Angela Abicht

4.9k total citations
124 papers, 2.1k citations indexed

About

Angela Abicht is a scholar working on Molecular Biology, Neurology and Cell Biology. According to data from OpenAlex, Angela Abicht has authored 124 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 41 papers in Neurology and 29 papers in Cell Biology. Recurrent topics in Angela Abicht's work include Myasthenia Gravis and Thymoma (38 papers), Mitochondrial Function and Pathology (28 papers) and Metabolism and Genetic Disorders (27 papers). Angela Abicht is often cited by papers focused on Myasthenia Gravis and Thymoma (38 papers), Mitochondrial Function and Pathology (28 papers) and Metabolism and Genetic Disorders (27 papers). Angela Abicht collaborates with scholars based in Germany, United Kingdom and Austria. Angela Abicht's co-authors include Hanns Lochmüller, Juliane S. Müller, Ulrike Schara, Rita Horváth, Elke Holinski‐Feder, Rolf Stucka, Angela Huebner, Violeta Mihaylova, Marina Dusl and Wolfgang Müller‐Felber and has published in prestigious journals such as Brain, Neurology and Human Molecular Genetics.

In The Last Decade

Angela Abicht

120 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Angela Abicht Germany 27 1.2k 864 537 341 269 124 2.1k
Helen Griffin United Kingdom 23 1.0k 0.9× 174 0.2× 160 0.3× 227 0.7× 247 0.9× 49 1.5k
Göknur Haliloğlu Türkiye 23 922 0.8× 210 0.2× 183 0.3× 183 0.5× 259 1.0× 116 1.7k
Christine Barnérias France 20 704 0.6× 139 0.2× 156 0.3× 236 0.7× 283 1.1× 73 1.4k
Roseline Froissart France 27 804 0.7× 172 0.2× 657 1.2× 185 0.5× 309 1.1× 90 2.8k
Michael P. Fautsch United States 32 1.3k 1.1× 293 0.3× 306 0.6× 34 0.1× 185 0.7× 122 3.5k
Teresa Sevilla Spain 27 759 0.6× 846 1.0× 245 0.5× 38 0.1× 141 0.5× 102 2.3k
Chaim Jalas United States 23 724 0.6× 191 0.2× 231 0.4× 87 0.3× 375 1.4× 60 1.7k
Sharon Keers United Kingdom 18 1.8k 1.6× 131 0.2× 326 0.6× 178 0.5× 134 0.5× 28 2.1k
Denise Cassandrini Italy 23 735 0.6× 106 0.1× 185 0.3× 228 0.7× 176 0.7× 62 1.3k
Julia Rankin United Kingdom 21 1.1k 1.0× 282 0.3× 258 0.5× 21 0.1× 314 1.2× 39 1.7k

Countries citing papers authored by Angela Abicht

Since Specialization
Citations

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

Fields of papers citing papers by Angela Abicht

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angela Abicht

This figure shows the co-authorship network connecting the top 25 collaborators of Angela Abicht. A scholar is included among the top collaborators of Angela Abicht 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 Angela Abicht. Angela Abicht 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.
Neuhann, Teresa, Eva‐Christina Prott, Jonas Leubner, et al.. (2024). LZTR1 loss-of-function variants associated with café au lait macules with or without freckling. Frontiers in Neurology. 15. 1391425–1391425. 1 indexed citations
2.
Marina, Adela Della, Andreas Hentschel, Ulrike Schara‐Schmidt, et al.. (2024). Novel Genetic and Biochemical Insights into the Spectrum of NEFL -Associated Phenotypes. Journal of Neuromuscular Diseases. 11(3). 625–645. 3 indexed citations
3.
Laner, Andreas, Philipp Arnold, Eileen Socher, et al.. (2023). Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes. 15(1). 14–14. 5 indexed citations
4.
Walter, Maggie C., Peter Reilich, Sabine Krause, et al.. (2021). Congenital myopathy and epidermolysis bullosa due to PLEC variant. Neuromuscular Disorders. 31(11). 1212–1217. 3 indexed citations
5.
Abicht, Angela, et al.. (2021). Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counseling. Cardiovascular Diagnosis and Therapy. 11(2). 637–649. 4 indexed citations
6.
Diebold, Isabel, et al.. (2020). Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes. Human Mutation. 41(5). 1025–1032. 8 indexed citations
7.
Eckenweiler, Matthias, Johannes A. Mayr, Sarah C. Grünert, Angela Abicht, & Rudolf Korinthenberg. (2020). Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants. Neuropediatrics. 52(2). 123–125. 6 indexed citations
8.
Abicht, Angela, Stephanie Kleinle, Elke Holinski‐Feder, et al.. (2018). Mitochondrial and nuclear disease panel (Mito‐aND‐Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost‐effective and sensitive NGS‐based method. Molecular Genetics & Genomic Medicine. 6(6). 1188–1198. 23 indexed citations
9.
Kölbel, Heike, Angela Abicht, Oliver Schwartz, et al.. (2018). Characteristic clinical and ultrastructural findings in nesprinopathies. European Journal of Paediatric Neurology. 23(2). 254–261. 7 indexed citations
10.
Köhler, Cornelia, Christoph M. Heyer, Sabine Hoffjan, et al.. (2015). Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene. Molecular and Cellular Probes. 29(5). 319–322. 14 indexed citations
11.
Ørstavik, Kristin, et al.. (2015). A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. Journal of Neuromuscular Diseases. 2(2). 181–184. 5 indexed citations
12.
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
13.
Abicht, Angela, et al.. (2012). Classical MERRF phenotype associated with mitochondrial tRNALeu (m.3243A>G) mutation. European Journal of Pediatrics. 171(5). 859–862. 16 indexed citations
14.
Seeger, Jürgen, Bertold Schrank, Angela Pyle, et al.. (2010). Clinical and neuropathological findings in patients with TACO1 mutations. Neuromuscular Disorders. 20(11). 720–724. 26 indexed citations
15.
Bulst, Stefanie, Angela Abicht, Elke Holinski‐Feder, et al.. (2009). In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes. Human Molecular Genetics. 18(9). 1590–1599. 44 indexed citations
16.
Schara, Ulrike, Marja Hietala, Carmelo Rodolico, et al.. (2007). G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Neuromuscular Disorders. 17(9-10). 818–818. 2 indexed citations
17.
Müller, Juliane, Angela Abicht, H.‐J. Christen, et al.. (2004). A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome. Neuromuscular Disorders. 14(11). 744–749. 19 indexed citations
18.
Barišić, Nina, Juliane S. Müller, Michaela A. Gazdik, et al.. (2004). Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants. European Journal of Paediatric Neurology. 9(1). 7–12. 28 indexed citations
19.
Abicht, Angela, Rolf Stucka, Veronika Karcagi, et al.. (1999). A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology. 53(7). 1564–1564. 77 indexed citations
20.
Abicht, Angela, Wolfgang Müller‐Felber, P.-A. Fischer, et al.. (1997). Congenital myasthenic syndromes: clinical and genetic analysis of 18 patients.. PubMed. 2(12). 515–22. 5 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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