Detalhe da pesquisa
1.
Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies.
Clin Chem
; 67(9): 1210-1219, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34077512
2.
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.
Clin Chem
; 61(4): 608-16, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25710461
3.
Factors affecting levels of circulating cell-free fetal DNA in maternal plasma and their implications for noninvasive prenatal testing.
Prenat Diagn
; 35(8): 816-22, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26013964
4.
Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.
Prenat Diagn
; 35(8): 810-5, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25967380
5.
Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies.
Genet Med
; 16(5): 419-22, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24091801
6.
Noninvasive detection of a balanced fetal translocation from maternal plasma.
Clin Chem
; 60(10): 1298-305, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25030021
7.
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.
Am J Obstet Gynecol
; 211(4): 365.e1-12, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24657131
8.
Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.
Prenat Diagn
; 33(6): 591-7, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23592550
9.
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.
Genet Med
; 14(3): 296-305, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22281937
10.
Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma.
Clin Chem
; 58(7): 1148-51, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22563040
11.
Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration.
Hum Genomics
; 5(5): 420-40, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21807600
12.
DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations.
Prenat Diagn
; 32(8): 730-4, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22585317
13.
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.
Genet Med
; 13(11): 913-20, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22005709
14.
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting.
Am J Obstet Gynecol
; 204(3): 205.e1-11, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21310373
15.
Comment on "Clinical application of massively parallel sequencing-based prenatal non-invasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors".
Prenat Diagn
; 33(13): 1310-3, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24327426
16.
Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domains.
Genome Biol
; 16: 78, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886572
17.
Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.
PLoS One
; 9(10): e109173, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25289665
18.
High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma.
PLoS One
; 8(3): e57381, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23483908
19.
A genomic analysis of the archaeal system Ignicoccus hospitalis-Nanoarchaeum equitans.
Genome Biol
; 9(11): R158, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19000309
20.
On the predictability of protein database search complexity and its relevance to optimization of distributed searches.
J Proteome Res
; 6(9): 3443-8, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17663575