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Finding Patients At Risk for Rare Disease

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[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

Extracting Electronic Health Record (EHR) Data Using Transfer Learning

January 9, 2023 by Corey Fournier, Senior Data Engineer

At ThinkGenetic, Inc. our goal is to reduce the time to diagnosis for genetic and rare conditions. Given they are rare, we must be cognizant of the time it takes […]

News, Technical Research algorithms, BERT model, clinical note, EHR, electronic health records, genetic conditino, genetic condition, Google, ICD-10, Medical Coding, medical record, misdiagnosed, Name Entity Recognition, Natural Language Processing, NLP, Procedures codes, Rare Disease, rare genetic disease, Relation Extraction, Semantic Role labeling, Shi and Lin, Snomed, structured data, T5, Text-to-text Transfer Transformers, undiagnosed, unstructured data

[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

Supporting Rare Disease Day 2022

February 25, 2022 by Jennifer Dykeman

February 28th is Rare Disease Day! In the United States, a disease is defined as rare if it affects less than 200,000 people. It is currently thought that there may be […]

Advocacy, Education, News advocacy, Find a Genetic Counselor, GARD, Genetic and Rare Disease Information Center, National Organization for Rare Diseases, National Society of Genetic Counselor, NIH, NORD, NSGC, patient services, Rare Disease Day

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

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Upcoming Events

Feb 1
February 1, 2026 - February 6, 2026

WORLDSymposium on Lysosomal Disease Research 2026

Mar 10
March 10, 2026 - March 14, 2026

ACMG Annual Clinical Genetics Meeting 2026

View Calendar

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

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