A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux typeKrista A. Geister, Sally A. Camper|Human Molecular Genetics|2012Cited by 69
Loss of function of <i>Colgalt1</i> disrupts collagen post-translational modification and causes musculoskeletal defectsKrista A. Geister, David R. Beier|Disease Models & Mechanisms|2019Cited by 34
The Genetic and Molecular Etiologies of Two Spontaneous Mouse Models of Skeletal Dysplasia and Infertility.Krista A. Geister|Deep Blue (University of Michigan)|2013Cited by 0