Sandra Gill
Texas A&M University(US)
Publications by Year
Research Areas
Hereditary Neurological Disorders, RNA Research and Splicing, RNA regulation and disease, Signaling Pathways in Disease, Cellular Mechanics and Interactions
Most-Cited Works
- → Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia(2001)593 cited
- → Tissue-Specific Reduction in Splicing Efficiency of IKBKAP Due to the Major Mutation Associated with Familial Dysautonomia(2003)140 cited
- → Linkage Analysis of Chromosome 1q Markers in 136 Prostate Cancer Families(1998)135 cited
- → Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia(2007)73 cited
- → Identification of the first non‐Jewish mutation in familial Dysautonomia(2003)72 cited
- → Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31(1999)69 cited
- → Fusion of the EWS Gene to a DNA segment from 9q22‐31 in a human myxoid chondrosarcoma(1995)44 cited
- → Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31(1999)38 cited
- → Drosophila RNase H1 is essential for development but not for proliferation(2001)32 cited
- → Of splice and men: what does the distribution of IKAP mRNA in the rat tell us about the pathogenesis of familial dysautonomia?(2003)29 cited