Richard B Parad

7PUBLICATIONS
23CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthCentral nervous system
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Publications (7)

|Jun 03, 2026
Germline Whole-Genome Sequencing in Early-Onset Pediatric Solid Tumors Implicates Novel Risk Factors.

|Dec 29, 2021
Genetic counseling access for parents of newborns who screen positive for cystic fibrosis: Consensus guidelines.

Elinor Langfelder-Schwind, Karen S Raraigh, Richard B Parad

|Nov 29, 2021
Implementation of Hospital-Based Supplemental Duchenne Muscular Dystrophy Newborn Screening (sDMDNBS): A Pathway to Broadening Adoption.

Richard B Parad, Yvonne Sheldon, Arindam Bhattacharjee

|Aug 26, 2021
Differences in clinical and laboratory biomarkers for short and long-term respiratory outcomes in preterm neonates.

Richard B Parad, Janis L Breeze, Norma Terrin

|Dec 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation.

Laura V Milko, Flavia Chen, Kee Chan

|Sep 25, 2019
Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen-positive diagnostic resolution process.

Elinor Langfelder-Schwind, Karen S Raraigh, Richard B Parad

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Frequent Collaborators

2 joint publications

Alan H Beggs

2 joint publications

Elinor Langfelder-Schwind

2 joint publications

Karen S Raraigh

1 joint publications

Ozge Ceyhan-Birsoy