André Schaller

2.6k total citations
74 papers, 1.2k citations indexed

About

André Schaller is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Clinical Biochemistry. According to data from OpenAlex, André Schaller has authored 74 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 11 papers in Cardiology and Cardiovascular Medicine and 10 papers in Clinical Biochemistry. Recurrent topics in André Schaller's work include Mitochondrial Function and Pathology (23 papers), RNA modifications and cancer (10 papers) and Metabolism and Genetic Disorders (9 papers). André Schaller is often cited by papers focused on Mitochondrial Function and Pathology (23 papers), RNA modifications and cancer (10 papers) and Metabolism and Genetic Disorders (9 papers). André Schaller collaborates with scholars based in Switzerland, France and Germany. André Schaller's co-authors include Sabina Gallati, Christopher B. Jackson, Jean‐Marc Nuoffer, Dagmar Hahn, Daniel Schümperli, Carolina Courage, Martin Konrad, Berndt Müller, Andrea Felser and María Eugenia Soriano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

André Schaller

69 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
André Schaller Switzerland 19 697 157 145 137 133 74 1.2k
Kenji E. Orii Japan 29 851 1.2× 317 2.0× 205 1.4× 78 0.6× 41 0.3× 71 2.4k
Vincent Laugel France 26 1.7k 2.4× 142 0.9× 475 3.3× 114 0.8× 18 0.1× 88 2.3k
Sang Hee Min United States 15 455 0.7× 125 0.8× 105 0.7× 69 0.5× 208 1.6× 22 1.4k
Tsugio Amemiya Japan 22 462 0.7× 48 0.3× 150 1.0× 112 0.8× 79 0.6× 168 1.8k
Mortaza Bonyadi Iran 19 651 0.9× 31 0.2× 157 1.1× 120 0.9× 19 0.1× 93 1.3k
Essam Al‐Sabban Saudi Arabia 10 911 1.3× 29 0.2× 107 0.7× 175 1.3× 239 1.8× 30 1.5k
Adriana M. Montaño United States 33 508 0.7× 58 0.4× 274 1.9× 62 0.5× 36 0.3× 79 2.9k
Pia Höglund Finland 21 867 1.2× 14 0.1× 332 2.3× 379 2.8× 159 1.2× 27 1.4k
Dominique Bozon France 23 745 1.1× 179 1.1× 232 1.6× 1.4k 10.2× 69 0.5× 57 2.4k
Peter Gustavsson Sweden 20 1.3k 1.8× 18 0.1× 476 3.3× 60 0.4× 37 0.3× 38 1.8k

Countries citing papers authored by André Schaller

Since Specialization
Citations

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

Fields of papers citing papers by André Schaller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of André Schaller

This figure shows the co-authorship network connecting the top 25 collaborators of André Schaller. A scholar is included among the top collaborators of André Schaller 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 André Schaller. André Schaller 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.
2.
Döring, Yvonne, André Schaller, Erik Vassella, et al.. (2024). Non‐Hotspot PIK3CA Variants Have Higher Variant Allele Frequency and are More Common in Syndromic Vascular Malformations. American Journal of Medical Genetics Part A. 197(2). e63883–e63883. 1 indexed citations
3.
Meyer, Christoph, et al.. (2023). Complex I, V, and MDH2 deficient human skin fibroblasts reveal distinct metabolic signatures by 1H HR‐MAS NMR. Journal of Inherited Metabolic Disease. 47(2). 270–279.
4.
Laubscher, Bernard, Amit V. Pandey, Sibylle Tschumi, et al.. (2023). Expanding the p.(Arg85Trp) Variant-Specific Phenotype of HNF4A: Features of Glycogen Storage Disease, Liver Cirrhosis, Impaired Mitochondrial Function, and Glomerular Changes. Molecular Syndromology. 14(4). 347–362. 4 indexed citations
5.
Schaller, André, et al.. (2023). Induced pluripotent stem cell technology as diagnostic tool in patients with suspected ornithine transcarbamylase deficiency lacking genetic confirmation. Molecular Genetics and Metabolism Reports. 37. 101007–101007. 1 indexed citations
6.
Gschwind, Markus, Nuria García Segarra, André Schaller, et al.. (2022). Early‐onset leukoencephalomyelopathy due to a biallelic NDUFV1 variant in a mid‐forties patient. Annals of Clinical and Translational Neurology. 9(6). 888–892. 1 indexed citations
7.
Laemmle, Alexander, André Schaller, Andrea Felser, et al.. (2021). Triheptanoin – Novel therapeutic approach for the ultra-rare disease mitochondrial malate dehydrogenase deficiency. Molecular Genetics and Metabolism Reports. 29. 100814–100814. 12 indexed citations
8.
Vaclavik, Veronika, et al.. (2020). Longitudinal case study and phenotypic multimodal characterization of McArdle disease-linked retinopathy: insight into pathomechanisms. Ophthalmic Genetics. 41(1). 73–78. 3 indexed citations
9.
Jackson, Christopher B., Martina Huemer, Franck Martin, et al.. (2018). A variant inMRPS14(uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement. Human Molecular Genetics. 28(4). 639–649. 33 indexed citations
10.
Mueller, Sandro Manuel, Jens A. Petersen, Sebastian Frese, et al.. (2017). Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients. Orphanet Journal of Rare Diseases. 12(1). 184–184. 15 indexed citations
11.
Jackson, Christopher B., et al.. (2014). Heterologous expression from the human D-Loop in organello. Mitochondrion. 17. 67–75. 6 indexed citations
12.
Jackson, Christopher B., Christoph Neuwirth, Dagmar Hahn, et al.. (2014). Novel mitochondrial tRNAIlem.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype. British Journal of Ophthalmology. 98(10). 1453–1459. 8 indexed citations
13.
Känel, Thomas von, Frauke Stanke, André Schaller, et al.. (2013). Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A. European Journal of Human Genetics. 21(12). 1462–1466. 10 indexed citations
14.
Konrad, Martin, Jianghui Hou, Stefanie Weber, et al.. (2007). CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis. Journal of the American Society of Nephrology. 19(1). 171–181. 82 indexed citations
15.
Schüpbach, Michaël, André Schaller, Caspar Brekenfeld, et al.. (2007). Mitochondrial neurogastrointestinal encephalomyopathy in three siblings. Journal of Neurology. 254(2). 146–153. 29 indexed citations
16.
Labuhn, Martin, Vincent Vuaroqueaux, Fréderic Fina, et al.. (2006). Simultaneous quantitative detection of relevant biomarkers in breast cancer by quantitative real-time PCR. The International Journal of Biological Markers. 21(1). 30–39. 13 indexed citations
17.
Schaller, André, Rolf Troller, Daniel Molina, et al.. (2005). Rapid typing of Moraxella catarrhalis subpopulations based on outer membrane proteins using mass spectrometry. PROTEOMICS. 6(1). 172–180. 20 indexed citations
18.
Rittinger, Olaf, et al.. (2005). Quantitative Heterozygotentestung und das therapeutische Dilemma bei Menkes-Syndrom. Klinische Pädiatrie. 217(5). 286–290. 1 indexed citations
19.
Pavlović, Mladen, André Schaller, Jean‐Pierre Pfammatter, et al.. (2004). Age-dependent suppression of SERCA2a mRNA in pediatric atrial myocardium. Biochemical and Biophysical Research Communications. 326(2). 344–348. 12 indexed citations
20.
Schaller, André. (1987). Schweizer Neutralität im West-Ost-Handel : das Hotz-Linder-Agreement vom 23. Juli 1951. 7 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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