Reena Jethva

628 total citations
13 papers, 410 citations indexed

About

Reena Jethva is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Reena Jethva has authored 13 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Reena Jethva's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Mesenchymal stem cell research (2 papers). Reena Jethva is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Mesenchymal stem cell research (2 papers). Reena Jethva collaborates with scholars based in United States and Italy. Reena Jethva's co-authors include Agustín Legido, Michael J. Goldenthal, Jerry Vockley, Michael J. Bennett, Edwin M. Horwitz, Satoru Otsuru, Massimo Dominici, Ted J. Hofmann, Charlotte L. Phillips and Masahiro Iwamoto and has published in prestigious journals such as Blood, Molecular Genetics and Metabolism and Cytotherapy.

In The Last Decade

Reena Jethva

12 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Reena Jethva United States	9	190	140	84	78	73	13	410
Maria Descartes United States	16	399 2.1×	431 3.1×	40 0.5×	51 0.7×	40 0.5×	34	720
Meena Balasubramanian United Kingdom	18	310 1.6×	555 4.0×	55 0.7×	25 0.3×	26 0.4×	74	802
Ardinger Hh United States	6	192 1.0×	124 0.9×	27 0.3×	10 0.1×	56 0.8×	287	402
Adam Mp	6	180 0.9×	113 0.8×	27 0.3×	10 0.1×	56 0.8×	286	388
Bean Ljh	6	180 0.9×	113 0.8×	26 0.3×	10 0.1×	56 0.8×	285	386
Rachel Sayuri Honjo Brazil	13	205 1.1×	174 1.2×	25 0.3×	11 0.1×	26 0.4×	60	460
Eri Takeshita Japan	14	526 2.8×	117 0.8×	78 0.9×	20 0.3×	35 0.5×	75	763
Ruen Yao China	15	385 2.0×	334 2.4×	25 0.3×	17 0.2×	23 0.3×	64	657
A Amemiya Japan	6	173 0.9×	104 0.7×	24 0.3×	9 0.1×	53 0.7×	269	377
Marjan M. Nezarati Canada	10	232 1.2×	198 1.4×	36 0.4×	11 0.1×	15 0.2×	17	447

Countries citing papers authored by Reena Jethva

Since Specialization

Citations

This map shows the geographic impact of Reena Jethva'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 Reena Jethva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reena Jethva more than expected).

Fields of papers citing papers by Reena Jethva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Reena Jethva. 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 Reena Jethva. The network helps show where Reena Jethva may publish in the future.

Co-authorship network of co-authors of Reena Jethva

This figure shows the co-authorship network connecting the top 25 collaborators of Reena Jethva. A scholar is included among the top collaborators of Reena Jethva 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 Reena Jethva. Reena Jethva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Schmidt, Sarah, Hélio Pedro, Reena Jethva, et al.. (2025). Newborn Screening for Gaucher Disease: The New Jersey Experience. International Journal of Neonatal Screening. 11(2). 34–34.

Prasad, Rajeev, et al.. (2017). 22q11.2 microduplication syndrome with associated esophageal atresia/tracheo‐esophageal fistula and vascular ring. Clinical Case Reports. 5(3). 351–356. 12 indexed citations

Goldenthal, Michael J., Shirish Damle, Nidhi Shah, et al.. (2015). Mitochondrial Enzyme Dysfunction in Autism Spectrum Disorders; A Novel Biomarker Revealed From Buccal Swab Analysis. Biomarkers in Medicine. 9(10). 957–965. 38 indexed citations

Imitola, Jaime, Divya S. Khurana, Nadiya M. Teplyuk, et al.. (2015). A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephaly. American Journal of Medical Genetics Part A. 167(11). 2808–2816. 7 indexed citations

Imitola, Jaime, Carol E. Anderson, Reena Jethva, et al.. (2014). Fraternal Twins With Autism, Severe Cognitive Deficit, and Epilepsy: Diagnostic Role of Chromosomal Microarray Analysis. Seminars in Pediatric Neurology. 21(2). 167–171. 14 indexed citations

Anderson, Carol E., et al.. (2014). Co‐occurrence of non‐mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: Case report and review of the literature. American Journal of Medical Genetics Part A. 164(12). 3187–3193. 7 indexed citations

Stabler, Sally P., Mark Korson, Reena Jethva, et al.. (2013). Metabolic Profiling of Total Homocysteine and Related Compounds in Hyperhomocysteinemia: Utility and Limitations in Diagnosing the Cause of Puzzling Thrombophilia in a Family. JIMD Reports. 11. 149–163. 25 indexed citations

Legido, Agustín, Reena Jethva, & Michael J. Goldenthal. (2013). Mitochondrial Dysfunction in Autism. Seminars in Pediatric Neurology. 20(3). 163–175. 72 indexed citations

Liu, Jinglan, et al.. (2013). Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cord. Birth Defects Research Part A Clinical and Molecular Teratology. 97(12). 812–815. 4 indexed citations

10.

Otsuru, Satoru, Patricia Gordon, Kengo Shimono, et al.. (2012). Transplanted bone marrow mononuclear cells and MSCs impart clinical benefit to children with osteogenesis imperfecta through different mechanisms. Blood. 120(9). 1933–1941. 115 indexed citations

11.

Hoban, Rebecca, Amy E. Roberts, Laurie Demmer, Reena Jethva, & B Shephard. (2012). Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant. American Journal of Medical Genetics Part A. 158A(6). 1411–1413. 22 indexed citations

12.

Jethva, Reena, Satoru Otsuru, Massimo Dominici, & Edwin M. Horwitz. (2009). Cell therapy for disorders of bone. Cytotherapy. 11(1). 3–17. 26 indexed citations

13.

Jethva, Reena, Michael J. Bennett, & Jerry Vockley. (2008). Short-chain acyl-coenzyme A dehydrogenase deficiency. Molecular Genetics and Metabolism. 95(4). 195–200. 68 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.

Explore authors with similar magnitude of impact