Chad VanSant‐Webb

Clinical utility of a next generation sequencing panel assay for Marfan and Marfan‐like syndromes featuring aortopathy

Whitney Wooderchak‐Donahue, Chad VanSant‐Webb, Tatiana Tvrdik et al. · American Journal of Medical Genetics Part A · 2015 · 68 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Large-scale Identification of Clonal Hematopoiesis and Mutations Recurrent in Blood Cancers

Julie Feusier, Sasi Arunachalam, Tsewang Tashi et al. · Blood Cancer Discovery · 2021 · 43 citations · Full text

Life Sciences, Genetics, Hematology +17

NF1 Somatic Mutation in Dystrophic Scoliosis

Rebecca L. Margraf, Chad VanSant‐Webb, Rong Mao et al. · Journal of Molecular Neuroscience · 2019 · 20 citations

Medicine, Genetics, Molecular Genetics +14

Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic Telangiectasia

Whitney Wooderchak‐Donahue, Jamie McDonald, Andrew Farrell et al. · Journal of Medical Genetics · 2018 · 16 citations

Life Sciences, Genetics, Molecular Genetics +17