☰

Julia Louise Wunderlich, Ph.D.

Affiliations: 
1990- Audiology Monash Medical Centre 
 1997-2003 Audiology and Speech Sciences University of Melbourne, Parkville, Victoria, Australia 
Area:
Audiology
Google:
"Julia Wunderlich"
Tree Publications Similar researchers PubMed Report error

Parents

Sign in to add mentor
Barbara Katherine Cone grad student 1997-2003 University of Melbourne
Robert K. Shepherd grad student 1997-2003 University of Melbourne

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Mao D, Wunderlich J, Savkovic B, et al. (2021) Speech token detection and discrimination in individual infants using functional near-infrared spectroscopy. Scientific Reports. 11: 24006
Wunderlich JL, Cone-Wesson BK. (2006) Maturation of CAEP in infants and children: a review. Hearing Research. 212: 212-23
Wunderlich JL, Cone-Wesson BK, Shepherd R. (2006) Maturation of the cortical auditory evoked potential in infants and young children. Hearing Research. 212: 185-202
Cone-Wesson B, Wunderlich J. (2003) Auditory evoked potentials from the cortex: audiology applications. Current Opinion in Otolaryngology & Head and Neck Surgery. 11: 372-7
Rance G, Cone-Wesson B, Wunderlich J, et al. (2002) Speech perception and cortical event related potentials in children with auditory neuropathy. Ear and Hearing. 23: 239-53
Dahl HH, Saunders K, Kelly TM, et al. (2001) Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness. The Medical Journal of Australia. 175: 191-4
Wunderlich JL, Cone-Wesson BK. (2001) Effects of stimulus frequency and complexity on the mismatch negativity and other components of the cortical auditory-evoked potential. The Journal of the Acoustical Society of America. 109: 1526-37
Wilcox SA, Saunders K, Osborn AH, et al. (2000) High frequency hearing loss correlated with mutations in the GJB2 gene. Human Genetics. 106: 399-405
See more...