Franz Rüschendorf

Max Delbrück Center for Molecular Medicine
Germany

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Genetics D-index 56 Citations 10,319 114 World Ranking 2711 National Ranking 196

Overview

What are the main themes of his work throughout his whole career to date

His studies link Brachydactyly with Pediatrics. His research on Brachydactyly often connects related areas such as Short stature. His study ties his expertise on Pediatrics together with the subject of Short stature. Franz Rüschendorf performs multidisciplinary study in Allergy and Hay fever in his work. His study in Immunology extends to Hay fever with its themes. As part of his studies on Immunology, Franz Rüschendorf frequently links adjacent subjects like Atopic dermatitis. In his research, Franz Rüschendorf performs multidisciplinary study on Atopic dermatitis and Asthma. Franz Rüschendorf integrates Asthma and Allergy in his research. He carries out multidisciplinary research, doing studies in Genome-wide association study and Single-nucleotide polymorphism.

Franz Rüschendorf most often published in these fields:

Pediatrics (50.00%)
Short stature (50.00%)
Brachydactyly (50.00%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

Anita Rauch;Juliane Hoyer;Sabine Guth;Christiane Zweier.
American Journal of Medical Genetics Part A (2006)

522 Citations

Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march.

Ingo Marenholz;Renate Nickel;Franz Rüschendorf;Florian Schulz.
The Journal of Allergy and Clinical Immunology (2006)

499 Citations

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.

Sandra M Pasternack;Ivar von Kügelgen;Khalid Al Aboud;Young-Ae Lee;Young-Ae Lee.
Nature Genetics (2008)

448 Citations

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2.

Louise A Metherell;J Paul Chapple;Sadani Cooray;Alessia David.
Nature Genetics (2005)

416 Citations

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21.

Young-Ae Lee;Ulrich Wahn;Rainer Kehrt;Luigi Tarani.
Nature Genetics (2000)

357 Citations

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

Manuel A. Ferreira;Judith M. Vonk;Hansjörg Baurecht;Ingo Marenholz;Ingo Marenholz.
Nature Genetics (2017)

355 Citations

A common variant on chromosome 11q13 is associated with atopic dermatitis

Jorge Esparza-Gordillo;Stephan Weidinger;Regina Fölster-Holst;Anja Bauerfeind.
Nature Genetics (2009)

342 Citations

Inflammatory Skin and Bowel Disease Linked to ADAM17 Deletion

Diana C. Blaydon;Paolo Biancheri;Wei Li Di;Vincent Plagnol.
The New England Journal of Medicine (2011)

321 Citations

Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease

Birgit Uhlenberg;Markus Schuelke;Franz Rüschendorf;Nico Ruf.
American Journal of Human Genetics (2004)

296 Citations

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.

Kirsten Huck;Oliver Feyen;Tim Niehues;Franz Rüschendorf.
Journal of Clinical Investigation (2009)

282 Citations

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Frequent Co-Authors

External Links

Personal Website for Franz Rüschendorf