Odelia Rajanayagam

Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

Erik Schoenmakers, Maura Agostini, Catherine Mitchell et al. · Journal of Clinical Investigation · 2010 · 308 citations · Full text

Spermatogenesis, Genetics, Lipid Peroxidation +18

A Dominant-negative Peroxisome Proliferator-activated Receptor γ (PPARγ) Mutant Is a Constitutive Repressor and Inhibits PPARγ-mediated Adipogenesis

Mark Gurnell, John M. Wentworth, Maura Agostini et al. · Journal of Biological Chemistry · 2000 · 264 citations · Full text

Retardation of post-natal development caused by a negatively acting thyroid hormone receptor α1

Alexander A. Tinnikov, Kristina Nordström, Peter Thorén et al. · The EMBO Journal · 2002 · 180 citations · Full text

Developmental Biology, Genetics, Thyroid Disease +8

Non-DNA binding, dominant-negative, human PPARγ mutations cause lipodystrophic insulin resistance

Maura Agostini, Erik Schoenmakers, Catherine Mitchell et al. · Cell Metabolism · 2006 · 180 citations · Full text

Digenic inheritance of severe insulin resistance in a human pedigree

David B. Savage, Maura Agostini, Inês Barroso et al. · Nature Genetics · 2002 · 145 citations

Insulin Resistance, Metabolic Syndrome, Genetic Determinant +8