Work

Hospital-level variation in genetic testing in children’s hospitals’ neonatal intensive care units from 2016 to 2021

Year: 2022

Type: article

Study design: Observational Study

Source: Genetics in Medicine

DOI: 10.1016/j.gim.2022.12.004

Authors: Katharine Press Callahan, Joshua Radack, Monica H. Wojcik, Sabrina Malone Jenkins, Russell T. Nye, Cara Skraban, Katherine Taylor Wild, Chris Feudtner

Institutions: Children's Hospital of Philadelphia, University of Pennsylvania, Boston Children's Hospital, Harvard University, University of Utah, University of Utah Health Care

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDGs: Good health and well-being, Reduced inequalities

Open Access status: bronze

Funders: Children's Hospital of Philadelphia, National Human Genome Research Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: The Burden of Genetic Disorders in Infant Mortality, Penn Postdoctoral Training Program in the Ethical, Legal and Social Implications of Genetics and Genomics

OpenAlex ID: W4311423537

FWCI: 2.553

Cites: 19

Cited by: 22

Related to: 10