Detalles de la búsqueda
1.
Genetics providers' perspectives on the use of digital tools in clinical practice.
Genet Med
; 26(6): 101122, 2024 Mar 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-38493336
2.
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
3.
Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Hum Genet
; 142(3): 321-330, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36629921
4.
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
5.
Genome screening, reporting, and genetic counseling for healthy populations.
Hum Genet
; 142(2): 181-192, 2023 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-36331656
6.
"I don't need any more unknowns hanging over my head": Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing.
Genet Med
; 25(12): 100960, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37577963
7.
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
8.
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings.
Hum Genet
; 141(12): 1875-1885, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35739291
9.
"Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome Management.
Oncologist
; 27(5): e393-e401, 2022 05 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35385106
10.
"Doctors shouldn't have to cheat the system": Clinicians' real-world experiences of the utility of genomic sequencing.
Genet Med
; 24(9): 1888-1898, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35612591
11.
Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Hum Genet
; 140(3): 493-504, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-32892247
12.
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
13.
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
14.
Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment.
Genet Med
; 22(12): 2011-2019, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32820245
15.
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
16.
Parents' attitudes towards research involving genome sequencing of their healthy children: a qualitative study.
Eur J Hum Genet
; 32(2): 171-175, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-37864046
17.
"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screening.
Eur J Hum Genet
; 32(2): 176-181, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-37821757
18.
Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.
BMJ Open
; 14(4): e081426, 2024 Apr 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38569677
19.
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol.
BMJ Open
; 13(6): e072999, 2023 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-37270192
20.
Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey.
Clin Biochem
; 118: 110607, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37406717