Detalhe da pesquisa
1.
Placental, maternal, fetal, and technical origins of false-positive cell-free DNA screening results.
Am J Obstet Gynecol
; 230(4): 381-389, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38008147
2.
The accuracy of cell-free DNA screening for fetal segmental copy number variants: A systematic review and meta-analysis.
BJOG
; 130(6): 549-559, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36655363
3.
Experiences of receiving an increased chance of sex chromosome aneuploidy result from non-invasive prenatal testing in Australia: "A more complicated scenario than what I had ever realized".
J Genet Couns
; 32(1): 213-223, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36114608
4.
Cell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalances.
Prenat Diagn
; 42(11): 1349-1357, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36068932
5.
Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study.
Am J Obstet Gynecol
; 225(5): 527.e1-527.e12, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33957116
6.
Ultrasound findings and detection of fetal abnormalities before 11 weeks of gestation.
Prenat Diagn
; 41(13): 1675-1684, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34643279
7.
Outcomes following the detection of fetal edema in early pregnancy prior to non-invasive prenatal testing.
Prenat Diagn
; 41(2): 241-247, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33067800
8.
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Hum Reprod
; 35(3): 694-704, 2020 03 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32207823
9.
Increasing maternal age is not a significant cause of false-positive results for monosomy X in non-invasive prenatal testing.
Prenat Diagn
; 40(11): 1466-1473, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32673423
10.
The importance of ultrasound preceding cell-free DNA screening for fetal chromosomal abnormalities.
Prenat Diagn
; 40(11): 1439-1446, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32662897
11.
Early Diagnosis and Differences in Progression of Fetal Encephalocele.
J Ultrasound Med
; 39(7): 1435-1440, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31944319
12.
Lipiodol flush under ultrasound guidance in Australia.
Aust N Z J Obstet Gynaecol
; 60(6): 965-969, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32909253
13.
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.
Prenat Diagn
; 39(13): 1254-1261, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31691307
14.
Cell-free fetal DNA testing in singleton IVF conceptions.
Hum Reprod
; 33(4): 572-578, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29462319
15.
Non-Invasive Prenatal Testing for Sex Chromosome Aneuploidy in Routine Clinical Practice.
Fetal Diagn Ther
; 44(2): 85-90, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-28873375
16.
Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.
Aust N Z J Obstet Gynaecol
; 56(6): 605-613, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27402530
17.
Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium.
Mol Cytogenet
; 17(1): 9, 2024 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38627791
18.
"Taking its toll": the challenges of working in fetal medicine.
Birth
; 40(1): 52-60, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24635425
19.
Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.
Front Genet
; 13: 975987, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36105088
20.
Preimplantation Genetic Testing for Monogenic Conditions: Is Cell-Free DNA Testing the Next Step?
Mol Diagn Ther
; 25(6): 683-690, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34495483