Work

Novel phenotype–disease matching tool for rare genetic diseases

Year: 2018

Type: article

Source: Genetics in Medicine

DOI: 10.1038/s41436-018-0050-4

Authors: Jing Chen, Huan Xu, Anil Jegga, Kejian Zhang, Pete S. White, Ge Zhang

Institutions: Cincinnati Children's Hospital Medical Center, University of Cincinnati

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Cincinnati Children's Hospital Medical Center, National Institutes of Health, National Human Genome Research Institute

Award: Better Outcomes for Children: Promoting Excellence in Healthcare Genomics to Inform Policy

OpenAlex ID: W2808672056

FWCI: 0.92

Cites: 24

Cited by: 26

Related to: 10