen, Asthma & Immunology, C1-inhibitor, Dave Jacob, Dawn Laney, EHR, HAE, Hereditary angioedema, Jessica Dronen, Jingjing Yang, LSDC, Marc Riedl, Marissa Shams, research, sensitivity, specificity, ThinkGenetic

[Press Release] Massachusetts Startup Wins Horizon Prize, Powered by MIT Solve, with Algorithm-Based FindEHR Solution for Finding Undiagnosed Genetic Disorder Patients using Electronic Medical Records

October 7, 2021 by Ruth O'Keefe

ThinkGenetic combines modern machine learning with practical information in genetics to solve a major concern in healthcare – the identification of patients living with undiagnosed rare genetic conditions Boston, MA, […]

Investor News, News, Press Releases AI, algorithm, artificial intelligence, Boston startup, Dave Jacob, electronic health records, FindEHR, Horizon Prize, Horizon Therapeutics, machine learning, Massachusetts Institute of Technology, medical health records, MIT Solve, ThinkGenetic, Tim Walbert, undiagnosed patients

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Upcoming Events

Oct 17
October 17 - October 21

NSGC Annual Conference 2023

Feb 4
February 4, 2024 - February 9, 2024

WORLDSymposium on Lysosomal Disease Research 2024

Mar 12
March 12, 2024 - March 16, 2024

ACMG Annual Clinical Genetics Meeting 2024

Feb 2
February 2, 2025 - February 7, 2025

WORLDSymposium on Lysosomal Disease Research 2025

Mar 18
March 18, 2025 - March 22, 2025

ACMG Annual Clinical Genetics Meeting 2025

View Calendar

Together let’s systematically accelerate detecting at-risk  individuals.

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