Frenny Sheth

1.9k total citations
96 papers, 839 citations indexed

About

Frenny Sheth is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Frenny Sheth has authored 96 papers receiving a total of 839 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Genetics, 37 papers in Molecular Biology and 26 papers in Physiology. Recurrent topics in Frenny Sheth's work include Genomic variations and chromosomal abnormalities (30 papers), Lysosomal Storage Disorders Research (23 papers) and Trypanosoma species research and implications (11 papers). Frenny Sheth is often cited by papers focused on Genomic variations and chromosomal abnormalities (30 papers), Lysosomal Storage Disorders Research (23 papers) and Trypanosoma species research and implications (11 papers). Frenny Sheth collaborates with scholars based in India, Poland and Germany. Frenny Sheth's co-authors include Jayesh Sheth, Mehul Mistri, Joris Andrieux, Raju Shah, Rama Vaidya, Chaitanya Datar, Mahesh Kamate, Manisha Desai, Thomas Liehr and N. J. Chinoy 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

Frenny Sheth

90 papers receiving 785 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frenny Sheth India 16 273 271 269 136 122 96 839
Jayesh Sheth India 18 277 1.0× 243 0.9× 318 1.2× 166 1.2× 136 1.1× 111 938
Francesca Menni Italy 17 271 1.0× 162 0.6× 208 0.8× 113 0.8× 115 0.9× 46 1.0k
Dominique Bozon France 23 745 2.7× 232 0.9× 295 1.1× 118 0.9× 217 1.8× 57 2.4k
Shuan-Pei Lin Taiwan 19 239 0.9× 158 0.6× 371 1.4× 64 0.5× 210 1.7× 39 793
Pranoot Tanpaiboon United States 18 285 1.0× 186 0.7× 329 1.2× 64 0.5× 110 0.9× 55 820
Marcos José Burle de Aguiar Brazil 19 296 1.1× 152 0.6× 121 0.4× 127 0.9× 81 0.7× 57 795
C B Whitley United States 17 287 1.1× 138 0.5× 556 2.1× 59 0.4× 214 1.8× 30 970
F. A. Beemer Netherlands 12 232 0.8× 167 0.6× 293 1.1× 101 0.7× 101 0.8× 21 714
A. H. Fensom United Kingdom 14 175 0.6× 89 0.3× 329 1.2× 103 0.8× 111 0.9× 31 725
Silvana Briuglia Italy 16 315 1.2× 215 0.8× 88 0.3× 113 0.8× 45 0.4× 52 812

Countries citing papers authored by Frenny Sheth

Since Specialization
Citations

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

Fields of papers citing papers by Frenny Sheth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frenny Sheth

This figure shows the co-authorship network connecting the top 25 collaborators of Frenny Sheth. A scholar is included among the top collaborators of Frenny 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 Frenny Sheth. Frenny 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
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Sheth, Harsh, et al.. (2022). The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndrome. BMC Genomics. 23(1). 458–458. 2 indexed citations
4.
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
5.
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
6.
Sheth, Jayesh, et al.. (2018). A case of Raine syndrome presenting with facial dysmorphy and review of literature. BMC Medical Genetics. 19(1). 76–76. 24 indexed citations
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Sheth, Frenny, et al.. (2016). Characterization of two novel FANCG mutations in Indian Fanconi anemia patients. Leukemia Research. 53. 50–56. 3 indexed citations
9.
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
10.
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
11.
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
12.
Sheth, Jayesh, Mehul Mistri, Chaitanya Datar, et al.. (2014). Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease. Molecular Genetics and Metabolism Reports. 1. 425–430. 9 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.
Asadollahi, Reza, Beatrice Oneda, Frenny Sheth, et al.. (2013). Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. European Journal of Human Genetics. 21(10). 1100–1104. 47 indexed citations
15.
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
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.
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
18.
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
19.
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
20.
Multani, Asha S., et al.. (1996). Three siblings with Harlequin Ichthyosis in an Indian family. Early Human Development. 45(3). 229–233. 6 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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