Examinant per Autoria "Graessner, Holm"
Resultats per pàgina
Opcions d'ordenació
Ítem Accés Obert Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report(Nature Research, 2023) Lagorce, David; Lebreton, Emeline; Matalonga, Leslie; Hongnat, Oscar; Chahdil, Maroua; Piscia, Davide; Paramonov, Ida; Ellwanger, Kornelia; Köhler, Sebastian; Robinson, Peter N.; Graessner, Holm; Beltran, Sergi; Lucano, Caterina; Hanauer, Marc; Rath, Ana
Ítem Accés Obert RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases(Nature Research, 2018) Lochmüller, Hanns; Badowska, Dorota M.; Thompson, Rachel; Knoers, Nine V.; Aartsma-Rus, Annemieke; Gut, Ivo Glynne; Wood, Libby; Harmuth, Tina; Durudas, Andre; Graessner, Holm; Schaefer, Franz; Riess, Olaf; RD-Connect consortium; NeurOmics consortium; EURenOmics consortium
Ítem Accés Obert Solving the unsolved rare diseases in Europe(Nature Research, 2021) Graessner, Holm; Zurek, Birte; Hoischen, Alexander; Beltran, Sergi
Ítem Accés Obert Solving unsolved rare neurological diseases-a Solve-RD viewpoint(Springer Nature, 2021) Matalonga, Leslie; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Solve-RD-DITF-RND; van de Warrenburg, Bart; Schöls, Ludger; Wilke, Carlo; Bevot, Andrea; Zuchner, Stephan; Beltran, Sergi; Laurie, Steven, 1973-; Matalonga, Leslie; Graessner, Holm; Synofzik, Matthis; Solve-RD Consortium