Astrid Eisenkölbl

1.2k total citations
8 papers, 27 citations indexed

About

Astrid Eisenkölbl is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Astrid Eisenkölbl has authored 8 papers receiving a total of 27 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Surgery, 2 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Astrid Eisenkölbl's work include Multiple Sclerosis Research Studies (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Congenital Anomalies and Fetal Surgery (2 papers). Astrid Eisenkölbl is often cited by papers focused on Multiple Sclerosis Research Studies (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Congenital Anomalies and Fetal Surgery (2 papers). Astrid Eisenkölbl collaborates with scholars based in Austria, Germany and Canada. Astrid Eisenkölbl's co-authors include Dieter Furthner, Ariane Biebl, Klaus Schmitt, Evelyn Lechner, Gudrun Gröppel, Christian Lechner, Markus Reindl, José Machado, Kevin Rostásy and Adi Klein and has published in prestigious journals such as Neuromuscular Disorders, Pediatric Neurology and Neuropediatrics.

In The Last Decade

Astrid Eisenkölbl

6 papers receiving 25 citations

Peers

Astrid Eisenkölbl

NEURO

SURGE

OTORH

GENET

PFM

Dorte Bechtold Denmark

L. Castillo United States

E. Sesenna Italy

Kenneth R. Fretwell United States

Ruba Kiwan Canada

A. Timochenko France

Alyssa K. Ovaitt United States

Tine Boiy Belgium

Kévin Janot France

Caroline Prégardien Belgium

Dorte Bechtold Denmark

Astrid Eisenkölbl

6 ×0.3

NEURO

8 ×0.6

SURGE

7 ×0.7

OTORH

3 ×0.8

GENET

3 ×0.8

PFM

Citations per year, relative to Astrid Eisenkölbl Astrid Eisenkölbl (= 1×) peers Dorte Bechtold

Countries citing papers authored by Astrid Eisenkölbl

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Eisenkölbl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Eisenkölbl

This figure shows the co-authorship network connecting the top 25 collaborators of Astrid Eisenkölbl. A scholar is included among the top collaborators of Astrid Eisenkölbl 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 Astrid Eisenkölbl. Astrid Eisenkölbl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Eisenkölbl, Astrid, et al.. (2025). Congenital-onset MLASA2 from a novel YARS2 variant: A literature review. Journal of Neuromuscular Diseases. 708676363–708676363.

2.

Machado, José, et al.. (2025). 559PThromboembolic events in myotonic dystrophy type 1 patients – a case series. Neuromuscular Disorders. 53. 105809–105809.

3.

Lechner, Christian, Markus Breu, Mareike Schimmel, et al.. (2024). Blood parameters in pediatric myelin oligodendrocyte glycoprotein antibody-associated disorders. European Journal of Paediatric Neurology. 50. 86–95. 2 indexed citations

4.

Eisenkölbl, Astrid, et al.. (2024). Repeated AAV9 Titer Determination in a Presymptomatic SMA Patient with Three SMN2 Gene Copies – A Case Report. Journal of Neuromuscular Diseases. 11(2). 493–498. 3 indexed citations

5.

Eisenkölbl, Astrid, et al.. (2023). Expanding the phenotype of RBCK1-associated polyglucosan body myopathy type 1. Molecular Genetics and Metabolism Reports. 38. 101031–101031. 2 indexed citations

6.

Eisenkölbl, Astrid. (2021). Neue Therapiemöglichkeiten der spinalen Muskelatrophie. Pädiatrie & Pädologie. 56(2). 59–66. 3 indexed citations

7.

Peternell, A., Markus Breu, Mareike Schimmel, et al.. (2021). Blood Parameter Analysis in Pediatric MOG-Antibody-Associated Disorders. Neuropediatrics. 1 indexed citations

8.

Biebl, Ariane, et al.. (2013). Facial Nerve Paralysis in Children: Is It as Benign as Supposed?. Pediatric Neurology. 49(3). 178–181. 16 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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