Neeta L. Vora

3.7k total citations · 1 hit paper
87 papers, 2.0k citations indexed

About

Neeta L. Vora is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Neeta L. Vora has authored 87 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Pediatrics, Perinatology and Child Health, 36 papers in Genetics and 20 papers in Molecular Biology. Recurrent topics in Neeta L. Vora's work include Prenatal Screening and Diagnostics (58 papers), Genomic variations and chromosomal abnormalities (22 papers) and Fetal and Pediatric Neurological Disorders (21 papers). Neeta L. Vora is often cited by papers focused on Prenatal Screening and Diagnostics (58 papers), Genomic variations and chromosomal abnormalities (22 papers) and Fetal and Pediatric Neurological Disorders (21 papers). Neeta L. Vora collaborates with scholars based in United States, Australia and United Kingdom. Neeta L. Vora's co-authors include Diana W. Bianchi, Lyn S. Chitty, Angie C. Jelin, Ronald J. Wapner, Emily Hardisty, Karen Wou, Sunayna Best, Louise Wilkins‐Haug, Lisa Hui and Judy E. Garber and has published in prestigious journals such as JAMA, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Neeta L. Vora

81 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2023 58 citations Lisa Hui, Katie Ellis et al. Prenatal Diagnosis profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Neeta L. Vora United States	23	1.4k	773	500	245	222	87	2.0k
José Carlos Ferreira United States	22	882 0.6×	764 1.0×	816 1.6×	162 0.7×	67 0.3×	39	1.6k
Kristin G. Monaghan United States	18	1.1k 0.8×	693 0.9×	454 0.9×	291 1.2×	110 0.5×	29	2.0k
Stephanie Allen United Kingdom	16	653 0.5×	316 0.4×	325 0.7×	183 0.7×	93 0.4×	43	1.1k
Constantin S. von Kaisenberg Germany	25	863 0.6×	166 0.2×	435 0.9×	374 1.5×	80 0.4×	75	2.2k
Banu Aygün United States	29	644 0.5×	131 0.2×	320 0.6×	151 0.6×	48 0.2×	114	2.8k
Robert Saura France	19	445 0.3×	318 0.4×	163 0.3×	83 0.3×	49 0.2×	50	868
Hyun Mee Ryu South Korea	19	739 0.5×	109 0.1×	307 0.6×	86 0.4×	96 0.4×	120	1.3k
Shuenn‐Dyh Chang Taiwan	19	672 0.5×	185 0.2×	205 0.4×	87 0.4×	47 0.2×	103	1.3k
Christine M. Armour Canada	20	358 0.3×	435 0.6×	340 0.7×	68 0.3×	68 0.3×	52	923
C Nessmann France	22	701 0.5×	225 0.3×	273 0.5×	89 0.4×	40 0.2×	45	1.4k

Countries citing papers authored by Neeta L. Vora

Since Specialization

Citations

This map shows the geographic impact of Neeta L. Vora's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Neeta L. Vora with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Neeta L. Vora more than expected).

Fields of papers citing papers by Neeta L. Vora

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Neeta L. Vora. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Neeta L. Vora. The network helps show where Neeta L. Vora may publish in the future.

Co-authorship network of co-authors of Neeta L. Vora

This figure shows the co-authorship network connecting the top 25 collaborators of Neeta L. Vora. A scholar is included among the top collaborators of Neeta L. Vora based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Neeta L. Vora. Neeta L. Vora is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gilmore, Kelly L., et al.. (2025). Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene. Prenatal Diagnosis. 45(2). 227–230. 1 indexed citations

Quintero, Rubén A., Neeta L. Vora, Neil S. Seligman, et al.. (2024). 866 Zygosity-based Twin Pregnancy Outcomes: Insights from SNP-Based cfDNA Screening. American Journal of Obstetrics and Gynecology. 230(1). S459–S459.

Vora, Neeta L.. (2024). Gynecologic Care of Transgender and Gender-Diverse People. Obstetrical & Gynecological Survey. 79(8). 466–467.

Gilmore, Kelly L., et al.. (2023). Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalities. Genetics in Medicine. 25(10). 100915–100915. 8 indexed citations

Chong, Karen, David Chitayat, Kelly L. Gilmore, et al.. (2023). Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy. American Journal of Medical Genetics Part A. 191(5). 1282–1292. 1 indexed citations

Hui, Lisa, Katie Ellis, Mark D. Pertile, et al.. (2023). 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. Prenatal Diagnosis. 43(7). 814–828. 58 indexed citations breakdown →

Harris, Sarah, et al.. (2023). Two unrelated fetuses with ITPR1 missense variants and fetal hydrops. Prenatal Diagnosis. 43(11). 1463–1466.

Townley-Tilson, W. H. Davin, et al.. (2023). Insulin Elevates ID2 Expression in Trophoblasts and Aggravates Preeclampsia in Obese ASB4-Null Mice. International Journal of Molecular Sciences. 24(3). 2149–2149. 3 indexed citations

Palomaki, Glenn E., Rossa W. K. Chiu, Mark D. Pertile, et al.. (2020). International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies. Prenatal Diagnosis. 41(10). 1222–1232. 41 indexed citations

10.

Vora, Neeta L., Kelly L. Gilmore, Alicia Brandt, et al.. (2020). An approach to integrating exome sequencing for fetal structural anomalies into clinical practice. Genetics in Medicine. 22(5). 954–961. 51 indexed citations

11.

Milko, Laura V., Julianne O’Daniel, Stephanie B. Crowley, et al.. (2019). An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening. The Journal of Pediatrics. 209. 68–76. 44 indexed citations

12.

Jelin, Angie C. & Neeta L. Vora. (2018). Whole Exome Sequencing. Obstetrics and Gynecology Clinics of North America. 45(1). 69–81. 87 indexed citations

13.

Vora, Neeta L. & Lisa Hui. (2018). Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development. Genetics in Medicine. 20(8). 791–799. 16 indexed citations

14.

Grace, Matthew R., Emily Hardisty, Sarah K. Dotters‐Katz, Neeta L. Vora, & Jeffrey A. Kuller. (2016). Cell-Free DNA Screening. Obstetrical & Gynecological Survey. 71(8). 477–487. 45 indexed citations

15.

Swortwood, Madeleine J., et al.. (2016). Naloxone and Metabolites Quantification in Cord Blood of Prenatally Exposed Newborns and Correlations with Maternal Concentrations. American Journal of Perinatology Reports. 6(4). e385–e390. 16 indexed citations

16.

Bianchi, Diana W., Darya Chudova, Amy J. Sehnert, et al.. (2015). Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies. Obstetrical & Gynecological Survey. 70(12). 744–746. 3 indexed citations

17.

Edlow, Andrea G., Neeta L. Vora, Lisa Hui, et al.. (2014). Maternal Obesity Affects Fetal Neurodevelopmental and Metabolic Gene Expression: A Pilot Study. PLoS ONE. 9(2). e88661–e88661. 59 indexed citations

18.

Siedhoff, Matthew T., et al.. (2013). Cornual Placenta Accreta Managed by Postpartum Total Laparoscopic Hysterectomy. Journal of Minimally Invasive Gynecology. 21(1). 17–22. 2 indexed citations

19.

Vora, Neeta L., Kirby L. Johnson, Geralyn Lambert‐Messerlian, et al.. (2010). Relationships Between Cell-Free DNA and Serum Analytes in the First and Second Trimesters of Pregnancy. Obstetrics and Gynecology. 116(3). 673–678. 9 indexed citations

20.

Vora, Neeta L., Kirby L. Johnson, Inga Peter, et al.. (2010). Circulating cell‐free DNA levels increase variably following chorionic villus sampling. Prenatal Diagnosis. 30(4). 325–328. 18 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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