Accès ouvert
2026
article
OpenAlex
Matthew H. Mossayebi, Sophie Adams, Megan E. Bunnell, Stephanie H. Guseh et autres
OBJECTIVES: We evaluated the diagnostic yield of karyotype (KT) and chromosomal microarray (CMA) with isolated severe FGR diagnosed before 32 weeks' gestation. Exome and genome sequencing (ES/GS) level data were available in a subset of this population. METHOD: We performed a retrospective …
us
(code pays fourni par la source)
2025
article
OpenAlex
Darren B. Orbach, Alireza Abdollah Shamshirsaz, Louise E. Wilkins-Haug
us
(code pays fourni par la source)
2025
editorial
OpenAlex
Christina Ronai, Louise E. Wilkins-Haug
us
(code pays fourni par la source)
2025
article
OpenAlex
Teresa N. Sparks, Louise E. Wilkins-Haug
The authors declare no conflicts of interest. Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.
us
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Darren B. Orbach, Alireza Abdollah Shamshirsaz, Louise E. Wilkins-Haug, Stephanie H. Guseh et autres
Importance: Vein of Galen malformation (VOGM) is the most common congenital cerebrovascular anomaly. Fetuses with VOGM and wide mediolateral falcine sinus diameters are at high risk for mortality, brain injury, and neurodevelopmental delay. In utero embolization may improve survival and outcomes. Objective: …
us
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
NN Lanners, S Morton, S. Blanco, Sara Mansoorshahi et autres
OBJECTIVE: Concurrent development of the placenta and heart during early gestation suggests a shared biological basis for the co-occurrence of abnormal placentation and congenital heart disease (CHD). This study investigated the association between placental vascular pathology and CHD type. METHODS: A retrospective …
us
(code pays fourni par la source)
2025
article
OpenAlex
Sophie Adams, Olivia Maher Trocki, Christina J. Miller, Courtney Studwell et autres
BACKGROUND: Genetic screening has advanced from prenatal cell-free DNA (cfDNA) screening for aneuploidies (cfDNA-ANP) to single-gene disorders (cfDNA-SGD). Clinical validation studies have been promising in pregnancies with anomalies but are limited in the general population. METHODS: Chart review and laboratory data identified …
us
(code pays fourni par la source)
2024
article
OpenAlex
Chrystalle Katte Carreon, Christina Ronai, Wayne Tworetzky, Sarah U. Morton et autres
OBJECTIVE: Impairments in the maternal-fetal environment are associated with adverse postnatal outcomes among infants with congenital heart disease. Therefore, we sought to investigate placental anomalies as they related to various forms of fetal congenital heart disease (FCHD). METHODS: We reviewed the placental …
us, de
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Lindsay R. Freud, Lynn L. Simpson, Louise E. Wilkins-Haug
The authors declare no conflicts of interest. Data sharing is not applicable to this article as no new data were created or analyzed in this study.
ca, us
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Radhika Viswanathan, Sarah E Little, Louise E. Wilkins-Haug, Ellen W. Seely et autres
BACKGROUND: Hypertensive disorders of pregnancy (HDP) are the most common cause of postpartum readmission. Prior research led to clinical guidelines for postpartum management; however, the patient experience is often missing from this work. The objective of this study is to understand the …
us
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Ryan M. Callahan, Kevin G. Friedman, Wayne Tworetzky, Jesse J. Esch et autres
FAV is offered to fetuses with severe aortic valve stenosis and evolving hypoplastic left heart syndrome. An inferential analysis of TS and SAE in a large series has not been reported. The purpose of this study was to determine factors associated with …
us
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Harrison Brand, Christopher W. Whelan, Michael Duyzend, John Lemanski et autres
us
(code pays fourni par la source)