Detalhe da pesquisa
1.
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Am J Hum Genet
; 110(9): 1454-1469, 2023 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595579
2.
Treatment for Mild Chronic Hypertension during Pregnancy.
N Engl J Med
; 386(19): 1781-1792, 2022 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35363951
3.
The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model.
Am J Obstet Gynecol
; 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38432413
4.
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.
Am J Obstet Gynecol
; 230(3): 368.e1-368.e12, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37717890
5.
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.
Prenat Diagn
; 44(2): 196-204, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37594370
6.
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.
Prenat Diagn
; 44(4): 422-431, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38054560
7.
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
N Engl J Med
; 383(18): 1746-1756, 2020 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33027564
8.
Performance of prenatal cfDNA screening for sex chromosomes.
Genet Med
; 25(8): 100879, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154148
9.
Prenatal exome and genome sequencing for fetal structural abnormalities.
Am J Obstet Gynecol
; 228(2): 140-149, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36027950
10.
Society for Maternal-Fetal Medicine Consult Series #64: Systemic lupus erythematosus in pregnancy.
Am J Obstet Gynecol
; 228(3): B41-B60, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36084704
11.
Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening results.
Am J Obstet Gynecol
; 229(3): 300.e1-300.e9, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36965866
12.
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.
Prenat Diagn
; 43(11): 1394-1405, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37752660
13.
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy.
Prenat Diagn
; 43(2): 133-143, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36588186
14.
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.
Prenat Diagn
; 43(13): 1574-1580, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38066724
15.
Cell-free DNA Screening for Aneuploidy.
Clin Obstet Gynecol
; 66(3): 557-567, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37650668
16.
Understanding Preterm Birth in Pregnancies Complicated by Nonimmune Hydrops Fetalis.
Am J Perinatol
; 40(9): 917-922, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36603834
17.
Evaluation of Hypoglycemia in Neonates of Women at Risk for Late Preterm Delivery: An Antenatal Late Preterm Steroids Trial Cohort Study.
Am J Perinatol
; 40(5): 532-538, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34044454
18.
Universal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing for Obstetric Inpatient Units Across the United States.
Clin Infect Dis
; 75(1): e322-e328, 2022 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34791093
19.
The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research.
Genet Med
; 24(2): 410-418, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906477
20.
Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.
Genet Med
; 24(6): 1206-1216, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396980