Shirley Rainier
University of Michigan–Ann Arbor(US)Michigan United(US)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Neurogenetic and Muscular Disorders Research, Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation
Most-Cited Works
- → Relaxation of imprinted genes in human cancer(1993)794 cited
- → Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour(1994)464 cited
- → Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia(2001)359 cited
- → Neuropathy Target Esterase Gene Mutations Cause Motor Neuron Disease(2008)243 cited
- → NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)(2003)206 cited
- → Myofibrillogenesis Regulator 1 Gene Mutations Cause Paroxysmal Dystonic Choreoathetosis(2004)179 cited
- Loss of imprinting in hepatoblastoma.(1995)
- Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.