Steffen Leiz

2.6k total citations
24 papers, 586 citations indexed

About

Steffen Leiz is a scholar working on Neurology, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Steffen Leiz has authored 24 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Neurology, 7 papers in Psychiatry and Mental health and 5 papers in Molecular Biology. Recurrent topics in Steffen Leiz's work include Epilepsy research and treatment (6 papers), Peripheral Neuropathies and Disorders (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Steffen Leiz is often cited by papers focused on Epilepsy research and treatment (6 papers), Peripheral Neuropathies and Disorders (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Steffen Leiz collaborates with scholars based in Germany, Austria and United States. Steffen Leiz's co-authors include Kevin Rostásy, Gerhard Kluger, Markus Reindl, Michael Karenfort, M. Steinborn, Rainer Seidl, Jutta Gärtner, Peter Huppke, Martin Griebel and Brenda Huppke and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Steffen Leiz

22 papers receiving 573 citations

Peers

Steffen Leiz

PMH

NEURO

PPCH

CMN

PFM

Reghann G. LaFrance‐Corey United States

Hiroyuki Torisu Japan

Melinda Nolan Australia

B. Dalla Bernardina Italy

Ichiro Kuki Japan

Juan José Garcı́a-Peñas Spain

Nobutsune Ishikawa Japan

Michael Karenfort Germany

A. Mrabet Tunisia

Silvia Vieker Germany

Reghann G. LaFrance‐Corey United States

Steffen Leiz

237 ×1.0

PMH

172 ×1.2

NEURO

106 ×0.7

PPCH

140 ×1.1

CMN

153 ×1.2

PFM

Citations per year, relative to Steffen Leiz Steffen Leiz (= 1×) peers Reghann G. LaFrance‐Corey

Countries citing papers authored by Steffen Leiz

Since Specialization

Citations

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

Fields of papers citing papers by Steffen Leiz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steffen Leiz

This figure shows the co-authorship network connecting the top 25 collaborators of Steffen Leiz. A scholar is included among the top collaborators of Steffen Leiz 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 Steffen Leiz. Steffen Leiz 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

Giorgi, Laetitia, Eva‐Maria Wendel, Michael Karenfort, et al.. (2024). Long-term follow-up MR imaging in children with transverse myelitis. Multiple Sclerosis and Related Disorders. 92. 105926–105926.

Bartels, Frederik, Annette Aigner, Graham Cooper, et al.. (2023). Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Acute Disseminated Encephalomyelitis. Neurology Neuroimmunology & Neuroinflammation. 10(2). 4 indexed citations

Vogel, Florian, Martin Krenn, Dominik S. Westphal, et al.. (2022). A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype. Epilepsia. 63(4). e35–e41. 8 indexed citations

Paprocka, Justyna, Pınar Tektürk, Betül Baykan, et al.. (2022). Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review. Seizure. 116. 14–23. 2 indexed citations

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

Kostić, Marko, Essam A. Assali, Yael Amitai, et al.. (2021). Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Communications Biology. 4(1). 666–666. 33 indexed citations

Kostić, Marko, Essam A. Assali, Yael Amitai, et al.. (2021). Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Communications Biology. 4(1). 755–755. 2 indexed citations

Rakete, Stefan, et al.. (2021). Mercury poisoning of a 4-year-old child by indirect contact to a mercury-containing facial cream: A case report. SHILAP Revista de lepidopterología. 9. 2050313X211025227–2050313X211025227. 1 indexed citations

Borggraefe, Ingo, Moritz Tacke, Lucia Gerstl, et al.. (2019). Epilepsy surgery in the first months of life: a large type IIb focal cortical dysplasia causing neonatal drug‐resistant epilepsy. Epileptic Disorders. 21(1). 122–127. 2 indexed citations

10.

Heussen, N, Steffen Leiz, Tilman Polster, et al.. (2018). Impact of Hippotherapy on Gross Motor Function and Quality of Life in Children with Bilateral Cerebral Palsy: A Randomized Open-Label Crossover Study. Neuropediatrics. 49(3). 185–192. 33 indexed citations

11.

Tate, Elizabeth D., et al.. (2017). Rituximab, IVIg, and Tetracosactide (ACTH1–24) Combination Immunotherapy (“RITE-CI”) for Pediatric Opsoclonus-Myoclonus Syndrome: Immunomarkers and Clinical Observations. Neuropediatrics. 49(2). 123–134. 5 indexed citations

12.

Koch, J., Johannes A. Mayr, Benjamin J.S. al-Haddad, et al.. (2017). Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations. Neuropediatrics. 48(S 01). S1–S45. 1 indexed citations

13.

Shen, Dingding, Ciria C. Hernández, Wangzhen Shen, et al.. (2016). De novo GABRG2mutations associated with epileptic encephalopathies. Brain. 140(1). 49–67. 78 indexed citations

14.

Hennes, E., Matthias Baumann, Mareike Schimmel, et al.. (2016). Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children. Neuropediatrics. 47(S 01). 4 indexed citations

15.

Baethmann, Martina, et al.. (2015). Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy. Neuropediatrics. 46(S 01).

16.

Spiczak, Sarah von, Thomas Bast, Edda Haberlandt, et al.. (2011). A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome. Epilepsia. 52(1). 175–178. 44 indexed citations

17.

Stülpnagel, Celina von, Gerhard Kluger, Steffen Leiz, & Hans Holthausen. (2010). Levetiracetam as add-on therapy in different subgroups of “benign” idiopathic focal epilepsies in childhood. Epilepsy & Behavior. 17(2). 193–198. 23 indexed citations

18.

Leiz, Steffen & Gerhard Kluger. (2008). Malignant migrating partial seizures in infancy. Neuropediatrics. 39(1). 8 indexed citations

19.

Steinborn, M., et al.. (2004). CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: distribution of lesions and prognostic value of imaging findings. Pediatric Radiology. 34(10). 805–10. 69 indexed citations

20.

Weidenbach, H, Steffen Leiz, Andreas K. Nüssler, et al.. (2000). Disturbed bile secretion and cytochrome P-450 function during the acute state of experimental colitis in rats. Journal of Hepatology. 32(5). 708–717. 12 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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