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.
Phthalate and phthalate replacement concentrations in relationship to adiposity in a multi-racial cohort of children.
Int J Obes (Lond)
; 2024 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38824227
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.
Multiethnic Growth Standards for Fetal Body Composition and Organ Volumes Derived from 3D Ultrasonography.
Am J Obstet Gynecol
; 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38838912
5.
Improving prenatal diagnosis through standards and aggregation.
Prenat Diagn
; 44(4): 454-464, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38242839
6.
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.
Prenat Diagn
; 44(3): 343-351, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38285371
7.
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical study.
Prenat Diagn
; 44(3): 304-316, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38411249
8.
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
9.
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
10.
Association of Mild Iodine Insufficiency during Pregnancy with Child Neurodevelopment in Patients with Subclinical Hypothyroidism or Hypothyroxinemia.
Am J Perinatol
; 41(S 01): e3326-e3332, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38228158
11.
Causal Genetic Variants in Stillbirth.
N Engl J Med
; 383(12): 1107-1116, 2020 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32786180
12.
Performance of prenatal cfDNA screening for sex chromosomes.
Genet Med
; 25(8): 100879, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154148
13.
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.
Genet Med
; 25(12): 100983, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37746849
14.
Association of Living in a Food Desert and Poor Periconceptional Diet Quality in a Cohort of Nulliparous Pregnant Individuals.
J Nutr
; 153(8): 2432-2441, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37364682
15.
Should we offer prenatal exome sequencing for intrauterine growth restriction or short long bones? A systematic review and meta-analysis.
Am J Obstet Gynecol
; 228(4): 409-417.e4, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36209938
16.
Comparing population-based fetal growth standards in a US cohort.
Am J Obstet Gynecol
; 2023 Dec 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38151220
17.
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
18.
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
19.
Sleep-disordered Breathing in Pregnancy and after Delivery: Associations with Cardiometabolic Health.
Am J Respir Crit Care Med
; 205(10): 1202-1213, 2022 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35144521
20.
Correlation of Ocular Plane-Wave Doppler With Optical Coherence Tomography Angiography in Preeclampsia.
J Ultrasound Med
; 42(12): 2815-2824, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37605863