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Diverging trajectories of trust in healthcare and on-line information seeking: what’s next with LLMs

Diverging trajectories of trust in healthcare and on-line information seeking: what’s next with LLMs

February 1, 2026February 1, 2026
Weekly Roundup – January 31, 2026

Weekly Roundup – January 31, 2026

January 31, 2026February 1, 2026
Embedding clinical intelligence to help close care gaps

Embedding clinical intelligence to help close care gaps

January 31, 2026January 31, 2026
Impact of Mobilization Facilitated by Wearable Device Enhanced Patient Monitoring/Electrophysiology Pod–Based Feedback on Postoperative Complications Following Colorectal Cancer Surgery: Randomized Controlled Trial

Impact of Mobilization Facilitated by Wearable Device Enhanced Patient Monitoring/Electrophysiology Pod–Based Feedback on Postoperative Complications Following Colorectal Cancer Surgery: Randomized Controlled Trial

January 31, 2026January 31, 2026
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Tag: rare diseases

Few shot learning for phenotype-driven diagnosis of patients with rare genetic diseases

Few shot learning for phenotype-driven diagnosis of patients with rare genetic diseases

June 20, 2025June 21, 2025npj Digital Medicine

There are over 7000 rare diseases, some affecting 3500 or fewer patients in the United States. Due to clinicians’ limited experience with such diseases and the heterogeneity of clinical presentations, ~70% of individuals seeking…

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Exclusive: Pangea Data, AstraZeneca's Alexion partner to spot rare disease with EHRs

Exclusive: Pangea Data, AstraZeneca’s Alexion partner to spot rare disease with EHRs

June 9, 2025June 9, 2025MobiHealthNews

Pangea Data, a company focused on detecting rare diseases in patients, is partnering with Alexion, a subsidiary of AstraZeneca focused on treating rare diseases, to co-develop, clinically validate and ultimately seek regulatory approval for…

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Exclusive: Pangaea Data, AstraZeneca's Alexion partner to spot rare disease with EHRs

Exclusive: Pangaea Data, AstraZeneca’s Alexion partner to spot rare disease with EHRs

June 9, 2025June 9, 2025MobiHealthNews

Pangaea Data, a company focused on detecting hard-to-diagnose diseases in patients, is partnering with Alexion, a subsidiary of AstraZeneca focused on treating rare diseases, to co-develop, clinically validate and ultimately seek regulatory approval for an…

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Orphan Drugs Reshape Pharmaceutical Market

Orphan Drugs Reshape Pharmaceutical Market

April 4, 2025DistilINFO Hospital IT

The Evolving Orphan Drug Landscape
Once considered specialized treatments for rare conditions, orphan drugs are now challenging the dominance of mainstream medications in the pharmaceutical industry. According to two recent Evaluate reports—”Are Orphans That Different?”…

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A phenotype-based AI pipeline outperforms human experts in differentially diagnosing rare diseases using EHRs

A phenotype-based AI pipeline outperforms human experts in differentially diagnosing rare diseases using EHRs

January 28, 2025January 29, 2025npj Digital Medicine

Rare diseases, affecting ~350 million people worldwide, pose significant challenges in clinical diagnosis due to the lack of experienced physicians and the complexity of differentiating between numerous rare diseases. To address these challenges, we…

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Korea starts recruiting for 1 billion bio data project

Korea starts recruiting for 1 billion bio data project

December 30, 2024December 30, 2024Healthcare IT news

Korea officially launches big bio data projectThe South Korean government has started recruiting participants for the National Integrated Bio Big Data Construction Project.
The ambitious 606 billion won (over $400 million) project is Korea’s largest healthcare project…

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Direct-to-patient platform uses AI to find gaps in care

Direct-to-patient platform uses AI to find gaps in care

December 13, 2024December 13, 2024Healthcare IT news

Unite Genomics announced a new clinical listening partnership with a “Top 10 pharma company” that can personalize and tailor patient psoriasis care insights based on their medical records on Monday.This direct-to-consumer platform uses artificial…

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Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

November 22, 2024November 22, 2024npj Digital Medicine

Patients with rare diseases often experience prolonged diagnostic delays. Ordering appropriate genetic tests is crucial yet challenging, especially for general pediatricians without genetic expertise. Recent American College of Medical Genetics (ACMG) guidelines embrace early…

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Citizen Health secures $14.5M in seed funding for rare disease drug development

Citizen Health secures $14.5M in seed funding for rare disease drug development

November 20, 2024November 20, 2024MobiHealthNews

Citizen Health, a company that helps patients oversee rare and complex health conditions, announced it raised $14.5 million in seed funding.Transformation Capital led the round with participation from Wavemaker 360 and prominent angel investors. 
The…

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Citizen Health Secures $14.5M for AI Platform for Rare Diseases

Citizen Health Secures $14.5M for AI Platform for Rare Diseases

November 19, 2024November 20, 2024HIT Consultant

What You Should Know:

– Citizen Health, an innovative AI-powered consumer health platform designed to support over 400 million individuals managing rare and complex conditions, has announced the successful closing of a $14.5 million seed round. 

–  The…

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