Steven L. Kugler

936 total citations
19 papers, 632 citations indexed

About

Steven L. Kugler is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Steven L. Kugler has authored 19 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Psychiatry and Mental health, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Steven L. Kugler's work include Epilepsy research and treatment (11 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (3 papers). Steven L. Kugler is often cited by papers focused on Epilepsy research and treatment (11 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (3 papers). Steven L. Kugler collaborates with scholars based in United States, Canada and United Kingdom. Steven L. Kugler's co-authors include David E. Mandelbaum, Michael H. Miller, Sandra J. England, Daniel Lewin, Arthur S. Walters, William G. Johnson, Deb K. Pal, Edward S. Stenroos, Tara Clarke and Lisa J. Strug and has published in prestigious journals such as PLoS ONE, Neurology and Epilepsia.

In The Last Decade

Steven L. Kugler

19 papers receiving 608 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven L. Kugler United States 13 365 169 163 137 124 19 632
Geoff Wallace Australia 14 237 0.6× 95 0.6× 168 1.0× 291 2.1× 134 1.1× 20 721
Tiziana Calarese Italy 11 315 0.9× 189 1.1× 78 0.5× 59 0.4× 98 0.8× 16 509
Akie Miyamoto Japan 17 178 0.5× 159 0.9× 201 1.2× 192 1.4× 74 0.6× 49 732
Richard Webster Australia 13 217 0.6× 132 0.8× 92 0.6× 96 0.7× 64 0.5× 28 426
G. D’Orsi Italy 15 439 1.2× 264 1.6× 198 1.2× 84 0.6× 260 2.1× 48 789
Reija Alén Finland 12 119 0.3× 333 2.0× 136 0.8× 152 1.1× 90 0.7× 14 700
Eliane Roulet‐Perez Switzerland 15 297 0.8× 224 1.3× 123 0.8× 95 0.7× 149 1.2× 39 682
Eileen Broomall United States 7 168 0.5× 131 0.8× 74 0.5× 74 0.5× 68 0.5× 16 437
Cristina Petrelli Italy 14 240 0.7× 74 0.4× 113 0.7× 141 1.0× 92 0.7× 28 562
Anna Volzone Italy 9 120 0.3× 92 0.5× 88 0.5× 49 0.4× 84 0.7× 15 451

Countries citing papers authored by Steven L. Kugler

Since Specialization
Citations

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

Fields of papers citing papers by Steven L. Kugler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven L. Kugler. 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 Steven L. Kugler. The network helps show where Steven L. Kugler may publish in the future.

Co-authorship network of co-authors of Steven L. Kugler

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

All Works

19 of 19 papers shown
1.
Cuddapah, Vishnu Anand, Holly Dubbs, Laura Adang, et al.. (2021). Understanding the phenotypic spectrum of ASXL‐related disease: Ten cases and a review of the literature. American Journal of Medical Genetics Part A. 185(6). 1700–1711. 18 indexed citations
2.
Addis, Laura, Theodore Chiang, Tara Clarke, et al.. (2013). Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes Brain & Behavior. 13(3). 333–340. 6 indexed citations
3.
Strug, Lisa J., Laura Addis, Theodore Chiang, et al.. (2012). The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy. PLoS ONE. 7(7). e40696–e40696. 12 indexed citations
4.
Cauley, Ryan P., et al.. (2010). Polyspike and Waves Do Not Predict Generalized Tonic-Clonic Seizures in Childhood Absence Epilepsy. Journal of Child Neurology. 25(4). 475–481. 14 indexed citations
5.
Strug, Lisa J., Tara Clarke, Theodore Chiang, et al.. (2009). Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4). European Journal of Human Genetics. 17(9). 1171–1181. 141 indexed citations
6.
Kugler, Steven L., Bhavna Bali, Philip Lieberman, et al.. (2008). An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder. Epilepsia. 49(6). 1086–1090. 24 indexed citations
7.
Anwar, Mujahid, Anne Koons, Barbara Ostfeld, et al.. (2005). Neurobehavioral consequences of intraventricular hemorrhage in the very low birthweight infant. 20(3). 149–153. 1 indexed citations
8.
Mandelbaum, David E., et al.. (2005). Efficacy of Levetiracetam at 12 Months in Children Classified by Seizure Type, Cognitive Status, and Previous Anticonvulsant Drug Use. Journal of Child Neurology. 20(7). 590–594. 22 indexed citations
9.
Mandelbaum, David E., et al.. (2005). Broad-Spectrum Efficacy of Zonisamide at 12 Months in Children With Intractable Epilepsy. Journal of Child Neurology. 20(7). 594–597. 12 indexed citations
10.
Pal, Deb K., Steven L. Kugler, David E. Mandelbaum, & Martina Durner. (2003). Phenotypic features of familial febrile seizures. Neurology. 60(3). 410–414. 15 indexed citations
11.
Kaufman, Kenneth R., Steven L. Kugler, & Rǎjesh C. Sachdeo. (2002). Tiagabine in the Management of Postencephalitic Epilepsy and Impulse Control Disorder. Epilepsy & Behavior. 3(2). 190–194. 16 indexed citations
12.
Walters, Arthur S., David E. Mandelbaum, Daniel Lewin, et al.. (2000). Dopaminergic therapy in children with restless legs/periodic limb movements in sleep and ADHD. Pediatric Neurology. 22(3). 182–186. 185 indexed citations
13.
Kugler, Steven L., et al.. (1998). Hereditary febrile seizures: Phenotype and evidence for a chromosome 19p locus. American Journal of Medical Genetics. 79(5). 354–361. 51 indexed citations
14.
Kugler, Steven L. & Rǎjesh C. Sachdeo. (1998). Topiramate efficacy in infancy. Pediatric Neurology. 19(4). 320–322. 11 indexed citations
15.
Kugler, Steven L. & William G. Johnson. (1998). Genetics of the febrile seizure susceptibility trait. Brain and Development. 20(5). 265–274. 27 indexed citations
16.
Johnson, William G., et al.. (1996). Pedigree analysis in families with febrile seizures. American Journal of Medical Genetics. 61(4). 345–352. 58 indexed citations
17.
Johnson, William G., et al.. (1996). Pedigree analysis in families with febrile seizures. American Journal of Medical Genetics. 61(4). 345–352. 8 indexed citations
18.
Kugler, Steven L., Asher Barzilai, David S. Hodes, et al.. (1991). Acute hemiplegia associated with HIV infection. Pediatric Neurology. 7(3). 207–210. 4 indexed citations
19.
Kugler, Steven L., et al.. (1990). Hypothermia and systemic lupus erythematosus.. PubMed. 17(5). 680–1. 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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