Denise Yan

Research Assistant Professor

  • 2224 Citations
19942019
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  • 22 Similar Profiles
Hearing Loss Medicine & Life Sciences
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Sensorineural Hearing Loss Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Hearing Medicine & Life Sciences

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Research Output 1994 2019

  • 2224 Citations
  • 86 Article
  • 5 Review article
  • 1 Comment/debate

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

Li, W., Mei, L., Chen, H., Cai, X., Liu, Y., Men, M., Liu, X. Z., Yan, D., Ling, J., Feng, Y. & Dorszewska, J., Jan 1 2019, In : Neural Plasticity. 2019, 7143458.

Research output: Contribution to journalArticle

Open Access
Waardenburg Syndrome
Genotype
Phenotype
Melanosis
Amblyopia
1 Citation (Scopus)

Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2-associated schwannomas reveals differences in efficacy and drug resistance development

Fuse, M. A., Dinh, C. T., Vitte, J., Kirkpatrick, J., Mindos, T., Plati, S. K., Young, J., Huang, J., Carlstedt, A., Franco, M. C., Brnjos, K., Nagamoto, J., Petrilli, A. M., Copik, A. J., Soulakova, J. N., Bracho, O., Yan, D., Mittal, R., Shen, R., Telischi, F. F. & 5 othersMorrison, H., Giovannini, M., Liu, X. Z., Chang, L. S. & Fernandez-Valle, C., Mar 18 2019, In : Neuro-Oncology. 21, 4, p. 486-497 12 p.

Research output: Contribution to journalArticle

Neurofibromatosis 2
Neurilemmoma
Drug Resistance
Acoustic Neuroma
Neurofibromin 2

Role of microRNAs in inner ear development and hearing loss

Mittal, R., Liu, G., Polineni, S. P., Bencie, N., Yan, D. & Liu, X. Z., Feb 20 2019, In : Gene. 686, p. 49-55 7 p.

Research output: Contribution to journalReview article

Inner Ear
MicroRNAs
Hearing Loss
Inner Auditory Hair Cells
Research

Zebrafish Model for Nonsyndromic X-Linked Sensorineural Deafness, DFNX1

DeSmidt, A. A., Zou, B., Grati, M., Yan, D., Mittal, R., Yao, Q., Richmond, M. T., Denyer, S., Liu, X. Z. & Lu, Z., Jan 1 2019, In : Anatomical Record.

Research output: Contribution to journalArticle

deafness
Ribose-Phosphate Pyrophosphokinase
Deafness
Zebrafish
Danio rerio
1 Citation (Scopus)

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

Wang, L., Feng, Y., Yan, D., Qin, L., Grati, M., Mittal, R., Li, T., Sundhari, A. K., Liu, Y., Chapagain, P., Blanton, S. H., Liao, S. & Liu, X. Z., Jun 2 2018, (Accepted/In press) In : Human Genetics. p. 1-10 10 p.

Research output: Contribution to journalArticle

Phosphoric Diester Hydrolases
Exome
Inner Auditory Hair Cells
Genes
Genetic Heterogeneity