Jennifer L. Dawkins
University of Sydney(AU)Concord Repatriation General Hospital(AU)Anzac Research Institute(AU)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Cellular transport and secretion, Endoplasmic Reticulum Stress and Disease, RNA regulation and disease, Hippo pathway signaling and YAP/TAZ
Most-Cited Works
- → Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I(2001)418 cited
- → The gene for hereditary sensory neuropathy type I (HSN–I) maps to chromosome 9q22.1–q22.3(1996)120 cited
- → Hereditary Sensory Neuropathy Type I: Haplotype Analysis Shows Founders in Southern England and Europe(2001)28 cited
- → Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy(2002)26 cited
- → Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1→q22.3: exclusion of GAS1 and XPA(1997)19 cited
- → A YAC-Based Transcript Map of Human Chromosome 9q22.1–q22.3 Encompassing the Loci for Hereditary Sensory Neuropathy Type I and Multiple Self-Healing Squamous Epithelioma(1998)18 cited
- → The Charcot–Marie–Tooth Binary Repeat Contains a Gene Transcribed from the Opposite Strand of a Partially Duplicated Region of theCOX10Gene(1997)18 cited
- → Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis(2000)10 cited