Maria Eriksson

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Maria Eriksson, W. Ted Brown, Leslie B. Gordon et al. · Nature · 2003 · 2.2K citations · Full text

Point Mutations, Genetic Disorder, Genetics +5

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome

Robert D. Goldman, Dale K. Shumaker, Michael R. Erdos et al. · Proceedings of the National Academy of Sciences · 2004 · 1.1K citations · Full text

Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging

Dale K. Shumaker, Thomas Dechat, Alexander Kohlmaier et al. · Proceedings of the National Academy of Sciences · 2006 · 751 citations · Full text

Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome

Renée Varga, Maria Eriksson, Michael R. Erdos et al. · Proceedings of the National Academy of Sciences · 2006 · 291 citations · Full text

Assessment of left ventricular structure and function in preeclampsia by echocardiography and cardiovascular biomarkers

Rangeen Rafik Hamad, Anders Larsson, John Pernow et al. · Journal of Hypertension · 2009 · 169 citations