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Beyond exploratory: a tailored framework for designing and assessing qualitative health research

BMJ open, 2019-08, Vol.9 (8), p.e030123

2019

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Community recommendations on biobank governance: Results from a deliberative community engagement in California

PloS one, 2017-02, Vol.12 (2), p.e0172582-e0172582

2017

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Patient and clinician perspectives on a patient‐facing dashboard that visualizes patient reported outcomes in rheumatoid arthritis

Health expectations : an international journal of public participation in health care and health policy, 2020-08, Vol.23 (4), p.846-859

2020

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Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease

Prion, 2022-12, Vol.16 (1), p.23-39

2022

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Practices, challenges, and opportunities when addressing the palliative care needs of people living with dementia: Specialty memory care provider perspectives

Alzheimer's & dementia : translational research & clinical interventions, 2021, Vol.7 (1), p.e12144-n/a

2021

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Barriers and facilitators to older adults' use of nonpharmacologic approaches for chronic pain: a person-focused model

Pain (Amsterdam), 2021-11, Vol.162 (11), p.2769-2779

2021

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Unintended Consequences of Opioid Regulations in Older Adults with Multiple Chronic Conditions

The Gerontologist, 2020-10, Vol.60 (7), p.1343-1352

2020

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"Captive by the Uncertainty"-Experiences with Anticipatory Guidance for People Living with Dementia and Their Caregivers at a Specialty Dementia Clinic

Journal of Alzheimer's disease, 2022-01, Vol.86 (2), p.787-800

2022

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Dementia Specialty Care Clinicians' Perspectives on Their Role in the Dementia Diagnostic Process and Diagnostic Disclosure

Journal of geriatric psychiatry and neurology, 2024-07, p.8919887241254468

2024

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Antibias Efforts in United States Maternity Care: A Scoping Review of the Publicly Funded Health Equity Intervention Pipeline

Clinical obstetrics and gynecology, 2023-03, Vol.66 (1), p.110

2023

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The Importance Of Integrating Narrative Into Health Care Decision Making

Health Affairs, 2016-04, Vol.35 (4), p.720-725

2016

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Decision-making about clinical trial options among older patients with metastatic cancer who have exhausted standard therapies

Journal of geriatric oncology, 2022-06, Vol.13 (5), p.594-599

2022

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"Relationships, Very Quickly, Turn to Nothing": Loneliness, Social Isolation, and Adaptation to Changing Social Lives Among Persons Living With Dementia and Care Partners

The Gerontologist, 2024-04, Vol.64 (4)

2024

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Caregiver Experiences Navigating the Diagnostic Journey in a Rapidly Progressing Dementia

Journal of geriatric psychiatry and neurology, 2023-07, Vol.36 (4), p.282-294

2023

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Approaches to decision-making among late-stage melanoma patients: a multifactorial investigation

Supportive care in cancer, 2019-03, Vol.27 (3), p.1059-1070

2019

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Hospice Staff Perspectives on Caring for People with Dementia: A Multisite, Multistakeholder Study

Journal of palliative medicine, 2020-08, Vol.23 (8), p.1013-1020

2020

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“Goals of Care Conversations Don't Fit in a Box”: Hospice Staff Experiences and Perceptions of Advance Care Planning Quality Measurement

Journal of pain and symptom management, 2021-05, Vol.61 (5), p.917-927

2021

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The Social Contexts of Birthing People with Public- and Private-Payer Prenatal Care: Illuminating an Understudied Aspect of the Patient Experience

Health equity, 2022-12, Vol.6 (1), p.898-908

2022

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"I Didn't Sign Up for This": Perspectives from Persons Living with Dementia and Care Partners on Challenges, Supports, and Opportunities to Add Geriatric Neuropalliative Care to Dementia Specialty Care

Journal of Alzheimer's disease, 2022-01, Vol.90 (3), p.1301-1320

2022

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The Continued Importance of Quality Parent-Adolescent Relationships During Late Adolescence

Journal of research on adolescence, 2008-03, Vol.18 (1), p.187-200

2008

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Characteristics of people with dementia lost to follow‐up from a dementia care center

International journal of geriatric psychiatry, 2022-01, Vol.37 (1), p.n/a

2022

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The promises of computational ethnography: Improving transparency, replicability, and validity for realist approaches to ethnographic analysis

Ethnography, 2018-06, Vol.19 (2), p.254-284

2018

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"It's Case by Case, and It's a Struggle": A Qualitative Study of Hospice Practices, Perspectives, and Ethical Dilemmas When Caring for Hospice Enrollees with Full-Code Status or Intensive Treatment Preferences

Journal of palliative medicine, 2021-04, Vol.24 (4), p.496-504

2021

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Linking Broad Consent to Biobank Governance: Support From a Deliberative Public Engagement in California

American journal of bioethics, 2015-09, Vol.15 (9), p.56-57

2015

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Community-Based Palliative Care Consultations: Comparing Dementia to Nondementia Serious Illnesses

Journal of palliative medicine, 2020-08, Vol.23 (8), p.1021-1029

2020

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Beyond exploratory: a tailored framework for designing and assessing qualitative health research

Community recommendations on biobank governance: Results from a deliberative community engagement in California

Patient and clinician perspectives on a patient‐facing dashboard that visualizes patient reported outcomes in rheumatoid arthritis

Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease

Practices, challenges, and opportunities when addressing the palliative care needs of people living with dementia: Specialty memory care provider perspectives

Barriers and facilitators to older adults' use of nonpharmacologic approaches for chronic pain: a person-focused model

Unintended Consequences of Opioid Regulations in Older Adults with Multiple Chronic Conditions

"Captive by the Uncertainty"-Experiences with Anticipatory Guidance for People Living with Dementia and Their Caregivers at a Specialty Dementia Clinic

Dementia Specialty Care Clinicians' Perspectives on Their Role in the Dementia Diagnostic Process and Diagnostic Disclosure

Antibias Efforts in United States Maternity Care: A Scoping Review of the Publicly Funded Health Equity Intervention Pipeline

The Importance Of Integrating Narrative Into Health Care Decision Making

Decision-making about clinical trial options among older patients with metastatic cancer who have exhausted standard therapies

"Relationships, Very Quickly, Turn to Nothing": Loneliness, Social Isolation, and Adaptation to Changing Social Lives Among Persons Living With Dementia and Care Partners

Caregiver Experiences Navigating the Diagnostic Journey in a Rapidly Progressing Dementia

Approaches to decision-making among late-stage melanoma patients: a multifactorial investigation

Hospice Staff Perspectives on Caring for People with Dementia: A Multisite, Multistakeholder Study

“Goals of Care Conversations Don't Fit in a Box”: Hospice Staff Experiences and Perceptions of Advance Care Planning Quality Measurement

The Social Contexts of Birthing People with Public- and Private-Payer Prenatal Care: Illuminating an Understudied Aspect of the Patient Experience

"I Didn't Sign Up for This": Perspectives from Persons Living with Dementia and Care Partners on Challenges, Supports, and Opportunities to Add Geriatric Neuropalliative Care to Dementia Specialty Care

The Continued Importance of Quality Parent-Adolescent Relationships During Late Adolescence

Characteristics of people with dementia lost to follow‐up from a dementia care center

The promises of computational ethnography: Improving transparency, replicability, and validity for realist approaches to ethnographic analysis

"It's Case by Case, and It's a Struggle": A Qualitative Study of Hospice Practices, Perspectives, and Ethical Dilemmas When Caring for Hospice Enrollees with Full-Code Status or Intensive Treatment Preferences

Linking Broad Consent to Biobank Governance: Support From a Deliberative Public Engagement in California

Community-Based Palliative Care Consultations: Comparing Dementia to Nondementia Serious Illnesses

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