Onderzoeker
Nina De Rocker
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 feb 2012 → 23 sep 2018
Publicaties
1 - 7 van 7
- Zebrafish collagen type I: molecular and biochemical characterization of the major structural protein in bone and skin(2016)
Auteurs: Charlotte Gistelinck, R Gioia, A Gagliardi, F Tonelli, L Marchese, L Bianchi, C Landi, L Bini, Ann Huysseune, Paul Witten, et al.
- Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity(2015)
Auteurs: Nina De Rocker, Sarah Vergult, David Koolen, Eva Jacobs, Alexander Hoischen, Susan Zeesman, Birgitte Bang, Frédérique Béna, Nele Bockaert, Ernie Bongers, et al.
Pagina's: 460 - 466 - BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment
Auteurs: Annekatrien Boel, Wouter Steyaert, Nina De Rocker, Bert Callewaert
- Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems
Auteurs: Anneke T Vulto-van Silfhout, Shivakumar Rajamanickam, Philip J Jensik, Sarah Vergult, Nina De Rocker, Kathryn J Newhall, Ramya Raghavan, Sara N Reardon, Kelsey Jarrett, Tara McIntyre, et al.
Pagina's: 649 - 661 - Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Auteurs: Daniela A Braun, Jia Rao, Geraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst-Schwan, et al.
Pagina's: 1529 - 1538 - BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment (vol 6, 30330, 2016)
Auteurs: Annekatrien Boel, Wouter Steyaert, Nina De Rocker, Bert Callewaert
- Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
Auteurs: Steve Lefever, Ellen De Meester, Nina De Rocker, Filip Pattyn, Françoise Meire, Jan Hellemans
Pagina's: 576 - 585