Dominic Thyagarajan

1.9k total citations
62 papers, 1.3k citations indexed

About

Dominic Thyagarajan is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, Dominic Thyagarajan has authored 62 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 19 papers in Neurology and 15 papers in Clinical Biochemistry. Recurrent topics in Dominic Thyagarajan's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (15 papers) and Neurological disorders and treatments (11 papers). Dominic Thyagarajan is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (15 papers) and Neurological disorders and treatments (11 papers). Dominic Thyagarajan collaborates with scholars based in Australia, United States and United Kingdom. Dominic Thyagarajan's co-authors include Edward Byrne, Susan Bressman, Kenneth K. Lau, Sangkot Marzuki, Robert M. I. Kapsa, Patcharee Lertrit, A.S. Noer, Sara Shanske, Terrence L. Cascino and Serge Przedborski and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Dominic Thyagarajan

61 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dominic Thyagarajan Australia 19 629 321 292 192 166 62 1.3k
Masumi Ito Japan 21 445 0.7× 205 0.6× 100 0.3× 169 0.9× 206 1.2× 77 1.3k
E Peeters Netherlands 23 447 0.7× 257 0.8× 113 0.4× 78 0.4× 197 1.2× 46 1.7k
Michele Carbonelli Italy 29 990 1.6× 184 0.6× 147 0.5× 159 0.8× 143 0.9× 63 2.7k
Tae‐Sung Ko South Korea 24 216 0.3× 213 0.7× 162 0.6× 219 1.1× 362 2.2× 116 1.7k
Lucia Fusco Italy 28 449 0.7× 277 0.9× 167 0.6× 129 0.7× 587 3.5× 87 2.2k
Yutaka Awaya Japan 18 376 0.6× 132 0.4× 68 0.2× 259 1.3× 622 3.7× 38 1.4k
G. Geoffroy Canada 22 563 0.9× 233 0.7× 195 0.7× 106 0.6× 648 3.9× 67 1.8k
Eray Dırık Türkiye 19 273 0.4× 92 0.3× 76 0.3× 143 0.7× 126 0.8× 72 1.2k
Hadassa Goldberg‐Stern Israel 23 378 0.6× 215 0.7× 108 0.4× 152 0.8× 429 2.6× 51 1.6k
Maja von der Hagen Germany 22 651 1.0× 417 1.3× 48 0.2× 82 0.4× 249 1.5× 80 1.5k

Countries citing papers authored by Dominic Thyagarajan

Since Specialization
Citations

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

Fields of papers citing papers by Dominic Thyagarajan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dominic Thyagarajan

This figure shows the co-authorship network connecting the top 25 collaborators of Dominic Thyagarajan. A scholar is included among the top collaborators of Dominic Thyagarajan 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 Dominic Thyagarajan. Dominic Thyagarajan 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.
Brosnan, Méadhbh, et al.. (2018). Dopamine restores cognitive motivation in Parkinson’s disease. Brain. 142(3). 719–732. 67 indexed citations
3.
Rao, Aravinda S., et al.. (2017). Arytenoid cartilage feature point detection using laryngeal 3D CT images in Parkinson's disease. PubMed. 11. 1820–1823. 1 indexed citations
4.
Glikmann‐Johnston, Yifat, et al.. (2017). Emotion recognition in Parkinson’s disease: Static and dynamic factors.. Neuropsychology. 32(2). 230–234. 8 indexed citations
5.
Thyagarajan, Dominic, et al.. (2013). MAGNETIC RESONANCE IMAGING TECHNOLOGY FOR PROCESS CONTROL AND QUALITY MAINTENANCE IN FOOD QUALITY OPERATION. 4 indexed citations
6.
Kelly, Linda, et al.. (2013). Delayed postirradiation camptocormia. BMJ Case Reports. 2013. bcr2013200083–bcr2013200083. 5 indexed citations
7.
Phan, Thanh G., Timur E. Gureyev, Yakov I. Nesterets, Henry Ma, & Dominic Thyagarajan. (2012). Novel Application of EEG Source Localization in the Assessment of the Penumbra. Cerebrovascular Diseases. 33(4). 405–407. 7 indexed citations
8.
Muyderman, Håkan, et al.. (2012). The mitochondrial T1095C mutation increases gentamicin-mediated apoptosis. Mitochondrion. 12(4). 465–471. 17 indexed citations
9.
Kumar, Kishore R., et al.. (2009). Transient Changes on Brain Magnetic Resonance Imaging in a Patient With Sturge-Weber Syndrome Presenting With Hemiparesis. The Neurologist. 15(6). 351–354. 12 indexed citations
10.
Krupa, Małgorzata, et al.. (2009). Clinical, electrophysiological and genetic features of a large Australian family with paramyotonia congenita. The Medical Journal of Australia. 190(6). 334–336. 4 indexed citations
11.
Day, Bruce, et al.. (2008). A unique case of cortical myoclonus sensitive to visual stimuli in the peripersonal space. Movement Disorders. 24(3). 422–425. 1 indexed citations
12.
Wilcox, Robert A., et al.. (2007). Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions. Movement Disorders. 22(7). 1020–1023. 10 indexed citations
13.
McKelvie, Penelope, Steven Collins, Dominic Thyagarajan, et al.. (2002). Meningoencephalomyelitis with vasculitis due to varicella zoster virus: a case report and review of the literature. Pathology. 34(1). 88–93. 30 indexed citations
14.
Hutchison, Wendy, et al.. (2002). Clinical and molecular features of adPEO due to mutations in the Twinkle gene. Journal of the Neurological Sciences. 201(1-2). 39–44. 37 indexed citations
15.
Quigley, Anita, et al.. (2001). A Novel Clinical Phenotype of Myopathy, Sensorimotor Neuropathy, Infertility, and Hypogonadism With Multiple Mitochondrial DNA Deletions. Journal of Clinical Neuromuscular Disease. 3(2). 77–82. 6 indexed citations
16.
Thyagarajan, Dominic, Susan Bressman, Claudio Bruno, et al.. (2000). A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Annals of Neurology. 48(5). 730–736. 146 indexed citations
17.
Thyagarajan, Dominic, Susan Bressman, Claudio Bruno, et al.. (2000). A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Annals of Neurology. 48(5). 730–736. 11 indexed citations
18.
Marzuki, Sangkot, Patcharee Lertrit, Robert M. I. Kapsa, et al.. (1992). Reply to Howell et al.: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA. The American Journal of Human Genetics. 50(6). 1337–1340. 9 indexed citations
19.
Lertrit, Patcharee, A.S. Noer, M.J.Bernadette Jean-François, et al.. (1992). A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.. PubMed. 51(3). 457–68. 55 indexed citations
20.
Noer, A.S., Herawati Sudoyo, Patcharee Lertrit, et al.. (1991). A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.. Europe PMC (PubMed Central). 49(4). 715–22. 64 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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