- ORCID iD
-
0000-0003-1337-1970
Show
Sort by
-
- Journal Article
- A1
- open access
Bmpr1aa modulates the severity of the skeletal phenotype in an fkbp10-deficient Bruck syndrome zebrafish model
-
- Journal Article
- A2
- open access
Crispant analysis in zebrafish as a tool for rapid functional screening of disease-causing genes for bone fragility
-
- Journal Article
- A1
- open access
MOXD1 is a lineage-specific gene and a tumor suppressor in neuroblastoma
-
- Journal Article
- A1
- open access
Zebrafish avatars : toward functional precision medicine in low-grade serous ovarian cancer
-
Syntaxin-18 defects in human and zebrafish cause traffic jams and unravel key roles in early bone development
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.394-394 -
Syntaxin 18 defects in human and zebrafish unravel key roles in early cartilage and bone development
-
- Conference Paper
- C3
- open access
Crispant analysis in zebrafish as a tool for rapid functional screening of disease-causing genes for Osteogenesis Imperfecta
-
SOX11 is a mediator of core regulatory circuit robustness : upregulation of SWI/SNF components and recruitment of transcriptional enhancer NONO
-
- Journal Article
- A1
- open access
A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract
-
- Conference Paper
- C3
- open access
A tapt1 knockout zebrafish line with aberrant lens development and impaired vision models human pediatric cataract