The NEUROMICS work plan integrates a group of expert centres with five aims: (i) to unravel a large portion of still unknown genetic causes of ten categories of NDD and NMD using next-generation genomics approaches; (ii) to provide a diagnostic strategy to detect most genetic causes in clinical practice; (iii) to develop biomarkers which better describe phenotype and predict progression using transcriptomic, proteomic, metabolomic, and lipidomic technologies; (iv) to use Omics approaches for disease pathway elucidation in animal models, as well as on patient derived iPSC and other cell types; and (v) to utilize Omics-based results for stratified therapy development for NMD/NDD.

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Project start date – October 2012
Project end date – September 2017

Funded by FP7

Coordinated by

Olaf Riess, Tübingen, Germany
Co-coordinators: Gert-Jan van Ommen, Leiden, Netherlands and Brunhilde Wirth, Köln, Germany