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Navigating responsible bio-political citizenship: Cross-country comparison of stigma in Covid-19 illness narratives in Germany, Japan, the UK and the USA

SSM. Qualitative research in health, 2023-12, Vol.4, p.100291-100291, Article 100291

2023

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The familial canopy as thought space for meaning making, emotional calibration and planful action around inherited cancer risk

SSM. Qualitative research in health, 2023-06, Vol.3, p.100282, Article 100282

2023

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Negotiation of collective and individual candidacy for long Covid healthcare in the early phases of the Covid-19 pandemic: Validated, diverted and rejected candidacy

SSM. Qualitative research in health, 2023-06, Vol.3, p.100207-100207, Article 100207

2023

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Talking about inequities: A comparative analysis of COVID-19 narratives in the UK, US, and Brazil

SSM. Qualitative research in health, 2023-06, Vol.3, p.100277-100277, Article 100277

2023

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A qualitative feasibility study of a prototype patient-centered video intervention to increase uptake of cancer genetic testing among Black Americans

Pilot and feasibility studies, 2024-04, Vol.10 (1), p.62-62, Article 62

2024

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Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized

The Hastings Center report, 2019-05, Vol.49 (S1), p.S72-S81

Grob, Rachel

2019

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Testing Baby: The Transformation of Newborn Screening, Parenting, and Policymaking

Grob, Rachel

1, 2011

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When Mistakes Multiply: How Inadequate Responses to Medical Mishaps Erode Trust in American Medicine

The Hastings Center report, 2023-09, Vol.53 (S2), p.S22-S32

2023

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Cross country analysis of qualitative interviews: Developing a method, a community and an understanding of how Covid has been experienced around the globe

SSM. Qualitative research in health, 2024-06, Vol.5, p.100396, Article 100396

2024

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Treating, Fast and Slow: Americans' Understanding of and Responses to Low-Value Care

The Milbank quarterly, 2017-03, Vol.95 (1), p.70-116

2017

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Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized

The Hastings Center report, 2019-06, Vol.49 (3), p.S72-S81

GROB, RACHEL

2019

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Developing catalyst films of health experiences: an analysis of a robust multi-stakeholder involvement journey

Research involvement and engagement, 2022-07, Vol.8 (1), p.34-34, Article 34

2022

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Why Physicians Should Trust in Patients

JAMA : the journal of the American Medical Association, 2019-04, Vol.321 (14), p.1347

2019

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Using Patient-Reported Information to Improve Clinical Practice

Health services research, 2015-12, Vol.50 (S2), p.2116-2154

2015

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The Heart of Patient-Centered Care

Journal of health politics, policy and law, 2013-04, Vol.38 (2), p.457-465

Grob, Rachel

2013

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Is my sick child healthy? Is my healthy child sick?: Changing parental experiences of cystic fibrosis in the age of expanded newborn screening

Social science & medicine (1982), 2008-10, Vol.67 (7), p.1056-1064

Grob, Rachel

2008

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Educating, Enrolling, And Engaging: The State Of Marketplace Consumer Assistance Under The Affordable Care Act

Health Affairs, 2015-12, Vol.34 (12), p.2052-2060

2015

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What is emerging for qualitative research in the COVID-19 emergency?: A rejoinder to ‘Collecting qualitative data during a pandemic’ by David Silverman

Communication & medicine, 2021-09, Vol.17 (1), p.85-87

2021

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Polyphonic perspectives on health and care: Reflections from two decades of the DIPEx project

Journal of health services research & policy, 2021-04, Vol.26 (2), p.133-140

2021

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Physicians' Trust in Patients-Reply

JAMA : the journal of the American Medical Association, 2019-08, Vol.322 (8), p.782

2019

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A framework for conceptualizing how narratives from health-care consumers might improve or impede the use of information about provider quality

Patient experience journal, 2018-04, Vol.5 (1), p.15-26

2018

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Stumbling Into Adulthood: Learning From Depression While Growing Up

Qualitative health research, 2020-07, Vol.30 (9), p.1392-1408

2020

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Wobbly moments: Trust considerations for evolving cystic fibrosis care models

Journal of cystic fibrosis, 2024-09

2024

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Leveraging Patients’ Creative Ideas for Innovation in Health Care

The Milbank quarterly, 2024-03, Vol.102 (1), p.233-269

2024

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CAHPS and Comments

Journal of patient experience, 2017-03, Vol.4 (1), p.37-45

2017

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Navigating responsible bio-political citizenship: Cross-country comparison of stigma in Covid-19 illness narratives in Germany, Japan, the UK and the USA

The familial canopy as thought space for meaning making, emotional calibration and planful action around inherited cancer risk

Negotiation of collective and individual candidacy for long Covid healthcare in the early phases of the Covid-19 pandemic: Validated, diverted and rejected candidacy

Talking about inequities: A comparative analysis of COVID-19 narratives in the UK, US, and Brazil

A qualitative feasibility study of a prototype patient-centered video intervention to increase uptake of cancer genetic testing among Black Americans

Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized

Testing Baby: The Transformation of Newborn Screening, Parenting, and Policymaking

When Mistakes Multiply: How Inadequate Responses to Medical Mishaps Erode Trust in American Medicine

Cross country analysis of qualitative interviews: Developing a method, a community and an understanding of how Covid has been experienced around the globe

Treating, Fast and Slow: Americans' Understanding of and Responses to Low-Value Care

Qualitative Research on Expanded Prenatal and Newborn Screening: Robust but Marginalized

Developing catalyst films of health experiences: an analysis of a robust multi-stakeholder involvement journey

Why Physicians Should Trust in Patients

Using Patient-Reported Information to Improve Clinical Practice

The Heart of Patient-Centered Care

Is my sick child healthy? Is my healthy child sick?: Changing parental experiences of cystic fibrosis in the age of expanded newborn screening

Educating, Enrolling, And Engaging: The State Of Marketplace Consumer Assistance Under The Affordable Care Act

What is emerging for qualitative research in the COVID-19 emergency?: A rejoinder to ‘Collecting qualitative data during a pandemic’ by David Silverman

Polyphonic perspectives on health and care: Reflections from two decades of the DIPEx project

Physicians' Trust in Patients-Reply

A framework for conceptualizing how narratives from health-care consumers might improve or impede the use of information about provider quality

Stumbling Into Adulthood: Learning From Depression While Growing Up

Wobbly moments: Trust considerations for evolving cystic fibrosis care models

Leveraging Patients’ Creative Ideas for Innovation in Health Care

CAHPS and Comments

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