Neeta Vora

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University of North Carolina at Chapel Hill

United States

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About

Neeta Vora is a Professor at the University of North Carolina at Chapel Hill, USA. Her research focuses on prenatal genetic counseling, congenital anomalies, and the implications of genetic variants in fetal development. Recent articles highlight her work on TGFBR1 variants, disparities in prenatal genetic screening, and the use of cell-free DNA in maternal cancer screening.

Recent Grants

Grant: Close

Early Genomic Diagnosis

Open Date: 2017-07-07

Close Date: 2021-06-30

Grant: Close

Determination of Fetal Gene Expression in Women with Preterm & Term Birth

Open Date: 2014-08-15

Close Date: 2017-01-31

Articles (18)

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2025

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2022

Collaborators (10)

Teresa N. Sparks

UNITED STATES

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Kristen Miller

Assistant Professor

Johns Hopkins University

UNITED STATES

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Mark Pertile

Head, Divisions of Reproductive Genetics and Biochemical Genetics

AUSTRALIA

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Lisa Hui

Associate Professor

University of Melbourne

AUSTRALIA

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Naomi Riches

Research Assistant Professor

University of Utah School of Medicine

UNITED STATES

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Asha Talati

University of North Carolina

UNITED STATES

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Joris Vermeesch

Professor

KULeuven

BELGIUM

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Kate Swanson

Assistant Professor

University of California, San Francisco

UNITED STATES

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Andrew M. Tidball

University of Michigan

UNITED STATES

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Marcella Boynton

Assistant Professor

University of North Carolina at Chapel Hill

UNITED STATES

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Neeta Vora

Research Interests

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About

Recent Grants

Articles (18)

Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys–Dietz Syndrome

Unequal Uptake: Insurance‐Related Disparities in Prenatal Genetic Counseling and Screening at a Quaternary Medical Center

Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene

Response to Wynn and Hokovec Regarding “The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use”

Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use

The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease

Cell-free DNA Screening and Maternal Cancer

Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin–Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features

Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies

Diagnostic yield and psychological outcomes among women pursuing trio‐exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes?

Understanding the experiences and perspectives of prenatal screening among a diverse cohort.

Two unrelated fetuses with ITPR1 missense variants and fetal hydrops

A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects

Sex-Dependent Differences in Mouse Placental Gene Expression following a Maternal High-Fat Diet

Prenatal exome and genome sequencing for fetal structural abnormalities

Prenatal phenotype of 47, XXY (Klinefelter syndrome)

Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series

RNA-Seq of amniotic fluid cell-free RNA: a discovery phase study of the pathophysiology of congenital cytomegalovirus infection

Collaborators (10)

Teresa N. Sparks

Kristen Miller

Mark Pertile

Lisa Hui

Naomi Riches

Asha Talati

Joris Vermeesch

Kate Swanson

Andrew M. Tidball

Marcella Boynton

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