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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents 2022 ·Neuropediatrics ·(unknown), Kevin Rostásy, Ronny Wickström, (unknown), Stefano Sartori, Margherita Nosadini, Ellen Knierim, Gerhard Kluger, Rudolf Korinthenberg, (unknown), Stephan Waltz, Steffen Leiz, Martin Häusler	1
2	Impaired mitochondrial maturation of sulfite oxidase in a patient with severe sulfite oxidase deficiency 2019 ·Human Molecular Genetics ·Daniel A. Bender, (unknown), José Angel Santamaria‐Araujo, (unknown), Stephan Waltz, Deniz Bartsch, Leo Kurian, Sebahattin Çırak, Günter Schwarz	21
3	Early vibration assisted physiotherapy in toddlers with cerebral palsy - a randomized controlled pilot trial. 2016 ·PubMed ·Christina Stark, Peter Herkenrath, (unknown), Stephan Waltz, Ingrid Becker, (unknown), Oliver Semler, Heike Hoyer‐Kuhn, İbrahim Duran, Barbara Hero, Mijna Hadders‐Algra, Eckhard Schöenau	20
4	Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy 2015 ·Brain ·Kerstin Hallmann, Alexei P. Kudin, Gábor Zsurka, Cornelia Kornblum, Jens Reimann, (unknown), Stephan Waltz, Elke Hattingen, Hölger Thiele, Peter Nürnberg, Cornelia Rüb, Wolfgang Voos, Jens Kopatz, Harald Neumann, Wolfram S. Kunz	47
5	Intervallrehabilitation mit häuslichem Training bei Kindern mit Zerebralparese 2013 ·Monatsschrift Kinderheilkunde ·Christina Stark, Oliver Semler, İbrahim Duran, Angelika Stabrey, (unknown), Peter Herkenrath, (unknown), Stephan Waltz, Eckhard Schönaü	6
6	Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families 2008 ·Movement Disorders ·Hiltrud Muhle, Anja Neumann, K. Lohmann-Hedrich, Thora Lohnau, Yang Lü, Susen Winkler, Stephan Waltz, (unknown), Patricia L. Kramer, Christine Klein, Ulrich Stephani	52
7	Photosensitivity in epileptic syndromes of childhood and adolescence 2008 ·Epileptic Disorders ·Lu Yang, Stephan Waltz, (unknown), Hiltrud Muhle, Ulrich Stephani	58
8	Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy 2005 ·Annals of Neurology ·Ulrike Tauer, Susanne Lorenz, Kirsten P. Lenzen, Armin Heils, Hiltrud Muhle, (unknown), Bernd A. Neubauer, Stephan Waltz, Gabrielle Rudolf, Manuel Mattheisen, Konstantin Strauch, Peter Nürnberg, Bettina Schmitz, Ulrich Stephani, Thomas Sander	65
9	Inheritance of Photosensitivity 2000 ·Neuropediatrics ·Stephan Waltz, Ulrich Stephani	53
10	Photic stimulation — standardization of screening methods 1999 ·Neurophysiologie Clinique ·Dorothée Kasteleijn‐Nolst Trenité, C.D. Binnie, G. F. A. Harding, Arnold J. Wilkins, (unknown), Orvar Eeg‐Olofsson, (unknown), Olaf Henriksen, Günter Krämer, (unknown), (unknown), (unknown), R Naquet, B. Pedersen, Stefano Ricci, Guido Rubboli, Henk Spekreijse, Stephan Waltz	39
11	Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures 1998 ·Neuropediatrics ·H. Doose, (unknown), (unknown), Stephan Waltz	45
12	Neuroborreliosis and isolated trochlear palsy 1998 ·European Journal of Paediatric Neurology ·Dominik N. Müller, Bernd A. Neubauer, Stephan Waltz, Ulrich Stephani	11
13	Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient 1997 ·Clinical Genetics ·Almuth Caliebe, Stephan Waltz, J. Jenderny	27
14	Benign Childhood Epilepsy with Centrotemporal Spikes and Electroencephalography Trait are Not Linked to EBN1 and EBN2 of Benign Neonatal Familial Convulsions 1997 ·Epilepsia ·Bernd A. Neubauer, Hans W. Moises, (unknown), Stephan Waltz, (unknown), Ulrich Stephani	18
15	Epileptische Anfälle bei Bildschirmspielen 1997 ·Monatsschrift Kinderheilkunde ·Stephan Waltz, Andreas Hahn, Ulrich Stephani	1
16	Akutes und chronisches fetofetales Transfusionssyndrom 1997 ·Klinische Pädiatrie ·Josef Sonntag, Thoralf Schollmeyer, Stephan Waltz, (unknown), (unknown), (unknown)	2
17	Serum creatinine concentration, urinary creatinine excretion and creatinine clearance during the first 9 weeks in preterm infants with a birth weight below 1500 g 1996 ·European Journal of Pediatrics ·Josef Sonntag, (unknown), Stephan Waltz	84
18	Morbidity and mortality of discordant twins up to 34 weeks of gestational age 1996 ·European Journal of Pediatrics ·(unknown), Josef Sonntag, Stephan Waltz, Thoralf Schollmeyer, (unknown), D. Weisner	41
19	Parental generalized EEG alpha activity predisposes to spike wave discharges in offspring 1995 ·Human Genetics ·Hermann Doose, (unknown), Stephan Waltz	7
20	The different patterns of the photoparoxysmal response — a genetic study 1992 ·Electroencephalography and Clinical Neurophysiology ·Stephan Waltz, H.‐J. Christen, H. Doose	171

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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