Stephan Waltz

1.5k total citations
21 papers, 771 citations indexed

About

Stephan Waltz is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stephan Waltz has authored 21 papers receiving a total of 771 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Psychiatry and Mental health, 7 papers in Pediatrics, Perinatology and Child Health and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stephan Waltz's work include Epilepsy research and treatment (8 papers), Neuroscience and Neuropharmacology Research (5 papers) and Genomics and Rare Diseases (2 papers). Stephan Waltz is often cited by papers focused on Epilepsy research and treatment (8 papers), Neuroscience and Neuropharmacology Research (5 papers) and Genomics and Rare Diseases (2 papers). Stephan Waltz collaborates with scholars based in Germany, Sweden and Italy. Stephan Waltz's co-authors include H. Doose, H.‐J. Christen, Ulrich Stephani, Josef Sonntag, Hiltrud Muhle, Lu Yang, Bernd A. Neubauer, J. Jenderny, Almuth Caliebe and D. Weisner and has published in prestigious journals such as Brain, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Stephan Waltz

21 papers receiving 749 citations

Peers

Stephan Waltz
Karin Edebol Eeg‐Olofsson Sweden
Arie Weinstock United States
Ulrich Brandl Germany
Alessandra Morano Italy
Su Jeong You South Korea
Biswaroop Chakrabarty India
Hélène Verhelst Belgium
Marianne Juel Kjeldsen Denmark
Jinane Fattouch Italy
H. Huntley Hardison United States
Karin Edebol Eeg‐Olofsson Sweden
Stephan Waltz
Citations per year, relative to Stephan Waltz Stephan Waltz (= 1×) peers Karin Edebol Eeg‐Olofsson

Countries citing papers authored by Stephan Waltz

Since Specialization
Citations

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

Fields of papers citing papers by Stephan Waltz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Waltz

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Waltz. A scholar is included among the top collaborators of Stephan Waltz 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 Stephan Waltz. Stephan Waltz 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.
Rostásy, Kevin, Ronny Wickström, Stefano Sartori, et al.. (2022). Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents. Neuropediatrics. 54(1). 14–19. 1 indexed citations
2.
Bender, Daniel A., José Angel Santamaria‐Araujo, Stephan Waltz, et al.. (2019). Impaired mitochondrial maturation of sulfite oxidase in a patient with severe sulfite oxidase deficiency. Human Molecular Genetics. 28(17). 2885–2899. 21 indexed citations
3.
Stark, Christina, Peter Herkenrath, Stephan Waltz, et al.. (2016). Early vibration assisted physiotherapy in toddlers with cerebral palsy - a randomized controlled pilot trial.. PubMed. 16(3). 183–92. 20 indexed citations
4.
Hallmann, Kerstin, Alexei P. Kudin, Gábor Zsurka, et al.. (2015). Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy. Brain. 139(2). 338–345. 47 indexed citations
5.
Stark, Christina, Oliver Semler, İbrahim Duran, et al.. (2013). Intervallrehabilitation mit häuslichem Training bei Kindern mit Zerebralparese. Monatsschrift Kinderheilkunde. 161(7). 625–632. 6 indexed citations
6.
Muhle, Hiltrud, Anja Neumann, K. Lohmann-Hedrich, et al.. (2008). Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families. Movement Disorders. 23(8). 1113–1121. 52 indexed citations
7.
Yang, Lu, et al.. (2008). Photosensitivity in epileptic syndromes of childhood and adolescence. Epileptic Disorders. 10(2). 136–143. 58 indexed citations
8.
Tauer, Ulrike, Susanne Lorenz, Kirsten P. Lenzen, et al.. (2005). Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Annals of Neurology. 57(6). 866–873. 65 indexed citations
9.
Waltz, Stephan & Ulrich Stephani. (2000). Inheritance of Photosensitivity. Neuropediatrics. 31(2). 82–85. 53 indexed citations
10.
Trenité, Dorothée Kasteleijn‐Nolst, C.D. Binnie, G. F. A. Harding, et al.. (1999). Photic stimulation — standardization of screening methods. Neurophysiologie Clinique. 29(4). 318–324. 39 indexed citations
11.
Doose, H., et al.. (1998). Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures. Neuropediatrics. 29(5). 229–238. 45 indexed citations
12.
Müller, Dominik N., Bernd A. Neubauer, Stephan Waltz, & Ulrich Stephani. (1998). Neuroborreliosis and isolated trochlear palsy. European Journal of Paediatric Neurology. 2(5). 275–276. 11 indexed citations
13.
Caliebe, Almuth, Stephan Waltz, & J. Jenderny. (1997). Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient. Clinical Genetics. 52(2). 116–119. 27 indexed citations
14.
15.
Waltz, Stephan, Andreas Hahn, & Ulrich Stephani. (1997). Epileptische Anfälle bei Bildschirmspielen. Monatsschrift Kinderheilkunde. 145(8). 845–849. 1 indexed citations
16.
Sonntag, Josef, et al.. (1997). Akutes und chronisches fetofetales Transfusionssyndrom. Klinische Pädiatrie. 209(5). 321–327. 2 indexed citations
17.
18.
Sonntag, Josef, et al.. (1996). Morbidity and mortality of discordant twins up to 34 weeks of gestational age. European Journal of Pediatrics. 155(3). 224–229. 41 indexed citations
19.
Doose, Hermann, et al.. (1995). Parental generalized EEG alpha activity predisposes to spike wave discharges in offspring. Human Genetics. 96(6). 695–704. 7 indexed citations
20.
Waltz, Stephan, H.‐J. Christen, & H. Doose. (1992). The different patterns of the photoparoxysmal response — a genetic study. Electroencephalography and Clinical Neurophysiology. 83(2). 138–145. 171 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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