Richard B. Parad

9.1k total citations · 1 hit paper
102 papers, 5.4k citations indexed

About

Richard B. Parad is a scholar working on Pulmonary and Respiratory Medicine, Surgery and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Richard B. Parad has authored 102 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Pulmonary and Respiratory Medicine, 25 papers in Surgery and 24 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Richard B. Parad's work include Neonatal Respiratory Health Research (46 papers), Cystic Fibrosis Research Advances (27 papers) and Congenital Diaphragmatic Hernia Studies (16 papers). Richard B. Parad is often cited by papers focused on Neonatal Respiratory Health Research (46 papers), Cystic Fibrosis Research Advances (27 papers) and Congenital Diaphragmatic Hernia Studies (16 papers). Richard B. Parad collaborates with scholars based in United States, United Kingdom and Australia. Richard B. Parad's co-authors include Frank J. Accurso, Philip M. Farrell, Terry B. White, Michael J. Rock, Elizabeth N. Allred, Anne Marie Comeau, Preston W. Campbell, Henry L. Dorkin, Judy A. Estroff and Peter R. Durie and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Richard B. Parad

101 papers receiving 5.2k citations

Hit Papers

Guidelines for Diagnosis of Cystic Fibrosis in Newborns t... 2008 2026 2014 2020 2008 200 400 600

Peers

Richard B. Parad
Charles R. Rosenfeld United States
Richard B. Parad
Citations per year, relative to Richard B. Parad Richard B. Parad (= 1×) peers Charles R. Rosenfeld

Countries citing papers authored by Richard B. Parad

Since Specialization
Citations

This map shows the geographic impact of Richard B. Parad's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Richard B. Parad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard B. Parad more than expected).

Fields of papers citing papers by Richard B. Parad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard B. Parad. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Richard B. Parad. The network helps show where Richard B. Parad may publish in the future.

Co-authorship network of co-authors of Richard B. Parad

This figure shows the co-authorship network connecting the top 25 collaborators of Richard B. Parad. A scholar is included among the top collaborators of Richard B. Parad based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Richard B. Parad. Richard B. Parad is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Green, Robert C., Nidhi Shah, Casie A. Genetti, et al.. (2023). Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. The American Journal of Human Genetics. 110(7). 1034–1045. 25 indexed citations
2.
Ahmed, Saima, Oludare A. Odumade, Patrick van Zalm, et al.. (2022). Urine Proteomics for Noninvasive Monitoring of Biomarkers in Bronchopulmonary Dysplasia. Neonatology. 119(2). 193–203. 22 indexed citations
3.
Lazow, Stefanie P., Sarah Tracy, Judy A. Estroff, et al.. (2021). A role for abdominal ultrasound in discriminating suspected necrotizing enterocolitis in congenital heart disease patients. Pediatric Surgery International. 38(2). 225–233. 5 indexed citations
4.
Parad, Richard B., et al.. (2020). Targeted next generation sequencing for newborn screening of Menkes disease. Molecular Genetics and Metabolism Reports. 24. 100625–100625. 7 indexed citations
5.
Davis, Jonathan M., Aprile L. Pilon, Jeffrey Shenberger, et al.. (2019). The role of recombinant human CC10 in the prevention of chronic pulmonary insufficiency of prematurity. Pediatric Research. 86(2). 254–260. 11 indexed citations
6.
Ceyhan‐Birsoy, Ozge, Kalotina Machini, Matthew S. Lebo, et al.. (2017). A curated gene list for reporting results of newborn genomic sequencing. Genetics in Medicine. 19(7). 809–818. 76 indexed citations
7.
Salinas, Danieli B., Colleen Azen, Suzanne Young, et al.. (2016). Phenotypes of California CF Newborn Screen-Positive Children with CFTR 5T Allele by TG Repeat Length. Genetic Testing and Molecular Biomarkers. 20(9). 496–503. 25 indexed citations
8.
Munck, À., Sarah Mayell, Anna Shawcross, et al.. (2015). Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening. Journal of Cystic Fibrosis. 14(6). 706–713. 123 indexed citations
9.
Glotzbecker, Michael P., Judy A. Estroff, Leslie A. Kalish, et al.. (2013). Prospective Evaluation of a Prenatal Sonographic Clubfoot Classification System. Fetal Diagnosis and Therapy. 34(4). 236–240. 8 indexed citations
10.
11.
Keiles, Steven, Ruth Koepke, Richard B. Parad, & Martin Kharrazi. (2011). Impact of IVS8-(TG)m(T)n on IRT and sweat chloride levels in newborns identified by California CF newborn screening. Journal of Cystic Fibrosis. 11(3). 257–260. 6 indexed citations
12.
Nguyen, Ruby H.N., et al.. (2010). US assessment of estrogen-responsive organ growth among healthy term infants: piloting methods for assessing estrogenic activity. Pediatric Radiology. 41(5). 633–642. 17 indexed citations
13.
Mitchell, Michael, et al.. (2009). Oropharyngeal flora in healthy infants: Observations and implications for cystic fibrosis care. Pediatric Pulmonology. 44(5). 497–502. 29 indexed citations
14.
Farrell, Philip M., Beryl J. Rosenstein, Terry B. White, et al.. (2008). Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report. The Journal of Pediatrics. 153(2). S4–S14. 747 indexed citations breakdown →
15.
Als, Heidelise, Linda Gilkerson, Frank H. Duffy, et al.. (2003). A Three-Center, Randomized, Controlled Trial of Individualized Developmental Care for Very Low Birth Weight Preterm Infants: Medical, Neurodevelopmental, Parenting, and Caregiving Effects. Journal of Developmental & Behavioral Pediatrics. 24(6). 399–408. 252 indexed citations
16.
Marter, L.J. Van, et al.. (2002). Urine Bombesin-like Peptide Elevation Precedes Clinical Evidence of Bronchopulmonary Dysplasia. American Journal of Respiratory and Critical Care Medicine. 165(8). 1093–1097. 48 indexed citations
17.
Marter, L.J. Van, et al.. (2001). Antenatal glucocorticoid treatment does not reduce chronic lung disease among surviving preterm infants. The Journal of Pediatrics. 138(2). 198–204. 36 indexed citations
18.
Chiba‐Falek, Ornit, Richard B. Parad, Eitan Kerem, & Batsheva Kerem. (1999). Variable Levels of Normal RNA in Different Fetal Organs Carrying a Cystic Fibrosis Transmembrane Conductance Regulator Splicing Mutation. American Journal of Respiratory and Critical Care Medicine. 159(6). 1998–2002. 33 indexed citations
19.
Bromley, Bryann, Judy A. Estroff, Stephen P. Sanders, et al.. (1992). Fetal echocardiography: Accuracy and limitations in a population at high and low risk for heart defects. American Journal of Obstetrics and Gynecology. 166(5). 1473–1481. 150 indexed citations
20.
Parad, Richard B. & Craig Gérard. (1992). A sequence variation in intron 17B of the cystic fibrosis transmembrane conductance regulator gene. Human Mutation. 1(3). 258–259. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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