Thomas Wieland - Concepedia

Author

Thomas Wieland

Also Known As

Aguilar, David, Not Available Not Available, T WIELAND, T Wieland, T. WIELAND, T. Wieland, THOMAS WIELAND, Tan, Sian-Tsung, Thomas WIELAND, Thomas Wieland

466

Publications

24.7K

Citations

H-Index

227

Concepts

All Affiliations

Heidelberg University University Hospital Heidelberg Helmholtz Zentrum München Technical University of Munich University Medical Centre Mannheim

About

Thomas Wieland is an author at Heidelberg University specializing in medicine, cell signaling, and signal transduction.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	53	117	13.4K
2	Natural Sciences	24	28	2.3K
3	Health Sciences	7	7	598
4	Engineering	2	2	129
5	Education	1	1	62

Thomas Wieland

221

Publications

22.2K

Citations

H-Index

Page 1

	Year	Citations
Transcriptome and genome sequencing uncovers functional variation in humans Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Nature Human VariationGeneticsGenomicsTranscriptomicsMedicine	2013	2.1K
The genetic architecture of type 2 diabetes Christian Fuchsberger, Jason Flannick, Tanya M. Teslovich, Nature Genetic DeterminantGeneticsDiabetesGenetic EpidemiologyType 2	2016	1.1K
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, The Lancet Genetic MutationsMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	1.1K
Fluorescent phallotoxin, a tool for the visualization of cellular actin. Elisabeth Wulf, Axel Deboben, Friedlinde A. Bautz, Proceedings of the National Academy of Sciences CytoskeletonCellular PhysiologyFluorescent DerivativeFluorescent PhallotoxinFilamentous Actin	1979	800
A deep proteome and transcriptome abundance atlas of 29 healthy human tissues Dongxue Wang, Basak Eraslan, Thomas Wieland, Molecular Systems Biology	2019	767
Enhanced Sarcoplasmic Reticulum Ca <sup>2+</sup> Leak and Increased Na <sup>+</sup> -Ca <sup>2+</sup> Exchanger Function Underlie Delayed Afterdepolarizations in Patients With Chronic Atrial Fibrillation Niels Voigt, Na Li, Qiongling Wang, Circulation	2012	603
Mutations in the deubiquitinase gene USP8 cause Cushing's disease Martín Reincke, Silviu Sbiera, Akira Hayakawa, Nature Genetics Disease MechanismMedicineGeneticsPathologyDisease Gene Identification	2014	573
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension Felix Beuschlein, Sheerazed Boulkroun, Thomas Wieland, Nature Genetics HypertensionSomatic MutationsGeneticsPhysiologySecondary Hypertension	2013	552
Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signaling Moritz Felcht, Robert Luck, Alexander Schering, Journal of Clinical Investigation Integrin ExpressionAngiopoietin SignalingAngiogenesisDevelopmental BiologySignal Transduction	2012	466
Constitutive Activation of PKA Catalytic Subunit in Adrenal Cushing's Syndrome Felix Beuschlein, Guillaume Assié, Davide Calebiro, New England Journal of Medicine	2014	423

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