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Susan G Stanton

Showing results (1-10 of 12) with videos related to

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Frontiers in Human Neuroscience|June 8, 2012
On Variability and Genes: Inter-individual Differences in Auditory Brain FunctionPeter Sörös, Susan G Stanton
Biomedical Engineering Education|January 19, 2026
Quantitative and Qualitative Assessments of the Impacts of a Summer Clinical Immersion Program for Biomedical Engineering StudentsEllen P Brennan-Pierce, Julie A Dunn, Susan G Stanton
Biomedical Engineering Education|February 28, 2025
Insights from a Virtual Clinical Immersion ProgramEllen P Brennan-Pierce, Susan G Stanton, Julie A Dunn
American Journal of Audiology|September 27, 2005
Hearing screening outcomes in infants of pregestational diabetic mothersSusan G Stanton, Elizabeth Ryerson, Shana L Moore, et al.
Hearing Research|August 26, 2006
N-Acetyl L-cysteine does not protect against premature age-related hearing loss in C57BL/6J mice: a pilot studyRickie R Davis, Ming-Wen Kuo, Susan G Stanton, et al.
American Journal of Audiology|April 2, 2014
X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical careSusan G Stanton, Anne Griffin, Tracy L Stockley, et al.
International Journal of Molecular Sciences|June 12, 2026
Heterozygous Nonsense Mutation in the Nuclear Transport Factor <i>KPNA7</i>, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant OtosclerosisTammy Benteau, Nelly Abdelfatah, Anne Griffin, et al.
Human Genetics|November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effectJustin A Pater, Tammy Benteau, Anne Griffin, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHLNelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
European Journal of Human Genetics : EJHG|April 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analysesSushma Singh, Cindy Penney, Anne Griffin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Frontiers in Human Neuroscience|June 8, 2012
On Variability and Genes: Inter-individual Differences in Auditory Brain FunctionPeter Sörös, Susan G Stanton
Biomedical Engineering Education|January 19, 2026
Quantitative and Qualitative Assessments of the Impacts of a Summer Clinical Immersion Program for Biomedical Engineering StudentsEllen P Brennan-Pierce, Julie A Dunn, Susan G Stanton
Biomedical Engineering Education|February 28, 2025
Insights from a Virtual Clinical Immersion ProgramEllen P Brennan-Pierce, Susan G Stanton, Julie A Dunn
American Journal of Audiology|September 27, 2005
Hearing screening outcomes in infants of pregestational diabetic mothersSusan G Stanton, Elizabeth Ryerson, Shana L Moore, et al.
Hearing Research|August 26, 2006
N-Acetyl L-cysteine does not protect against premature age-related hearing loss in C57BL/6J mice: a pilot studyRickie R Davis, Ming-Wen Kuo, Susan G Stanton, et al.
American Journal of Audiology|April 2, 2014
X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical careSusan G Stanton, Anne Griffin, Tracy L Stockley, et al.
International Journal of Molecular Sciences|June 12, 2026
Heterozygous Nonsense Mutation in the Nuclear Transport Factor <i>KPNA7</i>, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant OtosclerosisTammy Benteau, Nelly Abdelfatah, Anne Griffin, et al.
Human Genetics|November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effectJustin A Pater, Tammy Benteau, Anne Griffin, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHLNelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
European Journal of Human Genetics : EJHG|April 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analysesSushma Singh, Cindy Penney, Anne Griffin, et al.
Pageof 2