Kerry A. Miller
University of Oxford(GB)MRC Weatherall Institute of Molecular Medicine(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Genomic variations and chromosomal abnormalities, Hedgehog Signaling Pathway Studies, Genomics and Rare Diseases, Craniofacial Disorders and Treatments
Most-Cited Works
- → Factors influencing success of clinical genome sequencing across a broad spectrum of disorders(2015)386 cited
- → A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis(2017)195 cited
- A new formula for a half-oxidized hematoxylin solution that neither overstains nor requires differentiation.(1974)
- → Diagnostic value of exome and whole genome sequencing in craniosynostosis(2016)120 cited
- → Mutations in CDC45 , Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis(2016)118 cited
- → A Recurrent Mosaic Mutation in SMO , Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome(2016)91 cited
- → Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability(2015)