Mehul Mistri

507 total citations
30 papers, 253 citations indexed

About

Mehul Mistri is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Mehul Mistri has authored 30 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Physiology, 11 papers in Cell Biology and 10 papers in Molecular Biology. Recurrent topics in Mehul Mistri's work include Lysosomal Storage Disorders Research (18 papers), Cellular transport and secretion (9 papers) and Trypanosoma species research and implications (8 papers). Mehul Mistri is often cited by papers focused on Lysosomal Storage Disorders Research (18 papers), Cellular transport and secretion (9 papers) and Trypanosoma species research and implications (8 papers). Mehul Mistri collaborates with scholars based in India, Poland and United Kingdom. Mehul Mistri's co-authors include Jayesh Sheth, Frenny Sheth, Mahesh Kamate, Chaitanya Datar, Koumudi Godbole, Parag Tamhankar, Ashish Bavdekar, Mamta Muranjan, Sheela Nampoothiri and Raju Shah and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Molecular Genetics and Metabolism.

In The Last Decade

Mehul Mistri

28 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mehul Mistri India 10 193 81 78 68 49 30 253
Xinying Hong United States 12 303 1.6× 53 0.7× 136 1.7× 107 1.6× 63 1.3× 41 441
Sabrina Eichler Germany 10 251 1.3× 87 1.1× 111 1.4× 94 1.4× 77 1.6× 15 324
Mahesh Kamate India 11 149 0.8× 66 0.8× 142 1.8× 67 1.0× 33 0.7× 59 426
Amal Aqul United States 7 169 0.9× 27 0.3× 75 1.0× 53 0.8× 52 1.1× 14 286
Cate Walsh Vockley United States 6 274 1.4× 31 0.4× 85 1.1× 50 0.7× 94 1.9× 8 368
Kristiane Michelin‐Tirelli Brazil 11 288 1.5× 88 1.1× 98 1.3× 123 1.8× 83 1.7× 23 347
Sylvie Duthel France 6 278 1.4× 50 0.6× 75 1.0× 50 0.7× 102 2.1× 9 352
Hsuan-Chieh Liao Taiwan 8 247 1.3× 48 0.6× 86 1.1× 96 1.4× 56 1.1× 8 315
Agnes H. Chen United States 7 157 0.8× 42 0.5× 28 0.4× 43 0.6× 47 1.0× 9 199
Jessica de Ruijter Netherlands 8 333 1.7× 99 1.2× 68 0.9× 162 2.4× 64 1.3× 11 405

Countries citing papers authored by Mehul Mistri

Since Specialization
Citations

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

Fields of papers citing papers by Mehul Mistri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mehul Mistri

This figure shows the co-authorship network connecting the top 25 collaborators of Mehul Mistri. A scholar is included among the top collaborators of Mehul Mistri 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 Mehul Mistri. Mehul Mistri 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.
Aggarwal, Shagun, Sumita Danda, Shubha R. Phadke, et al.. (2023). Proband only exome sequencing in 403 Indian children with neurodevelopmental disorders: Diagnostic yield, utility and challenges in a resource-limited setting. European Journal of Medical Genetics. 66(5). 104730–104730. 5 indexed citations
2.
Mistri, Mehul, et al.. (2022). The diagnostic utility of exome‐based carrier screening in families with a positive family history. American Journal of Medical Genetics Part A. 188(4). 1323–1333. 2 indexed citations
3.
Mistri, Mehul, et al.. (2021). Bi‐allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family. Clinical Genetics. 100(6). 748–751. 7 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, Jayesh, et al.. (2018). Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India. BMC Medical Genetics. 19(1). 109–109. 3 indexed citations
6.
7.
Sheth, Jayesh, Mehul Mistri, Mahesh Kamate, et al.. (2018). Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patients. BMC Neurology. 18(1). 203–203. 12 indexed citations
8.
Sheth, Jayesh, et al.. (2017). Quantitative and Qualitative Analysis of Urinary Glycosaminoglycans (GAGs). 1 indexed citations
9.
Sheth, Jayesh, et al.. (2016). GM2 gangliosidosis AB variant: novel mutation from India – a case report with a review. BMC Pediatrics. 16(1). 88–88. 17 indexed citations
10.
Tamhankar, Parag, et al.. (2015). Clinical, biochemical and mutation profile in Indian patients with Sandhoff disease. Journal of Human Genetics. 61(2). 163–166. 5 indexed citations
11.
Sheth, Jayesh, et al.. (2015). Lysosomal storage disorders in Indian children with neuroregression attending a genetic center. Indian Pediatrics. 52(12). 1029–1033. 10 indexed citations
12.
Sheth, Jayesh, Mehul Mistri, Frenny Sheth, et al.. (2014). Prenatal Diagnosis of Lysosomal Storage Disorders by Enzymes Study Using Chorionic Villus and Amniotic Fluid. Journal of Fetal Medicine. 1(1). 17–24. 5 indexed citations
13.
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
14.
Mistri, Mehul, et al.. (2014). Prenatal diagnosis of autosomal recessive osteopetrosis: a case report. Molecular Cytogenetics. 7(S1). 1 indexed citations
15.
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
16.
Mistri, Mehul, et al.. (2014). Prenatal diagnosis of lysosomal storage disorders: our experience in 120 cases. Molecular Cytogenetics. 7(S1). 2 indexed citations
17.
Sheth, Jayesh, et al.. (2014). Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD). Molecular Cytogenetics. 7(Suppl 1). P52–P52. 2 indexed citations
18.
Sheth, Jayesh, Mehul Mistri, Frenny Sheth, et al.. (2013). Burden of Lysosomal Storage Disorders in India: Experience of 387 Affected Children from a Single Diagnostic Facility. JIMD Reports. 51–63. 43 indexed citations
19.
Mistri, Mehul, et al.. (2012). Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India. PLoS ONE. 7(6). e39122–e39122. 31 indexed citations
20.
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

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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