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1.
A model for the return and referral of all clinically significant secondary findings of genomic sequencing.
J Med Genet
; 60(8): 733-739, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37217257
2.
Great expectations: patients' preferences for clinically significant results from genomic sequencing.
Hum Genet
; 142(4): 553-562, 2023 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-36943453
3.
How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey.
Genet Med
; 25(5): 100819, 2023 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-36919843
4.
Patient and public preferences for being recontacted with updated genomic results: a mixed methods study.
Hum Genet
; 140(12): 1695-1708, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34537903
5.
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care.
Genet Med
; 23(6): 1086-1094, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33654192
6.
Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Genet Med
; 22(4): 727-735, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31822848
7.
Utility of prospective pathologic evaluation to inform clinical genetic testing for hereditary leiomyomatosis and renal cell carcinoma.
Cancer
; 123(13): 2452-2458, 2017 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28171700
8.
"I Don't Want to Be an Ostrich": Managing Mothers' Uncertainty during BRCA1/2 Genetic Counseling.
J Genet Couns
; 26(3): 455-468, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-27473644
9.
Educational and Psychosocial Support Needs in Lynch Syndrome: Implementation and Assessment of an Educational Workshop and Support Group.
J Genet Couns
; 26(2): 232-243, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-27734221
10.
Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General's My Family Health Portrait.
Genet Med
; 17(9): 753-6, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-25521335
11.
Assessment of individuals with BRCA1 and BRCA2 large rearrangements in high-risk breast and ovarian cancer families.
Breast Cancer Res Treat
; 145(3): 625-34, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24825132
12.
Talking about familial breast cancer risk: topics and strategies to enhance mother-daughter interactions.
Qual Health Res
; 24(4): 517-35, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24633365
13.
Sources of uncertainty about daughters' breast cancer risk that emerge during genetic counseling consultations.
J Genet Couns
; 21(2): 292-304, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21833819
14.
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.
BMJ Open
; 12(4): e060899, 2022 04 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-35487723
15.
PARC report: a health-systems focus on reimbursement and patient access to pharmacogenomics testing.
Pharmacogenomics
; 21(11): 785-796, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32748688
16.
PARC report: a perspective on the state of clinical pharmacogenomics testing.
Pharmacogenomics
; 21(11): 809-820, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32635876
17.
Quality of life drives patients' preferences for secondary findings from genomic sequencing.
Eur J Hum Genet
; 28(9): 1178-1186, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32424322
18.
Development of patient "profiles" to tailor counseling for incidental genomic sequencing results.
Eur J Hum Genet
; 27(7): 1008-1017, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-30846854
19.
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
BMJ Open
; 9(10): e031092, 2019 10 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31594892
20.
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
Eur J Hum Genet
; 26(7): 984-995, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29703952