Victoria R. Sanders

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy

Norine Voisin, Rhonda E. Schnur, Sofia Douzgou et al. · The American Journal of Human Genetics · 2021 · 44 citations · Full text

Epileptic Encephalopathy, Mendelian Disorder, Genetic Disorder +9

De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

Sandra Jansen, Ilse van der Werf, A. Micheil Innes et al. · European Journal of Human Genetics · 2019 · 42 citations · Full text

Neurodevelopmental Disorders, Mendelian Disorder, Genetic Disorder +11

A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects

David B. Beck, Megan T. Cho, Francisca Millan et al. · Neurogenetics · 2016 · 34 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +8

Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7

Laura Castilla‐Vallmanya, Kaja Kristine Selmer, Clémantine Dimartino et al. · Genetics in Medicine · 2020 · 32 citations · Full text

Biology, Medicine, Genetics +12

Cervical spinal cord compression in infants with achondroplasia: should neuroimaging be routine?

Victoria R. Sanders, Stephen H. Sheldon, Joel Charrow · Genetics in Medicine · 2018 · 31 citations · Full text

Spinal Cord Injury, Spinal Trauma, Pediatrics +6