Hans Joenje

Research output

Research output per year 1984 2003 2004 2005 2008 2009 2010 2012 2015 2022

• 71 Article
• 6 Meeting Abstract
• 2 Comment/Letter to the editor
• 1 Chapter
• 2 More
  • 1 Erratum/Corrigendum
  • 1 Letter

Research output per year

Research output per year

Search results

• 2010

  Ectopic ESCO2 Expression in Roberts Syndrome Fibroblasts Corrects Cohesion Defects and Sensitivity to DNA Damaging Agents

  van der Lelij, P., van Gosliga, D., Oostra, A. B., Steltenpool, J., de Groot, J., Waisfisz, Q., Scheper, R. J., Darroudi, F., Godthelp, B. C., Joenje, H. & de Winter, J. P., Jul 2010, In: American Journal of Medical Genetics Part A. 152A, 7, p. 1635-1636

  Research output: Contribution to journal › Meeting Abstract › Academic
• 2009

  Fanconi Anemia: Recent Advances and Perspectives

  Joenje, H., Dorsman, J. C., Waisfisz, Q., de Winter, J. P. & Bierings, M., 2009, In: Haematologica. 94, p. S7-S7

  Research output: Contribution to journal › Meeting Abstract › Other research output

  70 Citations (Scopus)
• 2007

  Roberts syndrome-SC phocomeliia: Clinical and molecular findings

  Vega, H., Jabs, E. W., Gordillo, M., Trainer, A., Luque, R., Kayserili, H., Skovby, F., Hennekam, R., Uzielli, M., Schnur, R., Manouvrier, S., Paznekas, W. A., Chang, S., Waisfisz, Q., Joenje, H., Hou, F. & Zou, H., 15 Jun 2007, In: American Journal of Medical Genetics Part A. 143A, 12, p. 1298-1299

  Research output: Contribution to journal › Meeting Abstract › Academic
• 2006

  Hypermethylation of FANCC and FANCL resulting in a mitomycine-C (MMC) sensitive cellular phenotype in sporadic acute leukemia.

  Hess, C. J., Ameziane, N., Schuurhuis, G. J., Errami, A., Denkers, F., Hubeeck, I., Kaspers, G. J. L., Joenje, H., Reinhardt, D., Ossenkoppele, G. J., Zwaan, C. M. & Waisfisz, Q., 16 Nov 2006, In: Blood. 108, 11, p. 630A-630A

  Research output: Contribution to journal › Meeting Abstract › Academic
• 2005

  Persistent chromosomal instability and cross-linker sensitivity in Fanconi anaemia derived leukaemia cell lines with bi-allelic FANCD1/BRCA2 mutations

  Meyer, S., Tonnies, H., Fergusson, WF., Oostra, AB., Medhurst, AL., Waisfisz, Q., De Winter, JP., Chen, F., Carr, TF., Green, M., Barber, L., Eden, OB., Will, AM., Joenje, H. & Taylor, GM., Apr 2005, In: British journal of haematology. 129, p. 81-81

  Research output: Contribution to journal › Meeting Abstract › Academic

  21 Citations (Scopus)
• 2004

  A Fanconi anemia core complex contains a ubiquitin ligase and is required for monoubiquitination of FANCD2

  Meetei, A. R., de Winter, J., Medhurst, A., Wallisch, M., Waisfisz, Q., van de Vrugt, H., Oostra, A., Yan, Z., Ling, C., Bishop, C., Hoatlin, M., Joenje, H. & Wang, OW., May 2004, In: CELL STRUCTURE AND FUNCTION. 29, p. 11-11

  Research output: Contribution to journal › Meeting Abstract › Academic