Diana C. Blaydon
Queen Mary University of London(GB)
Publications by Year
Research Areas
Skin and Cellular Biology Research, Wnt/β-catenin signaling in development and cancer, Kruppel-like factors research, Hearing, Cochlea, Tinnitus, Genetics, Ion Transport and Channel Regulation
Most-Cited Works
- → A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene(2000)324 cited
- → Inflammatory Skin and Bowel Disease Linked toADAM17Deletion(2011)306 cited
- → RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome(2012)202 cited
- → The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia(2006)190 cited
- → Genomewide Single Nucleotide Polymorphism Microarray Mapping in Basal Cell Carcinomas Unveils Uniparental Disomy as a Key Somatic Event(2005)165 cited
- → Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1(2000)132 cited
- → Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion(2011)117 cited
- → Assessment of the genetic causes of recessive childhood non‐syndromic deafness in the UK – implications for genetic testing(2005)114 cited
- → Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma(2013)113 cited
- → Role for WNT16B in human epidermal keratinocyte proliferation and differentiation(2007)78 cited