Author

Annmarie Sommer

Observed name: A. Sommer

Institutions: Nationwide Children's Hospital, The Ohio State University

Observed institutions: Nationwide Children's Hospital, The Ohio State University

OpenAlex ID: A5037019482

Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

2001 · Ernst Reichenberger, Valdenize Tiziani, et al. · The American Journal of Human Genetics · 198

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

2010 · Jennifer J. Johnston, Julie C. Sapp, et al. · Human Mutation · 130

Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expression

1992 · J. Wagstaff, J.H.M. Knoll, et al. · Nature Genetics · 100

Works count: 3

Citation count: 428

H-index: 3

I10-index: 3