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Researcher
Nina De Rocker
Profile
Projects
Publications
Activities
8
Results
2018
BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment (vol 6, 30330, 2016)
Annekatrien Boel
Wouter Steyaert
Nina De Rocker
Björn Menten
Bert Callewaert
Anne De Paepe
Paul Coucke
Andy Willaert
Correction
2018
2017
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Björn Menten
Sarah Vergult
Nina De Rocker
Marleen Praet
Agnieszka Prytula-Ebels
Bert Callewaert
A1
Journal Article
in
NATURE GENETICS
2017
2016
BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment
Annekatrien Boel
Wouter Steyaert
Nina De Rocker
Björn Menten
Bert Callewaert
Anne De Paepe
Paul Coucke
Andy Willaert
A1
Journal Article
in
SCIENTIFIC REPORTS
2016
CRISPR-Cas9 modeling of cell lines and zebrafish to study the TLX1-PHF6 cooperative interrelationship in T-cell acute lymphoblastic leukemia
Siebe Loontiens
Kaat Durinck
Nina De Rocker
Annekatrien Boel
Suzanne Vanhauwaert
Pieter Rondou
Inge Van de Walle
Tom Taghon
Björn Menten
Andy Willaert
Paul Coucke
Pieter Van Vlierberghe
Franki Speleman
C3
Conference
2016
Zebrafish collagen type I: molecular and biochemical characterization of the major structural protein in bone and skin
Charlotte Gistelinck
Ann Huysseune
Paul Witten
An Staes
Kris Gevaert
Nina De Rocker
Björn Menten
Fransiska Malfait
Anne De Paepe
Paul Coucke
Andy Willaert
A1
Journal Article
in
SCIENTIFIC REPORTS
2016
2015
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity
Nina De Rocker
Sarah Vergult
Eva Jacobs
Suzanne Vanhauwaert
Andy Willaert
Paul Coucke
Franki Speleman
Björn Menten
A1
Journal Article
in
GENETICS IN MEDICINE
2015
2014
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems
Sarah Vergult
Nina De Rocker
Andy Willaert
Björn Menten
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2014
2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
Frauke Coppieters
Bram De Wilde
Steve Lefever
Ellen De Meester
Nina De Rocker
Caroline Van Cauwenbergh
Filip Pattyn
Bart Leroy
Jan Hellemans
Jo Vandesompele
Elfride De Baere
A1
Journal Article
in
GENETICS IN MEDICINE
2012