Molly M. Crenshaw

A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome

Jennifer J. Johnston, Mónica Sánchez-Contreras, Kim M. Keppler‐Noreuil et al. · The American Journal of Human Genetics · 2015 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Compound heterozygous alterations in intraflagellar transport protein <i>CLUAP1</i> in a child with a novel Joubert and oral–facial–digital overlap syndrome

Jennifer J. Johnston, Chanjae Lee, Ingrid M. Wentzensen et al. · Molecular Case Studies · 2017 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype

Susan M. Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano et al. · The American Journal of Human Genetics · 2022 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Pathogenetic insights from quantification of the cerebriform connective tissue nevus in Proteus syndrome

Neera R. Nathan, Rachna Patel, Molly M. Crenshaw et al. · Journal of the American Academy of Dermatology · 2017 · 16 citations

Medicine, Neurology, Pathology +12

Orthopaedic Management of Leg-length Discrepancy in Proteus Syndrome: A Case Series

Molly M. Crenshaw, Cara Goerlich, Lauren E. Ivey et al. · Journal of Pediatric Orthopaedics · 2018 · 16 citations

Medicine, Orthopedic Surgery, Surgery +13