Maia V. Ouspenskaia

Measurement of Residual Leukemia during Remission in Childhood Acute Lymphoblastic Leukemia

William Roberts, Zeev Estrov, Maia V. Ouspenskaia et al. · New England Journal of Medicine · 1997 · 186 citations · Full text

Medicine, Hematology, Oncology +17

Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

Erich Roessler, Maia V. Ouspenskaia, Jayaprakash D. Karkera et al. · The American Journal of Human Genetics · 2008 · 174 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Loss-of-Function Mutations in Growth Differentiation Factor-1 (GDF1) Are Associated with Congenital Heart Defects in Humans

Jayaprakash D. Karkera, J.S. Lee, Erich Roessler et al. · The American Journal of Human Genetics · 2007 · 139 citations · Full text

Life Sciences, Cardiology, Genetics +16

Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation

Hélène Neyret‐Kahn, Moussa Benhamed, Tao Ye et al. · Genome Research · 2013 · 128 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

The mutational spectrum of holoprosencephaly-associated changes within the<i>SHH</i>gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis

Erich Roessler, Kênia Balbi El-Jaick, Christèle Dubourg et al. · Human Mutation · 2009 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16