Emma M. Wade

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

Emma M. Wade, Philip B. Daniel, Zandra A. Jenkins et al. · The American Journal of Human Genetics · 2016 · 73 citations · Full text

Life Sciences, Genetics, Molecular Biology +8

Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype

Emma M. Wade, Zandra A. Jenkins, Philip B. Daniel et al. · American Journal of Medical Genetics Part A · 2017 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Biallelic variants in EFEMP1 in a man with a pronounced connective tissue phenotype

Sean G. W. Driver, Meremaihi R. Jackson, Konrad Klaus Richter et al. · European Journal of Human Genetics · 2019 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Sulf1 modulates BMP signaling and is required for somite morphogenesis and development of the horizontal myoseptum

Jason R. Meyers, Jessica Planamento, Pierson Ebrom et al. · Developmental Biology · 2013 · 27 citations

Life Sciences, Developmental Biology, Molecular Biology +16

Fibulin-3 knockout mice demonstrate corneal dysfunction but maintain normal retinal integrity

Steffi Daniel, Marian Renwick, Viet Q. Chau et al. · Journal of Molecular Medicine · 2020 · 25 citations · Full text

Medicine, Genetics, Ophthalmology +9