Ramesh C. Juyal

4.6k total citations
51 papers, 1.5k citations indexed

About

Ramesh C. Juyal is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Ramesh C. Juyal has authored 51 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 18 papers in Molecular Biology and 12 papers in Neurology. Recurrent topics in Ramesh C. Juyal's work include Parkinson's Disease Mechanisms and Treatments (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ramesh C. Juyal is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ramesh C. Juyal collaborates with scholars based in India, United States and China. Ramesh C. Juyal's co-authors include B.K. Thelma, Pragna I. Patel, Antonio Baldini, Madhuri Behari, Uday B. Muthane, Frank Greenberg, Hiroko H. Dodge, Shyla T. Govindappa, Rajesh Pandav and Vijay Chandra and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Gut.

In The Last Decade

Ramesh C. Juyal

51 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ramesh C. Juyal India 23 499 470 251 233 201 51 1.5k
Gabriele Stumm Germany 15 145 0.3× 631 1.3× 401 1.6× 257 1.1× 72 0.4× 23 1.6k
Bruno Maranda Canada 23 394 0.8× 714 1.5× 39 0.2× 288 1.2× 129 0.6× 57 1.4k
Margarita Raygada United States 23 407 0.8× 455 1.0× 188 0.7× 128 0.5× 52 0.3× 49 2.2k
Nancy Wu United States 18 469 0.9× 1.3k 2.8× 125 0.5× 124 0.5× 60 0.3× 35 2.1k
Thomas Opladen Germany 24 478 1.0× 782 1.7× 199 0.8× 191 0.8× 378 1.9× 84 1.9k
Colin Delaney United States 15 113 0.2× 480 1.0× 117 0.5× 238 1.0× 91 0.5× 20 1.1k
Hiroko Okuda Japan 19 180 0.4× 383 0.8× 359 1.4× 98 0.4× 375 1.9× 50 1.3k
Luca Lovrečić Slovenia 19 335 0.7× 606 1.3× 124 0.5× 88 0.4× 47 0.2× 58 1.2k
Yves de Keyzer France 25 110 0.2× 765 1.6× 174 0.7× 252 1.1× 121 0.6× 56 2.2k
Gen Wen United States 19 134 0.3× 584 1.2× 199 0.8× 165 0.7× 76 0.4× 34 1.3k

Countries citing papers authored by Ramesh C. Juyal

Since Specialization
Citations

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

Fields of papers citing papers by Ramesh C. Juyal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ramesh C. Juyal. 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 Ramesh C. Juyal. The network helps show where Ramesh C. Juyal may publish in the future.

Co-authorship network of co-authors of Ramesh C. Juyal

This figure shows the co-authorship network connecting the top 25 collaborators of Ramesh C. Juyal. A scholar is included among the top collaborators of Ramesh C. Juyal 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 Ramesh C. Juyal. Ramesh C. Juyal 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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Senapati, Sabyasachi, Shalini Singh, Ashok Kumar, et al.. (2014). Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation. Pharmacogenetics and Genomics. 24(4). 211–219. 41 indexed citations
3.
Nagarajan, Perumal, et al.. (2011). Sex and strain-related differences in the peripheral blood cell values of mutant mouse strains. Comparative Clinical Pathology. 21(6). 1577–1585. 3 indexed citations
4.
Mittal, Kirti, Neerja Gupta, Madhulika Kabra, Ramesh C. Juyal, & B.K. Thelma. (2011). Distinct De Novo deletions in a brother–sister pair with RTT: A case report. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 859–863. 5 indexed citations
5.
Negi, Sapna, Ashok Kumar, B.K. Thelma, & Ramesh C. Juyal. (2011). Association of Cullin1 haplotype variants with rheumatoid arthritis and response to methotrexate. Pharmacogenetics and Genomics. 21(9). 590–593. 10 indexed citations
6.
Punia, Sohan, Madhuri Behari, Shyla T. Govindappa, et al.. (2011). Leads from xenobiotic metabolism genes for Parkinson’s disease among north Indians. Pharmacogenetics and Genomics. 21(12). 790–797. 6 indexed citations
7.
Punia, Sohan, Madhuri Behari, Shyla T. Govindappa, et al.. (2010). Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinson's disease among North Indians. Pharmacogenetics and Genomics. 20(7). 435–441. 22 indexed citations
8.
Punia, Sohan, et al.. (2008). Genetic Profiling of Genes from the Oxidative Stress Pathway Among North and South Indians. Human Biology. 80(2). 161–179. 2 indexed citations
9.
Behari, Madhuri, Shyla T. Govindappa, Vinay Goyal, et al.. (2006). Parkin mutations in familial and sporadic Parkinson's disease among Indians. Parkinsonism & Related Disorders. 12(4). 239–245. 40 indexed citations
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Punia, Sohan, Madhuri Behari, Shyla T. Govindappa, et al.. (2006). Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients. Neuroscience Letters. 409(2). 83–88. 59 indexed citations
12.
Mittal, Uma, Sangeeta Sharma, Subhabrata Chakrabarti, et al.. (2003). Complex phenotypes in an Indian family with homozygous SCA2 mutations. Annals of Neurology. 55(1). 130–133. 23 indexed citations
13.
Thelma, B.K., Ramesh C. Juyal, Hiroko H. Dodge, et al.. (2001). APOE Polymorphism in a Rural Older Population-Based Sample in India. Human Biology. 73(1). 135–144. 19 indexed citations
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Elsea, Sarah H., Smita M. Purandare, Ramesh C. Juyal, et al.. (1997). Definition of the critical interval for Smith-Magenis syndrome. Cytogenetic and Genome Research. 79(3-4). 276–281. 25 indexed citations
16.
Juyal, Ramesh C., et al.. (1996). Mosaicism for del(17) (p11.2p11.2) underlying the Smith-Magenis syndrome. American Journal of Medical Genetics. 66(2). 193–196. 20 indexed citations
17.
Juyal, Ramesh C., Frank Greenberg, James R. Lupski, et al.. (1995). Smith‐Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization. American Journal of Medical Genetics. 58(3). 286–291. 22 indexed citations
18.
Thelma, B.K., Rita Tewari, Ramesh C. Juyal, & Satyawada Rama Rao. (1991). Random/nonrandom X-chromosome inactivation in <i>Nesokia indica: </i>possible influence of heterochromatin. Cytogenetic and Genome Research. 56(2). 87–90. 2 indexed citations
19.
Thelma, B.K., et al.. (1988). Does heterochromatin variation potentiate speciation?. Cytogenetic and Genome Research. 47(4). 204–208. 15 indexed citations
20.
Tewari, Rita, Ramesh C. Juyal, B.K. Thelma, B.C. Das, & Satyawada Rama Rao. (1987). Folate-sensitive fragile sites on the X-chromosome heterochromatin of the Indian mole rat, <i>Nesokia indic</i><i>a</i>. Cytogenetic and Genome Research. 44(1). 11–17. 17 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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