Venkateswaran Ramesh

2.5k total citations
20 papers, 846 citations indexed

About

Venkateswaran Ramesh is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Venkateswaran Ramesh has authored 20 papers receiving a total of 846 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Clinical Biochemistry. Recurrent topics in Venkateswaran Ramesh's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Venkateswaran Ramesh is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Venkateswaran Ramesh collaborates with scholars based in United Kingdom, Canada and United States. Venkateswaran Ramesh's co-authors include Patrick F. Chinnery, Rita Horváth, Helen Griffin, Angela Pyle, Jennifer Duff, Vijeya Ganesan, Sara Kivity, Ailsa McLellan, Anne M. McIntosh and Deepak Gill and has published in prestigious journals such as Brain, Neurology and Archives of Disease in Childhood.

In The Last Decade

Venkateswaran Ramesh

20 papers receiving 837 citations

Peers

Venkateswaran Ramesh

CMN

PMH

GENET

PPCH

Sumimasa Yamashita Japan

Mizue Iai Japan

Kaja Kristine Selmer Norway

Bernhard Weschke Germany

Birgit Uhlenberg Germany

Liesbet Deprez Belgium

Rita Cittadella Italy

Takahito Inoue Japan

Afshin Saffari Germany

Taoyun Ji China

Sumimasa Yamashita Japan

Venkateswaran Ramesh

568 ×1.3

231 ×0.9

CMN

110 ×0.5

PMH

143 ×1.0

GENET

67 ×0.5

PPCH

Citations per year, relative to Venkateswaran Ramesh Venkateswaran Ramesh (= 1×) peers Sumimasa Yamashita

Countries citing papers authored by Venkateswaran Ramesh

Since Specialization

Citations

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

Fields of papers citing papers by Venkateswaran Ramesh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Venkateswaran Ramesh

This figure shows the co-authorship network connecting the top 25 collaborators of Venkateswaran Ramesh. A scholar is included among the top collaborators of Venkateswaran Ramesh 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 Venkateswaran Ramesh. Venkateswaran Ramesh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Chatterjee, Fiona, et al.. (2020). Severe cortical damage associated with COVID-19 case report. Seizure. 84. 66–68. 7 indexed citations

Boczonadi, Veronika, Martin King, Anthony C. Smith, et al.. (2018). Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease. Genetics in Medicine. 20(10). 1224–1235. 40 indexed citations

Ng, Yi Shiau, Rebecca Scott, Venkateswaran Ramesh, et al.. (2017). The adjunctive application of transcranial direct current stimulation in the management of de novo refractory epilepsia partialis continua in adolescent‐onset POLG‐related mitochondrial disease. Epilepsia Open. 3(1). 103–108. 13 indexed citations

Bánsági, Boglárka, Helen Griffin, Roger G. Whittaker, et al.. (2017). Genetic heterogeneity of motor neuropathies. Neurology. 88(13). 1226–1234. 69 indexed citations

Cooper, Monica S., Anne M. McIntosh, Douglas E. Crompton, et al.. (2016). Mortality in Dravet syndrome. Epilepsy Research. 128. 43–47. 225 indexed citations

Lewis‐Smith, David, Kimberli J. Kamer, Helen Griffin, et al.. (2016). Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood. Neurology Genetics. 2(2). e59–e59. 79 indexed citations

Splitt, Miranda, Venkateswaran Ramesh, Suzanne D. DeBrosse, et al.. (2016). FHF1 (FGF12) epileptic encephalopathy. Neurology Genetics. 2(6). e115–e115. 29 indexed citations

Pyle, Angela, Venkateswaran Ramesh, Marina Bartsakoulia, et al.. (2014). Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene. Journal of Neuromuscular Diseases. 1(1). 55–63. 14 indexed citations

Keogh, Michael J., Angela Pyle, Jennifer Duff, et al.. (2014). A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism. Neurogenetics. 16(1). 65–67. 30 indexed citations

10.

Pyle, Angela, David Bargiela, Helen Griffin, et al.. (2014). Exome sequencing in undiagnosed inherited and sporadic ataxias. Brain. 138(2). 276–283. 94 indexed citations

11.

Ramesh, Venkateswaran, et al.. (2013). Cytochrome P450 2C9 gene polymorphism in phenytoin induced gingival enlargement: A case report. Journal of Pharmacy And Bioallied Sciences. 5(3). 237–237. 11 indexed citations

12.

Cross, J. Helen, Rolf A. Heckemann, Roxana Gunny, et al.. (2013). Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome. Developmental Medicine & Child Neurology. 55(9). 846–856. 43 indexed citations

13.

Montgomery, Tara, et al.. (2012). TUBA1A Mutation-Associated Lissencephaly: Case Report and Review of the Literature. Pediatric Neurology. 46(2). 127–131. 36 indexed citations

14.

Kathuria, Sushruta, Shikha Arora, & Venkateswaran Ramesh. (2012). Sjogren-Larsson syndrome: Importance of early diagnosis and aggressive physiotherapy. Dermatology Online Journal. 18(9). 11–11. 4 indexed citations

15.

Ramesh, Venkateswaran, Bruno De Bernardi, Caterina Garone, et al.. (2010). Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis. Developmental Medicine & Child Neurology. 52(8). 725–732. 73 indexed citations

16.

McFarland, Robert, Gavin Hudson, Rachael W. Taylor, et al.. (2009). Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1). BMJ Case Reports. 2009. bcr1220081303–bcr1220081303. 7 indexed citations

17.

Basu, Anna, et al.. (2009). Coma Blisters in 2 Children on Anticonvulsant Medication. Journal of Child Neurology. 24(8). 1021–1025. 8 indexed citations

18.

McFarland, Robert, Gavin Hudson, Rachael W. Taylor, et al.. (2008). Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ ( POLG1 ). Archives of Disease in Childhood. 93(2). 151–153. 47 indexed citations

19.

Slatter, Mary, Clive Taylor, Venkateswaran Ramesh, et al.. (2007). Outcome of Hematopoietic Stem Cell Transplantation in Severe Combined Immune Deficiency With Central Nervous System Viral Infection. The Pediatric Infectious Disease Journal. 26(2). 129–133. 10 indexed citations

20.

Ramesh, Venkateswaran & D. Gardner‐Medwin. (1992). Familial Paroxysmal Rhabdomyolysis: Management of Two Cases of the Non‐exertional Type. Developmental Medicine & Child Neurology. 34(1). 73–79. 7 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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