Partnership to Boost Pediatric Precision Medicine, Genomics

Partnership to Boost Pediatric Precision Medicine, Genomics

Publication date: Nov 05, 2019

November 04, 2019 – Shriners Hospitals for Children is partnering with Genome Medical to offer high-quality genomic services and precision medicine for pediatric patients.

The collaboration will ensure that families and patients receiving next-generation DNA sequencing through the new Genomics Institute at Shriners Hospital will have access to Genome Medical’s network of clinical genetic specialists.

-Genome Medical is excited to be part of this strategic partnership with Shriners Hospitals for Children to advance pediatric genomics research and improve the quality of care through genome-informed diagnosis and treatment,” said Lisa Alderson, co-founder and CEO of Genome Medical.

We are changing that by joining together with Shriners Hospitals to offer easy access to leading clinical genetics specialists via virtual care, typically with next day appointments, to ensure every child has access to appropriate genetic care to guide personalized treatment plans. “

Nicklaus Children’s Hospital of Miami partnered with Rady Children’s Institute for Genomic Medicine and Sanford Health to offer whole genome sequencing tests to pediatric patients.

Concepts Keywords
CEO Travel distances
Cerebral Palsy Care healthcare system
Childrens Hospital Counseling
Cleft Lip Branches of biology
Club Foot Genetics
Day Care Genomics
Florida Medical genetics
Genetic Biotechnology
Genetic Counseling Emerging technologies
Genetic Diseases Applied genetics
Genetic Sequencing Whole genome sequencing
Genetic Testing Genetic counseling
Genetics Precision medicine
Genome
Genomic Sequencing
Healthcare
Hospital
Leading Edge
Miami
North America
Osteogenesis Imperfecta
Palate
Pediatric
Pediatrics
PhD
Physician
Precision Medicine
President
Sanford
Scoliosis
Sequencing
Shriners
Shriners Hospital
Tampa

Semantics

Type Source Name
gene UNIPROT CD69
gene UNIPROT DNMT1
gene UNIPROT PDC
gene UNIPROT PTPN5
disease MESH cerebral palsy
disease DOID cerebral palsy
disease MESH cleft lip
disease DOID cleft lip
disease MESH scoliosis
disease DOID scoliosis
disease MESH osteogenesis imperfecta
disease DOID osteogenesis imperfecta
disease MESH diagnosis
disease MESH lifestyle
gene UNIPROT ANP32B
gene UNIPROT TNFSF13

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