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Jean L Raphael

Biographic Data

ID5382195
NAMEJean L Raphael
GIVEN NAMESJean L
FAMILY NAMERaphael
SIGNATURERAPHAEL J L
AFFILIATIONSBaylor College of Medicine
ORCID0000-0002-8612-1705
VERIFIEDYes
TOTAL WORKS5
TOTAL CITATIONS0
WORKS AS AUTHOR5
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2013
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Inclusion of Community-Based Participatory Research in High-Impact Medical Journals

    Open Access•Michelle Dougherty, Yesmina Salib et al.•ARTICLE•Health Equity•2025

    Community-based participatory research (CBPR) is essential for addressing health care inequities; however, it is unclear to what extent articles published in high-impact medical journals use CPBR. We reviewed original research articles in nine journals across 4 years to determine how frequently CBPR was used and, for articles using CBPR, details about partnerships. Of 5,624 articles, only 6 (0.1%) used CBPR. Five identified community partners and…

  • Psychologists as leaders in equitable science

    Open Access•Desireé N Williford, Emily McTate et al.•ARTICLE•American Psychologist•2023•References: 7

    Psychologists have an ethical responsibility to advance health equity and can play a significant role in improving health care experiences for families racialized as Black, including those with sickle cell disease (SCD), a group of genetic blood disorders primarily affecting communities of color. Parents of children with SCD report experiences of stigma and discrimination due to racism in the health care system. The current commentary describes t…

  • Relationship-focused vs. Structural Activities in Medical Home Measurement in Pediatrics

    Open Access•Christopher J Stille, Jean L Raphael et al.•ARTICLE•Maternal and Child Health Journal•2018

  • Shared Decision Making Among Parents of Children with Mental Health Conditions Compared to Children with Chronic Physical Conditions

    Open Access•Ashley M Butler, Sara Elkins et al.•ARTICLE•Maternal and Child Health Journal•2014

  • Integration of Administrative Data and Chart Review for Reporting Health Care Utilization Among Children With Sickle Cell Disease

    Open Access•Jean L Raphael, Xuan G Tran et al.•ARTICLE•SAGE Open•2013

    Health care utilization of children with sickle cell disease (SCD) has been well documented due to an increase in the use of administrative data sets. While use of such data sources is relatively efficient and low cost, questions remain as to whether they provide sufficient information to fully characterize health care use. The aim of this study was to determine whether administrative data have the capacity to fully assess health care utilization…

No prominent works on this page.

  • Integration of Administrative Data and Chart Review for Reporting Health Care Utilization Among Children With Sickle Cell Disease

    Open Access•Jean L Raphael, Xuan G Tran et al.•ARTICLE•SAGE Open•2013

    Health care utilization of children with sickle cell disease (SCD) has been well documented due to an increase in the use of administrative data sets. While use of such data sources is relatively efficient and low cost, questions remain as to whether they provide sufficient information to fully characterize health care use. The aim of this study was to determine whether administrative data have the capacity to fully assess health care utilization…

  • Shared Decision Making Among Parents of Children with Mental Health Conditions Compared to Children with Chronic Physical Conditions

    Open Access•Ashley M Butler, Sara Elkins et al.•ARTICLE•Maternal and Child Health Journal•2014

  • Relationship-focused vs. Structural Activities in Medical Home Measurement in Pediatrics

    Open Access•Christopher J Stille, Jean L Raphael et al.•ARTICLE•Maternal and Child Health Journal•2018

  • Psychologists as leaders in equitable science

    Open Access•Desireé N Williford, Emily McTate et al.•ARTICLE•American Psychologist•2023•References: 7

    Psychologists have an ethical responsibility to advance health equity and can play a significant role in improving health care experiences for families racialized as Black, including those with sickle cell disease (SCD), a group of genetic blood disorders primarily affecting communities of color. Parents of children with SCD report experiences of stigma and discrimination due to racism in the health care system. The current commentary describes t…

  • Inclusion of Community-Based Participatory Research in High-Impact Medical Journals

    Open Access•Michelle Dougherty, Yesmina Salib et al.•ARTICLE•Health Equity•2025

    Community-based participatory research (CBPR) is essential for addressing health care inequities; however, it is unclear to what extent articles published in high-impact medical journals use CPBR. We reviewed original research articles in nine journals across 4 years to determine how frequently CBPR was used and, for articles using CBPR, details about partnerships. Of 5,624 articles, only 6 (0.1%) used CBPR. Five identified community partners and…

Medicine (5 works) · Medical education (3 works) · Psychology (3 works) · Community-based participatory research (2 works) · Computer Science (2 works) · Environmental health (2 works) · Family and Disability Support Research (2 works) · Family medicine (2 works) · Health care (2 works) · Nursing (2 works)

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