Ignatia B Van den Veyver
Overview
Explore the profile of Ignatia B Van den Veyver including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
87
Citations
1247
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Hutchinson J, Potocki L, Van den Veyver I
Prenat Diagn
. 2025 Feb;
PMID: 39916310
A comprehensive postmortem examination is an essential component of a work-up after stillbirth. Its findings can support accurate counseling of parents about causes and risk of recurrence. It also supports...
2.
Zemet R, Van den Veyver I
Best Pract Res Clin Obstet Gynaecol
. 2024 Sep;
97:102545.
PMID: 39265228
Genetic testing for prenatal diagnosis in the pre-genomic era primarily focused on detecting common fetal aneuploidies, using methods that combine maternal factors and imaging findings. The genomic era, ushered in...
3.
Zemet R, Maktabi M, Tinfow A, Giordano J, Heisler T, Yan Q, et al.
Am J Obstet Gynecol
. 2024 Jun;
PMID: 38914189
Background: Amniocentesis for genetic diagnosis is most commonly done between 15 and 22 weeks of gestation but can be performed at later gestational ages. The safety and genetic diagnostic accuracy...
4.
Cacheiro P, Lawson S, Van den Veyver I, Marengo G, Zocche D, Murray S, et al.
Genet Med
. 2024 Apr;
26(7):101141.
PMID: 38629401
Purpose: Existing resources that characterize the essentiality status of genes are based on either proliferation assessment in human cell lines, viability evaluation in mouse knockouts, or constraint metrics derived from...
5.
Cacheiro P, Lawson S, Van den Veyver I, Marengo G, Zocche D, Murray S, et al.
medRxiv
. 2024 Jan;
PMID: 38260283
Essential genes are those whose function is required for cell proliferation and/or organism survival. A gene's intolerance to loss-of-function can be allocated within a spectrum, as opposed to being considered...
6.
Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Su L, Anikar S, et al.
Reprod Sci
. 2023 Sep;
31(1):173-189.
PMID: 37658178
Human embryonic stem cells (hESCs) cultured in media containing bone morphogenic protein 4 (BMP4; B) differentiate into trophoblast-like cells. Supplementing media with inhibitors of activin/nodal signaling (A83-01) and of fibroblast...
7.
Maktabi M, Vossaert L, Van den Veyver I
Clin Obstet Gynecol
. 2023 Aug;
66(3):636-648.
PMID: 37650673
Considering the diagnostic limitations of cfDNA-based noninvasive prenatal testing (NIPT), scientists have long been interested in isolating and analyzing rare intact fetal and trophoblast cells from maternal blood or endocervical...
8.
Jolly A, Du H, Borel C, Chen N, Zhao S, Grochowski C, et al.
HGG Adv
. 2023 May;
4(3):100188.
PMID: 37124138
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by aplasia of the female reproductive tract; the syndrome can include renal anomalies, absence or dysgenesis, and skeletal anomalies. While functional models have elucidated several...
9.
Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Nasiotis E, Su L, et al.
Reprod Sci
. 2023 Mar;
30(9):2780-2793.
PMID: 36976514
The subcortical maternal complex (SCMC) is a multiprotein complex in oocytes and preimplantation embryos that is encoded by maternal effect genes. The SCMC is essential for zygote-to-embryo transition, early embryogenesis,...
10.
Sakyu T, Stover S, Wang Y, Ward P, Gandhi M, Braun M, et al.
Clin Case Rep
. 2023 Feb;
11(2):e6692.
PMID: 36846174
We present a fetus with bilaterally enlarged and echogenic kidneys. Prenatal testing detected compound heterozygosity for a 0.676 Mb de novo deletion and an inherited pathogenic variant in . This...