Subaashini Natarajan

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Clare V. Logan, György Szabadkai, Jenny A. Sharpe et al. · Nature Genetics · 2013 · 365 citations

Mitochondrial Myopathy, Mitochondrial Calcium, Muscle Disorder +11

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans et al. · Nature Cell Biology · 2015 · 245 citations · Full text

Ciliopathy Genes, Functional Genomics, Glioma +10

FGF‐2 modulates Wnt signaling in undifferentiated hESC and iPS cells through activated PI3‐K/GSK3β signaling

Vanessa Ding, Ling Ling, Subaashini Natarajan et al. · Journal of Cellular Physiology · 2010 · 121 citations

Signal Transduction, Developmental Biology, Fibroblast Growth Factor-2 +14

Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects

Zakia A. Abdelhamed, Gabrielle Wheway, Katarzyna Szymańska et al. · Human Molecular Genetics · 2013 · 107 citations · Full text

Tyrosine Phosphorylation Profiling in FGF-2 Stimulated Human Embryonic Stem Cells

Vanessa Ding, Paul J. Boersema, Leong Yan Foong et al. · PLoS ONE · 2011 · 63 citations · Full text

Cell Proliferation, Unique Phosphotyrosine Peptides, Fgf Receptors +17