Genome-wide identification of microRNA-related variants associated with risk of Alzheimer’s disease

por Ghanbari, Mohsen, Ikram, M. Arfan, de Looper, Hans W. J., Hofman, Albert, Erkeland, Stefan J., Franco, Oscar H., Dehghan, Abbas
Publicado 2016

Truncated CSF3 receptors induce pro‐inflammatory responses in severe congenital neutropenia

por Olofsen, Patricia A., Bosch, Dennis A., de Looper, Hans W. J., van Strien, Paulina M. H., Hoogenboezem, Remco M., Roovers, Onno, van der Velden, Vincent H. J., Bindels, Eric M. J., De Pater, Emma M., Touw, Ivo P.
Publicado 2022

Malignant Transformation Involving CXXC4 Mutations Identified in a Leukemic Progression Model of Severe Congenital Neutropenia

por Olofsen, Patricia A., Fatrai, Szabolcs, van Strien, Paulina M.H., Obenauer, Julia C., de Looper, Hans W.J., Hoogenboezem, Remco M., Erpelinck-Verschueren, Claudia A.J., Vermeulen, Michael P.W.M., Roovers, Onno, Haferlach, Torsten, Jansen, Joop H., Ghazvini, Mehrnaz, Bindels, Eric M.J., Schneider, Rebekka K., de Pater, Emma M., Touw, Ivo P.
Publicado 2020