On the public citation graph

Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

https://doi.org/10.1371/journal.pone.0133522
0 signed · 74 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.a.31860openalex-snapshot
A novel splice site mutation in EYA4 causes DFNA10 hearing loss
inferredcites →https://doi.org/10.1002/ajmg.a.32134openalex-snapshot
A novel splice site mutation in EYA4 causes DFNA10 hearing loss (Am J Med Genet 143(14): 1599–1604)
inferredcites →https://doi.org/10.1002/humu.21400openalex-snapshot
Novel genomic techniques open new avenues in the analysis of monogenic disorders
inferredcites →https://doi.org/10.1006/bbrc.1997.6865openalex-snapshot
Expression, Nuclear Localization and Interactions of Human MCM/P1 Proteins
inferredcites →https://doi.org/10.1016/j.ajhg.2010.05.011openalex-snapshot
Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
inferredcites →https://doi.org/10.1016/j.heares.2011.07.002openalex-snapshot
Apoptosis in acquired and genetic hearing impairment: The programmed death of the hair cell
inferredcites →https://doi.org/10.1016/j.leukres.2008.10.025openalex-snapshot
A novel role for acinus and MCM2 as host-specific signaling enhancers of DNA-damage-induced apoptosis in association with viral protein gp70
inferredcites →https://doi.org/10.1016/j.molcel.2006.01.030openalex-snapshot
Localization of MCM2-7, Cdc45, and GINS to the Site of DNA Unwinding during Eukaryotic DNA Replication
inferredcites →https://doi.org/10.1016/j.molcel.2008.05.020openalex-snapshot
The Mcm2-7 Complex Has In Vitro Helicase Activity
inferredcites →https://doi.org/10.1016/j.yexmp.2011.11.003openalex-snapshot
Overexpression of MCM2 in myelodysplastic syndromes: Association with bone marrow cell apoptosis and peripheral cytopenia
inferredcites →https://doi.org/10.1017/s0022215113003265openalex-snapshot
Non-syndromic hereditary sensorineural hearing loss: review of the genes involved
inferredcites →https://doi.org/10.1038/ng0793-289openalex-snapshot
Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness
inferredcites →https://doi.org/10.1038/nrg1377openalex-snapshot
Genetic insights into the morphogenesis of inner ear hair cells
inferredcites →https://doi.org/10.1046/j.1432-1033.2002.03224.xopenalex-snapshot
Distinct parts of minichromosome maintenance protein 2 associate with histone H3/H4 and RNA polymerase II holoenzyme
inferredcites →https://doi.org/10.1073/pnas.1222285110openalex-snapshot
Mutation of the ATP-gated P2X 2 receptor leads to progressive hearing loss and increased susceptibility to noise
inferredcites →https://doi.org/10.1074/jbc.273.14.8369openalex-snapshot
Biochemical Function of Mouse Minichromosome Maintenance 2 Protein
inferredcites →https://doi.org/10.1074/jbc.m011556200openalex-snapshot
Replication Factors MCM2 and ORC1 Interact with the Histone Acetyltransferase HBO1
inferredcites →https://doi.org/10.1086/381133openalex-snapshot
Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family
inferredcites →https://doi.org/10.1091/mbc.e06-03-0241openalex-snapshot
Essential Role of Phosphorylation of MCM2 by Cdc7/Dbf4 in the Initiation of DNA Replication in Mammalian Cells
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1097/00129492-200407000-00035openalex-snapshot
Caspases, the Enemy Within, and Their Role in Oxidative Stress-Induced Apoptosis of Inner Ear Sensory Cells
inferredcites →https://doi.org/10.1101/cshperspect.a012807openalex-snapshot
The Minichromosome Maintenance Replicative Helicase
inferredcites →https://doi.org/10.1111/cge.12006openalex-snapshot
Whole exome sequencing identifies a novel DFNA9 mutation, C162Y
inferredcites →https://doi.org/10.1111/j.1399-0004.2010.01585.xopenalex-snapshot
Whole-exome sequencing: a powerful technique for identifying novel genes of complex disorders
inferredcites →https://doi.org/10.1128/mmbr.68.1.109-131.2004openalex-snapshot
Eukaryotic MCM Proteins: Beyond Replication Initiation
inferredcites →https://doi.org/10.1136/jmg.40.7.479openalex-snapshot
Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9
inferredcites →https://doi.org/10.1159/000091090openalex-snapshot
An Overview of Hereditary Hearing Loss
inferredcites →https://doi.org/10.1186/gb-2011-12-9-r95openalex-snapshot
Comprehensive comparison of three commercial human whole-exome capture platforms
inferredcites →https://doi.org/10.1200/jco.2001.19.22.4259openalex-snapshot
MCM2 Is an Independent Predictor of Survival in Patients With Non–Small-Cell Lung Cancer
inferredcites →https://doi.org/10.1371/journal.pone.0040129openalex-snapshot
Minichromosome Maintenance 2 Bound with Retroviral Gp70 Is Localized to Cytoplasm and Enhances DNA-Damage-Induced Apoptosis
inferredcites →https://doi.org/10.1371/journal.pone.0069549openalex-snapshot
Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
inferredcites →https://doi.org/10.1523/jneurosci.1690-14.2014openalex-snapshot
Characterization of Transcriptomes of Cochlear Inner and Outer Hair Cells
inferredcites →https://doi.org/10.2174/1381612054367346openalex-snapshot
Molecular Pathways Involved in Apoptotic Cell Death in the Injured Cochlea: Cues to Novel Therapeutic Strategies
inferredcites →https://doi.org/10.2174/156652409788488775openalex-snapshot
Function and Expression Pattern of Nonsyndromic Deafness Genes
inferredcites →https://doi.org/10.4161/cc.25336openalex-snapshot
The ORC/Cdc6/MCM2–7 complex, a new power player for regulated helicase loading

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4677331openalex-extracted
Association of Sheep Mcm2 And Mxd3 Gene Polymorphisms with Body Weight and Average Daily Gain In Hu Sheep
inferred← citeshttps://doi.org/10.1002/lary.28646openalex-snapshot
Genetics of Postlingual Sensorineural Hearing Loss
inferred← citeshttps://doi.org/10.1002/path.4828openalex-snapshot
The pathological consequences of impaired genome integrity in humans; disorders of the DNA replication machinery
inferred← citeshttps://doi.org/10.1007/s00439-022-02441-0openalex-snapshot
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants
inferred← citeshttps://doi.org/10.1007/s00439-023-02569-7openalex-snapshot
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues
inferred← citeshttps://doi.org/10.1007/s10875-023-01437-3openalex-snapshot
Unwinding the Role of the CMG Helicase in Inborn Errors of Immunity
inferred← citeshttps://doi.org/10.1007/s42764-023-00108-2openalex-snapshot
Chromatin-based DNA replication initiation regulation in eukaryotes
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.24165-5openalex-snapshot
Development and Deafness
inferred← citeshttps://doi.org/10.1016/b978-0-12-815234-8.00003-3openalex-snapshot
Hereditary Hearing Impairment
inferred← citeshttps://doi.org/10.1016/j.ajhg.2024.07.008openalex-snapshot
Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder
inferred← citeshttps://doi.org/10.1016/j.cell.2022.12.008openalex-snapshot
The human pre-replication complex is an open complex
inferred← citeshttps://doi.org/10.1016/j.cub.2022.03.005openalex-snapshot
Isolation, profiling, and tracking of extracellular vesicle cargo in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.06.019openalex-snapshot
Dormant origins as a built-in safeguard in eukaryotic DNA replication against genome instability and disease development
inferred← citeshttps://doi.org/10.1016/j.heares.2020.107906openalex-snapshot
Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss
inferred← citeshttps://doi.org/10.1016/j.heares.2020.107912openalex-snapshot
Dual and triple AAV delivery of large therapeutic gene sequences into the inner ear
inferred← citeshttps://doi.org/10.1016/j.heares.2020.107934openalex-snapshot
Practical aspects of inner ear gene delivery for research and clinical applications
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.122350openalex-snapshot
RNA-seq analysis highlights DNA replication and DNA repair associated with early-onset hearing loss in the cochlea of DBA/2J mice
inferred← citeshttps://doi.org/10.1038/s41434-020-0177-1openalex-snapshot
Gene therapy development in hearing research in China
inferred← citeshttps://doi.org/10.1080/09513590.2023.2206912openalex-snapshot
Mutational analysis of minichromosome maintenance complex component ( MCM ) family genes in Chinese Han women with polycystic ovarian syndrome
inferred← citeshttps://doi.org/10.1097/mop.0000000000000410openalex-snapshot
Navigating genetic diagnostics in patients with hearing loss
inferred← citeshttps://doi.org/10.1101/2021.09.23.461577openalex-snapshot
Tracking extracellular vesicle (EV) cargo as a platform for studying EVomics, signaling, and targeting in vivo
inferred← citeshttps://doi.org/10.1136/bcr-2024-262338openalex-snapshot
Novel variant in OTOG gene in consanguineous family with sensorineural hearing loss
inferred← citeshttps://doi.org/10.1136/jmedgenet-2020-107518openalex-snapshot
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability
inferred← citeshttps://doi.org/10.1155/2021/7928937openalex-snapshot
The Alterations and Potential Roles of MCMs in Breast Cancer
inferred← citeshttps://doi.org/10.1159/000444599openalex-snapshot
Genetic Elucidation of Nonsyndromic Hearing Loss in the High-Throughput Sequencing Era
inferred← citeshttps://doi.org/10.11606/d.5.2020.tde-23012020-114342openalex-snapshot
Estudos genético-moleculares em surdez não sindrômica e sindrômica
inferred← citeshttps://doi.org/10.17430/895541openalex-snapshot
NOVEL TRENDS IN THE MOLECULAR GENETICS OF HEARING LOSS
inferred← citeshttps://doi.org/10.17431/na/156389openalex-snapshot
Autosomal dominant hearing loss – literature review
inferred← citeshttps://doi.org/10.20944/preprints202008.0308.v1openalex-snapshot
A Comprehensive Review on Inherited Sensorineural Hearing Loss and Their Syndromes
inferred← citeshttps://doi.org/10.3389/fimmu.2019.00869openalex-snapshot
Immunomodulatory Effects and Induction of Apoptosis by Different Molecular Weight Chitosan Oligosaccharides in Head Kidney Macrophages From Blunt Snout Bream (Megalobrama amblycephala)
inferred← citeshttps://doi.org/10.3390/biomedicines11061616openalex-snapshot
Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review
inferred← citeshttps://doi.org/10.3390/genes10050331openalex-snapshot
Post-Translational Modifications of the Mini-Chromosome Maintenance Proteins in DNA Replication
inferred← citeshttps://doi.org/10.3390/genes12111666openalex-snapshot
Discovering of Genomic Variations Associated to Growth Traits by GWAS in Braunvieh Cattle
inferred← citeshttps://doi.org/10.3390/genes14061225openalex-snapshot
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies—Expanding the Phenotype
inferred← citeshttps://doi.org/10.3390/ijms22020911openalex-snapshot
Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms
inferred← citeshttps://doi.org/10.3390/ijms26031020openalex-snapshot
Identification of MCM2-Interacting Proteins Associated with Replication Initiation Using APEX2-Based Proximity Labeling Technology
inferred← citeshttps://doi.org/10.47749/t/unicamp.2017.986482openalex-snapshot
Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva
inferred← citeshttps://doi.org/10.47749/t/unicamp.2020.1127185openalex-snapshot
Etiologia da perda auditiva em indivíduos heterozigotos para o locus DFNB1
inferred← citeshttps://doi.org/10.5808/gi.2018.16.4.e20openalex-snapshot
Genetic Hearing Loss and Gene Therapy
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.