Jayesh Sheth

1.7k total citations
111 papers, 938 citations indexed

About

Jayesh Sheth is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Jayesh Sheth has authored 111 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 39 papers in Molecular Biology and 39 papers in Physiology. Recurrent topics in Jayesh Sheth's work include Lysosomal Storage Disorders Research (34 papers), Genomic variations and chromosomal abnormalities (22 papers) and Cellular transport and secretion (17 papers). Jayesh Sheth is often cited by papers focused on Lysosomal Storage Disorders Research (34 papers), Genomic variations and chromosomal abnormalities (22 papers) and Cellular transport and secretion (17 papers). Jayesh Sheth collaborates with scholars based in India, Poland and Germany. Jayesh Sheth's co-authors include Frenny Sheth, Mehul Mistri, Rama Vaidya, Raju Shah, Koumudi Godbole, Chaitanya Datar, David H. McKenna, Mahesh Kamate, Manisha Desai and Thomas Liehr and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Jayesh Sheth

107 papers receiving 885 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jayesh Sheth India 18 318 277 243 166 136 111 938
Frenny Sheth India 16 269 0.8× 273 1.0× 271 1.1× 136 0.8× 122 0.9× 96 839
Carolina Fischinger Moura de Souza Brazil 19 427 1.3× 507 1.8× 183 0.8× 103 0.6× 170 1.3× 110 1.2k
Francesca Menni Italy 17 208 0.7× 271 1.0× 162 0.7× 113 0.7× 115 0.8× 46 1.0k
Simona Fecarotta Italy 17 299 0.9× 207 0.7× 127 0.5× 39 0.2× 165 1.2× 41 775
Agnieszka Jurecka Poland 21 649 2.0× 405 1.5× 143 0.6× 84 0.5× 446 3.3× 63 1.2k
Dominique Bozon France 23 295 0.9× 745 2.7× 232 1.0× 118 0.7× 217 1.6× 57 2.4k
Serena Gasperini Italy 16 443 1.4× 223 0.8× 83 0.3× 110 0.7× 146 1.1× 64 880
J. E. Wraith United Kingdom 20 692 2.2× 381 1.4× 84 0.3× 147 0.9× 242 1.8× 35 1.3k
Pranoot Tanpaiboon United States 18 329 1.0× 285 1.0× 186 0.8× 64 0.4× 110 0.8× 55 820
Adel Shalata Israel 15 88 0.3× 706 2.5× 212 0.9× 89 0.5× 154 1.1× 42 1.2k

Countries citing papers authored by Jayesh Sheth

Since Specialization
Citations

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

Fields of papers citing papers by Jayesh Sheth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayesh Sheth

This figure shows the co-authorship network connecting the top 25 collaborators of Jayesh Sheth. A scholar is included among the top collaborators of Jayesh Sheth 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 Jayesh Sheth. Jayesh Sheth 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.
Anderson, Glenn, et al.. (2024). Maculopathy and adult‐onset ataxia in patients with biallelic MFSD8 variants. Molecular Genetics & Genomic Medicine. 12(8). e2505–e2505. 2 indexed citations
2.
3.
Saxena, Deepti, Madhulika Kabra, Neerja Gupta, et al.. (2022). Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II. European Journal of Medical Genetics. 65(3). 104447–104447. 3 indexed citations
4.
5.
Zeng, Xue, et al.. (2021). Giant axonal neuropathy with novel GAN pathogenic variant in a patient of consanguineous origin from Poonch Jammu and Kashmir-India. Molecular Biology Reports. 48(2). 1607–1614. 2 indexed citations
6.
Tamhankar, Parag, Lakshmi Vasudevan, Rita Christopher, et al.. (2020). Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1. Journal of Pediatric Genetics. 10(3). 213–221. 5 indexed citations
7.
Sheth, Jayesh, et al.. (2020). Lysosomal Storage Disorders: An Underdiagnosed Metabolic Disorder. 73(6). 26–32. 1 indexed citations
8.
Mistri, Mehul, Mahesh Kamate, Neerja Gupta, et al.. (2019). Identification of novel variants in a large cohort of children with Tay–Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India. Journal of Human Genetics. 64(10). 985–994. 3 indexed citations
9.
Sheth, Frenny, et al.. (2018). A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 114–114. 7 indexed citations
10.
Sheth, Frenny, et al.. (2015). Pure interstitial dup(6)(q22.31q22.31) – a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 5–5. 3 indexed citations
11.
Sheth, Harsh, Faye Elliott, Michael S. Jackson, et al.. (2014). Point of care testing for improving risk- benefit ratio of aspirin and warfarin. Molecular Cytogenetics. 7(Suppl 1). I54–I54. 1 indexed citations
12.
Mistri, Mehul, Ashish Bavdekar, Mamta Muranjan, et al.. (2014). Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease. Journal of Human Genetics. 59(4). 223–228. 22 indexed citations
13.
Sheth, Frenny, et al.. (2013). Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter. Molecular Cytogenetics. 6(1). 24–24. 1 indexed citations
14.
Sheth, Jayesh, Mehul Mistri, Mahesh Kamate, S. Vaja, & Frenny Sheth. (2012). Diagnostic strategy for mucolipidosis II/III. Indian Pediatrics. 49(12). 975–977. 10 indexed citations
15.
McKenna, David H. & Jayesh Sheth. (2011). Umbilical cord blood: current status & promise for the future.. PubMed. 134. 261–9. 22 indexed citations
16.
Sheth, Frenny, Joris Andrieux, Elisabeth Ewers, et al.. (2011). Characterization of sSMC by FISH and molecular techniques. European Journal of Medical Genetics. 54(3). 247–255. 14 indexed citations
17.
Jain, Shalu, Inusha Panigrahi, Jayesh Sheth, & Sarita Agarwal. (2011). STR markers for detecting heterogeneity in Indian population. Molecular Biology Reports. 39(1). 461–465. 6 indexed citations
18.
Sheth, Frenny, Joris Andrieux, & Jayesh Sheth. (2010). Supernumerary marker chromosome in a child with microcephaly and mental retardation. Indian Pediatrics. 47(3). 277–279. 7 indexed citations
19.
Vinci, G, Raja Brauner, Attila Tar, et al.. (2009). Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. Fertility and Sterility. 92(4). 1347–1350. 17 indexed citations
20.
Sheth, Frenny, Elisabeth Ewers, Nadezda Kosyakova, et al.. (2009). A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report. Molecular Cytogenetics. 2(1). 22–22. 13 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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