Detalhe da pesquisa
1.
Barriers and facilitators to collaborative care implementation within the New York State Collaborative Care Medicaid Program.
BMC Health Serv Res
; 24(1): 505, 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38654291
2.
Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: An observational study of 4 clinical workflows.
Genet Med
; 25(5): 100802, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36906849
3.
Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior.
Am J Hum Genet
; 105(1): 122-131, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204012
4.
A Study Examining the Usefulness of a New Measure of Research Engagement.
J Gen Intern Med
; 37(Suppl 1): 50-56, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35349011
5.
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer.
Cancer Causes Control
; 32(5): 483-492, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33591484
6.
Population-based implementation of behavioral health detection and treatment into primary care: early data from New York state.
BMC Health Serv Res
; 21(1): 922, 2021 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34488741
7.
Patient-reported outcomes in the Translational Breast Cancer Research Consortium.
Cancer
; 126(5): 922-930, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31743427
8.
A pilot study of a telehealth family-focused melanoma preventive intervention for children with a family history of melanoma.
Psychooncology
; 29(1): 148-155, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31520429
9.
Implementing collaborative care to reduce depression for rural native American/Alaska native people.
BMC Health Serv Res
; 20(1): 34, 2020 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31931791
10.
Women's beliefs about what causes obesity: variation by race/ethnicity and acculturation in a Washington State sample.
Ethn Health
; 25(2): 243-254, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29243503
11.
Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassification.
J Genet Couns
; 29(5): 857-866, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31916645
12.
Development of FamilyTalk: an Intervention to Support Communication and Educate Families About Colorectal Cancer Risk.
J Cancer Educ
; 35(3): 470-478, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30737640
13.
Randomized trial of a web-based survivor intervention on melanoma prevention behaviors of first-degree relatives.
Cancer Causes Control
; 30(3): 225-233, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30483971
14.
Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance.
Genet Med
; 21(6): 1435-1442, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30374176
15.
MAGENTA (Making Genetic testing accessible): a prospective randomized controlled trial comparing online genetic education and telephone genetic counseling for hereditary cancer genetic testing.
BMC Cancer
; 19(1): 648, 2019 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31266460
16.
Comparing provider and patient views of issues for low-resourced breast cancer patients.
Psychooncology
; 28(5): 1018-1024, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30785226
17.
Patients' perspectives of variants of uncertain significance and strategies for uncertainty management.
J Genet Couns
; 28(2): 313-325, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30636062
18.
Patient goals, motivations, and attitudes in a patient-driven variant reclassification study.
J Genet Couns
; 28(3): 558-569, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31163102
19.
Content validation of a quantitative stakeholder engagement measure.
J Community Psychol
; 47(8): 1937-1951, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31475370
20.
Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.
Genet Med
; 20(11): 1438-1445, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29493582