Astrid Blaschek

5.5k total citations
74 papers, 1.7k citations indexed

About

Astrid Blaschek is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Astrid Blaschek has authored 74 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 23 papers in Pathology and Forensic Medicine and 18 papers in Genetics. Recurrent topics in Astrid Blaschek's work include Multiple Sclerosis Research Studies (20 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Peripheral Neuropathies and Disorders (9 papers). Astrid Blaschek is often cited by papers focused on Multiple Sclerosis Research Studies (20 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Peripheral Neuropathies and Disorders (9 papers). Astrid Blaschek collaborates with scholars based in Germany, Austria and United States. Astrid Blaschek's co-authors include Florian Heinen, Wolfgang Müller‐Felber, Andreas Straube, Katharina Vill, Rüdiger von Kries, Kevin Rostásy, Astrid Milde‐Busch, Ingo Borggräfe, Heike Kölbel and Inga K. Koerte and has published in prestigious journals such as Brain, Neurology and Diabetes Care.

In The Last Decade

Astrid Blaschek

69 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Astrid Blaschek Germany 24 762 598 388 356 348 74 1.7k
B. Mamoli Austria 23 418 0.5× 723 1.2× 247 0.6× 266 0.7× 143 0.4× 113 1.7k
Nancy L. Kuntz United States 28 794 1.0× 1.9k 3.1× 740 1.9× 90 0.3× 521 1.5× 102 3.5k
Suketaka Momoshima Japan 27 1.1k 1.4× 361 0.6× 294 0.8× 144 0.4× 186 0.5× 68 2.6k
Pierre Labauge France 23 506 0.7× 1.2k 1.9× 716 1.8× 190 0.5× 100 0.3× 119 2.4k
Frank Vandenabeele Belgium 20 391 0.5× 121 0.2× 480 1.2× 122 0.3× 300 0.9× 55 1.7k
Laura Papetti Italy 21 320 0.4× 426 0.7× 269 0.7× 720 2.0× 139 0.4× 106 1.6k
Gianni Boris Bradač Italy 27 269 0.4× 1.1k 1.8× 192 0.5× 113 0.3× 305 0.9× 145 2.2k
Lori Billinghurst United States 18 136 0.2× 441 0.7× 598 1.5× 472 1.3× 275 0.8× 26 2.3k
Arjun V. Pendharkar United States 21 252 0.3× 404 0.7× 157 0.4× 170 0.5× 274 0.8× 93 1.5k
Jean‐Philippe Neau France 21 238 0.3× 548 0.9× 106 0.3× 142 0.4× 116 0.3× 79 1.5k

Countries citing papers authored by Astrid Blaschek

Since Specialization
Citations

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

Fields of papers citing papers by Astrid Blaschek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Blaschek

This figure shows the co-authorship network connecting the top 25 collaborators of Astrid Blaschek. A scholar is included among the top collaborators of Astrid Blaschek 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 Blaschek. Astrid Blaschek 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.
Breu, Markus, Ruxandra‐Iulia Milos, J Svoboda, et al.. (2024). Rituximab treatment in pediatric‐onset multiple sclerosis. European Journal of Neurology. 31(5). e16228–e16228. 12 indexed citations
2.
Saffari, Afshin, Claire Cannet, Astrid Blaschek, et al.. (2024). Identification of Biochemical Determinants for Diagnosis and Prediction of Severity in 5q Spinal Muscular Atrophy Using 1H-Nuclear Magnetic Resonance Metabolic Profiling in Patient-Derived Biofluids. International Journal of Molecular Sciences. 25(22). 12123–12123. 2 indexed citations
3.
Schönberg, Nils, David R. Howell, Johanna Wagner, et al.. (2024). Instrumented Balance Error Scoring System in Children and Adolescents—A Cross Sectional Study. Diagnostics. 14(5). 513–513. 1 indexed citations
4.
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
5.
Kölbel, Heike, Astrid Blaschek, Ulrike Schara‐Schmidt, et al.. (2023). P206 Impaired neurodevelopment in children with 5q-SMA - 2 years after newborn screening. Neuromuscular Disorders. 33. S86–S86. 1 indexed citations
6.
Marina, Adela Della, Marina Flotats‐Bastardas, Felix Distelmaier, et al.. (2022). Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initially. European Journal of Paediatric Neurology. 41. 27–35. 6 indexed citations
7.
Kölbel, Heike, Katharina Vill, Oliver Schwartz, et al.. (2021). Neugeborenenscreeningprogramm für die spinale Muskelatrophie. Der Nervenarzt. 93(2). 135–141. 2 indexed citations
8.
Müller‐Felber, Wolfgang, Katharina Vill, Oliver Schwartz, et al.. (2020). Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening – Opportunity or Burden?. Journal of Neuromuscular Diseases. 7(2). 109–117. 42 indexed citations
9.
Zech, Michael, Theresa Brunet, Matěj Škorvánek, et al.. (2020). Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia. Parkinsonism & Related Disorders. 77. 70–75. 4 indexed citations
10.
Oertel, Frederike Cosima, Olivier Outteryck, Benjamin Knier, et al.. (2019). Optical coherence tomography in myelin-oligodendrocyte-glycoprotein antibody-seropositive patients: a longitudinal study. Journal of Neuroinflammation. 16(1). 154–154. 44 indexed citations
11.
Vill, Katharina, Heike Kölbel, Oliver Schwartz, et al.. (2019). One Year of Newborn Screening for SMA – Results of a German Pilot Project. Journal of Neuromuscular Diseases. 6(4). 503–515. 108 indexed citations
12.
Vill, Katharina, Wolfgang Müller‐Felber, Dieter Gläser, et al.. (2018). SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy. Human Genetics. 137(11-12). 911–919. 15 indexed citations
13.
Milos, Ruxandra‐Iulia, Fritz Leutmezer, Kevin Rostásy, et al.. (2018). Clinical and magnetic resonance imaging features of children, adolescents, and adults with a clinically isolated syndrome. European Journal of Paediatric Neurology. 22(6). 1087–1094. 2 indexed citations
14.
Vill, Katharina, Astrid Blaschek, Ulrike Schara, et al.. (2017). Spinale Muskelatrophie: Zeit für das Neugeborenenscreening?. Der Nervenarzt. 3 indexed citations
15.
Vill, Katharina, Wolfgang Müller‐Felber, Veronika Teusch, et al.. (2016). Proximal muscular atrophy and weakness: An unusual adverse effect of deferasirox iron chelation therapy. Neuromuscular Disorders. 26(4-5). 322–325. 4 indexed citations
16.
Vill, Katharina, Joachim Schessl, Veronika Teusch, et al.. (2014). Muscle ultrasound in classic infantile and adult Pompe disease: A useful screening tool in adults but not in infants. Neuromuscular Disorders. 25(2). 120–126. 25 indexed citations
17.
Gallenmüller, Constanze, Wolfgang Müller‐Felber, Marina Dusl, et al.. (2013). Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK. Neuromuscular Disorders. 24(1). 31–35. 47 indexed citations
18.
Kornek, Barbara, Fahmy Aboul‐Enein, Kevin Rostásy, et al.. (2013). Natalizumab Therapy for Highly Active Pediatric Multiple Sclerosis. JAMA Neurology. 70(4). 469–469. 58 indexed citations
19.
Goebel, Hans H. & Astrid Blaschek. (2011). Protein Aggregation in Congenital Myopathies. Seminars in Pediatric Neurology. 18(4). 272–276. 13 indexed citations
20.
Milde‐Busch, Astrid, Astrid Blaschek, Ingo Borggräfe, et al.. (2010). Besteht ein Zusammenhang zwischen der verkürzten Gymnasialzeit und Kopfschmerzen und gesundheitlichen Belastungen bei Schülern im Jugendalter?. Klinische Pädiatrie. 222(4). 255–260. 24 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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