Research Explorer

Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.

Researcher

Nina De Rocker

8 Results

2018

BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment (vol 6, 30330, 2016)

Annekatrien BoelWouter SteyaertNina De RockerBjörn MentenBert CallewaertAnne De PaepePaul CouckeAndy Willaert

2017

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Björn MentenSarah VergultNina De RockerMarleen PraetAgnieszka Prytula-EbelsBert Callewaert

A1 Journal Article in NATURE GENETICS

2016

BATCH-GE : batch analysis of next-generation sequencing data for genome editing assessment

Annekatrien BoelWouter SteyaertNina De RockerBjörn MentenBert CallewaertAnne De PaepePaul CouckeAndy Willaert

A1 Journal Article in SCIENTIFIC REPORTS

CRISPR-Cas9 modeling of cell lines and zebrafish to study the TLX1-PHF6 cooperative interrelationship in T-cell acute lymphoblastic leukemia

Siebe LoontiensKaat DurinckNina De RockerAnnekatrien BoelSuzanne VanhauwaertPieter RondouInge Van de WalleTom TaghonBjörn MentenAndy WillaertPaul CouckePieter Van VlierbergheFranki Speleman

Zebrafish collagen type I: molecular and biochemical characterization of the major structural protein in bone and skin

Charlotte GistelinckAnn HuysseunePaul WittenAn StaesKris GevaertNina De RockerBjörn MentenFransiska MalfaitAnne De PaepePaul CouckeAndy Willaert

A1 Journal Article in SCIENTIFIC REPORTS

2015

Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Nina De RockerSarah VergultEva JacobsSuzanne VanhauwaertAndy WillaertPaul CouckeFranki SpelemanBjörn Menten

A1 Journal Article in GENETICS IN MEDICINE

2014

Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems

Sarah VergultNina De RockerAndy WillaertBjörn Menten

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

2012

Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis

Frauke CoppietersBram De WildeSteve LefeverEllen De MeesterNina De RockerCaroline Van CauwenberghFilip PattynBart LeroyJan HellemansJo VandesompeleElfride De Baere

A1 Journal Article in GENETICS IN MEDICINE