Rachel Hardisty
Mary Lyon Centre at MRC Harwell(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Muscle Physiology and Disorders, Genomics and Chromatin Dynamics, Epigenetics and DNA Methylation, Vestibular and auditory disorders
Most-Cited Works
- → A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse(2000)656 cited
- → Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31(2003)339 cited
- → A radiation hybrid map of mouse genes(2001)93 cited
- → The Deaf Mouse Mutant Jeff (Jf) is a Single Gene Model of Otitis Media(2002)82 cited
- → Mutagenesis strategies for identifying novel loci associated with disease phenotypes(2003)42 cited
- → Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)(2001)26 cited
- → Enu Mutagenesis and the Search for Deafness Genes(1999)20 cited
- → Towards a mutant map of the mouse ? new models of neurological, behavioural, deafness, bone, renal and blood disorders(2004)18 cited
- → The molecular genetics of inherited deafness – current knowledge and recent advances(1998)13 cited