Frenny Sheth

1.9k citations
97 papers · 865 · h-index 17

Impact in

  • Physiology top 10%
    • Lysosomal Storage Disorders Research
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 26
    • Genetics and Neurodevelopmental Disorders 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5

Frenny Sheth

90 papers receiving 811 citations

Peers

Frenny Sheth
Comparison fields: 5 of 82
  • Physiology 251
  • Genetics 233
  • Physiology 35
  • Pediatrics, Perinatology and Child Health 116
  • Cell Biology 96
Replace Jayesh Sheth with:
Jayesh Sheth India
M. F. Niermeijer Netherlands
A. H. Fensom United Kingdom
Agnieszka Jurecka Poland
Francesca Menni Italy
F. A. Beemer Netherlands
Keith Pohl United Kingdom
J. E. Wraith United Kingdom
Pranoot Tanpaiboon United States
Ercan Mıhçı Türkiye
Frenny Sheth relative to Jayesh Sheth India Jayesh Sheth's profile →
Citations per field
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Jayesh Sheth · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Frenny Sheth, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Frenny Sheth Line = papers co-authored together Frenny Sheth links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 97 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201554
2 201349
3 201344
4 201536
5 201232
6
Gene polymorphism and folate metabolism: a maternal risk factor for Down syndrome.
200331
7 200628
8 200927
9 201825
10
Cytogenetic analysis of Down syndrome in Gujarat.
200725
11 199724
12 201422
13 201718
14 200917
15 201617
16 201617
17 200716
18 201516
19 202314
20 200814

About Frenny Sheth

Frenny Sheth is a scholar working on Genetics, Molecular Biology, Physiology, Epidemiology and Cell Biology, having authored 97 papers that have together received 865 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Lysosomal Storage Disorders Research (22 papers), Prenatal Screening and Diagnostics (8 papers), Trypanosoma species research and implications (7 papers), Chromosomal and Genetic Variations (7 papers), Cellular transport and secretion (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Physiology (251 citations), Genetics (233 citations), Physiology (35 citations), Pediatrics, Perinatology and Child Health (116 citations) and Cell Biology (96 citations). Frenny Sheth has collaborated with scholars based in India, Poland and Germany. Frequent co-authors include Jayesh Sheth, Mehul Mistri, Joris Andrieux, Chaitanya Datar, Rama Vaidya, Mahesh Kamate, Raju Shah, Manisha Desai, Thomas Liehr and Asha S. Multani. Their work appears in journals such as Molecular Cytogenetics, BMC Pediatrics, BMC Neurology, Fertility and Sterility and Journal of Assisted Reproduction and Genetics.

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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