Kathryn M. Harper

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Margot A. Cousin, Blake A. Creighton, Keith A. Breau et al. · Nature Genetics · 2021 · 98 citations · Full text

Developmental Anomaly, Pathogenic Sptbn1 Variants, Brain Development +7

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice

Go Suzuki, Kathryn M. Harper, Tetsuya Hiramoto et al. · Human Molecular Genetics · 2009 · 86 citations · Full text

Internalised White Ideal, Skin Tone Surveillance, and Hair Surveillance Predict Skin and Hair Dissatisfaction and Skin Bleaching among African American and Indian Women

Kathryn M. Harper, Becky L. Choma · Sex Roles · 2018 · 79 citations

Ethnicity, Skin Tone Surveillance, Gender Studies +13

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain

Kathryn M. Harper, Takeshi Hiramoto, Kenji Tanigaki et al. · Human Molecular Genetics · 2012 · 62 citations · Full text

Brain Mechanism, Genetics, Social Behavior Dysfunction +20

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice

Go Suzuki, Kathryn M. Harper, Tetsuya Hiramoto et al. · Human Molecular Genetics · 2009 · 53 citations · Full text