Andreas Hahn

3.9k total citations
93 papers, 1.3k citations indexed

About

Andreas Hahn is a scholar working on Molecular Biology, Physiology and Rheumatology. According to data from OpenAlex, Andreas Hahn has authored 93 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 18 papers in Physiology and 16 papers in Rheumatology. Recurrent topics in Andreas Hahn's work include Glycogen Storage Diseases and Myoclonus (16 papers), Lysosomal Storage Disorders Research (15 papers) and Muscle Physiology and Disorders (10 papers). Andreas Hahn is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (16 papers), Lysosomal Storage Disorders Research (15 papers) and Muscle Physiology and Disorders (10 papers). Andreas Hahn collaborates with scholars based in Germany, United States and Switzerland. Andreas Hahn's co-authors include Bernd A. Neubauer, Anne Schänzer, Ulrich Stephani, Y Rideau, John R. Bach, Anne Delaubier, Claire Le Guillou, Ulrich Müller, Dietmar Schranz and Maria Kontaridis and has published in prestigious journals such as Circulation, PLoS ONE and Circulation Research.

In The Last Decade

Andreas Hahn

88 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Hahn Germany 21 680 224 198 192 183 93 1.3k
Jean‐Marie Cuisset France 23 820 1.2× 184 0.8× 151 0.8× 343 1.8× 194 1.1× 64 1.5k
Christine Barnérias France 20 704 1.0× 193 0.9× 133 0.7× 113 0.6× 283 1.5× 73 1.4k
Günther Bernert Austria 21 486 0.7× 149 0.7× 130 0.7× 121 0.6× 88 0.5× 57 1.4k
Marc L. Otten United States 29 407 0.6× 168 0.8× 131 0.7× 90 0.5× 128 0.7× 61 2.1k
Maja von der Hagen Germany 22 651 1.0× 196 0.9× 101 0.5× 82 0.4× 215 1.2× 80 1.5k
Diana M. Escolar United States 20 1.5k 2.2× 288 1.3× 195 1.0× 373 1.9× 168 0.9× 49 2.0k
A. Reha United States 11 953 1.4× 281 1.3× 163 0.8× 165 0.9× 145 0.8× 29 1.5k
Michael A. Nigro United States 21 618 0.9× 318 1.4× 180 0.9× 126 0.7× 211 1.2× 36 1.4k
Byung Chan Lim South Korea 23 750 1.1× 176 0.8× 481 2.4× 130 0.7× 436 2.4× 165 1.8k
Andrea Klein Switzerland 22 837 1.2× 513 2.3× 93 0.5× 164 0.9× 136 0.7× 70 1.5k

Countries citing papers authored by Andreas Hahn

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Hahn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Hahn

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Hahn. A scholar is included among the top collaborators of Andreas Hahn 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 Andreas Hahn. Andreas Hahn 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.
Martakis, Κyriakos, et al.. (2025). N-Acetyl-leucine in progressive CACNA1A ataxia: A case series. European Journal of Paediatric Neurology. 54. 64–67.
2.
Hahn, Andreas, Heinrich Garn, Markus Waser, et al.. (2025). Standardized low-resolution brain electromagnetic tomography does not improve EEG Alzheimer's disease assessment. NeuroImage. 310. 121144–121144.
3.
Patterson, Marc C., Uma Ramaswami, Aimée Donald, et al.. (2025). Disease-Modifying, Neuroprotective Effect of N-Acetyl- l -Leucine in Adult and Pediatric Patients With Niemann-Pick Disease Type C. Neurology. 105(1). e213589–e213589.
4.
Trollmann, Regina, Jessika Johannsen, Katharina Vill, et al.. (2024). Postnatal management of preterm infants with spinal muscular atrophy: experience from German newborn screening. Orphanet Journal of Rare Diseases. 19(1). 353–353. 2 indexed citations
5.
Weiss, Deike, Anna Perez, P. Weber, et al.. (2024). Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life. European Journal of Paediatric Neurology. 51. 17–23. 12 indexed citations
6.
Waitz, Markus, et al.. (2024). Effects of liberalising visiting policy and staff education on parental visiting duration in the neonatal unit. Acta Paediatrica. 113(4). 684–691. 1 indexed citations
7.
8.
Savarese, Marco, Susanne Rinné, Anne Schänzer, et al.. (2023). Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking. Acta Neuropathologica Communications. 11(1). 4–4. 4 indexed citations
9.
Hahn, Andreas, René Günther, Albert C. Ludolph, et al.. (2022). Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany. Orphanet Journal of Rare Diseases. 17(1). 276–276. 20 indexed citations
10.
Westphal, Dominik S., Elisa Mastantuono, Heide Seidel, et al.. (2022). There is more to it than just congenital heart defects – The phenotypic spectrum of TAB2-related syndrome. Gene. 814. 146167–146167. 2 indexed citations
11.
Fazeli, Walid, Somayeh Bakhtiari, Abbas Tafakhori, et al.. (2021). The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature. European Journal of Paediatric Neurology. 36. 7–13. 5 indexed citations
12.
Rupp, Stefan, Anne Schänzer, Dietmar Schranz, et al.. (2018). Genetic basis of hypertrophic cardiomyopathy in children. Clinical Research in Cardiology. 108(3). 282–289. 20 indexed citations
13.
Schänzer, Anne, et al.. (2017). Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American Myopathy. Neuropediatrics. 48(6). 451–455. 26 indexed citations
14.
Friedburg, Christoph, Hakan Akintuerk, Saskia Biskup, et al.. (2017). Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome. American Journal of Medical Genetics Part A. 173(4). 959–965. 6 indexed citations
15.
Weber, Axel, Angelika Köhler, Andreas Hahn, & Ulrich Müller. (2014). 8p23.1 duplication syndrome: narrowing of critical interval to 1.80 Mbp. Molecular Cytogenetics. 7(1). 94–94. 11 indexed citations
16.
Hahn, Andreas, Nesrin Karabul, Dorle Schmidt, et al.. (2014). Outcome of Patients with Classical Infantile Pompe Disease Receiving Enzyme Replacement Therapy in Germany. JIMD Reports. 20. 65–75. 47 indexed citations
17.
Lal, Dennis, Eva M. Reinthaler, Mohammad R. Toliat, et al.. (2013). Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy. PLoS ONE. 8(10). 18 indexed citations
18.
Weber, Axel, Angelika Köhler, Andreas Hahn, Bernd A. Neubauer, & Ulrich Müller. (2013). Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome. Neurogenetics. 14(3-4). 251–253. 27 indexed citations
19.
Zirn, Birgit, Maja Hempel, Andreas Hahn, et al.. (2008). Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype. American Journal of Medical Genetics Part A. 146A(22). 2960–2965. 6 indexed citations
20.
Hahn, Andreas, et al.. (2004). Induction of epileptic negative myoclonus by oxcarbazepine in symptomatic epilepsy. Epileptic Disorders. 6(4). 271–274. 12 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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