Michael Pike

2.8k total citations
61 papers, 1.9k citations indexed

About

Michael Pike is a scholar working on Neurology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michael Pike has authored 61 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 11 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michael Pike's work include Autoimmune Neurological Disorders and Treatments (9 papers), Spinal Dysraphism and Malformations (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Michael Pike is often cited by papers focused on Autoimmune Neurological Disorders and Treatments (9 papers), Spinal Dysraphism and Malformations (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Michael Pike collaborates with scholars based in United Kingdom, United States and Canada. Michael Pike's co-authors include James J. Lipsky, David J. Atherton, Bethan Lang, Dennis C. Mays, William J. Sandborn, Franz Blaes, Catherine J. Huntoon, Michael P. Bell, D J McKean and Laurence J. Egan and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Michael Pike

59 papers receiving 1.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Michael Pike 616 459 385 246 237 61 1.9k
Liling Warren 281 0.5× 497 1.1× 507 1.3× 107 0.4× 124 0.5× 26 1.6k
William E. Karnes 456 0.7× 240 0.5× 186 0.5× 224 0.9× 56 0.2× 50 2.0k
Mira Irons 283 0.5× 1.8k 3.9× 632 1.6× 217 0.9× 253 1.1× 82 3.2k
Antonio Agostino Sinisi 298 0.5× 639 1.4× 584 1.5× 321 1.3× 74 0.3× 118 3.3k
Sirui Zhou 235 0.4× 640 1.4× 504 1.3× 230 0.9× 162 0.7× 84 1.8k
Leslie A. Lange 458 0.7× 1.2k 2.5× 654 1.7× 455 1.8× 102 0.4× 87 3.0k
Huichun Xu 291 0.5× 1.3k 2.9× 272 0.7× 379 1.5× 55 0.2× 61 2.4k
Mefkûre Eraksoy 810 1.3× 498 1.1× 111 0.3× 236 1.0× 398 1.7× 97 2.4k
N. Scott Litofsky 583 0.9× 655 1.4× 79 0.2× 391 1.6× 77 0.3× 102 2.4k
Brahim Tabarki 327 0.5× 567 1.2× 240 0.6× 258 1.0× 142 0.6× 89 1.8k

Countries citing papers authored by Michael Pike

Since Specialization
Citations

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

Fields of papers citing papers by Michael Pike

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Pike

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Pike. A scholar is included among the top collaborators of Michael Pike 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 Michael Pike. Michael Pike 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.
Iro, Mildred A., Manish Sadarangani, Michael Absoud, et al.. (2023). Intravenous immunoglobulin treatment in childhood encephalitis (IgNiTE): a randomised controlled trial. BMJ Open. 13(11). e072134–e072134. 3 indexed citations
2.
Verity, Christopher, Anne Marie Winstone, Robert Will, et al.. (2018). Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?. Archives of Disease in Childhood. 104(4). 360–365. 6 indexed citations
3.
Anand, Geetha, Michael Pike, Sanjay R. Mehta, et al.. (2018). Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population. Archives of Disease in Childhood. 103(5). 463–469. 17 indexed citations
4.
Hacohen, Yael, Michael Absoud, Mark Woodhall, et al.. (2013). Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort. Journal of Neurology Neurosurgery & Psychiatry. 85(4). 456–461. 60 indexed citations
5.
MacPherson, Lesley, Katharine Foster, Peter Lunt, et al.. (2010). Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis. Molecular Genetics and Metabolism. 100(2). 207–212. 27 indexed citations
6.
Blaes, Franz, Michael Pike, & Bethan Lang. (2008). Autoantibodies in childhood opsoclonus–myoclonus syndrome. Journal of Neuroimmunology. 201-202. 221–226. 33 indexed citations
7.
Matthay, Katherine K., Franz Blaes, Barbara Hero, et al.. (2005). Opsoclonus myoclonus syndrome in neuroblastoma a report from a workshop on the dancing eyes syndrome at the advances in neuroblastoma meeting in Genoa, Italy, 2004. Cancer Letters. 228(1-2). 275–282. 102 indexed citations
8.
Cordeiro, Nuno, Kate Gardner, Susan Huson, et al.. (2005). Renal vascular disease in neurofibromatosis type 2: association or coincidence?. Developmental Medicine & Child Neurology. 48(1). 58–59. 10 indexed citations
9.
Tay, S K, Hasan O. Akman, Wendy K. Chung, et al.. (2004). Fatal infantile neuromuscular presentation of glycogen storage disease type IV. Neuromuscular Disorders. 14(4). 253–260. 48 indexed citations
10.
Dalton, Paola, Robert M. J. Deacon, Andrew M. Blamire, et al.. (2003). Maternal neuronal antibodies associated with autism and a language disorder. Annals of Neurology. 53(4). 533–537. 165 indexed citations
11.
Gallagher, Andrew, et al.. (2001). ‘HHH syndrome associated with callosal agenesis and disordered neuronal migration’. Developmental Medicine & Child Neurology. 43(6). 430–1. 1 indexed citations
12.
Pike, Michael, et al.. (2001). Improved methods for determining the concentration of 6-thioguanine nucleotides and 6-methylmercaptopurine nucleotides in blood. Journal of Chromatography B Biomedical Sciences and Applications. 757(1). 1–9. 31 indexed citations
13.
Ruggieri, Martino, Alexander K. Smárason, & Michael Pike. (1999). Spinal cord insults in the prenatal, perinatal, and neonatal periods. Developmental Medicine & Child Neurology. 41(5). 311–317. 10 indexed citations
14.
Matteson, Eric L., et al.. (1999). Induction therapy with an intravenous loading dose of azathioprine for treatment of refractory, active rheumatoid arthritis. Arthritis & Rheumatism. 42(1). 186–187. 7 indexed citations
15.
Egan, Laurence J., Dennis C. Mays, Catherine J. Huntoon, et al.. (1999). Inhibition of Interleukin-1-stimulated NF-κB RelA/p65 Phosphorylation by Mesalamine Is Accompanied by Decreased Transcriptional Activity. Journal of Biological Chemistry. 274(37). 26448–26453. 182 indexed citations
16.
Rae, Caroline, Richard B. Scott, Campbell Thompson, et al.. (1998). Brain biochemistry in Duchenne muscular dystrophy: A 1H magnetic resonance and neuropsychological study. Journal of the Neurological Sciences. 160(2). 148–157. 47 indexed citations
17.
Pike, Michael, Peter K. H. Wong, Olof Flodmark, et al.. (1990). Electrophysiologic studies, computed tomography, and neurologic outcome in acute bacterial meningitis. The Journal of Pediatrics. 116(5). 702–706. 20 indexed citations
18.
Pike, Michael, Derek A. Applegarth, Henry G. Dunn, et al.. (1990). Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction. The Journal of Pediatrics. 116(1). 88–94. 18 indexed citations
19.
Pike, Michael, et al.. (1989). A family with X-linked ichthyosis and hypogonadism. European Journal of Pediatrics. 148(5). 442–444. 10 indexed citations
20.
Pike, Michael. (1989). Neurological and Developmental Findings in Children With Cataracts. Archives of Pediatrics and Adolescent Medicine. 143(6). 706–706. 10 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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