Burkhard Simma

1.3k total citations
36 papers, 765 citations indexed

About

Burkhard Simma is a scholar working on Genetics, Neurology and Physiology. According to data from OpenAlex, Burkhard Simma has authored 36 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Neurology and 6 papers in Physiology. Recurrent topics in Burkhard Simma's work include Diabetes Management and Research (5 papers), Diabetes and associated disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Burkhard Simma is often cited by papers focused on Diabetes Management and Research (5 papers), Diabetes and associated disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Burkhard Simma collaborates with scholars based in Austria, United States and Germany. Burkhard Simma's co-authors include R. Burger, Peter Sacher, Sergio Fanconi, Markus Falk, Helmut Ellemunter, Rudolf Trawöger, Martina Huemer, Thomas Müller, Hanno Ulmer and Alfred Königsrainer and has published in prestigious journals such as The Lancet, Critical Care Medicine and The Journal of Pediatrics.

In The Last Decade

Burkhard Simma

36 papers receiving 705 citations

Peers

Burkhard Simma
D. Bohn United States
J. Matthew Lacy United States
Akira Kurokawa Japan
Glenn Neil-Dwyer United Kingdom
José Quero Spain
Matthew B. Wallenstein United States
J Kyttä Finland
Joseph D. Burns United States
John F. Valente United States
Alejandro Forteza United States
D. Bohn United States
Burkhard Simma
Citations per year, relative to Burkhard Simma Burkhard Simma (= 1×) peers D. Bohn

Countries citing papers authored by Burkhard Simma

Since Specialization
Citations

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

Fields of papers citing papers by Burkhard Simma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Burkhard Simma

This figure shows the co-authorship network connecting the top 25 collaborators of Burkhard Simma. A scholar is included among the top collaborators of Burkhard Simma 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 Burkhard Simma. Burkhard Simma 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.
Kerbl, Reinhold, et al.. (2022). SARS-CoV-2-Seroprävalenz in Österreich. Die Situation vor der Omikronwelle. Monatsschrift Kinderheilkunde. 170(6). 487–489. 3 indexed citations
2.
Simma, Burkhard, et al.. (2018). Adherence to Guidelines in the Treatment of Diabetic Ketoacidosis in Children. Pediatric Emergency Care. 37(5). 245–249. 3 indexed citations
3.
4.
Biebl, Ariane, Axel Muendlein, Heinz Drexel, et al.. (2015). Confirmation of Host Genetic Determinants in the CFH Region and Susceptibility to Meningococcal Disease in a Central European Study Sample. The Pediatric Infectious Disease Journal. 34(10). 1115–1117. 7 indexed citations
5.
Fuchs, Martin, et al.. (2015). Cross-sectional study to evaluate the longitudinal development of child and adolescent psychiatric diagnoses of inpatients in Vorarlberg, Austria. European Journal of Pediatrics. 175(2). 221–228. 1 indexed citations
6.
Revençu, Nicole, Birgit Krabichler, Véronique Beauloye, et al.. (2013). Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22. American Journal of Medical Genetics Part A. 161(12). 3176–3181. 17 indexed citations
7.
Schober, Hans‐Christof, et al.. (2012). Central nervous system Lyme disease - Presentation of two cases. Neuropediatrics. 43(2). 1 indexed citations
8.
Huemer, Martina, Burkhard Simma, Adolf Mühl, et al.. (2010). Low Levels of Asymmetric Dimethylarginine in Children with Diabetes Mellitus Type I Compared with Healthy Children. The Journal of Pediatrics. 158(4). 602–606.e1. 17 indexed citations
9.
Patch, Ann‐Marie, et al.. (2009). Neonatal diabetes mellitus due to pancreas agenesis: a new case report and review of the literature. Pediatric Diabetes. 10(7). 487–491. 7 indexed citations
10.
Simma, Burkhard, et al.. (2007). Risk Factors for Pediatric Stroke: Consequences for Therapy and Quality of Life. Pediatric Neurology. 37(2). 121–126. 39 indexed citations
11.
Huemer, Martina, et al.. (2005). Hyperhomocysteinemia in Children Treated with Antiepileptic Drugs Is Normalized by Folic Acid Supplementation. Epilepsia. 46(10). 1677–1683. 56 indexed citations
12.
Kapelari, Klaus, Andreas Heitger, Alfred Königsrainer, et al.. (2005). Loss of intrahepatic bile ducts: an important feature of familial hemophagocytic lymphohistiocytosis. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 446(6). 619–625. 8 indexed citations
13.
Biebl, Ariane, Christian Bernhard, Martin Frühwirth, et al.. (2005). Vaccine strategies of meningococcal disease: results of a 10-year population-based study. European Journal of Pediatrics. 164(12). 735–740. 6 indexed citations
14.
Janecke, Andreas, Susanne Dertinger, Uwe‐Peter Ketelsen, et al.. (2004). Neonatal type IV glycogen storage disease associated with “null” mutations in glycogen branching enzyme 1. The Journal of Pediatrics. 145(5). 705–709. 27 indexed citations
15.
Frühwirth, Martin, Andreas Janecke, Thomas Müller, et al.. (2003). Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome. The Journal of Pediatrics. 142(4). 441–447. 13 indexed citations
16.
Petek, Erwin, Christian Windpassinger, Burkhard Simma, et al.. (2003). Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. Journal of Human Genetics. 48(6). 283–287. 18 indexed citations
17.
Frühwirth, Martin, Harald E. Fischer, Burkhard Simma, et al.. (2001). Rotavirus infection as cause of tacrolimus elevation in solid‐organ‐transplanted children. Pediatric Transplantation. 5(2). 88–92. 28 indexed citations
18.
19.
Simma, Burkhard, R. Burger, Markus Falk, Peter Sacher, & Sergio Fanconi. (1998). A prospective, randomized, and controlled study of fluid management in children with severe head injury. Critical Care Medicine. 26(7). 1265–1270. 257 indexed citations
20.
Simma, Burkhard, Wolfgang Sperl, & I Hammerer. (1990). GM1 Gangliosidose und dilatative Cardiomyopathie. Klinische Pädiatrie. 202(3). 183–185. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by D. Bohn Breakdown of academic impact, for papers by J. Matthew Lacy Breakdown of academic impact, for papers by Akira Kurokawa Breakdown of academic impact, for papers by Glenn Neil-Dwyer Breakdown of academic impact, for papers by José Quero Breakdown of academic impact, for papers by Matthew B. Wallenstein Breakdown of academic impact, for papers by J Kyttä Breakdown of academic impact, for papers by Joseph D. Burns Breakdown of academic impact, for papers by John F. Valente Breakdown of academic impact, for papers by Alejandro Forteza
Rankless by CCL
2026