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Angela Snyder

Biographic Data

ID4238005
NAMEAngela Snyder
GIVEN NAMESAngela
FAMILY NAMESnyder
SIGNATURESNYDER A
AFFILIATIONSGeorgia State University
ORCID0000-0002-5149-6355
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS0
WORKS AS AUTHOR4
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2017
LATEST PUBLICATION YEAR2026
H-INDEX0
  • The impact of social vulnerability on primary vaccine coverage in children with sickle cell disease

    Open Access•J Shi, Jiajing Scarlette Shi et al.•ARTICLE•Frontiers in Public Health•2026

    Introduction This study examines the relationship between social vulnerability and up-to-date (UTD) primary vaccine coverage among children with sickle cell disease (SCD). Methods This retrospective cohort study included children with SCD born in Georgia between 2008 and 2019, identified through the state newborn screening program. Immunization records were obtained from the state registry, and birth addresses were matched to census tract level S…

  • Newborn Screening for Sickle Cell Disease and Thalassemia

    Open Access•Maa-Ohui Quarmyne, Fiona Bock et al.•ARTICLE•JAMA Health Forum•2025

    The time has come for a paradigm shift in newborn screening for hemoglobinopathies through the adoption of universal molecular genetic testing

  • An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model

    Open Access•Marsha Treadwell, Swapandeep Mushiana et al.•ARTICLE•Quality of Life Research•2022

    Study results highlight the importance of the biopsychosocial model to enhance understanding of the needs of this complex population, and to design multi-dimensional approaches for providing more effective interventions to improve outcomes

  • Caring by Numbers

    Open Access•Beth M Hartzler, Angela Snyder•ARTICLE•Journal of Racial and Ethnic…•2017•References: 50

No prominent works on this page.

  • Caring by Numbers

    Open Access•Beth M Hartzler, Angela Snyder•ARTICLE•Journal of Racial and Ethnic…•2017•References: 50

  • An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model

    Open Access•Marsha Treadwell, Swapandeep Mushiana et al.•ARTICLE•Quality of Life Research•2022

    Study results highlight the importance of the biopsychosocial model to enhance understanding of the needs of this complex population, and to design multi-dimensional approaches for providing more effective interventions to improve outcomes

  • Newborn Screening for Sickle Cell Disease and Thalassemia

    Open Access•Maa-Ohui Quarmyne, Fiona Bock et al.•ARTICLE•JAMA Health Forum•2025

    The time has come for a paradigm shift in newborn screening for hemoglobinopathies through the adoption of universal molecular genetic testing

  • The impact of social vulnerability on primary vaccine coverage in children with sickle cell disease

    Open Access•J Shi, Jiajing Scarlette Shi et al.•ARTICLE•Frontiers in Public Health•2026

    Introduction This study examines the relationship between social vulnerability and up-to-date (UTD) primary vaccine coverage among children with sickle cell disease (SCD). Methods This retrospective cohort study included children with SCD born in Georgia between 2008 and 2019, identified through the state newborn screening program. Immunization records were obtained from the state registry, and birth addresses were matched to census tract level S…

Disease (4 works) · Hemoglobinopathies and Related Disorders (3 works) · Medicine (3 works) · Public health (3 works) · Blood groups and transfusion (2 works) · Gerontology (2 works) · Internal Medicine (2 works) · Population (2 works) · Biopsychosocial model (1 work) · Clinical Psychology (1 work)

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