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American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.Journal of Translational Medicine|December 11, 2014
Melanoma expression of matrix metalloproteinase-23 is associated with blunted tumor immunity and poor responses to immunotherapyDuane Moogk, Ines Pires da Silva, Michelle W Ma, et al.Journal of Translational Medicine|August 4, 2012
Serum microRNAs as biomarkers for recurrence in melanomaErica B Friedman, Shulian Shang, Eleazar Vega-Saenz de Miera, et al.Science Advances|October 9, 2024
SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sacHyun Jae Lee, Cristina Fenollar-Ferrer, Kevin Isgrig, et al.American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.Journal of Clinical and Translational Science|December 10, 2024
Evaluation and lessons learned from the dissemination and implementation science scholars program in the national cancer prevention and control research networkDaniela B Friedman, Cam Escoffery, Elaine H Morrato, et al.Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.JBMR Plus|April 3, 2025
How neighborhood socioeconomic status, green space, and walkability are associated with risk for fracture among postmenopausal womenMarilyn E Wende, Matthew C Lohman, Daniela B Friedman, et al.Journal of Medical Genetics|August 7, 2017
A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueductParna Chattaraj, Tina Munjal, Keiji Honda, et al.Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, et al.Pageof 97