Denise Yan, Ph.D.

Research Assistant Professor

  • 2096 Citations
19942019
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  • 20 Similar Profiles
Hearing Loss Medicine & Life Sciences
Mutation Medicine & Life Sciences
Deafness Medicine & Life Sciences
Genes Medicine & Life Sciences
Usher Syndromes Medicine & Life Sciences
Sensorineural Hearing Loss Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Hearing Medicine & Life Sciences

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Research Output 1994 2019

  • 2096 Citations
  • 83 Article
  • 5 Review article
  • 1 Comment/debate

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
Mutation
Inner Auditory Hair Cells
1 Citations

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

Amino acid 118 in the deafness causing (DFNA20/26) ACTG1 gene is a mutational hot spot

Wang, L., Yan, D., Qin, L., Li, T., Liu, H., Li, W., Mittal, R., Yong, F., Chapagain, P., Liao, S. & Liu, X. Z., Jun 1 2018, In : Gene Reports. 11, p. 264-269 6 p.

Research output: Contribution to journalArticle

Deafness
Hearing Loss
Amino Acids
Genes
Mutation
2 Citations

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss

Niu, Z., Yan, D., Bressler, S., Mei, L., Feng, Y. & Liu, X. Z., Jan 1 2018, In : International Journal of Pediatric Otorhinolaryngology. 104, p. 47-50 4 p.

Research output: Contribution to journalArticle

Hearing Loss
Exome
Mutation
Frameshift Mutation
Nonsense Codon

An update on phosphodiesterase mutations underlying genetic etiology of hearing loss and retinitis pigmentosa

Mittal, R., Bencie, N., Parrish, J. M., Liu, G., Mittal, J., Yan, D. & Liu, X. Z., Feb 8 2018, In : Frontiers in Genetics. 9, FEB, 9.

Research output: Contribution to journalComment/debate

Usher Syndromes
Retinitis Pigmentosa
Phosphoric Diester Hydrolases
Hearing Loss
Mutation