Detalhe da pesquisa
1.
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey.
Prenat Diagn
; 42(7): 934-946, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35476801
2.
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies.
Clin Genet
; 100(6): 647-658, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34155632
3.
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.
Prenat Diagn
; 41(6): 720-732, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33724493
4.
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han's taxonomy of uncertainty.
J Genet Couns
; 30(1): 198-210, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32638447
5.
Psychosocial Impact of a True-Positive, False-Positive, or Inconclusive Newborn Bloodspot Screening Result: A Questionnaire Study among Parents.
Int J Neonatal Screen
; 10(1)2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38535122
6.
Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing.
Appl Clin Genet
; 16: 89-97, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37216148
7.
The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis.
Eur J Med Genet
; 66(10): 104844, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37709011
8.
Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design.
PLoS One
; 17(1): e0261898, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35089945
9.
Parents' views on accepting, declining, and expanding newborn bloodspot screening.
PLoS One
; 17(8): e0272585, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35980961
10.
Response to the comment on Diderich et al. "The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis" (EJMG 66(10),104844).
Eur J Med Genet
; 67: 104884, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37972850