Richard Parad

Richard Parad

Harvard University

H-index: 42

North America-United States

About Richard Parad

Richard Parad, With an exceptional h-index of 42 and a recent h-index of 26 (since 2020), a distinguished researcher at Harvard University, specializes in the field of Neonatology, Pediatric Pulmonary, Cystic Fibrosis, Newborns, Bronchopulmonary Dysplasia.

His recent articles reflect a diverse array of research interests and contributions to the field:

The Early Care (0–3 Years) In Duchenne Muscular Dystrophy Meeting Report

341 Stakeholder feedbackon feasibilityof leveraging telehealth to optimize cystic fibrosis genetic counseling access

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

Spherical indentation of polycrystalline cubic boron nitride (PcBN): Contact damage evolution with increasing load and microstructural effects

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

P410: The effect of newborn genomic screening on downstream health care utilization and costs: Evidence from the BabySeq Project

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

A role for abdominal ultrasound in discriminating suspected necrotizing enterocolitis in congenital heart disease patients

Richard Parad Information

University

Position

Department of Pediatric Newborn Medicine, Brigham and Women's Hospital, Harvard Medical School

Citations(all)

9509

Citations(since 2020)

2872

Cited By

7823

hIndex(all)

42

hIndex(since 2020)

26

i10Index(all)

87

i10Index(since 2020)

52

Email

University Profile Page

Google Scholar

Richard Parad Skills & Research Interests

Neonatology

Pediatric Pulmonary

Cystic Fibrosis

Newborns

Bronchopulmonary Dysplasia

Top articles of Richard Parad

The Early Care (0–3 Years) In Duchenne Muscular Dystrophy Meeting Report

Journal of neuromuscular diseases

2024/1/4

Katherine Mathews
Katherine Mathews

H-Index: 35

Richard Parad
Richard Parad

H-Index: 26

341 Stakeholder feedbackon feasibilityof leveraging telehealth to optimize cystic fibrosis genetic counseling access

Journal of Cystic Fibrosis

2023/10/1

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

The American Journal of Human Genetics

2023/7/6

Spherical indentation of polycrystalline cubic boron nitride (PcBN): Contact damage evolution with increasing load and microstructural effects

International Journal of Refractory Metals and Hard Materials

2023/2/1

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

Genetics in Medicine

2023/3/1

P410: The effect of newborn genomic screening on downstream health care utilization and costs: Evidence from the BabySeq Project

Genetics in Medicine Open

2023/1/1

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

medRxiv

2022/3/18

A role for abdominal ultrasound in discriminating suspected necrotizing enterocolitis in congenital heart disease patients

Pediatric Surgery International

2022/2/1

An oversight regarding the Club cell?

Authorea Preprints

2022/5/2

Richard Parad
Richard Parad

H-Index: 26

Parental attitudes toward standard newborn screening and newborn genomic sequencing: findings from the BabySeq study

Frontiers in Genetics

2022/4/27

Genetic counseling access for parents of newborns who screen positive for cystic fibrosis: Consensus guidelines

Pediatric Pulmonology

2022/4

Urine proteomics for noninvasive monitoring of biomarkers in bronchopulmonary dysplasia

Neonatology

2022

Differences in clinical and laboratory biomarkers for short and long‐term respiratory outcomes in preterm neonates

Pediatric pulmonology

2021/12

Implementation of hospital-based supplemental Duchenne muscular dystrophy newborn screening (sDMDNBS): a pathway to broadening adoption

International Journal of Neonatal Screening

2021/11/15

Improving genetic counseling access for parents of newborns who screen positive for cystic fibrosis: consensus guidelines

2021/11/2

Richard Parad
Richard Parad

H-Index: 26

Psychosocial effect of newborn genomic sequencing on families in the BabySeq Project: a randomized clinical trial

JAMA pediatrics

2021/11/1

Abdominal ultrasound findings contribute to a multivariable predictive risk score for surgical necrotizing enterocolitis: A pilot study

The American Journal of Surgery

2021/11/1

Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project

Genetics in Medicine

2021/7

Specificity of International Classification of Diseases codes for bronchopulmonary dysplasia: an investigation using electronic health record data and a large insurance database

Journal of Perinatology

2021/4

Targeted next generation sequencing for newborn screening of Menkes disease

Molecular Genetics and Metabolism Reports

2020/9/1

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