PhenoTips is Named One of Canada’s Best Startup Employers

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London North West University Healthcare NHS Trust Finds Digital Way Forward with PhenoTips' Genomic Health Record

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The NHS East Genomic Medicine Service Alliance Harnesses PhenoTips’ Genomic Health Record in a Milestone Regional Transformation Project

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PhenoTips Announces Appointment of Dr. Pawel Buczkowicz As New CEO

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PhenoTips Pledges 1% Equity to Support CORD, CHEO Foundation, and SickKids Foundation

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PhenoTips® Closes CAD $2.5M Funding Round Led by GreenSky Capital for Software to Transform Medical Genetics

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PhenoTips® Secures $2.5 Million CAD to Expand Reach of Medical Genetics Software

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PhenoTips®, a U of T-SickKids genetic software startup, raises $2.5 million

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PhenoTips® launches Pre-Visit Patient Questionnaires that automatically generate pedigrees using patient-entered data

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World’s First Genomic Health Record™, PhenoTips®, Graduates From the Creative Destruction Lab

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To Aid with COVID-19 Efforts, PhenoTips® Offers Free Cloud-Hosted Genomics Software

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Software company Gene42 Rebrands as PhenoTips®

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Gene42 Rebrands As PhenoTips® in Preparation for Long-Term Growth

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Precision Medicine Software Market Worth $2.0 Billion by 2024 - Exclusive Report by MarketsandMarkets™

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Gene42, Care4Rare launch Canada’s first national rare disease research platform

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Gene42 Launches Rare Disease Platform Genomics4RD

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All-New Canadian Rare Disease Research Platform Begins Operations

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Gene42 Standardizes Phenotypic Data to Improve Variant Classification, Rare Disease Dx

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NIH-Backed Data Center for Pediatric Cancer Launches Research Portal

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Precision medicine: We know there's a market, but who are the top vendors?

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Gene42, SeqOne Partner for Rare Disease Diagnosis

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Canadian Government and Gene42 Team up to Tackle Big-Data Precision Healthcare

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Recognizing Digital Health in Canada

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Translation, Translation, Translation

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UofT experts on the revolution of artificial intelligence in medicine

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Big Data Takes On Mysterious Medical Conditions

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Human phenotyping on a population scale

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Appistry Launches CloudDx Translational from NIH Tool

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How to accelerate rare disease research

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