Usha Dave

503 total citations
22 papers, 287 citations indexed

About

Usha Dave is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Usha Dave has authored 22 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Clinical Biochemistry. Recurrent topics in Usha Dave's work include Metabolism and Genetic Disorders (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Usha Dave is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Usha Dave collaborates with scholars based in India, United Kingdom and Sri Lanka. Usha Dave's co-authors include Darab K. Dastur, Jayesh Sheth, Frenny Sheth, Raju Shah, Isamu Matsumoto, Lakshmi Mehta, Sanjeev V. Kothare, Ying Wang, Keming Xu and Amit Agarwal and has published in prestigious journals such as Epilepsia, Journal of the Royal Society of Medicine and Annals of Human Biology.

In The Last Decade

Usha Dave

19 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Usha Dave India 11 63 61 58 53 51 22 287
Vicki Shanker United States 13 98 1.6× 42 0.7× 114 2.0× 49 0.9× 48 0.9× 41 603
Jason Lockrow United States 8 99 1.6× 95 1.6× 107 1.8× 39 0.7× 56 1.1× 13 368
Giorgia Tascini Italy 9 99 1.6× 174 2.9× 39 0.7× 36 0.7× 40 0.8× 14 449
Pablo Lema Canada 11 71 1.1× 17 0.3× 40 0.7× 38 0.7× 80 1.6× 14 347
Prabhakar Singh India 8 107 1.7× 68 1.1× 62 1.1× 9 0.2× 33 0.6× 22 389
Evan A. Bordt United States 12 140 2.2× 17 0.3× 66 1.1× 16 0.3× 45 0.9× 17 591
Celia van der Merwe South Africa 11 125 2.0× 58 1.0× 69 1.2× 52 1.0× 5 0.1× 16 371
Runa Lindblom Australia 10 166 2.6× 53 0.9× 69 1.2× 165 3.1× 14 0.3× 12 497
Hitoshi Sejima Japan 9 37 0.6× 10 0.2× 24 0.4× 18 0.3× 40 0.8× 25 241
Manuel Velasco Venezuela 5 72 1.1× 41 0.7× 56 1.0× 19 0.4× 9 0.2× 8 306

Countries citing papers authored by Usha Dave

Since Specialization
Citations

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

Fields of papers citing papers by Usha Dave

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Usha Dave

This figure shows the co-authorship network connecting the top 25 collaborators of Usha Dave. A scholar is included among the top collaborators of Usha Dave 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 Usha Dave. Usha Dave 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.
2.
Dave, Usha, et al.. (2024). Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort. Indian Journal of Clinical Biochemistry. 40(2). 254–262.
3.
Abdelkreem, Elsayed, Radha Rama Devi Akella, Usha Dave, et al.. (2016). Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency. JIMD Reports. 35. 59–65. 13 indexed citations
4.
Dave, Usha. (2016). Genetic Counseling in Developmental Disability. International Journal of Human Genetics. 16(3-4). 89–97. 1 indexed citations
5.
Dave, Usha, et al.. (2014). Brain-Derived Neurotrophic Factor (BDNF) in Children with Autism Spectrum Disorder. Annals of Neurosciences. 21(4). 1 indexed citations
6.
Dave, Usha, et al.. (2014). Brain-Derived Neurotrophic Factor in children with Autism Spectrum Disorder. Annals of Neurosciences. 21(4). 129–33. 57 indexed citations
7.
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
8.
Dave, Usha, et al.. (2014). An open-label study to elucidate the effects of standardized Bacopa monnieri extract in the management of symptoms of attention-deficit hyperactivity disorder in children.. PubMed. 28(2). 10–5. 23 indexed citations
9.
Dave, Usha, et al.. (2013). Mutational Screening and Prenatal Diagnosis in Cornelia de Lange syndrome. The Journal of Obstetrics and Gynecology of India. 64(1). 27–31. 3 indexed citations
10.
Sheth, Jayesh, et al.. (2009). Plasma chitotriosidase activity in children with lysosomal storage disorders. The Indian Journal of Pediatrics. 77(2). 203–205. 27 indexed citations
11.
Dave, Usha, et al.. (2006). Trisomy 9p Syndrome in a Mentally Retarded Female Inherited from Maternal Reciprocal Translocation. International Journal of Human Genetics. 6(3). 203–207. 1 indexed citations
12.
Dave, Usha, et al.. (2005). A community genetics approach to population screening in India for mental retardation—a model for developing countries. Annals of Human Biology. 32(2). 195–203. 13 indexed citations
13.
Hodson, Kenneth, et al.. (2004). Meningococcal chest pain. Journal of the Royal Society of Medicine. 97(9). 434–435.
14.
Kothare, Sanjeev V., et al.. (2002). Maternal Age and Chromosomal Profile in 160 Down Syndrome Cases – Experience of a Tertiary Genetic Centre from India. International Journal of Human Genetics. 2(1). 49–53. 11 indexed citations
15.
Dave, Usha, et al.. (2001). Chemical Diagnosis of Congenital Metabolic Disorders by Gas Chromatography / Mass Spectrometry (GC/MS) in India. International Journal of Human Genetics. 1(3). 211–217. 2 indexed citations
16.
Xu, Keming, et al.. (2000). Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center. Journal of Chromatography B Biomedical Sciences and Applications. 746(1). 41–49. 22 indexed citations
17.
Dave, Usha, et al.. (1993). Evaluation of BR-16 A (mentat) in cognitive and behavioural dysfunction of mentally retarded children—A placebo-controlled study. The Indian Journal of Pediatrics. 60(3). 423–428. 27 indexed citations
18.
19.
Dastur, Darab K. & Usha Dave. (1986). Fine structure of cellular and vascular reaction in brain tuberculomas:. Pathology - Research and Practice. 181(6). 721–732. 6 indexed citations
20.
Dastur, Darab K. & Usha Dave. (1977). Ultrastructural basis of the vasculopathy in and around brain tuberculomas. Possible significance of altered basement membrane.. PubMed. 89(1). 35–50. 26 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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