Monika Hiller

Years Active: 2018-2020
Publications (10 Years): 2

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

Publications

Pietro Spitali, Irina Zaharieva, Stefan Bohringer, Monika Hiller, Amina Chaouch, Andreas Roos, Chiara Scotton, Mireille Claustres, Luca Bello, Craig M McDonald, Eric P Hoffman, null null, Zaida Koeks, Eka H E D Suchiman, Sebahattin Cirak, Mariacristina Scoto, Mojgan Reza, Peter A C 't Hoen, Erik H Niks, Sylvie Tuffery-Giraud, Hanns Lochmüller, Alessandra Ferlini, Francesco Muntoni, Annemieke M Aartsma-Rus
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy. European journal of human genetics : EJHG 28 (6) (2020)
Monika Hiller, Maria Sofia Falzarano, Iker Garcia-Jimenez, Valentina Sardone, Ruurd C Verheul, Linda Popplewell, Karen Anthony, Estibaliz Ruiz-Del-Yerro, Hana Osman, Jelle J Goeman, Kamel Mamchaoui, George Dickson, Alessandra Ferlini, Francesco Muntoni, Annemieke Aartsma-Rus, Virginia Arechavala-Gomeza, Nicole A Datson, Pietro Spitali
A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures. PloS one 13 (10) (2018)

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