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Neeta Vora

26PUBLICATIONS

78CO-AUTHORS

Women's studies (incl. girls' studies)Gene mappingCancer diagnosisGene expression (incl. microarray and other genome-wide approaches)Foetal development and medicine

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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 08, 2025

Cell-free DNA Screening and Maternal Cancer.

Neeta L Vora

|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

|Oct 10, 2024

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.

Rachel A Veazey, Allan J Fisher, Asha N Talati

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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

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

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