Kenneth Silver

2.0k total citations
32 papers, 1.0k citations indexed

About

Kenneth Silver is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Kenneth Silver has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Neurology and 7 papers in Genetics. Recurrent topics in Kenneth Silver's work include Metabolism and Genetic Disorders (4 papers), Epilepsy research and treatment (4 papers) and Genomics and Rare Diseases (3 papers). Kenneth Silver is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Epilepsy research and treatment (4 papers) and Genomics and Rare Diseases (3 papers). Kenneth Silver collaborates with scholars based in Canada, United States and United Kingdom. Kenneth Silver's co-authors include Frédérick Andermann, Barbara Mazer, Kathryn J. Swoboda, Martha C. Piper, Maria Ramsay, Douglas L. Arnold, Augustin M. O’Gorman, Diana M. Willis, Gordon V. Watters and Fahed Halal and has published in prestigious journals such as Brain, Neurology and PEDIATRICS.

In The Last Decade

Kenneth Silver

32 papers receiving 983 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kenneth Silver Canada 18 326 311 271 193 108 32 1.0k
Johan Lundgren Sweden 20 333 1.0× 271 0.9× 200 0.7× 226 1.2× 180 1.7× 28 1.3k
Johannes Lang Germany 16 173 0.5× 253 0.8× 291 1.1× 185 1.0× 39 0.4× 74 1000
Sotiris Youroukos Greece 16 327 1.0× 289 0.9× 187 0.7× 168 0.9× 124 1.1× 33 899
B. Wilken Germany 21 306 0.9× 108 0.3× 194 0.7× 114 0.6× 119 1.1× 38 1.2k
F Vassella Switzerland 19 205 0.6× 332 1.1× 100 0.4× 268 1.4× 71 0.7× 79 914
Christine Soufflet France 20 298 0.9× 492 1.6× 109 0.4× 417 2.2× 181 1.7× 48 1.5k
Evangelos Pavlou Greece 15 171 0.5× 203 0.7× 255 0.9× 98 0.5× 55 0.5× 48 747
S. Binelli Italy 20 209 0.6× 387 1.2× 188 0.7× 260 1.3× 109 1.0× 43 926
Güzide Turanlı Türkiye 15 111 0.3× 367 1.2× 80 0.3× 269 1.4× 71 0.7× 51 736
Maria Margherita Mancardi Italy 15 178 0.5× 149 0.5× 133 0.5× 113 0.6× 146 1.4× 86 696

Countries citing papers authored by Kenneth Silver

Since Specialization
Citations

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

Fields of papers citing papers by Kenneth Silver

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kenneth Silver

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth Silver. A scholar is included among the top collaborators of Kenneth Silver 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 Kenneth Silver. Kenneth Silver 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.
Silver, Kenneth. (2019). Habitual Weakness. Thought A Journal of Philosophy. 8(4). 270–277. 5 indexed citations
2.
Maas, Roderick P.P.W.M., Erik‐Jan Kamsteeg, Salvatore Mangano, et al.. (2018). Benign nocturnal alternating hemiplegia of childhood: A clinical and nomenclatural reappraisal. European Journal of Paediatric Neurology. 22(6). 1110–1117. 6 indexed citations
3.
Silver, Kenneth, et al.. (2017). Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation. Pediatric Neurology. 73. 101–105. 47 indexed citations
4.
Cole, Stephen, Martin Karrenbach, Kevin Boone, et al.. (2017). Effective Diffusivity Estimates from Distributed Fiber-optic Strain and Microseismic Measurements. 6 indexed citations
5.
Skjørringe, Tina, et al.. (2011). Exon duplications in the ATP7A gene: Frequency and Transcriptional Behaviour. Orphanet Journal of Rare Diseases. 6(1). 73–73. 8 indexed citations
6.
Silver, Kenneth, et al.. (2009). Dystonic storm due to Batten's disease treated with pallidotomy and deep brain stimulation. Movement Disorders. 24(7). 1048–1053. 48 indexed citations
7.
MacLeod, Heather, Peter Pytel, Robert L. Wollmann, et al.. (2007). A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscular Disorders. 17(4). 285–289. 16 indexed citations
8.
Jansen, Anna, Henian Cao, Paige Kaplan, et al.. (2007). Sanfilippo Syndrome Type D. Archives of Neurology. 64(11). 1629–1629. 26 indexed citations
9.
Swoboda, Kathryn J., Emmanuel Kanavakis, Athina Xaidara, et al.. (2004). Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel ATP1A2 mutation. Annals of Neurology. 55(6). 884–887. 119 indexed citations
10.
Mittal, Sandeep, Jean‐Pierre Farmer, Chantal Poulin, & Kenneth Silver. (2001). Reliability of intraoperative electrophysiological monitoring in selective posterior rhizotomy. Journal of neurosurgery. 95(1). 67–75. 35 indexed citations
11.
Arbour, Laura, Kenneth Silver, Peter Hechtman, Eileen P. Treacy, & Marion B. Coulter-Mackie. (2000). Variable onset of metachromatic leukodystrophy in a Vietnamese family. Pediatric Neurology. 23(2). 173–176. 19 indexed citations
12.
Cendes, Fernando, Frédérick Andermann, Kenneth Silver, & Douglas L. Arnold. (1995). Imaging of axonal damage in vivo in Rasmussen's syndrome. Brain. 118(3). 753–758. 40 indexed citations
13.
Pratt, Victoria M., et al.. (1995). Pelizaeus‐Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene. American Journal of Medical Genetics. 55(4). 402–404. 9 indexed citations
14.
Otero, Lucy J., Garry K. Brown, Kenneth Silver, Douglas L. Arnold, & Paul M. Matthews. (1995). Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1α subunit mutations in females. Pediatric Neurology. 13(4). 327–332. 10 indexed citations
15.
Arnold, Douglas L., Kenneth Silver, & Frédérick Andermann. (1993). Evidence for mitochondrial dysfunction in patients with alternating hemiplegia of childhood. Annals of Neurology. 33(6). 604–607. 29 indexed citations
16.
Shevell, Michael, Kenneth Silver, Gordon V. Watters, & Bernard Rosenblatt. (1993). Transient oculosympathetic paresis (group II Raeder paratrigeminal neuralgia) of childhood: Migraine variant. Pediatric Neurology. 9(4). 289–292. 4 indexed citations
17.
Chitayat, David, Kathleen Meagher‐Villemure, Orval Mamer, et al.. (1992). Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria. The Journal of Pediatrics. 121(1). 86–89. 31 indexed citations
18.
Halal, Fahed & Kenneth Silver. (1989). Slowly progressive macrocephaly with hamartomas: A new syndrome?. American Journal of Medical Genetics. 33(2). 182–185. 14 indexed citations
19.
Shevell, Michael, et al.. (1989). Neonatal dural sinus thrombosis. Pediatric Neurology. 5(3). 161–165. 71 indexed citations
20.
Piper, Martha C., Barbara Mazer, Kenneth Silver, & Maria Ramsay. (1988). RESOLUTION OF NEUROLOGICAL SYMPTOMS IN HIGH‐RISK INFANTS DURING THE FIRST TWO YEARS OF LIFE. Developmental Medicine & Child Neurology. 30(1). 26–35. 41 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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