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Genomenon connects patient’s DNA with the billions of dollars of genomic research to help doctors diagnose & cure cancer patients and babies with rare diseases, and researchers understand diseases at a molecular level.
Genomenon B2B Case Studies & Customer Successes
Case Studies
Showing 32 Genomenon Customer Success Stories
Alexion Expands Hypophosphatasia Diagnosis with Genomenon
Alexion
Amicus Therapeutics - Customer Case Study
Amicus Therapeutics
Amicus Therapeutics expands the Fabry disease treatment label with Genomenon
Amicus Therapeutics
Amicus Therapeutics de-risks IND prep with Genomenon’s literature-derived real-world evidence
Amicus Therapeutics
Lurie Children’s Hospital Accelerates Accurate Molecular Diagnoses Using Genomenon’s Mastermind Intelligence Platform
Ann & Robert H. Lurie Children's Hospital of Chicago
Kai Lee Yap
Director of Molecular Diagnostics
CDC accelerates newborn screening variant interpretation with Genomenon Mastermind
Centers for Disease Control and Prevention (CDC)
Hartwig Medical Foundation accelerates cancer diagnostics with Genomenon CKB
Hartwig Medical Foundation
Inozyme achieves a 3.1x increase in ENPP1 deficiency prevalence with Genomenon
Inozyme
Inozyme strengthens rare disease trial design with Genomenon’s literature-derived real world evidence
Inozyme
How Inozyme is Partnering with Genomenon to Raise Awareness and Promote Earlier Diagnosis of ENPP1 Deficiency
Inozyme
Intermountain Health accelerates endometrial cancer variant interpretation with Genomenon Mastermind
Intermountain Health
Limb-Girdle Muscular Dystrophy Foundation - Customer Case Study
Limb-Girdle Muscular Dystrophy Foundation
William Lowery
Chief Executive Officer
Limb-Girdle Muscular Dystrophy Foundation improves LGMD diagnosis and variant classification with Genomenon Mastermind
Limb-Girdle Muscular Dystrophy Foundation
How Loxo@Lilly Partnered with Genomenon to Refine the CDx Submission for Retevmo®
Loxo@Lilly
Loxo@Lilly expands Retevmo’s label with Genomenon
Loxo@Lilly
Loxo@Lilly expands Retevmo label in thyroid cancer with Genomenon
Loxo@Lilly
Loxo@Lilly advances RET companion diagnostic approval in Japan with Genomenon
Loxo@Lilly
a mid-size biopharma company expands its Fabry label with Genomenon
Mid-size Biopharma Company
Northwestern Medicine accelerates evidence-based oncology workflows with Genomenon’s CKB FLEX
Northwestern Medicine
Pharming improves APDS diagnosis with Genomenon
Pharming
How Pharming is Partnering with Genomenon to Democratize Access to Genetic Evidence and Promote Earlier APDS Diagnosis
Pharming Company
Rady Children’s Institute for Genomic Medicine - Customer Case Study
Rady Children’s Institute for Genomic Medicine
Kasia Ellsworth
Associate Lab Director
Rady Children’s Institute for Genomic Medicine improves newborn genetic screening with Genomenon
Rady Children’s Institute for Genomic Medicine (rcigm)
Rady Children’s Institute for Genomic Medicine speeds rare disease diagnosis with Genomenon Mastermind
Rady Children’s Institute for Genomic Medicine (rcigm)
Understanding the Comprehensive Variant Landscape of Rare Obesity Disorders
Rare Disease Pharmaceutical Company
Rare Genomics Institute achieves a rare disease diagnosis with Genomenon
Rare Genomics Institute
Rare Genomics Institute - Customer Case Study
Rare Genomics Institute
Lipika Ray
Rare Genomics Institute
Rhythm Pharmaceuticals accelerates rare obesity trial design with Genomenon
Rhythm Pharmaceuticals
UCB improves rare disease variant interpretation and earlier diagnosis with Genomenon
UCB
UCB Accelerates TK2D Diagnosis with Genomenon
UCB
University of Vermont Health Network standardizes genomic literature review with Genomenon Mastermind
University of Vermont Health Network
University of Vermont Health Network - Customer Case Study
University of Vermont Health Network
Nikoletta Sidiropoulos
Medical Director of Genomic Medicine
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