Denisa Weis (Denisa Ilencikova)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 4

Top Topics

Duchenne Muscular Dystrophy

Genome Wide Analysis

Top Venues

Pediatric blood & cancer

This page only lists publications with an associated author ORCID identifier.

Publications

Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
Bernhard Csillag, Denisa Weis, Manfred Meissl, Gerald Webersinke, Franco Laccone, Satoshi Narumi, Oskar Haas, Hans-Christoph Duba
Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation. Pediatric blood & cancer 66 (4) (2018)