Neeta Vora
26PUBLICATIONS
78CO-AUTHORS
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Publications (26)
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|Dec 03, 2025
The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies.Lisa S Weingarten, Allison Rosenbaum, Jessica de Voest
|May 06, 2025
Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys-Dietz Syndrome.Mia B Hodges, Sally Harris, Brianna Murphy
|Jan 05, 2025
Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene.Cordelia R Muir, Kelly L Gilmore, Smriti Singh
|Nov 29, 2024
Unequal Uptake: Insurance-Related Disparities in Prenatal Genetic Counseling and Screening at a Quaternary Medical Center.Divya Mallampati, Marcella Boynton, Asha Nikesh Talati
|Jan 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.Emily Zhao, Miles Bomback, Atlas Khan
|Dec 06, 2023
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.Gillian V Blayney, Eoghan Laffan, Preethi A Jacob
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Frequent Collaborators
4 joint publications
Lyn S Chitty
4 joint publications
Asha Nikesh Talati
4 joint publications
Jessica L Giordano
3 joint publications
Sarah Harris
3 joint publications
Teresa N Sparks
3 joint publications
Ignatia Van den Veyver
2 joint publications
Sylvie Langlois
2 joint publications
Kelly L Gilmore
2 joint publications
Angie C Jelin
1 joint publications
Kathryn J Gray
