Neeta L Vora
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Explore the profile of Neeta L Vora including associated specialties, affiliations and a list of published articles.
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84
Citations
895
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Recent Articles
1.
Grace M, Goodhue B, Vora N
Curr Opin Obstet Gynecol
. 2025 Jan;
37(2):55-59.
PMID: 39774459
Purpose Of Review: Despite the availability of Rh(D) immune globulin (RhIg) to prevent alloimmunization in Rh(D)-negative pregnant patients, anti-Rh(D) alloimmunization remains a prevalent cause of hemolytic disease of the fetus...
2.
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Muir C, Gilmore K, Singh S, Vora N
Prenat Diagn
. 2025 Jan;
45(2):227-230.
PMID: 39757347
Objective: To report a case of a fetus with multiple congenital anomalies and suspected Barth syndrome, highlighting potential phenotypic expansion of the syndrome. Methods: A 32-year-old G4P2011 patient was referred...
4.
Goralski J, Talati A, Hardisty E, Vora N
Obstet Gynecol
. 2024 Dec;
145(1):47-54.
PMID: 39666984
With improvements in overall health attributable to newly available medications called highly effective modulator therapy, an increasing number of people with cystic fibrosis (CF) are pursuing pregnancy. However, the safety...
5.
Veazey R, Fisher A, Talati A, Hardisty E, Gilmore K, Vora N
Prenat Diagn
. 2024 Oct;
44(12):1522-1525.
PMID: 39389935
No abstract available.
6.
Vora N, Langlois S, Chitty L
Prenat Diagn
. 2024 Sep;
44(12):1500-1501.
PMID: 39275903
No abstract available.
7.
Sneddon T, Gilmore K, Xiong M, Weck K, Powell B, Vora N
Am J Med Genet A
. 2024 Sep;
197(1):e63861.
PMID: 39235309
Gain-of-function variants in the WDR44 gene have recently been associated with an X-linked ciliopathy-related neurodevelopmental phenotype. Here, we report on a WDR44 loss-of-function (LOF) variant identified in the genome sequence...
8.
Roychaudhury A, Lee Y, Choi T, Thomas M, Khan T, Yousaf H, et al.
Ann Neurol
. 2024 Jul;
96(5):914-931.
PMID: 39073169
Objective: Intellectual disability is often the outcome of neurodevelopmental disorders and is characterized by significant impairments in intellectual and adaptive functioning. X-linked intellectual disability (XLID) is a subset of these...
9.
Talati A, Mallampati D, Hardisty E, Gilmore K, Vora N
Genet Med
. 2024 Jul;
26(11):101221.
PMID: 39045791
Purpose: To describe the association between geographic location of residence and use of aneuploidy screening or prenatal genetic counseling and how it is modified by maternal race and ethnicity. Methods:...
10.
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...