Concepedia
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Publications
17
Citations
1.5K
H-Index
16
Active since
2008
Affiliations
University of Oxford(Current)
John Radcliffe Hospital
MRC Weatherall Institute of Molecular Medicine
Oxford University Hospitals NHS Trust
Centre for Human Genetics
Aimée L Fenwick is an author at University of Oxford specializing in molecular genetics, genetics, and craniosynostosis genetics.
Publications per year
2008–2019
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, Hilary C. Martin, Stefano Lise et al. · Nature Genetics · 2015 · 388 citations · Full text
Life Sciences, Genetics, Molecular Genetics +14
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis
Vikram Sharma, Aimée L Fenwick, Mia Brockop et al. · Nature Genetics · 2013 · 224 citations
Dentistry, Molecular Biology, Molecular Genetics +16
Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth
Pekka Nieminen, Neil V. Morgan, Aimée L Fenwick et al. · The American Journal of Human Genetics · 2011 · 194 citations · Full text
Dentistry, Genetics, Molecular Genetics +17
Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis
Stephen R.F. Twigg, Elena Vorgia, Simon J. McGowan et al. · Nature Genetics · 2013 · 174 citations
Dentistry, Cell Biology, Craniofacial Biology +12
Diagnostic value of exome and whole genome sequencing in craniosynostosis
Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan et al. · Journal of Medical Genetics · 2016 · 123 citations · Full text
Life Sciences, Genetics, Molecular Genetics +16
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