Sandeep Jayawant

3.8k total citations
57 papers, 1.7k citations indexed

About

Sandeep Jayawant is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Sandeep Jayawant has authored 57 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 19 papers in Neurology and 9 papers in Surgery. Recurrent topics in Sandeep Jayawant's work include Myasthenia Gravis and Thymoma (16 papers), Muscle Physiology and Disorders (7 papers) and Metabolism and Genetic Disorders (7 papers). Sandeep Jayawant is often cited by papers focused on Myasthenia Gravis and Thymoma (16 papers), Muscle Physiology and Disorders (7 papers) and Metabolism and Genetic Disorders (7 papers). Sandeep Jayawant collaborates with scholars based in United Kingdom, United States and Netherlands. Sandeep Jayawant's co-authors include Jeremy Parr, Jacqueline Palace, David Beeson, S. Robb, Alison Kemp, Daniel Lashley, Pedro M. Rodríguez Cruz, Angela Vincent, P M Sharples and Frances Gibbon and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Sandeep Jayawant

54 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandeep Jayawant United Kingdom 26 713 584 315 203 185 57 1.7k
Maja von der Hagen Germany 22 417 0.6× 651 1.1× 155 0.5× 214 1.1× 249 1.3× 80 1.5k
Tuula Lönnqvist Finland 29 186 0.3× 1.4k 2.4× 278 0.9× 150 0.7× 347 1.9× 80 2.4k
E Peeters Netherlands 23 257 0.4× 447 0.8× 560 1.8× 97 0.5× 197 1.1× 46 1.7k
Günther Bernert Austria 21 283 0.4× 486 0.8× 152 0.5× 66 0.3× 153 0.8× 57 1.4k
Ekkehard M. Kasper United States 26 616 0.9× 321 0.5× 94 0.3× 38 0.2× 523 2.8× 97 2.0k
Jan E. Leestma United States 22 349 0.5× 537 0.9× 597 1.9× 49 0.2× 407 2.2× 50 2.2k
Mariasavina Severino Italy 26 431 0.6× 515 0.9× 819 2.6× 100 0.5× 236 1.3× 188 2.5k
Andrew D. Parent United States 26 832 1.2× 300 0.5× 227 0.7× 52 0.3× 258 1.4× 65 1.8k
Waney Squier United Kingdom 17 186 0.3× 255 0.4× 343 1.1× 50 0.2× 170 0.9× 34 901
Simone Mandelstam Australia 23 121 0.2× 726 1.2× 478 1.5× 99 0.5× 384 2.1× 60 2.1k

Countries citing papers authored by Sandeep Jayawant

Since Specialization
Citations

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

Fields of papers citing papers by Sandeep Jayawant

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandeep Jayawant

This figure shows the co-authorship network connecting the top 25 collaborators of Sandeep Jayawant. A scholar is included among the top collaborators of Sandeep Jayawant 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 Sandeep Jayawant. Sandeep Jayawant 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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Steel, Dora, Federica Rachele Danti, Benjamin Kamien, et al.. (2023). Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants. Neurology. 100(21). e2214–e2223. 1 indexed citations
3.
Magrinelli, Francesca, Clarissa Rocca, Roberto Simone, et al.. (2022). Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2‐1‐Related Disorder. Movement Disorders. 38(2). 347–353. 4 indexed citations
4.
Vecchio, Domizia, Sithara Ramdas, Pinki Munot, et al.. (2019). Paediatric myasthenia gravis: Prognostic factors for drug free remission. Neuromuscular Disorders. 30(2). 120–127. 24 indexed citations
5.
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Watson, Lauren M., Ricardo Parolin Schnekenberg, Jonathan P. Williams, et al.. (2017). Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. The American Journal of Human Genetics. 101(3). 451–458. 55 indexed citations
7.
Kilich, Eliz, et al.. (2016). Symptomatic stroke complicating central skull base osteomyelitis following otitis media in a 2-year old boy: Case report and review of the literature. International Journal of Pediatric Otorhinolaryngology. 89. 140–144. 5 indexed citations
8.
Logan, Clare V., Judith Cossins, Pedro M. Rodríguez Cruz, et al.. (2015). Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. The American Journal of Human Genetics. 97(6). 878–885. 55 indexed citations
9.
Brunklaus, Andreas, Rachael Ellis, Helen Stewart, et al.. (2015). Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families. European Journal of Paediatric Neurology. 19(4). 484–488. 20 indexed citations
10.
Anand, Geetha, Shelley Segal, Andrea H. Németh, et al.. (2014). H1N1 Triggered Recurrent Acute Necrotizing Encephalopathy in a Family With a T653I Mutation in the RANBP2 Gene. The Pediatric Infectious Disease Journal. 34(3). 318–320. 13 indexed citations
11.
Jayawant, Sandeep, Jeremy Parr, & Angela Vincent. (2013). Autoimmune myasthenia gravis. Handbook of clinical neurology. 113. 1465–1468. 14 indexed citations
12.
Pagnamenta, Alistair T., Stefano Lise, Victoria Harrison, et al.. (2011). Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies. Journal of Human Genetics. 57(1). 70–72. 46 indexed citations
13.
Palace, Jacqueline, Daniel Lashley, Stephen Bailey, et al.. (2011). Clinical features in a series of fast channel congenital myasthenia syndrome. Neuromuscular Disorders. 22(2). 112–117. 27 indexed citations
14.
Anand, Geetha, et al.. (2010). X‐linked hereditary motor sensory neuropathy (type 1) presenting with a stroke‐like episode. Developmental Medicine & Child Neurology. 52(7). 677–679. 33 indexed citations
15.
Lashley, Daniel, et al.. (2009). EPHEDRINE TREATMENT RESULTS IN PROFOUND FUNCTIONAL IMPROVEMENTS IN DOK-7 CONGENITAL MYASTHENIA. Journal of Neurology Neurosurgery & Psychiatry. 80. 1 indexed citations
16.
Ashley, Neil, Sandeep Jayawant, Jeremy Parr, et al.. (2007). Mutations in the mitochondrial DNA gamma polymerase (POLG-G) may cause Alpers syndrome, mitochondrial DNA depletion and apparent non-syndromic status epilepticus: implications for valproate therapy. Journal of Medical Genetics. 44. 1 indexed citations
17.
Morten, Karl, Neil Ashley, Frits A. Wijburg, et al.. (2007). Liver mtDNA content increases during development: A comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion. Mitochondrion. 7(6). 386–395. 45 indexed citations
18.
Parr, Jeremy & Sandeep Jayawant. (2007). Childhood myasthenia: clinical subtypes and practical management. Developmental Medicine & Child Neurology. 49(8). 629–635. 30 indexed citations
19.
Jayawant, Sandeep & Susan E. Libretto. (2004). Topiramate in the treatment of myoclonic-astatic epilepsy in children: a retrospective hospital audit.. SHILAP Revista de lepidopterología. 49(3). 202–5; discussion 205. 10 indexed citations
20.
Hadjikoutis, S, Sandeep Jayawant, & Neil Stoodley. (2002). Isolated hypoglossal nerve palsy in a 14-year-old girl. European Journal of Paediatric Neurology. 6(4). 225–228. 11 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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