Frank Hanisch

1.5k total citations
38 papers, 845 citations indexed

About

Frank Hanisch is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Frank Hanisch has authored 38 papers receiving a total of 845 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 9 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Frank Hanisch's work include Genetic Neurodegenerative Diseases (7 papers), Amyotrophic Lateral Sclerosis Research (7 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Frank Hanisch is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Amyotrophic Lateral Sclerosis Research (7 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Frank Hanisch collaborates with scholars based in Germany, United Kingdom and Hungary. Frank Hanisch's co-authors include Stephan Zierz, Malte Kornhuber, Marcus Deschauer, Ilka Schneider, Tobias Müller, Joachim Weis, Martin Winterholler, Torsten Kraya, Stefan Vielhaber and Benedikt Schoser and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Frank Hanisch

38 papers receiving 822 citations

Peers

Frank Hanisch

NEURO

PHYSI

GENET

RHEUM

Roberto Fernández‐Torrón Spain

Mette Cathrine Ørngreen Denmark

Megumi Yamada Japan

Zenji Shiozawa Japan

F. Muntoni United Kingdom

Akio Yokoseki Japan

Tina D. Jeppesen Denmark

Gaetano Bernardi Italy

Werner Poewe Austria

Roberto Fernández‐Torrón Spain

Frank Hanisch

388 ×1.2

290 ×0.9

NEURO

146 ×0.7

PHYSI

136 ×0.7

GENET

63 ×0.4

RHEUM

Citations per year, relative to Frank Hanisch Frank Hanisch (= 1×) peers Roberto Fernández‐Torrón

Countries citing papers authored by Frank Hanisch

Since Specialization

Citations

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

Fields of papers citing papers by Frank Hanisch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Hanisch

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

All Works

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20 of 20 papers shown

Rosenbohm, Angela, Steffen Hirsch, Alexander E. Volk, et al.. (2018). The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy. Journal of Neurology. 265(5). 1026–1036. 26 indexed citations

Mori, Kohji, Yoshihiro Nihei, Thomas Arzberger, et al.. (2016). Reduced hn RNPA 3 increases C9orf72 repeat RNA levels and dipeptide‐repeat protein deposition. EMBO Reports. 17(9). 1314–1325. 36 indexed citations

Schneider, Ilka, Malte Kornhuber, & Frank Hanisch. (2015). Long-term observation of incremental response and antibodies to voltage-gated calcium channels in patients with Lambert–Eaton myasthenic syndrome: two case reports. Journal of Medical Case Reports. 9(1). 59–59. 1 indexed citations

Dorst, Johannes, Luc Dupuis, Susanne Petri, et al.. (2015). Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study. Journal of Neurology. 262(4). 849–858. 64 indexed citations

Hübers, Annemarie, Susanne Petri, Katja Kollewe, et al.. (2015). Clinical features and differential diagnosis of flail arm syndrome. Journal of Neurology. 263(2). 390–395. 23 indexed citations

Hanisch, Frank & Stephan Zierz. (2015). C-Reactive Protein in Idiopathic Inflammatory Myopathies. 23(1-2). 45–51. 4 indexed citations

Hanisch, Frank, Malte Kornhuber, Charlotte L. Alston, et al.. (2014). SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions. Journal of Neurology Neurosurgery & Psychiatry. 86(6). 630–634. 37 indexed citations

Katona, István, Joachim Weis, & Frank Hanisch. (2014). Glycogenosome accumulation in the arrector pili muscle in Pompe disease. Orphanet Journal of Rare Diseases. 9(1). 17–17. 13 indexed citations

Joshi, Pushpa Raj, et al.. (2014). Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis. Journal of Clinical Neuroscience. 21(11). 1959–1963. 17 indexed citations

10.

Karabul, Nesrin, Cornelia Kornblum, Rudolf A. Kley, et al.. (2014). Pregnancy and delivery in women with Pompe disease. Molecular Genetics and Metabolism. 112(2). 148–153. 14 indexed citations

11.

Hanisch, Frank, Wenke Weidemann, Pushpa Raj Joshi, et al.. (2013). Sialylation and Muscle Performance: Sialic Acid Is a Marker of Muscle Ageing. PLoS ONE. 8(12). e80520–e80520. 25 indexed citations

12.

Schrøder, Thomas B., et al.. (2013). Eosinophils in hereditary and inflammatory myopathies.. PubMed. 32(3). 148–53. 22 indexed citations

13.

Schneider, Ilka, Frank Hanisch, Tobias Müller, Bernd Schmidt, & Stephan Zierz. (2012). Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 months. Wiener Medizinische Wochenschrift. 163(1-2). 40–44. 24 indexed citations

14.

Menzel, Matthias, Jens Soukup, Alexander Scharf, et al.. (2007). Endothelin-1 and cerebral blood flow in a porcine model. Journal of Clinical Neuroscience. 14(7). 650–657. 4 indexed citations

15.

Hanisch, Frank, Ylva Hellsten, & Stephan Zierz. (2006). Ecto- and cytosolic 5′-nucleotidases in normal and AMP deaminase-deficient human skeletal muscle. Biological Chemistry. 387(1). 53–8. 4 indexed citations

16.

Mittelbronn, Michel, Frank Hanisch, Marc Gleichmann, et al.. (2006). Myofiber Degeneration in Autosomal Dominant Emery–Dreifuss Muscular Dystrophy (AD‐EDMD) (LGMD1B). Brain Pathology. 16(4). 266–272. 13 indexed citations

17.

Gaul, Charly, Frank Hanisch, Daniel Neureiter, et al.. (2005). Intravascular lymphomatosis mimicking disseminated encephalomyelitis and encephalomyelopathy. Clinical Neurology and Neurosurgery. 108(5). 486–489. 5 indexed citations

18.

Hanisch, Frank, et al.. (2004). Die kongenitale Fibrose der äußeren Augenmuskeln (CFEOM) und andere Phänotypen der kongenitalen kranialen Dysinnervationssyndrome (CCDD). Der Nervenarzt. 76(4). 395–402. 5 indexed citations

19.

Clausen, Tobias, Alexander Scharf, Matthias Menzel, et al.. (2004). Influence of moderate and profound hyperventilation on cerebral blood flow, oxygenation and metabolism. Brain Research. 1019(1-2). 113–123. 28 indexed citations

20.

Vytopil, Michal, Enzo Ricci, Antonio Dello Russo, et al.. (2002). Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy. Neuromuscular Disorders. 12(10). 958–963. 42 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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