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.
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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)
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)
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)
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)
A major susceptibility locus for atopic dermatitis maps to chromosome 3q21.
Young-Ae Lee;Ulrich Wahn;Rainer Kehrt;Luigi Tarani.
Nature Genetics (2000)
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)
A common variant on chromosome 11q13 is associated with atopic dermatitis
Jorge Esparza-Gordillo;Stephan Weidinger;Regina Fölster-Holst;Anja Bauerfeind.
Nature Genetics (2009)
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)
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)
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)
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