Kathy Gardner

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Arkadiusz Piotrowski, Jing Xie, Ying F Liu et al. · Nature Genetics · 2013 · 315 citations

Developmental Anomaly, Rare Diseases, Somatic Variant +12

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.

Kevin M. Flanigan, Kathy Gardner, Kathy Alderson et al. · PubMed · 1996 · 248 citations

A new locus for hemiplegic migraine maps to chromosome 1q31

Kathy Gardner, M. Michael Barmada, Louis J. Ptáček et al. · Neurology · 1997 · 198 citations

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation

Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes et al. · Human Mutation · 2015 · 188 citations · Full text

Genetics, Genetic Epidemiology, Pathology +17

Early life experience alters behavior during social defeat: Focus on serotonergic systems

Kathy Gardner, K. V. Thrivikraman, Stafford L. Lightman et al. · Neuroscience · 2005 · 169 citations

Behavioral Sciences, Psychopathology, Psychiatry +15