D. Yan

F. Telischi, X. Liu, D. Yan, 2021, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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

X. Liu, D. Yan, R. Mittal, 2015, Genetic testing and molecular biomarkers.

Association of PRPS1 Mutations with Disease Phenotypes

X. Liu, D. Yan, R. Mittal, 2015, Disease markers.

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

X. Liu, J. Christodoulou, D. Yan, 2013, International journal of audiology.

Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment.

M. Tekin, X. Liu, D. Yan, 2011, Genetic testing and molecular biomarkers.

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

M. Tekin, C. Morton, X. Liu, 2017, PloS one.

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.

M. Ramsay, X. Liu, C. Penn, 2011, International journal of pediatric otorhinolaryngology.

Cochlear implantation in individuals with Usher type 1 syndrome.

F. Telischi, X. Liu, A. Eshraghi, 2008, International journal of pediatric otorhinolaryngology.

Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis

X. Liu, S. Blanton, Zhengmao Hu, 2019, Genetics in Medicine.

Audiological and genetic features of the mtDNA mutations

X. Liu, D. Yan, S. Angeli, 2008, Acta oto-laryngologica.

Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II

S. Jacobson, X. Liu, D. Yan, 2009, Journal of Human Genetics.

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

S. Z. Yang, D. Yan, G. Feng, 2008, Clinical genetics.

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

K. Arnos, A. Pandya, D. Corey, 2003, Human molecular genetics.

Pseudomonas aeruginosa Activates PKC-Alpha to Invade Middle Ear Epithelial Cells

X. Liu, D. Yan, R. Mittal, 2016, Front. Microbiol..

Otopathogenic Pseudomonas aeruginosa Enters and Survives Inside Macrophages

X. Liu, K. Mathee, D. Yan, 2016, Front. Microbiol..

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

Recent Perspectives on Gene-Microbe Interactions Determining Predisposition to Otitis Media

X. Liu, D. Yan, R. Mittal, 2019, Front. Genet..

Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions

Amit P. Patel, X. Liu, D. Yan, 2016, Journal of cellular physiology.

Otopathogenic Staphylococcus aureus Invades Human Middle Ear Epithelial Cells Primarily through Cholesterol Dependent Pathway

Amit P. Patel, X. Liu, D. Yan, 2019, Scientific Reports.

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

D. Yan, H. Lang, X. Ouyang, 2012, International journal of experimental pathology.

Neurotransmitters: The Critical Modulators Regulating Gut–Brain Axis

Sylvia Daunert, Amit P. Patel, S. Daunert, 2017, Journal of cellular physiology.

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

H. Rehm, C. Cremers, C. Möller, 1998, Science.

The genetic bases for non-syndromic hearing loss among Chinese

X. Liu, D. Yan, X. Ouyang, 2009, Journal of Human Genetics.

Cochlear molecules and hereditary deafness.

X. Liu, D. Yan, 2008, Frontiers in bioscience : a journal and virtual library.

The genetic deafness in Chinese population

D. Yan, Liu Xuezhong, Ouyang Xiaomei, 2006 .

Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating

X. Liu, D. Yan, L. Du, 2014, PloS one.

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

M. Tekin, X. Liu, D. Duman, 2015, Molecular Genetics and Genomics.

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis

X. Liu, S. Blanton, D. Yan, 2018, BioMed research international.

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.

X. Liu, K. Johnson, D. Yan, 2005, Human molecular genetics.

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population

Steve D. M. Brown, S. Jacobson, X. Liu, 2005, Human Genetics.

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

D. Yan, Yong Feng, L. Mei, 2019, Neural plasticity.

Genetic screening revealed usher syndrome in a paediatric Chinese patient

X. Liu, D. Yan, Q. Long, 2017, Hearing, balance and communication.

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

X. Liu, D. Yan, X. Ouyang, 2011, International journal of experimental pathology.

Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse

X. Liu, D. Yan, Chantal M. Longo-Guess, 2010, Brain Research.

An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C).

D. Yan, C. Giallourakis, V. Yajnik, 2006, Journal of molecular biology.

Next-generation sequencing in genetic hearing loss.

M. Tekin, X. Liu, S. Blanton, 2013, Genetic testing and molecular biomarkers.

Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2.

Juan I. Young, M. Tekin, F. Telischi, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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

T. Walsh, M. King, Hong-Bo Zhao, 2013, Proceedings of the National Academy of Sciences.

Role of microRNAs in inner ear development and hearing loss.

X. Liu, D. Yan, R. Mittal, 2019, Gene.

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians

A. Pandya, X. Liu, N. Matsushiro, 2003, Human Genetics.

Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cells

F. Telischi, X. Liu, D. Bradley, 2017, Oncotarget.

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

M. Tekin, X. Liu, S. Blanton, 2016, Human Genetics.

A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes

M. Tekin, X. Liu, S. Blanton, 2016, Hearing Research.

Modifiers of Hearing Impairment in Humans and Mice

X. Liu, D. Yan, 2010, Current genomics.

Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

Amit P. Patel, X. Liu, S. Blanton, 2018, Gene.

Indispensable Role of Ion Channels and Transporters in the Auditory System

Amit P. Patel, X. Liu, A. Eshraghi, 2017, Journal of cellular physiology.

Recent Advancements in Understanding the Role of Epigenetics in the Auditory System.

Juan I. Young, X. Liu, S. Blanton, 2020, Gene.

In Vitro Interaction of Pseudomonas aeruginosa with Human Middle Ear Epithelial Cells

X. Liu, Jian-Dong Li, D. Yan, 2014, PloS one.

[11]Isolation of candidate genes for inherited diseases: Application to X-linked retinal degenerations

A. Swaroop, D. Yan, R. Fujita, 1996 .

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

Amit P. Patel, X. Liu, D. Yan, 2016, Journal of cellular physiology.

Otopathogenic Pseudomonas aeruginosa induces MyD88-dependent auditory hair cell damage

X. Liu, D. Yan, R. Mittal, 2016, Cell Death Discovery.

Etiologic diagnosis of sensorineural hearing loss in adults

F. Telischi, X. Liu, T. Balkany, 2005, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Amino acid 118 in the Deafness Causing (DFNA20/26) ACTG1 gene is a Mutational Hot Spot.

X. Liu, D. Yan, R. Mittal, 2018, Gene reports.

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

X. Liu, D. Yan, S. Angeli, 2011, The Laryngoscope.

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

J. Chen, X. Liu, D. Yan, 2011, Journal of Human Genetics.

Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channel.

A. Swaroop, D. Yan, A. Sharma, 2000, American journal of physiology. Cell physiology.

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

T. Walsh, M. King, M. Tekin, 2016, Human mutation.

Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa.

P. Sieving, S. Jacobson, A. Swaroop, 1999, American journal of human genetics.

Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

X. Liu, D. Yan, Yong Feng, 2019, Human molecular genetics.

Characterization of ATPase Activity of P2RX2 Cation Channel

X. Liu, Yanbin Zhang, F. Yuan, 2016, Front. Physiol..

Antioxidant enzymes, presbycusis, and ethnic variability

Xue Zhong Liu, Anthony Bared, X. Liu, 2010, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Preimplantation genetic testing for hereditary hearing loss in Chinese population

S. Blanton, D. Yan, Yuanqing Yao, 2023, Journal of Assisted Reproduction and Genetics.

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12

A. Pandya, S. Blanton, D. Yan, 2005, Journal of Medical Genetics.

Functional characterization of a novel loss‐of‐function mutation of PRPS1 related to early‐onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic intervention

W. Park, B. Choi, D. Yan, 2016, The journal of gene medicine.

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

Abhiraami Kannan Sundhari, X. Liu, S. Blanton, 2018, Human Genetics.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

The genetic basis of deafness in populations of African descent.

X. Liu, S. Blanton, D. Yan, 2017, Journal of genetics and genomics = Yi chuan xue bao.

Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss

D. Yan, S. Angeli, X. Ouyang, 2007, American journal of medical genetics. Part A.

Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous Mutations

X. Liu, S. Blanton, D. Yan, 2021, Genes.

Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review

F. Telischi, X. Liu, A. Eshraghi, 2020, Journal of otology.

Audiological and genetic studies on large families with non-syndromic deafness

X. Liu, D. Yan, S. Angeli, 2008 .

The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 System

M. Tekin, X. Liu, D. Yan, 2020, Anatomical record.

Diagnostic and Therapeutic Applications of Genomic Medicine in Progressive, Late-Onset, Nonsyndromic Sensorineural Hearing Loss.

S. Blanton, D. Yan, R. Mittal, 2020, Gene.

Immunity genes and susceptibility to otitis media: a comprehensive review.

X. Liu, D. Yan, R. Mittal, 2014, Journal of genetics and genomics = Yi chuan xue bao.

Audiologic and genetic features of the A3243G mtDNA mutation.

X. Liu, D. Yan, X. Ouyang, 2013, Genetic testing and molecular biomarkers.

Review of Genotype-Phenotype Correlations in Usher Syndrome.

A. El-Amraoui, X. Liu, S. Blanton, 2021, Ear and hearing.

Cloning and functional expression of human retinal Kir2.4, a pH-sensitive inwardly rectifying K 1 channel

A. Swaroop, D. Yan, T. Yang-Feng, 2000 .

Elucidation of repeat motifs R1‐ and R2‐related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals

X. Liu, D. Yan, M. Pepper, 2022, Molecular genetics & genomic medicine.

Refinement of the DFNA41 locus and candidate genes analysis

Xiaofeng Zhu, X. Liu, D. Yan, 2005, Journal of Human Genetics.

A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60

M. Tekin, X. Liu, D. Yan, 2016, Human Genetics.

Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations

X. Liu, D. Yan, S. Angeli, 2011, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

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

Abhiraami Kannan Sundhari, X. Liu, S. Blanton, 2018, Human Genetics.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing Function

Amit P. Patel, X. Liu, A. Eshraghi, 2017, Journal of Cellular Physiology.