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Richard Parad, MD, Neonat/Perinatology, Boston, MA

RichardBParadMDMPH

Neonat/Perinatology Boston, MA

Birth Defect Genetics, Neonatal Respiratory Failure & Lung Development

Director, Newborn Genomic Medicine Program, Department of Pediatric Newborn Medicine, Brigham and Women's Hospital

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  • Office

    75 Francis St Cwn 418
    Brigham & Women's Hospital
    Boston, MA 02115
    Phone+1 617-732-7371
    Fax+1 617-278-6983

Summary

  • Dr. Richard Parad is a neonatologist in Boston, MA and is affiliated with multiple hospitals in the area, including Brigham and Women's Hospital, Boston Children's Hospital, Beth Israel Deaconess Medical Center, Massachusetts General Hospital, and Newton-Wellesley Hospital. He received his medical degree from University of California San Diego School of Medicine and has been in practice 36 years. He specializes in birth defect genetics and neonatal respiratory failure & lung development.

Education & Training

  • Harvard School of Public Health
    Harvard School of Public HealthMPH, Quantitative Methods, 1994 - 1997
  • Boston Children’s Hospital/Boston Medical Center
    Boston Children’s Hospital/Boston Medical CenterFellowship, Neonatal-Perinatal Medicine, 1984 - 1987
  • Boston Children’s Hospital/Boston Medical Center
    Boston Children’s Hospital/Boston Medical CenterResidency, Pediatrics, 1981 - 1984
  • University of California San Diego School of Medicine
    University of California San Diego School of MedicineClass of 1981

Certifications & Licensure

  • ME State Medical License
    ME State Medical License Current
  • MA State Medical License
    MA State Medical License 1984 - 2025
  • FL State Medical License
    FL State Medical License 1993 - 2012
  • American Board of Pediatrics Pediatrics
  • American Board of Pediatrics Neonatal-Perinatal Medicine

Clinical Trials

Publications & Presentations

PubMed

Press Mentions

  • Cureduchenne Launches Innovative Supplemental Newborn Screening Initiative Offering Opportunity for Early Diagnosis of Rare, Fatal Disease
    Cureduchenne Launches Innovative Supplemental Newborn Screening Initiative Offering Opportunity for Early Diagnosis of Rare, Fatal DiseaseJuly 22nd, 2021
  • Brigham and Women's Hospital Partners with CureDuchenne on Newborn Screening Program
    Brigham and Women's Hospital Partners with CureDuchenne on Newborn Screening ProgramJuly 22nd, 2021
  • Increase in Genetic Testing Brings Decrease in Some Hereditary Diseases
    Increase in Genetic Testing Brings Decrease in Some Hereditary DiseasesFebruary 24th, 2010
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