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Beth A Tarini

Biographic Data

ID6763242
NAMEBeth A Tarini
GIVEN NAMESBeth A
FAMILY NAMETarini
SIGNATURETARINI B A
AFFILIATIONSChildren's National
ORCID0000-0003-4272-8668
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS1
WORKS AS AUTHOR8
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2013
LATEST PUBLICATION YEAR2023
H-INDEX1
  • Healthcare team communication training in the United States

    Julia Hathaway, Beth A Tarini et al.•ARTICLE•Health Communication•2023

    The purpose of this literature review was to identify interventions designed to improve healthcare team communication in the United States. We conducted a review of peer-reviewed, English-language articles describing interventions aimed at improving healthcare team communication. We analyzed articles that met pre-specified inclusion and exclusion criteria and characterized who is testing communication interventions, the rationale for testing, and…

  • Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research

    Open Access•Erin Rothwell, Erin Johnson et al.•ARTICLE•Journal of Empirical Research on…•2020•References: 1

    Obtaining informed consent for bloodspot research from newborn screening is particularly challenging due to the hectic environment of the postnatal period and the relatively abstract nature of future, unspecified research on the biospecimens. A randomized controlled trial was conducted in three Michigan hospitals to compare two different consent processes (video and interactive tablet "app") with standard brochure-based consent in the Michigan Bi…

  • Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result

    Open Access•Anne Atkins, Beth A Tarini et al.•ARTICLE•Journal of Community Genetics•2019

  • Newborn Screening Collection and Delivery Processes in Michigan Birthing Hospitals

    Open Access•Amy L Cochran, Beth A Tarini et al.•ARTICLE•Maternal and Child Health Journal•2018

  • Survey of family history taking and genetic testing in pediatric practice

    Open Access•Robert A Saul, Tracy L Trotter et al.•ARTICLE•Journal of Community Genetics•2017

  • An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots

    Open Access•Erin Rothwell, Aaron J Goldenberg et al.•ARTICLE•Journal of Empirical Research on…•2017•Cited by: 1•References: 3

    As state newborn screening programs develop approaches to parental permission for the storage and use of residual dried newborn screening samples, it is important to understand how the public comprehends the consent elements. Focus groups in Utah, California, and Michigan ( n = 7 groups, 69 participants) were conducted to evaluate the language on a shortened consent form. Outcomes from the analysis included barriers to conceptualizing biospecimen…

  • Biobank participant support of newborn screening for disorders with variable treatment and intervention options

    Open Access•Megan E Bunnell, Beth A Tarini et al.•ARTICLE•Journal of Community Genetics•2016

  • Anticipating the arrival of low-penetrance genetic testing to primary care medicine

    Open Access•Beth A Tarini, Nicole Exe et al.•ARTICLE•Journal of Community Genetics•2013

  • An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots

    Open Access•Erin Rothwell, Aaron J Goldenberg et al.•ARTICLE•Journal of Empirical Research on…•2017•Cited by: 1•References: 3

    As state newborn screening programs develop approaches to parental permission for the storage and use of residual dried newborn screening samples, it is important to understand how the public comprehends the consent elements. Focus groups in Utah, California, and Michigan ( n = 7 groups, 69 participants) were conducted to evaluate the language on a shortened consent form. Outcomes from the analysis included barriers to conceptualizing biospecimen…

  • Anticipating the arrival of low-penetrance genetic testing to primary care medicine

    Open Access•Beth A Tarini, Nicole Exe et al.•ARTICLE•Journal of Community Genetics•2013

  • Biobank participant support of newborn screening for disorders with variable treatment and intervention options

    Open Access•Megan E Bunnell, Beth A Tarini et al.•ARTICLE•Journal of Community Genetics•2016

  • Survey of family history taking and genetic testing in pediatric practice

    Open Access•Robert A Saul, Tracy L Trotter et al.•ARTICLE•Journal of Community Genetics•2017

  • An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots

    Open Access•Erin Rothwell, Aaron J Goldenberg et al.•ARTICLE•Journal of Empirical Research on…•2017•Cited by: 1•References: 3

    As state newborn screening programs develop approaches to parental permission for the storage and use of residual dried newborn screening samples, it is important to understand how the public comprehends the consent elements. Focus groups in Utah, California, and Michigan ( n = 7 groups, 69 participants) were conducted to evaluate the language on a shortened consent form. Outcomes from the analysis included barriers to conceptualizing biospecimen…

  • Newborn Screening Collection and Delivery Processes in Michigan Birthing Hospitals

    Open Access•Amy L Cochran, Beth A Tarini et al.•ARTICLE•Maternal and Child Health Journal•2018

  • Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result

    Open Access•Anne Atkins, Beth A Tarini et al.•ARTICLE•Journal of Community Genetics•2019

  • Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research

    Open Access•Erin Rothwell, Erin Johnson et al.•ARTICLE•Journal of Empirical Research on…•2020•References: 1

    Obtaining informed consent for bloodspot research from newborn screening is particularly challenging due to the hectic environment of the postnatal period and the relatively abstract nature of future, unspecified research on the biospecimens. A randomized controlled trial was conducted in three Michigan hospitals to compare two different consent processes (video and interactive tablet "app") with standard brochure-based consent in the Michigan Bi…

  • Healthcare team communication training in the United States

    Julia Hathaway, Beth A Tarini et al.•ARTICLE•Health Communication•2023

    The purpose of this literature review was to identify interventions designed to improve healthcare team communication in the United States. We conducted a review of peer-reviewed, English-language articles describing interventions aimed at improving healthcare team communication. We analyzed articles that met pre-specified inclusion and exclusion criteria and characterized who is testing communication interventions, the rationale for testing, and…

Medicine (8 works) · Family medicine (5 works) · Genomics and Rare Diseases (4 works) · Nursing (4 works) · Psychology (4 works) · BRCA gene mutations in cancer (3 works) · Medical education (3 works) · Metabolism and Genetic Disorders (3 works) · Public health (3 works) · Alternative medicine (2 works)

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