Marianne Blockmans

INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

Monique Jacoby, James J. Cox, Stéphanie Gayral et al. · Nature Genetics · 2009 · 354 citations · Full text

Inpp5e Mutations, Molecular Physiology, Signal Transduction +6

Management and 1‐Year Outcomes of Patients With Newly Diagnosed Atrial Fibrillation and Chronic Kidney Disease: Results From the Prospective GARFIELD‐AF Registry

Shinya Goto, Pantep Angchaisuksiri, Jean‐Pierre Bassand et al. · Journal of the American Heart Association · 2019 · 54 citations · Full text

Developmental defects and rescue from glucose intolerance of a catalytically-inactive novel Ship2 mutant mouse

Eléonore Dubois, Monique Jacoby, Marianne Blockmans et al. · Cellular Signalling · 2012 · 30 citations

Knockout Mouse, Developmental Biology, Developmental Defects +6

The association between the SH2‐containing inositol polyphosphate 5‐Phosphatase 2 (SHIP2) and the adaptor protein APS has an impact on biochemical properties of both partners

Sheela Onnockx, Julie De Schutter, Marianne Blockmans et al. · Journal of Cellular Physiology · 2007 · 23 citations

Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry

Jitendra PS. Sawhney, V A Kothiwale, Vikas Bisne et al. · Indian Heart Journal · 2018 · 21 citations · Full text