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Institution

University of Düsseldorf

EducationDüsseldorf, Germany
About: University of Düsseldorf is a education organization based out in Düsseldorf, Germany. It is known for research contribution in the topics: Population & Diabetes mellitus. The organization has 25225 authors who have published 49155 publications receiving 1946434 citations.


Papers
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Journal ArticleDOI
TL;DR: These maps of Brodmann's areas 17 and 18 are the first of their kind and contain precise stereotaxic information on both interhemispheric and interindividual differences.

651 citations

Journal ArticleDOI
Dominik Sturm1, Dominik Sturm2, Brent A. Orr3, Umut H. Toprak1, Volker Hovestadt1, David T.W. Jones1, David Capper2, David Capper1, Martin Sill1, Ivo Buchhalter1, Paul A. Northcott1, Irina Leis2, Marina Ryzhova, Christian Koelsche2, Christian Koelsche1, Elke Pfaff2, Elke Pfaff1, Sariah Allen3, Gnanaprakash Balasubramanian1, Barbara C. Worst1, Barbara C. Worst2, Kristian W. Pajtler1, Sebastian Brabetz1, Pascal Johann2, Pascal Johann1, Felix Sahm2, Felix Sahm1, Jüri Reimand4, Jüri Reimand5, Alan Mackay6, Diana Carvalho6, Marc Remke4, Joanna J. Phillips7, Arie Perry7, Cynthia Cowdrey7, Rachid Drissi8, Maryam Fouladi8, Felice Giangaspero9, Maria Łastowska10, Wiesława Grajkowska10, Wolfram Scheurlen11, Torsten Pietsch12, Christian Hagel13, Johannes Gojo14, Daniela Lötsch14, Walter Berger14, Irene Slavc14, Christine Haberler14, Anne Jouvet15, Stefan Holm16, Silvia Hofer, Marco Prinz17, Catherine Keohane18, Iris Fried19, Christian Mawrin20, David Scheie21, Bret C. Mobley22, Matthew Schniederjan, Mariarita Santi23, Anna Maria Buccoliero11, Sonika Dahiya24, Christof M. Kramm25, André O. von Bueren25, Katja von Hoff13, Stefan Rutkowski13, Christel Herold-Mende2, Michael C. Frühwald26, Till Milde2, Till Milde1, Martin Hasselblatt27, Pieter Wesseling28, Pieter Wesseling29, Jochen Rößler30, Ulrich Schüller31, Martin Ebinger, Jens Schittenhelm32, Stephan Frank33, Rainer Grobholz, Istvan Vajtai, Volkmar Hans, Reinhard Schneppenheim13, Karel Zitterbart34, V. Peter Collins35, Eleonora Aronica36, Pascale Varlet, Stéphanie Puget37, Christelle Dufour38, Jacques Grill38, Dominique Figarella-Branger39, Marietta Wolter40, Martin U. Schuhmann32, Tarek Shalaby11, Michael A. Grotzer11, Timothy E. Van Meter41, Camelia M. Monoranu42, Jörg Felsberg40, Guido Reifenberger40, Matija Snuderl43, Lynn Ann Forrester43, Jan Koster36, Rogier Versteeg36, Richard Volckmann36, Peter van Sluis36, Stephan Wolf1, Tom Mikkelsen44, Amar Gajjar3, Kenneth Aldape45, Andrew S. Moore46, Michael D. Taylor4, Chris Jones6, Nada Jabado47, Matthias A. Karajannis43, Roland Eils, Matthias Schlesner1, Peter Lichter1, Andreas von Deimling1, Andreas von Deimling2, Stefan M. Pfister2, Stefan M. Pfister1, David W. Ellison3, Andrey Korshunov1, Andrey Korshunov2, Marcel Kool1 
25 Feb 2016-Cell
TL;DR: It is demonstrated that a significant proportion of institutionally diagnosed CNS-PNETs display molecular profiles indistinguishable from those of various other well-defined CNS tumor entities, facilitating diagnosis and appropriate therapy for patients with these tumors.

648 citations

Journal ArticleDOI
TL;DR: This article shows that all of these divergence-time estimates were generated through improper methodology on the basis of a single calibration point that has been unjustly denuded of error.

646 citations

Journal ArticleDOI
TL;DR: Adaptation of the liver ("hepatic mitochondrial flexibility") at early stages of obesity-related insulin resistance, which is subsequently lost in NASH is suggested.

646 citations

Journal ArticleDOI
TL;DR: The susceptibility gene (CYLD) has been identified by detecting germline mutations in 21 cylindromatosis families and somatic mutations in 1 sporadic and 5 familialcylindromas, all mutations predict truncation or absence of the encoded protein.
Abstract: Familial cylindromatosis is an autosomal dominant genetic predisposition to multiple tumours of the skin appendages. The susceptibility gene (CYLD) has previously been localized to chromosome 16q and has the genetic attributes of a tumour-suppressor gene (recessive oncogene). Here we have identified CYLD by detecting germline mutations in 21 cylindromatosis families and somatic mutations in 1 sporadic and 5 familial cylindromas. All mutations predict truncation or absence of the encoded protein. CYLD encodes three cytoskeletal-associated-protein-glycine-conserved (CAP-GLY) domains, which are found in proteins that coordinate the attachment of organelles to microtubules. CYLD also has sequence homology to the catalytic domain of ubiquitin carboxy-terminal hydrolases (UCH).

644 citations


Authors

Showing all 25575 results

NameH-indexPapersCitations
Karl J. Friston2171267217169
Roderick T. Bronson169679107702
Stanley B. Prusiner16874597528
Ralph A. DeFronzo160759132993
Monique M.B. Breteler15954693762
Thomas Meitinger155716108491
Karl Zilles13869272733
Ruben C. Gur13674161312
Alexis Brice13587083466
Michael Schmitt1342007114667
Michael Weller134110591874
Helmut Sies13367078319
Peter T. Fox13162283369
Yuri S. Kivshar126184579415
Markus M. Nöthen12594383156
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023139
2022470
20213,130
20202,721
20192,507
20182,439