L. M. Peters

Development of a qPCR Method to Measure Mitochondrial and Genomic DNA Damage with Application to Chemotherapy-Induced DNA Damage and Cryopreserved Cells

G. Jacobson, M. Jameson, R. Cursons, 2016, Biology.

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

H. Ostrer, B. Keats, S. Riazuddin, 2002, Nature Genetics.

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.

David W. Anderson, A. Griffith, T. Friedman, 2002, Human molecular genetics.

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

M. Bitner-Glindzicz, S. Riazuddin, Z. Ahmed, 2001, American journal of human genetics.

Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.

James F Battey, T. Friedman, J. Battey, 2007, Genomics.

Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.

Y. Raphael, M. Brilliant, S. Riazuddin, 2010, American journal of human genetics.

Supradiaphragmatic Hodgkin's disease: significance of large mediastinal masses.

L. Prosnitz, L. Farber, A. Knowlton, 1980, International journal of radiation oncology, biology, physics.