S Vlaho

856 total citations
24 papers, 513 citations indexed

About

S Vlaho is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, S Vlaho has authored 24 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in S Vlaho's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Amino Acid Enzymes and Metabolism (2 papers). S Vlaho is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Amino Acid Enzymes and Metabolism (2 papers). S Vlaho collaborates with scholars based in Germany, United States and Austria. S Vlaho's co-authors include Boris Gebhardt, Matthias Kieslich, Hansjosef Böhles, Franziska Hoche, Ralf Schubert, Stefan Zielen, Christian G. Bien, Kay Seidel, Luciana Porto and Doris Fischer and has published in prestigious journals such as Neurology, Gene and Epilepsia.

In The Last Decade

S Vlaho

20 papers receiving 507 citations

Peers

S Vlaho
Ewa Jamroz Poland
Gözde Yeşil Türkiye
Geetha Anand United Kingdom
Marios Kaliakatsos United Kingdom
Ewa Jamroz Poland
S Vlaho
Citations per year, relative to S Vlaho S Vlaho (= 1×) peers Ewa Jamroz

Countries citing papers authored by S Vlaho

Since Specialization
Citations

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

Fields of papers citing papers by S Vlaho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Vlaho

This figure shows the co-authorship network connecting the top 25 collaborators of S Vlaho. A scholar is included among the top collaborators of S Vlaho 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 S Vlaho. S Vlaho 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.
Kiefer, Alexander, Andreas Ambrosch, Benedikt Lampl, et al.. (2025). Timely Association of RSV Hospitalisation Waves in Children with the Detection of SARS-CoV-2 in the General Population in Eastern Bavaria. Viruses. 17(12). 1584–1584.
3.
Becker, Johanna Sabine, Nikolaus Haas, S Vlaho, et al.. (2021). Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Cause of Hypoglycemia-Induced Seizure and Death. Neuropediatrics. 52(5). 398–402. 7 indexed citations
4.
Schulz, Andrea, et al.. (2021). Focal Epilepsy as the First Clinical Manifestation of NCL2 without Dementia. Neuropediatrics.
7.
Balint, Bettina, Jürgen Haas, Alexander Schwarz, et al.. (2013). T-cell homeostasis in pediatric multiple sclerosis. Neurology. 81(9). 784–792. 56 indexed citations
8.
Bien, Christian G., Henning Tiemeier, Robert Sassen, et al.. (2012). Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins. Epilepsia. 54(3). 543–550. 106 indexed citations
9.
Vlaho, S, et al.. (2012). Encephalopathy and sinustachycardia in childhood a possible differential diagnosis. Journal of Pediatric Endocrinology and Metabolism. 25(1-2). 149–51. 5 indexed citations
10.
Hoche, Franziska, et al.. (2012). Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention. Neuropediatrics. 43(2). 1 indexed citations
11.
Hoche, Franziska, Kay Seidel, S Vlaho, et al.. (2012). Neurodegeneration in Ataxia Telangiectasia: What Is New? What Is Evident?. Neuropediatrics. 43(3). 119–129. 67 indexed citations
12.
Hoche, Franziska, Sabine Pfeifenbring, S Vlaho, et al.. (2011). Rare brain biopsy findings in a first ADEM-like event of pediatric MS: histopathologic, neuroradiologic and clinical features. Journal of Neural Transmission. 118(9). 1311–1317. 6 indexed citations
13.
Wittekindt, Boris, Annemarie Berger, Luciana Porto, et al.. (2009). Human herpes virus‐6 DNA in cerebrospinal fluid of children undergoing therapy for acute leukaemia. British Journal of Haematology. 145(4). 542–545. 13 indexed citations
14.
Kieslich, Matthias, Franziska Hoche, Janine Reichenbach, et al.. (2009). Extracerebellar MRI—Lesions in Ataxia Telangiectasia Go Along with Deficiency of the GH/IGF-1 Axis, Markedly Reduced Body Weight, High Ataxia Scores and Advanced Age. The Cerebellum. 9(2). 190–197. 32 indexed citations
15.
Porto, Luciana, Matthias Kieslich, Kea Franz, et al.. (2009). Spectroscopy of untreated pilocytic astrocytomas: do children and adults share some metabolic features in addition to their morphologic similarities?. Child s Nervous System. 26(6). 801–806. 16 indexed citations
16.
Vlaho, S, Luciana Porto, Elke Hattingen, et al.. (2007). Differenzialdiagnostische Abgrenzung Enzephalitis versus Gliom mittels Magnetresonanzspektroskopie. Klinische Pädiatrie. 219(4). 222–224. 3 indexed citations
17.
Gebhardt, Boris, et al.. (2005). N‐Carbamylglutamate protects patients with decompensated propionicaciduria from hyperammonaemia. Journal of Inherited Metabolic Disease. 28(2). 241–244. 52 indexed citations
18.
Vlaho, S, Boris Gebhardt, Rüdiger Gerlach, Stephan Weidauer, & Matthias Kieslich. (2003). Cyst of the third ventricle as an unusual cause of acquired hydrocephalus. Pediatric Neurology. 28(3). 225–227. 14 indexed citations
19.
Gebhardt, Boris, S Vlaho, Doris Fischer, A Sewell, & Hansjosef Böhles. (2003). N-carbamylglutamate enhances ammonia detoxification in a patient with decompensated methylmalonic aciduria. Molecular Genetics and Metabolism. 79(4). 303–304. 39 indexed citations
20.
Kieslich, Matthias, et al.. (2002). Midline Developmental Anomalies in Down Syndrome. Journal of Child Neurology. 17(6). 460–462. 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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