Jaya Ganesh

2.6k total citations
43 papers, 575 citations indexed

About

Jaya Ganesh is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Jaya Ganesh has authored 43 papers receiving a total of 575 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 14 papers in Physiology. Recurrent topics in Jaya Ganesh's work include Metabolism and Genetic Disorders (17 papers), Lysosomal Storage Disorders Research (12 papers) and Mitochondrial Function and Pathology (9 papers). Jaya Ganesh is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Lysosomal Storage Disorders Research (12 papers) and Mitochondrial Function and Pathology (9 papers). Jaya Ganesh collaborates with scholars based in United States, Italy and United Kingdom. Jaya Ganesh's co-authors include Salvatore DiMauro, Sara Shanske, Joel A. Fein, Elizabeth R. Alpern, Michio Hirano, Jorida Çoku, Kurenai Tanji, Ali Naini, Sindu Krishna and Jiesheng Lu and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and eLife.

In The Last Decade

Jaya Ganesh

37 papers receiving 563 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jaya Ganesh United States 14 376 239 77 62 55 43 575
Sunita Arya United States 9 185 0.5× 125 0.5× 94 1.2× 36 0.6× 71 1.3× 18 431
Ebru Canda Türkiye 9 105 0.3× 77 0.3× 29 0.4× 45 0.7× 56 1.0× 55 326
Elisabeth Jameson United Kingdom 11 120 0.3× 102 0.4× 49 0.6× 35 0.6× 185 3.4× 22 402
Soledad Kleppe United States 8 153 0.4× 160 0.7× 82 1.1× 57 0.9× 49 0.9× 12 333
Eric P. Wartchow United States 11 152 0.4× 58 0.2× 73 0.9× 15 0.2× 49 0.9× 21 395
Isabelle Redonnet‐Vernhet France 13 179 0.5× 85 0.4× 51 0.7× 43 0.7× 147 2.7× 26 398
Atsumi Tsuji‐Hosokawa Japan 10 165 0.4× 44 0.2× 43 0.6× 28 0.5× 18 0.3× 31 257
Cihan Öner Türkiye 10 120 0.3× 46 0.2× 48 0.6× 19 0.3× 44 0.8× 19 410
Ingrid Nermoen Norway 12 394 1.0× 62 0.3× 248 3.2× 31 0.5× 28 0.5× 27 706
G. Sabetta Italy 11 103 0.3× 145 0.6× 18 0.2× 41 0.7× 43 0.8× 29 279

Countries citing papers authored by Jaya Ganesh

Since Specialization
Citations

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

Fields of papers citing papers by Jaya Ganesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jaya Ganesh

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

All Works

20 of 20 papers shown
1.
Simpson, William, Andrew Ting, Louise Bier, et al.. (2025). Benefits of early intervention with olipudase alfa in symptomatic children with acid sphingomyelinase deficiency: A sibling case-comparison study. Molecular Genetics and Metabolism Reports. 43. 101210–101210.
2.
Scarpa, Maurizio, George A. Díaz, Roberto Giugliani, et al.. (2025). Long‐Term Safety and Clinical Outcomes With Olipudase Alfa Enzyme Replacement Therapy in Children and Adolescents With Acid Sphingomyelinase Deficiency. Journal of Inherited Metabolic Disease. 48(5). e70086–e70086.
3.
Hughes, Derralynn, Robert J. Hopkin, Jaya Ganesh, et al.. (2025). Isaralgagene civaparvovec (ST-920) gene therapy in adults with Fabry disease: Updated results from an ongoing phase 1/2 study (STAAR). Molecular Genetics and Metabolism. 144(2). 108773–108773. 1 indexed citations
4.
Ganesh, Jaya, et al.. (2024). Use of dichloroacetate as novel therapy in ECHS1 deficiency. Molecular Genetics and Metabolism. 141(4). 108315–108315.
5.
Estrella, Lissette, et al.. (2024). A Case of DNAJC12-Deficient Hyperphenylalaninemia Detected on Newborn Screening: Clinical Outcomes from Early Detection. International Journal of Neonatal Screening. 10(1). 7–7. 2 indexed citations
6.
7.
Ganesh, Jaya, et al.. (2023). PPA2 Deficiency in 2 Sisters. JACC Case Reports. 24. 102024–102024. 2 indexed citations
8.
Webb, Bryn D., Sara M. Nowinski, Ashley Solmonson, et al.. (2023). Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency. eLife. 12. 4 indexed citations
9.
Kelly, Nicole, Joseph J. Orsini, Aaron J. Goldenberg, et al.. (2023). ScreenPlus: A comprehensive, multi-disorder newborn screening program. Molecular Genetics and Metabolism Reports. 38. 101037–101037. 5 indexed citations
10.
Ganetzky, Rebecca, Kosuke Izumi, Andrew C. Edmondson, et al.. (2015). Fetal akinesia deformation sequence due to a congenital disorder of glycosylation. American Journal of Medical Genetics Part A. 167(10). 2411–2417. 11 indexed citations
11.
Keller, Michael D., Jaya Ganesh, Michele Paessler, et al.. (2013). Severe Combined Immunodeficiency Resulting From Mutations in MTHFD1. PEDIATRICS. 131(2). e629–e634. 35 indexed citations
12.
Wang, Guo-Li, Jing Wang, Ganka Douglas, et al.. (2011). Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis. Molecular Genetics and Metabolism. 103(4). 349–357. 23 indexed citations
13.
Swarr, Daniel T., Beth D. Kaufman, Mark A. Fogel, Richard S. Finkel, & Jaya Ganesh. (2011). Unusual Cardiac “Masses” in a Newborn with Infantile Pompe Disease. JIMD Reports. 5. 17–20. 4 indexed citations
14.
Coughlin, Curtis R., Ian D. Krantz, Eric Schmitt, et al.. (2010). Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism. 100(3). 296–299. 7 indexed citations
15.
Peña, Andrès, et al.. (2009). Partial splenic embolization in a child with Gaucher disease, massive splenomegaly and severe thrombocytopenia. Pediatric Radiology. 39(9). 1006–1009. 7 indexed citations
16.
Bornstein, Belén, Estela Área-Gómez, Kevin M. Flanigan, et al.. (2008). Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscular Disorders. 18(6). 453–459. 65 indexed citations
17.
Deardorff, Matthew A., Paige Kaplan, Pedro A. Sanchez‐Lara, et al.. (2008). Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: A role for detailed molecular analysis in complex presentations of classical diseases. Molecular Genetics and Metabolism. 94(4). 498–502. 19 indexed citations
18.
Spinazzola, Antonella, René Santer, Xiaoqi Ding, et al.. (2008). Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome. Archives of Neurology. 65(8). 1108–13. 48 indexed citations
19.
Katz, Lorraine E. Levitt, et al.. (2007). Fasting c-peptide and insulin-like growth factor-binding protein-1 levels help to distinguish childhood type 1 and type 2 diabetes at diagnosis. Pediatric Diabetes. 8(2). 53–59. 34 indexed citations
20.
Fein, Joel A., Jaya Ganesh, & Elizabeth R. Alpern. (2004). Medical Staff Attitudes Toward Family Presence During Pediatric Procedures. Pediatric Emergency Care. 20(4). 224–227. 54 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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