André Schaller

2.6k citations

74 papers · 1.2k indexed · h-index 19

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Nephrology top 5%

Papers in ⓘ

Molecular Biology 43
- Mitochondrial Function and Pathology 23
- RNA modifications and cancer 10
- ATP Synthase and ATPases Research 7
- RNA and protein synthesis mechanisms 7
Cardiology and Cardiovascular Medicine 11
- Cardiac electrophysiology and arrhythmias 6

Co-authors: Sabina Gallati (27 shared papers)Christopher B. Jackson (13 shared papers)Jean‐Marc Nuoffer (18 shared papers)Dagmar Hahn (9 shared papers)Daniel Schümperli (2 shared papers)Carolina Courage (2 shared papers)Martin Konrad (2 shared papers)Berndt Müller (2 shared papers)
Journals: European Journal of Human Genetics (5 papers)Biochemical and Biophysical Research Communications (4 papers)BMC Neurology (2 papers)Mitochondrion (2 papers)The International Journal of Biological Markers (2 papers)
Partner nations: Switzerland Germany France

In The Last Decade

André Schaller

69 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside André Schaller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with André Schaller Line = papers co-authored together André Schaller links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 74 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Neutrophil extracellular trap formation requires OPA1-dependent glycolytic ATP production Nature Communications ·Poorya Amini, Darko Stojkov, Andrea Felser, Christopher B. Jackson, Carolina Courage, André Schaller, Laurent Gelman, María Eugenia Soriano, Jean‐Marc Nuoffer, Luca Scorrano, Charaf Benarafa, Shída Yousefi, Hans‐Uwe Simon	2018	138
2	Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy Proceedings of the National Academy of Sciences ·Anil V. Nair, Berthold Hocher, Sjoerd Verkaart, Femke van Zeeland, Thiemo Pfab, Torsten Slowinski, Youpeng Chen, Karl P. Schlingmann, André Schaller, Sabina Gallati, René J.M. Bindels, Martin Konrad, Joost G.J. Hoenderop	2012	111
3	CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Journal of the American Society of Nephrology ·Martin Konrad, Jianghui Hou, Stefanie Weber, JoCombining Diaeresisrg DoCombining Diaeresistsch, Jameela A. Kari, Tomáš Seeman, Eberhard Kuwertz-BroCombining Diaeresisking, Amira Peco‐Antić, Velibor Tasić, Katalin Dittrich, Hammad O. Alshaya, Rodo O. von Vigier, Sabina Gallati, Daniel A. Goodenough, André Schaller	2007	82
4	Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency Journal of Medical Genetics ·Christopher B. Jackson, Jean‐Marc Nuoffer, Dagmar Hahn, Holger Prokisch, Birgit Haberberger, Matthias Gautschi, Annemarie Häberli, Sabina Gallati, André Schaller	2013	67
5	The stem–loop binding protein stimulates histone translation at an early step in the initiation pathway RNA ·Barbara Gorgoni, Stuart Andrews, André Schaller, Daniel Schümperli, Nicola K. Gray, Berndt Müller	2005	58
6	Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin? European Journal of Human Genetics ·Núria Camats, Mónica Fernández‐Cancio, Laura Audí, André Schaller, Christa E. Flück	2018	43
7	The Vacuolar H+-ATPase B1 Subunit Polymorphism p.E161K Associates with Impaired Urinary Acidification in Recurrent Stone Formers Journal of the American Society of Nephrology ·Nasser A. Dhayat, André Schaller, Giuseppe Albano, John Poindexter, Carolyn Griffith, Andreas Pasch, Sabina Gallati, Bruno Vogt, Orson W. Moe, Daniel G. Fuster	2015	40
8	The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutatedCFTR Alleles Human Mutation ·Bernhard Steiner, Kaspar Truninger, Javier Sanz, André Schaller, Sabina Gallati	2004	38
9	A variant inMRPS14(uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement Human Molecular Genetics ·Christopher B. Jackson, Martina Huemer, Ramona Bolognini, Franck Martin, Gabor Szinnai, Birgit Donner, Uwe Richter, Brendan J. Battersby, Jean‐Marc Nuoffer, Anu Suomalainen, André Schaller	2018	33
10	SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement American Journal of Medical Genetics Part A ·Carolina Courage, Christopher B. Jackson, Dagmar Hahn, Liliya Euro, Jean‐Marc Nuoffer, Sabina Gallati, André Schaller	2016	32
11	Mitochondrial neurogastrointestinal encephalomyopathy in three siblings Journal of Neurology ·Michaël Schüpbach, K. Madhavi Vadday, André Schaller, Caspar Brekenfeld, Liliane Kappeler, Jean‐François Benoist, C. Nguyen-Thi Xuan-Huong, J‐M. Burgunder, Frank Seibold, Sabina Gallati, Heinrich P. Mattle	2007	29
12	Molecular and biochemical characterisation of a novel mutation in POLGassociated with Alpers syndrome BMC Neurology ·André Schaller, Dagmar Hahn, Christopher B. Jackson, Ilse Kern, Christophe Chardot, Dominique C. Belli, Sabina Gallati, Jean‐Marc Nuoffer	2011	29
13	Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum Movement Disorders ·Sebastian R. Schreglmann, Franz Riederer, Marian Galovic, Christos Ganos, Georg Kägi, Daniel Waldvogel, Zane Jaunmuktane, André Schaller, Ute Hidding, Ernst Krasemann, Lars Michels, Christian R. Baumann, Kailash P. Bhatia, Hans H. Jung	2017	24
14	Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes – a case report BMC Neurology ·Tim Sinnecker, Michaela Andělová, Michael Mayr, Stephan Rüegg, Michael Sinnreich, Juergen Hench, Stephan Frank, André Schaller, Christoph Stippich, Jens Wuerfel, Leo H. Bonati	2019	23
15	A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy European Journal of Medical Genetics ·Christopher B. Jackson, Dagmar Hahn, Barbara Schröter, Uwe Richter, Brendan J. Battersby, Thomas Schmitt‐Mechelke, Paula Marttinen, Jean‐Marc Nuoffer, André Schaller	2017	22
16	Quantitative 1-Step DNA Methylation Analysis with Native Genomic DNA as Template Clinical Chemistry ·Thomas von Känel, Dominik Gerber, André Schaller, Alessandra Baumer, Eva Wey, Christopher B. Jackson, F.M. Gisler, Karl Heinimann, Sabina Gallati	2010	22
17	Functional importance of conserved nucleotides at the histone RNA 3' processing site. PubMed ·André Furger, André Schaller, Daniel Schümperli	1998	22
18	Rapid typing of *Moraxella catarrhalis* subpopulations based on outer membrane proteins using mass spectrometry PROTEOMICS ·André Schaller, Rolf Troller, Daniel Molina, Sabina Gallati, Christoph Aebi, Patricia Stutzmann Meier	2005	20
19	Prevalence and characteristics of genetic disease in adult kidney stone formers Nephrology Dialysis Transplantation ·Manuel Anderegg, Eric Olinger, Matteo Bargagli, Robert Geraghty, Lea Taylor, Alexander Nater, Rémy Bruggmann, John A. Sayer, Bruno Vogt, André Schaller, Daniel G. Fuster	2024	19
20	qPCR-based mitochondrial DNA quantification: Influence of template DNA fragmentation on accuracy Biochemical and Biophysical Research Communications ·Christopher B. Jackson, Sabina Gallati, André Schaller	2012	18

About André Schaller

André Schaller is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Clinical Biochemistry, Genetics and Pulmonary and Respiratory Medicine, having authored 74 papers that have together received 1.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (23 papers), RNA modifications and cancer (10 papers), Metabolism and Genetic Disorders (9 papers), ATP Synthase and ATPases Research (7 papers), RNA and protein synthesis mechanisms (7 papers), Cardiac electrophysiology and arrhythmias (6 papers), Cystic Fibrosis Research Advances (6 papers) and Neonatal Respiratory Health Research (5 papers). The work is most often cited by research in Clinical Biochemistry (157 citations), Nephrology (102 citations), Molecular Biology (697 citations), Nutrition and Dietetics (133 citations) and Neurology (60 citations). André Schaller has collaborated with scholars based in Switzerland, Germany and France. Frequent co-authors include Sabina Gallati, Christopher B. Jackson, Jean‐Marc Nuoffer, Dagmar Hahn, Daniel Schümperli, Carolina Courage, Martin Konrad, Berndt Müller, Andrea Felser and Shída Yousefi. Their work appears in journals such as European Journal of Human Genetics, Biochemical and Biophysical Research Communications, BMC Neurology, Mitochondrion and The International Journal of Biological Markers.

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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