Penelope L. Friedman
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Ion channel regulation and function, Connexins and lens biology, Cancer-related molecular mechanisms research, Barrier Structure and Function Studies
Most-Cited Works
- → Tricellulin Is a Tight-Junction Protein Necessary for Hearing(2006)282 cited
- → Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering(2010)264 cited
- → Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness(2005)110 cited
- → A RANDOMIZED PILOT STUDY OF SYSTEMIC IMMUNOSUPPRESSION IN THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION WITH CHOROIDAL NEOVASCULARIZATION(2010)87 cited
- → Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86(2014)86 cited
- → Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome(2009)86 cited
- → Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome(2016)50 cited
- → Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss(2015)21 cited