André Schaller - Concepedia

Author

André Schaller

Also Known As

A SCHALLER, A Schaller, A. Schaller, ANDRÉ SCHALLER, Andre Schaller, Andre[Combining Acute Accent] Schaller, André Schaller, André Schaller, Andr� Schaller, Belgium: Brussels (BELULB)

110

Publications

2.6K

Citations

H-Index

100

Concepts

All Affiliations

University Hospital of Bern University of Bern University Children’s Hospital Bern University of Helsinki University of Zurich

About

André Schaller is an author at University Hospital of Bern specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	21	1.2K
2	Engineering	4	4	73
3	Natural Sciences	2	2	41
4	Health Sciences	1	1	144
5	Public Health	1	1	58

André Schaller

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement Martin Konrad, André Schaller, Dominik Seelow, The American Journal of Human Genetics UrologyOphthalmologyMedicineGeneticsRenal Failure	2006	511
Neutrophil extracellular trap formation requires OPA1-dependent glycolytic ATP production Poorya Amini, Darko Stojkov, Andrea Felser, Nature Communications	2018	175
Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy Anil V. Nair, Berthold Hocher, Sjoerd Verkaart, Proceedings of the National Academy of Sciences GynecologyMolecular BiologyInsulin-induced ActivationInsulin SignalingCell Signaling	2012	144
CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Martin Konrad, Jianghui Hou, Stefanie Weber, Journal of the American Society of Nephrology	2007	126
Deficiency of <scp>ECHS</scp>1 causes mitochondrial encephalopathy with cardiac involvement Tobias B. Haack, Christopher B. Jackson, Kei Murayama, Annals of Clinical and Translational Neurology	2015	116
Mutations in <i>SDHD</i> lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency Christopher B. Jackson, Jean‐Marc Nuoffer, Dagmar Hahn, Journal of Medical Genetics	2013	83
The stem–loop binding protein stimulates histone translation at an early step in the initiation pathway Barbara Gorgoni, Stuart Andrews, André Schaller, RNA	2005	68
Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin? Núria Camats, Mónica Fernández‐Cancio, Laura Audí, European Journal of Human Genetics Broad PhenotypesInfertilityXy PatientsDevelopmental BiologyMendelian Disorder	2018	64
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, The American Journal of Human Genetics Mendelian DisorderFemale InfertilityWhole-exome Sequencing StudyGenetic DisorderGenetics	2021	58
The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutatedCFTR Alleles Bernhard Steiner, Kaspar Truninger, Javier Sanz, Human Mutation	2004	53

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