Vikram Sharma

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 · 218 citations · Full text

Frequent Cause, Molecular Biology, Craniofacial Development +6

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

Sclerostin, Developmental Biology, Signal Transduction +11

Effect of Preoperative Pain on Inferior Alveolar Nerve Block

Vivek Aggarwal, Mamta Singla, Arunajatesan Subbiya et al. · Anesthesia Progress · 2015 · 53 citations · Full text

<i>De novo</i> and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

Christian Babbs, Deborah Lloyd, Alistair T. Pagnamenta et al. · Journal of Medical Genetics · 2014 · 41 citations · Full text

Mutations of 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. · The Lancet · 2013 · 34 citations · Full text

Basic-helix-loop-helix Partner, Frequent Cause, Molecular Biology +6