Xue Z Liu

Professor

  • 6427 Citations
1993 …2023
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Research Output 1993 2019

2016
60 Citations (Scopus)

Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions

Mittal, R., Patel, A. P., Debs, L. H., Nguyen, D., Patel, K., Grati, M., Mittal, J., Yan, D., Chapagain, P. & Liu, X. Z., Dec 1 2016, In : Journal of Cellular Physiology. 231, 12, p. 2599-2621 23 p.

Research output: Contribution to journalReview article

Matrix Metalloproteinases
Extracellular Matrix
Chemical activation
Tissue Inhibitor of Metalloproteinases
Enzyme Precursors
7 Citations (Scopus)

MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform

Grati, M., Yan, D., Raval, M. H., Walsh, T., Ma, Q., Chakchouk, I., Kannan-Sundhari, A., Mittal, R., Masmoudi, S., Blanton, S. H., Tekin, M., King, M. C., Yengo, C. M. & Liu, X. Z., 2016, (Accepted/In press) In : Human Mutation.

Research output: Contribution to journalArticle

Stereocilia
Deafness
Protein Isoforms
Molecular Motor Proteins
Hearing Loss
4 Citations (Scopus)

Otopathogenic Pseudomonas aeruginosa enters and survives inside macrophages

Mittal, R., Lisi, C. V., Kumari, H., Grati, M., Blackwelder, P., Yan, D., Jain, C., Mathee, K., Weckwerth, P. H. & Liu, X. Z., Nov 18 2016, In : Frontiers in Microbiology. 7, NOV, 1828.

Research output: Contribution to journalArticle

Pseudomonas aeruginosa
Macrophages
Suppurative Otitis Media
Otitis Media
Host-Pathogen Interactions
12 Citations (Scopus)

PDZD7-MYO7A complex identified in enriched stereocilia membranes

Morgan, C. P., Krey, J. F., Grati, M., Zhao, B., Fallen, S., Kannan-Sundhari, A., Liu, X. Z., Choi, D., Müller, U. & Barr-Gillespie, P. G., Aug 15 2016, In : eLife. 5, AUGUST, e18312.

Research output: Contribution to journalArticle

Stereocilia
Cells
Membranes
Deafness
Genes
5 Citations (Scopus)

Pseudomonas aeruginosa activates PKC-alpha to invade middle ear epithelial cells

Mittal, R., Grati, M., Yan, D. & Liu, X. Z., Mar 4 2016, In : Frontiers in Microbiology. 7, MAR, 255.

Research output: Contribution to journalArticle

Middle Ear
Suppurative Otitis Media
Pseudomonas aeruginosa
Epithelial Cells
Otitis Media

Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase inhibitor p19Ink4d

Ma, Q., Grati, M., Bai, F., Pei, J., Pei, X-H. & Liu, X. Z., Mar 10 2016, In : Cell death & disease. 7, p. e2131

Research output: Contribution to journalLetter

Cyclin-Dependent Kinase Inhibitor p19
Auditory Hair Cells
Animal Disease Models
Cyclin-Dependent Kinases
Hearing Loss
8 Citations (Scopus)

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

Diaz-Horta, O., Abad, C., Sennaroglu, L., Ii, J. F., DeSmidt, A., Bademci, G., Tokgoz-Yilmaz, S., Duman, D., Cengiz, F. B., Grati, MH., Fitoz, S., Liu, X. Z., Farooq, A., Imtiaz, F., Currall, B. B., Morton, C. C., Nishita, M., Minami, Y., Lu, Z., Walz, K. & 1 others, Tekin, M., May 24 2016, In : Proceedings of the National Academy of Sciences of the United States of America. 113, 21, p. 5993-5998 6 p.

Research output: Contribution to journalArticle

Auditory Hair Cells
Inner Ear
Receptor Tyrosine Kinase-like Orphan Receptors
Hearing
Spiral Ganglion
20 Citations (Scopus)

Serotonin Activates Bacterial Quorum Sensing and Enhances the Virulence of Pseudomonas aeruginosa in the Host

Knecht, L. D., O'Connor, G., Mittal, R., Liu, X. Z., Daftarian, P., Deo, S. K. & Daunert, S., Feb 2 2016, (Accepted/In press) In : EBioMedicine.

Research output: Contribution to journalArticle

Quorum Sensing
Pseudomonas aeruginosa
Virulence
Serotonin
Bacteria
39 Citations (Scopus)

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Yan, D., Tekin, D., Bademci, G., Foster, J., Cengiz, F. B., Kannan-Sundhari, A., Guo, S., Mittal, R., Zou, B., Grati, M., Kabahuma, R. I., Kameswaran, M., Lasisi, T. J., Adedeji, W. A., Lasisi, A. O., Menendez, I., Herrera, M., Carranza, C., Maroofian, R., Crosby, A. H. & 11 others, Bensaid, M., Masmoudi, S., Behnam, M., Mojarrad, M., Feng, Y., Duman, D., Mawla, A. M., Nord, A. S., Blanton, S. H., Liu, X. Z. & Tekin, M., Aug 1 2016, In : Human Genetics. 135, 8, p. 953-961 9 p.

Research output: Contribution to journalArticle

Deafness
DNA
Guatemala
Genes
Iran
5 Citations (Scopus)

Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil

Manzoli, G. N., Bademci, G., Acosta, A. X., Félix, T. M., Cengiz, F. B., Foster, J., Da Silva, D. S. D., Menendez, I., Sanchez-Pena, I., Tekin, D., Blanton, S. H., Abe-Sandes, K., Liu, X. Z. & Tekin, M., Nov 1 2016, In : Annals of Human Genetics. 80, 6, p. 327-331 5 p.

Research output: Contribution to journalArticle

Deafness
Hearing Loss
Brazil
Genes
Genetic Heterogeneity
12 Citations (Scopus)

The genetic basis of deafness in populations of African descent

Rudman, J. R., Kabahuma, R. I., Bressler, S. E., Feng, Y., Blanton, S. H., Yan, D. & Liu, X. Z., Dec 20 2016, (Accepted/In press) In : Journal of Genetics and Genomics.

Research output: Contribution to journalArticle

Deafness
Hearing Loss
Mutation
Population
Connexins

The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation

Zhou, Y., Qing, J., Dong, Y., Nie, J., Li, J., Wang, C., Liu, Y., Peng, T., Duan, M., Liu, X. Z. & Xie, DI., Mar 3 2016, In : Acta Oto-Laryngologica. 136, 3, p. 277-282 6 p.

Research output: Contribution to journalArticle

Sensorineural Hearing Loss
Inner Ear
Transcription Factors
Genes
Control Groups
2015
44 Citations (Scopus)

Amissense mutation in DCDC2 causeshuman recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

Grati, M., Chakchouk, I., Ma, Q., Bensaid, M., Desmidt, A., Turki, N., Yan, D., Baanannou, A., Mittal, R., Driss, N., Blanton, S. H., Farooq, A., Lu, Z., Liu, X. Z. & Masmoudi, S., 2015, In : Human Molecular Genetics. 24, 9, p. 2482-2491 10 p.

Research output: Contribution to journalArticle

Cilia
Deafness
Mutation
Microtubules
Zebrafish
27 Citations (Scopus)

Association of PRPS1 Mutations with Disease Phenotypes

Mittal, R., Patel, K., Mittal, J., Chan, B., Yan, D., Grati, MH. & Liu, X. Z., 2015, In : Disease Markers. 2015, 127013.

Research output: Contribution to journalArticle

Ligases
Phenotype
Mutation
Audition
S-Adenosylmethionine
43 Citations (Scopus)

Current concepts in the pathogenesis and treatment of chronic suppurative otitis media

Mittal, R., Lisi, C. V., Gerring, R., Mittal, J., Mathee, K., Narasimhan, G., Azad, R. K., Yao, Q., Grati, MH., Yan, D., Eshraghi, A., Angeli, S. I., Telischi, F. F. & Liu, X. Z., Oct 1 2015, In : Journal of Medical Microbiology. 64, 10, p. 1103-1116 14 p.

Research output: Contribution to journalArticle

Suppurative Otitis Media
Otitis Media
Inner Ear
Ear Oval Window
Ear
12 Citations (Scopus)

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

Wang, H., Wang, X., He, C., Li, H., Qing, J., Grati, M., Hu, Z., Li, J., Hu, Y., Xia, K., Mei, L., Wang, X., Yu, J., Chen, H., Jiang, L., Liu, Y., Men, M., Zhang, H., Guan, L., Xiao, J. & 3 others, Zhang, J., Liu, X. Z. & Feng, Y., Mar 27 2015, In : Journal of Human Genetics. 60, 3, p. 119-126 8 p.

Research output: Contribution to journalArticle

Exome
Mutation
Genes
Carcinoembryonic Antigen
Cell Adhesion Molecules
1 Citation (Scopus)

Imaging assessment of profound sensorineural deafness with inner ear anatomical abnormalities

Wu, W. J., He, X. B., Tan, L. H., Hu, P., Peng, A. Q., Xiao, Z. A., Yang, S., Wang, T., Qing, J., Chen, X., Li, J. K., Peng, T., Dong, Y. P., Liu, X. Z. & Xie, D. H., Mar 1 2015, In : Journal of Otology. 10, 1, p. 29-38 10 p.

Research output: Contribution to journalArticle

Open Access
Cochlea
Deafness
Inner Ear
Cochlear Implants
Vestibular Aqueduct
8 Citations (Scopus)

Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System

Mittal, R., Chan, B., Grati, M., Mittal, J., Patel, K., Debs, L. H., Patel, A. P., Yan, D., Chapagain, P. & Liu, X. Z., 2015, (Accepted/In press) In : Journal of Cellular Physiology.

Research output: Contribution to journalArticle

Purinergic P2X2 Receptors
Molecular Structure
Molecular structure
Purinergic P2X4 Receptors
Purinergic P2X Receptors
14 Citations (Scopus)

Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53

Chakchouk, I., Grati, M., Bademci, G., Bensaid, M., Ma, Q., Chakroun, A., Foster, J., Yan, D., Duman, D., Diaz-Horta, O., Ghorbel, A., Mittal, R., Farooq, A., Tekin, M., Masmoudi, S. & Liu, X. Z., Aug 25 2015, In : Molecular Genetics and Genomics. 290, 4, p. 1327-1334 8 p.

Research output: Contribution to journalArticle

Hearing Loss
Mutation
Collagen Type XI
Exome
Trinucleotide Repeats
15 Citations (Scopus)

Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China

Qing, J., Zhou, Y., Lai, R., Hu, P., Ding, Y., Wu, W., Xiao, Z., Ho, P. T., Liu, Y., Liu, J., Du, L., Yan, D., Goldstein, B. J., Liu, X. Z. & Xie, D., Jan 1 2015, In : Genetic Testing and Molecular Biomarkers. 19, 1, p. 52-58 7 p.

Research output: Contribution to journalArticle

Sensorineural Hearing Loss
Mitochondrial DNA
China
Mutation
Mutation Rate

Role of p19ink4d in the pathogenesis of hearing loss

Lai, R., Li, J., Hu, P., Wen, J., Jie, Q., Dong, Y., Peng, T., Liu, X. Z. & Xie, D., 2015, In : International Journal of Clinical and Experimental Pathology. 8, 10, p. 12243-12251 9 p.

Research output: Contribution to journalArticle

Hearing Loss
Cisplatin
Deafness
Inner Ear
Mutation
30 Citations (Scopus)

The application of genome editing in studying hearing loss

Zou, B., Mittal, R., Grati, M., Lu, Z., Shu, Y., Tao, Y., Feng, Y., Xie, D., Kong, W., Yang, S., Chen, Z. Y. & Liu, X. Z., Sep 1 2015, In : Hearing Research. 327, p. 102-108 7 p.

Research output: Contribution to journalArticle

Clustered Regularly Interspaced Short Palindromic Repeats
Hearing Loss
Hearing
Inner Ear
Technology
7 Citations (Scopus)

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations

Yan, D., Kannan-Sundhari, A., Vishwanath, S., Qing, J., Mittal, R., Kameswaran, M. & Liu, X. Z., Sep 1 2015, In : Genetic Testing and Molecular Biomarkers. 19, 9, p. 512-527 16 p.

Research output: Contribution to journalArticle

Deafness
Population
Bilateral Hearing Loss
Inborn Genetic Diseases
Sensorineural Hearing Loss
2014
1 Citation (Scopus)

Cochlear implants in genetic deafness

Liu, X., Dec 1 2014, In : Journal of Otology. 9, 4, p. 156-162 7 p.

Research output: Contribution to journalArticle

Open Access
Cochlear Implantation
Cochlear Implants
Deafness
Spiral Ganglion
Sensorineural Hearing Loss
39 Citations (Scopus)

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

Diaz-Horta, O., Subasioglu-Uzak, A., Grati, M., DeSmidt, A., Foster, J., Cao, L., Bademci, G., Tokgoz-Yilmaz, S., Duman, D., Cengiz, F. B., Abad, C., Mittal, R., Blanton, S. H., Liu, X. Z., Farooq, A., Walz, K., Lu, Z. & Tekin, M., Jul 8 2014, In : Proceedings of the National Academy of Sciences of the United States of America. 111, 27, p. 9864-9868 5 p.

Research output: Contribution to journalArticle

Stereocilia
Hearing
Membrane Proteins
Inclusion Bodies
Cell Membrane
17 Citations (Scopus)

Immunity genes and susceptibility to otitis media: A comprehensive review

Mittal, R., Robalino, G., Gerring, R., Chan, B., Yan, D., Grati, M. & Liu, X. Z., Jan 1 2014, In : Journal of Genetics and Genomics. 41, 11, p. 567-581 15 p.

Research output: Contribution to journalArticle

Otitis Media
Immunity
Genes
Suppurative Otitis Media
Twin Studies
11 Citations (Scopus)

In Vitro interaction of Pseudomonas aeruginosa with human middle ear epithelial cells

Mittal, R., Grati, MH., Gerring, R., Blackwelder, P., Yan, D., Li, J. D. & Liu, X. Z., Mar 14 2014, In : PLoS One. 9, 3, e91885.

Research output: Contribution to journalArticle

Middle Ear
Pseudomonas aeruginosa
ears
epithelial cells
otitis media
16 Citations (Scopus)

Role of innate immunity in the pathogenesis of otitis media

Mittal, R., Kodiyan, J., Gerring, R., Mathee, K., Li, J. D., Grati, M. & Liu, X. Z., Dec 1 2014, In : International Journal of Infectious Diseases. 29, p. e259-e267

Research output: Contribution to journalArticle

Otitis Media
Innate Immunity
Middle Ear
Suppurative Otitis Media
Microbial Drug Resistance
8 Citations (Scopus)

Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating

Qing, J., Yan, D., Zhou, Y., Liu, Q., Wu, W., Xiao, Z., Liu, Y., Liu, J., Du, L., Xie, D. & Liu, X. Z., Oct 7 2014, In : PLoS One. 9, 10, e109178.

Research output: Contribution to journalArticle

Exome
deafness
Genetic Heterogeneity
Audition
hearing
2013
4 Citations (Scopus)

Audiologic and genetic features of the A3243G mtDNA mutation

Vivero, R. J., Ouyang, X., Kim, Y. G., Liu, W., Du, L., Yan, D. & Liu, X. Z., May 1 2013, In : Genetic Testing and Molecular Biomarkers. 17, 5, p. 383-389 7 p.

Research output: Contribution to journalArticle

Mitochondrial DNA
Mutation
Hearing Loss
Bilateral Hearing Loss
DNA
16 Citations (Scopus)

Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy

Liu, X. Z., Xie, D., Yuan, H. J., De Brouwer, A. P. M., Christodoulou, J. & Yan, D., Jan 1 2013, In : International Journal of Audiology. 52, 1, p. 23-28 6 p.

Research output: Contribution to journalArticle

deafness
Ligases
Hearing Loss
Phenotype
tooth disease
66 Citations (Scopus)

Mutation of the ATP-gated P2X2 receptor leads to progressive hearing loss and increased susceptibility to noise

Yan, D., Zhu, Y., Walsh, T., Xie, D., Yuan, H., Sirmaci, A., Fujikawa, T., Wong, A. C. Y., Loh, T. L., Du, L., Grati, M., Vlajkovic, S. M., Blanton, S. H., Ryan, A. F., Chen, Z. Y., Thorne, P. R., Kachar, B., Tekin, M., Zhao, H. B., Housley, G. D. & 2 others, King, M. C. & Liu, X. Z., Feb 5 2013, In : Proceedings of the National Academy of Sciences of the United States of America. 110, 6, p. 2228-2233 6 p.

Research output: Contribution to journalArticle

Purinergic P2X2 Receptors
Hearing Loss
Noise
Adenosine Triphosphate
Mutation
23 Citations (Scopus)

Next-generation sequencing in genetic hearing loss

Yan, D., Tekin, M., Blanton, S. H. & Liu, X. Z., Aug 1 2013, In : Genetic Testing and Molecular Biomarkers. 17, 8, p. 581-587 7 p.

Research output: Contribution to journalArticle

Hearing Loss
Genetic Association Studies
Deafness
Genes
Technology
2012
11 Citations (Scopus)

Analysis of miR-376 RNA cluster members in the mouse inner ear

Yan, D., Xing, Y., Ouyang, X., Zhu, J., Chen, Z. Y., Lang, H. & Liu, X. Z., Dec 1 2012, In : International Journal of Experimental Pathology. 93, 6, p. 450-457 8 p.

Research output: Contribution to journalArticle

Ribose-Phosphate Pyrophosphokinase
Inner Ear
RNA
Stria Vascularis
Sensory Ganglia
6 Citations (Scopus)

Audioprofiles and antioxidant enzyme genotypes in presbycusis

Angeli, S. I., Bared, A., Ouyang, X., Du, L. L., Yan, D. & Liu, X. Z., Nov 1 2012, In : Laryngoscope. 122, 11, p. 2539-2542 4 p.

Research output: Contribution to journalArticle

Presbycusis
Antioxidants
Genotype
Enzymes
Alleles

Cochlear implants in individuals with usher syndrome

Herman, B., Vivero, R. & Liu, X. Z., Dec 1 2012, Usher Syndrome: Pathogenesis, Diagnosis and Therapy. Nova Science Publishers, Inc., p. 347-352 6 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Usher Syndromes
Cochlear implants
Cochlear Implants
8 Citations (Scopus)

Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations

King, P. J., Ouyang, X., Du, L., Yan, D., Angeli, S. I. & Liu, X. Z., Nov 1 2012, In : Otolaryngology - Head and Neck Surgery (United States). 147, 5, p. 932-936 5 p.

Research output: Contribution to journalArticle

Sensorineural Hearing Loss
Pediatrics
Mutation
Mitochondrial DNA
Deafness
8 Citations (Scopus)

Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct

Lai, R., Hu, P., Zhu, F., Zhu, G., Vivero, R., Peng, A., Wu, W., Xiao, Z., Liu, X. Z. & Xie, D., Apr 1 2012, In : Journal of Laryngology and Otology. 126, 4, p. 349-355 7 p.

Research output: Contribution to journalArticle

Cochlear Implantation
Mutation
Speech Perception
Cochlear Implants
Enlarged Vestibular Aqueduct
47 Citations (Scopus)

Genetics of Hearing and Deafness

Angeli, S. I., Lin, X. & Liu, X. Z., Nov 1 2012, In : Anatomical Record. 295, 11, p. 1812-1829 18 p.

Research output: Contribution to journalArticle

deafness
hearing
Deafness
Hearing
gene
6 Citations (Scopus)

Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort

Vivero, R. J., Ouyang, X., Yan, D., Du, L., Liu, W., Angeli, S. I. & Liu, X. Z., Sep 1 2012, In : Genetic Testing and Molecular Biomarkers. 16, 9, p. 1146-1148 3 p.

Research output: Contribution to journalArticle

Mitochondrial DNA
Mutation
Deafness
Mutation Rate
Hearing Loss
60 Citations (Scopus)

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss

Yariz, K. O., Duman, D., Seco, C. Z., Dallman, J., Huang, M., Peters, T. A., Sirmaci, A., Lu, N., Schraders, M., Skromne, I., Oostrik, J., Diaz-Horta, O., Young, J., Tokgoz-Yilmaz, S., Konukseven, O., Shahin, H., Hetterschijt, L., Kanaan, M., Oonk, A. M. M., Edwards, Y. J. K. & 10 others, Li, H., Atalay, S., Blanton, S. H., Desmidt, A. A., Liu, X. Z., Pennings, R. J. E., Lu, Z., Chen, Z. Y., Kremer, H. & Tekin, M., Nov 2 2012, In : American Journal of Human Genetics. 91, 5, p. 872-882 11 p.

Research output: Contribution to journalArticle

Sensorineural Hearing Loss
Inner Ear
Mutation
Proteins
Morpholinos
2011
32 Citations (Scopus)

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

Kabahuma, R. I., Ouyang, X., Du, L. L., Yan, D., Hutchin, T., Ramsay, M., Penn, C. & Liu, X. Z., May 1 2011, In : International Journal of Pediatric Otorhinolaryngology. 75, 5, p. 611-617 7 p.

Research output: Contribution to journalArticle

Sequence Deletion
Mutation
Population
Genes
Restriction Fragment Length Polymorphisms
45 Citations (Scopus)

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

Schultz, J. M., Bhatti, R., Madeo, A. C., Turriff, A., Muskett, J. A., Zalewski, C. K., King, K. A., Ahmed, Z. M., Riazuddin, S., Ahmad, N., Hussain, Z., Qasim, M., Kahn, S. N., Meltzer, M. R., Liu, X. Z., Munisamy, M., Ghosh, M., Rehm, H. L., Tsilou, E. T., Griffith, A. J. & 4 others, Zein, W. M., Brewer, C. C., Riazuddin, S. & Friedman, T. B., Nov 1 2011, In : Journal of Medical Genetics. 48, 11, p. 767-775 9 p.

Research output: Contribution to journalArticle

Usher Syndromes
Deafness
Heterozygote
Alleles
Mutation
8 Citations (Scopus)

Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice

Yan, D., Kamiya, K., Ouyang, X. M. & Liu, X. Z., Feb 1 2011, In : International Journal of Experimental Pathology. 92, 1, p. 66-71 6 p.

Research output: Contribution to journalArticle

Stereocilia
Knockout Mice
Auditory Hair Cells
Usher Syndromes
Cochlea

Clinical application of genetic testing for sensorineural hearing loss

King, P., Grobman, A. & Liu, X. Z., Apr 1 2011, Hearing Loss: Classification, Causes and Treatment. Nova Science Publishers, Inc., p. 399-410 12 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Sensorineural Hearing Loss
Genetic Testing
Hearing Loss
Genes
Sensation Disorders
11 Citations (Scopus)

Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations

Lipan, M., Ouyang, X., Yan, D., Angeli, S. I., Du, L. L. & Liu, X. Z., Apr 1 2011, In : Laryngoscope. 121, 4, p. 811-814 4 p.

Research output: Contribution to journalArticle

Heterozygote
Hearing
Mutation
Hearing Loss
Incidence
23 Citations (Scopus)

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64

Cheng, J., Zhu, Y., He, S., Lu, Y., Chen, J., Han, B., Petrillo, M., Wrzeszczynski, K. O., Yang, S., Dai, P., Zhai, S., Han, D., Zhang, M. Q., Li, W., Liu, X. Z., Li, H., Chen, Z. Y. & Yuan, H., Jul 15 2011, In : American Journal of Human Genetics. 89, 1, p. 56-66 11 p.

Research output: Contribution to journalArticle

Mitochondrial Proteins
Hearing Loss
Inner Auditory Hair Cells
Mitochondria
Inhibitor of Apoptosis Proteins
9 Citations (Scopus)

Influence of DFNB1 status on expressive language in deaf children with cochlear implants

Angeli, S. I., Suarez, H., Lopez, A., Balkany, T. J. & Liu, X. Z., Dec 1 2011, In : Otology and Neurotology. 32, 9, p. 1437-1443 7 p.

Research output: Contribution to journalArticle

Cochlear Implants
Language
Deafness
Nonparametric Statistics
Child Language
1 Citation (Scopus)

Mutation Screening of the GJA7 (Cx45) Gene in a Large International Series of Probands with Nonsyndromic Hearing Impairment

Ouyang, X. M., Yan, D., Aslan, I., Du, L. L., Tekin, M. & Liu, X. Z., May 1 2011, In : Genetic Testing and Molecular Biomarkers. 15, 5, p. 333-336 4 p.

Research output: Contribution to journalArticle

Mutation
Connexins
Genes
Connexin 43
Sensorineural Hearing Loss
14 Citations (Scopus)

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Sun, Y., Chen, J., Sun, H., Cheng, J., Li, J., Lu, Y., Lu, Y., Jin, Z., Zhu, Y., Ouyang, X., Yan, D., Dai, P., Han, D., Yang, W., Wang, R., Liu, X. Z. & Yuan, H., Jan 1 2011, In : Journal of Human Genetics. 56, 1, p. 64-70 7 p.

Research output: Contribution to journalArticle

Missense Mutation
Hearing Loss
China
Myosins
Mutation