Detalhe da pesquisa
1.
Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsy.
Am J Hum Genet
; 110(10): 1616-1627, 2023 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37802042
2.
Digital health-enabled genomics: Opportunities and challenges.
Am J Hum Genet
; 109(7): 1190-1198, 2022 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35803232
3.
The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination.
Trends Genet
; 37(11): 951-954, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34503867
4.
Genetics providers' perspectives on the use of digital tools in clinical practice.
Genet Med
; 26(6): 101122, 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38493336
5.
Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?
Genet Med
; 26(2): 101033, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38007624
6.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-37217257
7.
Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Hum Genet
; 142(3): 321-330, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36629921
8.
Great expectations: patients' preferences for clinically significant results from genomic sequencing.
Hum Genet
; 142(4): 553-562, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36943453
9.
Genome screening, reporting, and genetic counseling for healthy populations.
Hum Genet
; 142(2): 181-192, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36331656
10.
"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.
Artigo
em Inglês
| MEDLINE | ID: mdl-37577963
11.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-36919843
12.
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.
J Med Genet
; 59(8): 817-826, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34544841
13.
Access to novel drugs and therapeutics for children and youth: Eliciting citizens' values to inform public funding decisions.
Health Expect
; 26(2): 715-727, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36639959
14.
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings.
Hum Genet
; 141(12): 1875-1885, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35739291
15.
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Am J Hum Genet
; 104(4): 578-595, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30951675
16.
"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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385106
17.
"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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35612591
18.
"I have to start learning how to live with becoming sick": A scoping review of the lived experiences of people with Huntington's disease.
Clin Genet
; 101(1): 3-19, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34216010
19.
Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study.
J Med Genet
; 58(4): 275-283, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32581083
20.
The clinical utility of exome and genome sequencing across clinical indications: a systematic review.
Hum Genet
; 140(10): 1403-1416, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34368901