Kathy Gardner
Alameda Health System(US)
Publications by Year
Research Areas
Migraine and Headache Studies, Neurofibromatosis and Schwannoma Cases, Neuroscience of respiration and sleep, Genetic Neurodegenerative Diseases, Peptidase Inhibition and Analysis
Most-Cited Works
- → Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas(2013)319 cited
- Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.(1996)
- → A new locus for hemiplegic migraine maps to chromosome 1q31(1997)198 cited
- → High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation(2015)189 cited
- → Early life experience alters behavior during social defeat: Focus on serotonergic systems(2005)169 cited
- → qPrimerDepot: a primer database for quantitative real time PCR(2006)159 cited
- → Adverse experience during early life and adulthood interact to elevate tph2 mRNA expression in serotonergic neurons within the dorsal raphe nucleus(2009)96 cited
- → Current whole-body MRI applications in the neurofibromatoses(2016)86 cited
- → Update on the genetics of migraine(2004)85 cited
- → Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia(2004)84 cited