Nina De Rocker
Ghent University Hospital(BE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, CRISPR and Genetic Engineering, Genomic variations and chromosomal abnormalities, Chromatin Remodeling and Cancer, Ocular Disorders and Treatments
Most-Cited Works
- → Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly(2017)218 cited
- → Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin(2016)126 cited
- → BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment(2016)97 cited
- → Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral Problems(2014)67 cited
- → Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity(2014)59 cited
- → Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis(2012)45 cited
- → Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment(2018)2 cited
- Leber Congenital Amaurosis: Development Of A Comprehensive Molecular Genetic Test Panel Using Next-generation Sequencing(2011)
- CRISPR-Cas9 modeling of cell lines and zebrafish to study the TLX1-PHF6 cooperative interrelationship in T-cell acute lymphoblastic leukemia(2016)