Laurie S. Sadler

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran et al. · The American Journal of Human Genetics · 2005 · 276 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10

Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia

Deborah Krakow, Joris Vriens, Natalia Camacho et al. · The American Journal of Human Genetics · 2009 · 207 citations · Full text

Molecular Physiology, Natural Sciences, Genetics +9

<i>HCN1</i>mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

Carla Marini, Alessandro Porro, Agnès Rastetter et al. · Brain · 2018 · 134 citations · Full text

Rationale and Design for the Blood Pressure Intervention of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trial

William C. Cushman, Richard H. Grimm, Jeffrey A. Cutler et al. · The American Journal of Cardiology · 2007 · 122 citations

Non-pharmacological Intervention, Hypertension, Diabetes Management +10

The Williams syndrome: Evidence for possible autosomal dominant inheritance

Laurie S. Sadler, Luther K. Robinson, Kathleen R. Verdaasdonk et al. · American Journal of Medical Genetics · 1993 · 71 citations