Debra Brooker
Mary Lyon Centre at MRC Harwell(GB)Medical Research Council(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Congenital heart defects research, Genomics and Chromatin Dynamics, Developmental Biology and Gene Regulation, Epigenetics and DNA Methylation
Most-Cited Works
- → A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse(2000)656 cited
- → A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains(2013)522 cited
- → The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period(2007)481 cited
- → Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media(2006)95 cited
- → Mouse mutagenesis identifies novel roles for left–right patterning genes in pulmonary, craniofacial, ocular, and limb development(2009)35 cited
- → The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon(2003)32 cited
- → Analysis of the mouse mutant Cloth‐ears shows a role for the voltage‐gated sodium channel Scn8a in peripheral neural hearing loss(2009)15 cited
- A G3 recessive screen for mutations affecting left-right patterning(2005)
- Identification of the regulatory elements responsible for cathepsin D expression and activation in retinal pigment epithelium cells(1999)