Franz Rüschendorf - Max Delbrück Center for Molecular Medicine in the Helmholtz Association

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Papers共 85 篇Author StatisticsCo-AuthorSimilar Experts

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Rare Variant Analysis in Eczema Identifies Exonic Variants in DUSP1, NOTCH4 and SLC9A4

Sarah Grosche,Ingo Marenholz,Jorge Esparza-Gordillo,Aleix Arnau-Soler,Erola Pairo-Castineira,Franz Rüschendorf,Tarunveer S. Ahluwalia,Catarina Almqvist,Andreas Arnold,Hansjörg Baurecht,Hans Bisgaard,Klaus Bønnelykke,Sara J. Brown,Mariona Bustamante,John A. Curtin,Adnan Custovic,Shyamali C. Dharmage,Ana Esplugues,Mario Falchi,Dietmar Fernandez-Orth,Manuel A. R. Ferreira,Andre Franke,Sascha Gerdes,Christian Gieger,Hakon Hakonarson,Patrick G. Holt,Georg Homuth,Norbert Hubner,Pirro G. Hysi,Marjo-Riitta Jarvelin,Robert Karlsson,Gerard H. Koppelman,Susanne Lau,Manuel Lutz,Patrik K. E. Magnusson,Guy B. Marks,Martina Müller-Nurasyid,Markus M. Nöthen,Lavinia Paternoster,Craig E. Pennell,Annette Peters,Konrad Rawlik,Colin F. Robertson,Elke Rodriguez,Sylvain Sebert,Angela Simpson,Patrick M. A. Sleiman,Marie Standl,Dora Stölzl,Konstantin Strauch,Agnieszka Szwajda,Albert Tenesa,Philip J. Thompson,Vilhelmina Ullemar,Alessia Visconti,Judith M. Vonk,Carol A. Wang,Stephan Weidinger,Matthias Wielscher,Catherine L. Worth, Chen-Jian Xu,Young-Ae Lee

Nature Communications（2021）

Cited16Views0WOSNATUREBibtex

Phosphatidylinositol 4-Kinase Β Mutations Cause Nonsyndromic Sensorineural Deafness and Inner Ear Malformation

Journal of genetics and genomics/Journal of Genetics and Genomicsno. 10 (2020): 618-626

Cited4Views0WOSBibtex

Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family with a Novel KCNQ1 Loss-of-Function Mutation

Harald Pruess,Guido Gessner,Stefan H. Heinemann,Franz Rueschendorf,Ann-Kathrin Ruppert,Herbert Schulz,Thomas Sander,Wilhelm Rimpau

Frontiers in Neurology（2019）

Cited5Views0WOSBibtex

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