Michaela Brunner‐Krainz

1.1k total citations
22 papers, 393 citations indexed

About

Michaela Brunner‐Krainz is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michaela Brunner‐Krainz has authored 22 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michaela Brunner‐Krainz's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Biochemical and Molecular Research (3 papers). Michaela Brunner‐Krainz is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Biochemical and Molecular Research (3 papers). Michaela Brunner‐Krainz collaborates with scholars based in Austria, Switzerland and Germany. Michaela Brunner‐Krainz's co-authors include Barbara Plecko, Kevin Rostásy, Dorothea Möslinger, Sabine Scholl‐Bürgi, Wolfgang Sperl, Daniela Karall, Oskar Maier, Viktoria Gredler, Thomas Berger and Giorgi Kuchukhidze and has published in prestigious journals such as Oxidative Medicine and Cellular Longevity, Journal of Neurology and Multiple Sclerosis Journal.

In The Last Decade

Michaela Brunner‐Krainz

20 papers receiving 388 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Michaela Brunner‐Krainz Austria 10 147 146 129 112 89 22 393
Deborah L. Renaud United States 11 233 1.6× 180 1.2× 88 0.7× 14 0.1× 42 0.5× 41 470
BN Harding United Kingdom 9 178 1.2× 46 0.3× 120 0.9× 69 0.6× 58 0.7× 12 402
Khalid Al‐Thihli Oman 13 219 1.5× 19 0.1× 135 1.0× 37 0.3× 50 0.6× 50 456
A. Al‐Memar United Kingdom 9 138 0.9× 106 0.7× 29 0.2× 13 0.1× 29 0.3× 13 336
J.M.F. Niermeijer Netherlands 8 66 0.4× 158 1.1× 81 0.6× 13 0.1× 31 0.3× 13 336
Ahmed Alfares Saudi Arabia 11 234 1.6× 16 0.1× 108 0.8× 36 0.3× 46 0.5× 38 474
Marwan Nashabat Saudi Arabia 13 229 1.6× 53 0.4× 130 1.0× 8 0.1× 66 0.7× 25 422
Guazzi Gc Italy 12 158 1.1× 72 0.5× 40 0.3× 29 0.3× 41 0.5× 58 359
Sarah Macklin United States 9 176 1.2× 17 0.1× 121 0.9× 33 0.3× 39 0.4× 21 423
Patrick A. Lundquist United States 8 130 0.9× 29 0.2× 20 0.2× 42 0.4× 40 0.4× 16 440

Countries citing papers authored by Michaela Brunner‐Krainz

Since Specialization
Citations

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

Fields of papers citing papers by Michaela Brunner‐Krainz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michaela Brunner‐Krainz. 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 Michaela Brunner‐Krainz. The network helps show where Michaela Brunner‐Krainz may publish in the future.

Co-authorship network of co-authors of Michaela Brunner‐Krainz

This figure shows the co-authorship network connecting the top 25 collaborators of Michaela Brunner‐Krainz. A scholar is included among the top collaborators of Michaela Brunner‐Krainz 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 Michaela Brunner‐Krainz. Michaela Brunner‐Krainz 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.
Herle, Marion, Michaela Brunner‐Krainz, Daniela Karall, et al.. (2021). A retrospective study on disease management in children and adolescents with phenylketonuria during the Covid-19 pandemic lockdown in Austria. Orphanet Journal of Rare Diseases. 16(1). 367–367. 4 indexed citations
2.
Beghini, Marianna, Dorothea Möslinger, Vassiliki Konstantopoulou, et al.. (2021). Project “Backtoclinic I”: An overview on the state of care of adult PKU patients in Austria. Molecular Genetics and Metabolism. 133(3). 257–260. 9 indexed citations
3.
Brunner‐Krainz, Michaela, Gérard Cortina, René G. Feichtinger, et al.. (2018). Severe Deoxyguanosine Kinase Deficiency in Austria. Journal of Pediatric Gastroenterology and Nutrition. 68(1). e1–e6. 11 indexed citations
4.
Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations
5.
Löscher, Wolfgang N., Martina Huemer, Thomas M. Stulnig, et al.. (2017). Pompe disease in Austria: clinical, genetic and epidemiological aspects. Journal of Neurology. 265(1). 159–164. 27 indexed citations
6.
Fabian, Elisabeth, Hermann Toplak, Michaela Brunner‐Krainz, et al.. (2017). Clinical-Pathological Conference Series from the Medical University of Graz. Wiener klinische Wochenschrift. 130(3-4). 151–160. 4 indexed citations
7.
Haberlandt, Edda, U Gruber‐Sedlmayr, Barbara Plecko, et al.. (2016). Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitis. European Journal of Paediatric Neurology. 21(3). 457–464. 29 indexed citations
8.
Behrens, R., et al.. (2015). Konsensus zur Ernährung in der pädiatrischen Palliativmedizin. Monatsschrift Kinderheilkunde. 163(9). 928–933. 1 indexed citations
9.
Karall, Daniela, Michaela Brunner‐Krainz, Vassiliki Konstantopoulou, et al.. (2015). Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD). Orphanet Journal of Rare Diseases. 10(1). 21–21. 43 indexed citations
10.
Strickland, Alleene V., Maria Schabhüttl, H. Offenbacher, et al.. (2015). Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1. Journal of Neurology. 262(9). 2124–2134. 49 indexed citations
11.
Behrens, R., et al.. (2015). Leitlinien zur Ernährung in der pädiatrischen Palliativmedizin. Pädiatrie & Pädologie. 50(S1). 4–24. 1 indexed citations
12.
Schwinger, Wolfgang, Petra Sovinz, Martin Benesch, et al.. (2014). Unrelated CD3/CD19-Depleted Peripheral Stem Cell Transplantation for Hurler Syndrome. Pediatric Hematology and Oncology. 31(8). 723–730. 2 indexed citations
13.
Paschke, Eduard, Johannes Zschocke, Michaela Brunner‐Krainz, et al.. (2012). Prevalence of tetrahydrobiopterine (BH4)‐responsive alleles among Austrian patients with PAH deficiency: comprehensive results from molecular analysis in 147 patients. Journal of Inherited Metabolic Disease. 36(1). 7–13. 18 indexed citations
14.
Rostásy, Kevin, Simone Mader, Kathrin Schanda, et al.. (2012). Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica. Multiple Sclerosis Journal. 19(8). 1052–1059. 117 indexed citations
15.
Brunner‐Krainz, Michaela, et al.. (2011). Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients. Neuropediatrics. 42(S 01). 1 indexed citations
16.
Haberlandt, Edda, Michaela Brunner‐Krainz, Dorothea Möslinger, et al.. (2009). Epilepsy in Patients with Propionic Acidemia. Neuropediatrics. 40(3). 120–125. 25 indexed citations
17.
Deutsch, J., et al.. (2006). Copper concentration of liver tissue under long‐term copper‐histidine therapy in a patient with Menkes disease. Journal of Inherited Metabolic Disease. 29(4). 593–593. 2 indexed citations
18.
19.
Brunner‐Krainz, Michaela, U Gruber‐Sedlmayr, Werner Zenz, Josef Simbrunner, & Barbara Plecko. (2004). Diagnostic findings in acute encephalitis. Neuropediatrics. 35(1).
20.
Sass, Jörn Oliver, Daniela Skladal, & Michaela Brunner‐Krainz. (1999). Normal Ascorbic Acid in Cerebrospinal Fluid of Patients with Infantile Neuronal Ceroid-Lipofuscinosis. Metabolic Brain Disease. 14(1). 67–70. 3 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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