Image-based characterization of thrombus formation in time-lapse DIC microscopy

by Brieu, Nicolas, Navab, Nassir, Serbanovic-Canic, Jovana, Ouwehand, Willem H., Stemple, Derek L., Cvejic, Ana, Groher, Martin
Published 2012

Single-Cell RNA-Sequencing Reveals a Continuous Spectrum of Differentiation in Hematopoietic Cells

by Macaulay, Iain C., Svensson, Valentine, Labalette, Charlotte, Ferreira, Lauren, Hamey, Fiona, Voet, Thierry, Teichmann, Sarah A., Cvejic, Ana
Published 2016

A Loss of Function Screen of Identified Genome-Wide Association Study Loci Reveals New Genes Controlling Hematopoiesis

by Bielczyk-Maczyńska, Ewa, Serbanovic-Canic, Jovana, Ferreira, Lauren, Soranzo, Nicole, Stemple, Derek L., Ouwehand, Willem H., Cvejic, Ana
Published 2014

CD4-Transgenic Zebrafish Reveal Tissue-Resident Th2- and Regulatory T Cell–like Populations and Diverse Mononuclear Phagocytes

by Dee, Christopher T., Nagaraju, Raghavendar T., Athanasiadis, Emmanouil I., Gray, Caroline, Fernandez del Ama, Laura, Johnston, Simon A., Secombes, Christopher J., Cvejic, Ana, Hurlstone, Adam F. L.
Published 2016

Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators

by Tijssen, Marloes R., Cvejic, Ana, Joshi, Anagha, Hannah, Rebecca L., Ferreira, Rita, Forrai, Ariel, Bellissimo, Dana C., Oram, S. Helen, Smethurst, Peter A., Wilson, Nicola K., Wang, Xiaonan, Ottersbach, Katrin, Stemple, Derek L., Green, Anthony R., Ouwehand, Willem H., Göttgens, Berthold
Published 2011

The Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish

by Bielczyk-Maczyńska, Ewa, Lam Hung, Laure, Ferreira, Lauren, Fleischmann, Tobias, Weis, Félix, Fernández-Pevida, Antonio, Harvey, Steven A., Wali, Neha, Warren, Alan J., Barroso, Inês, Stemple, Derek L., Cvejic, Ana
Published 2015

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

by Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Published 2011

Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR

by Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Christel, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric
Published 2012