Cambria I. Wethey

Exome Sequencing Identifies a Rare <i>HSPG2</i> Variant Associated with Familial Idiopathic Scoliosis

Erin E. Baschal, Cambria I. Wethey, Kandice Swindle et al. · G3 Genes Genomes Genetics · 2014 · 53 citations · Full text

Hspg2 Gene, Rare Diseases, Genetic Disorder +14

Mutations in <i>KIF7</i> implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish

Elizabeth Terhune, Melissa T. Cuevas, Anna M. Monley et al. · Human Mutation · 2020 · 28 citations · Full text

Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology

Erin E. Baschal, Elizabeth Terhune, Cambria I. Wethey et al. · G3 Genes Genomes Genetics · 2018 · 21 citations · Full text

Neurogenomics, Disease Etiology, Genetics +29

Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease

Elizabeth Terhune, Cambria I. Wethey, Melissa T. Cuevas et al. · Genes · 2021 · 17 citations · Full text

Family Members, Exome Sequencing, Genetics +28

Severity of Idiopathic Scoliosis Is Associated with Differential Methylation: An Epigenome-Wide Association Study of Monozygotic Twins with Idiopathic Scoliosis

Patrick M. Carry, Elizabeth Terhune, G. Devon Trahan et al. · Genes · 2021 · 17 citations · Full text