Heidi A. Heilstedt

Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome

Heidi A. Heilstedt, Blake C. Ballif, L A Howard et al. · The American Journal of Human Genetics · 2003 · 296 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

<i>GFAP</i> mutations, age at onset, and clinical subtypes in Alexander disease

Morgan J. Prust, Jiaxian Wang, Hiroki Morizono et al. · Neurology · 2011 · 256 citations · Full text

Medicine, Neurology, Neuroscience +15

Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure

Marzena Gajęcka, Wei Yu, Blake C. Ballif et al. · European Journal of Human Genetics · 2004 · 149 citations

Dentistry, Genetics, Molecular Genetics +15

Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice

Clemencia Colmenares, Heidi A. Heilstedt, Lisa G. Shaffer et al. · Nature Genetics · 2001 · 129 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Loss of the Potassium Channel β‐Subunit Gene, <i>KCNAB2</i>, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome

Heidi A. Heilstedt, Daniel L. Burgess, Anne E. Anderson et al. · Epilepsia · 2001 · 92 citations

Life Sciences, Genetics, Molecular Genetics +17