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Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0142(19990715)86:2<364::aid-cncr21>3.0.co;2-7openalex-snapshot
The International Neuroblastoma Pathology Classification (the Shimada system)
inferredcites →https://doi.org/10.1002/gcc.20926openalex-snapshot
Copy number defects of G1‐Cell cycle genes in neuroblastoma are frequent and correlate with high expression of E2F target genes and a poor prognosis
inferredcites →https://doi.org/10.1002/jcb.22146openalex-snapshot
HACE1: A novel repressor of RAR transcriptional activity
inferredcites →https://doi.org/10.1007/978-1-4612-4380-9_25openalex-snapshot
Nonparametric Estimation from Incomplete Observations
inferredcites →https://doi.org/10.1016/j.ajhg.2010.03.010openalex-snapshot
Distinct Variants at LIN28B Influence Growth in Height from Birth to Adulthood
inferredcites →https://doi.org/10.1016/j.cell.2009.10.014openalex-snapshot
An Epigenetic Switch Involving NF-κB, Lin28, Let-7 MicroRNA, and IL6 Links Inflammation to Cell Transformation
inferredcites →https://doi.org/10.1016/j.cell.2011.08.033openalex-snapshot
The Lin28/let-7 Axis Regulates Glucose Metabolism
inferredcites →https://doi.org/10.1016/j.cell.2011.10.039openalex-snapshot
Lin28A and Lin28B Inhibit let-7 MicroRNA Biogenesis by Distinct Mechanisms
inferredcites →https://doi.org/10.1016/j.stem.2010.06.011openalex-snapshot
MicroRNA Gene Regulatory Pathways in the Establishment and Maintenance of ESC Identity
inferredcites →https://doi.org/10.1038/nature07261openalex-snapshot
Identification of ALK as a major familial neuroblastoma predisposition gene
inferredcites →https://doi.org/10.1038/nature07398openalex-snapshot
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
inferredcites →https://doi.org/10.1038/nature08035openalex-snapshot
Copy number variation at 1q21.1 associated with neuroblastoma
inferredcites →https://doi.org/10.1038/nature08210openalex-snapshot
A role for Lin28 in primordial germ-cell development and germ-cell malignancy
inferredcites →https://doi.org/10.1038/nature08725openalex-snapshot
Opposing microRNA families regulate self-renewal in mouse embryonic stem cells
inferredcites →https://doi.org/10.1038/nature09609openalex-snapshot
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
inferredcites →https://doi.org/10.1038/ng.374openalex-snapshot
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
inferredcites →https://doi.org/10.1038/ng.382openalex-snapshot
Genetic variation in LIN28B is associated with the timing of puberty
inferredcites →https://doi.org/10.1038/ng.383openalex-snapshot
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche
inferredcites →https://doi.org/10.1038/ng.392openalex-snapshot
Lin28 promotes transformation and is associated with advanced human malignancies
inferredcites →https://doi.org/10.1038/ng1547openalex-snapshot
A genome-wide scalable SNP genotyping assay using microarray technology
inferredcites →https://doi.org/10.1038/ng2088openalex-snapshot
A new multipoint method for genome-wide association studies by imputation of genotypes
inferredcites →https://doi.org/10.1038/nm1621openalex-snapshot
The E3 ligase HACE1 is a critical chromosome 6q21 tumor suppressor involved in multiple cancers
inferredcites →https://doi.org/10.1038/nmeth842openalex-snapshot
Whole-genome genotyping with the single-base extension assay
inferredcites →https://doi.org/10.1038/sj.neo.7900146openalex-snapshot
Detection of MYCN Gene Amplification in Neuroblastoma by Fluorescence In Situ Hybridization: A Pediatric Oncology Group Study
inferredcites →https://doi.org/10.1056/nejmoa0708698openalex-snapshot
Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma
inferredcites →https://doi.org/10.1056/nejmoa0911123openalex-snapshot
Anti-GD2 Antibody with GM-CSF, Interleukin-2, and Isotretinoin for Neuroblastoma
inferredcites →https://doi.org/10.1056/nejmra0804577openalex-snapshot
Recent Advances in Neuroblastoma
inferredcites →https://doi.org/10.1080/01621459.1958.10501452openalex-snapshot
Nonparametric Estimation from Incomplete Observations
inferredcites →https://doi.org/10.1086/383253openalex-snapshot
Germline Mutations of the Paired–Like Homeobox 2B (PHOX2B) Gene in Neuroblastoma
inferredcites →https://doi.org/10.1086/424530openalex-snapshot
Germline PHOX2B Mutation in Hereditary Neuroblastoma
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1093/bioinformatics/btq419openalex-snapshot
LocusZoom: regional visualization of genome-wide association scan results
inferredcites →https://doi.org/10.1093/hmg/ddh215openalex-snapshot
Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney
inferredcites →https://doi.org/10.1126/science.1151526openalex-snapshot
Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells
inferredcites →https://doi.org/10.1126/science.1216557openalex-snapshot
Lin28b Reprograms Adult Bone Marrow Hematopoietic Progenitors to Mediate Fetal-Like Lymphopoiesis
inferredcites →https://doi.org/10.1136/jmg.2009.072983openalex-snapshot
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene
inferredcites →https://doi.org/10.1158/0008-5472.can-10-4167openalex-snapshot
LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3703openalex-snapshot
Common Variation at BARD1 Results in the Expression of an Oncogenic Isoform That Influences Neuroblastoma Susceptibility and Oncogenicity
inferredcites →https://doi.org/10.1158/1055-9965.epi-11-0830openalex-snapshot
Replication of Neuroblastoma SNP Association at the BARD1 Locus in African-Americans
inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-5090openalex-snapshot
Molecular Characterization of the Pediatric Preclinical Testing Panel
inferredcites →https://doi.org/10.1158/1541-7786.mcr-07-2102openalex-snapshot
A Functional Screen Identifies miR-34a as a Candidate Neuroblastoma Tumor Suppressor Gene
inferredcites →https://doi.org/10.1200/jco.1991.9.4.581openalex-snapshot
Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study.
inferredcites →https://doi.org/10.1200/jco.1993.11.8.1466openalex-snapshot
Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment.
inferredcites →https://doi.org/10.1200/jco.2010.29.6103openalex-snapshot
Racial and Ethnic Disparities in Risk and Survival in Children With Neuroblastoma: A Children's Oncology Group Study
inferredcites →https://doi.org/10.1371/journal.pgen.1000529openalex-snapshot
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
inferredcites →https://doi.org/10.1371/journal.pgen.1002026openalex-snapshot
Phenotype Restricted Genome-Wide Association Study Using a Gene-Centric Approach Identifies Three Low-Risk Neuroblastoma Susceptibility Loci
inferredcites →https://doi.org/10.1534/g3.111.001198openalex-snapshot
Genotype Imputation with Thousands of Genomes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Determining the Role of Single Nucleotide Polymorphisms of ANRIL Gene in Patients with Oral SCC
inferred← citeshttps://doi.org/10.1001/jamaoncol.2016.5945openalex-snapshot
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases
inferred← citeshttps://doi.org/10.1002/adbi.202400730openalex-snapshot
LIN28B Promotes Cancer Cell Dissemination and Angiogenesis
inferred← citeshttps://doi.org/10.1002/advs.202415181openalex-snapshot
The Non‐Coding Regulatory Variant rs2863002 at chr11p11.2 Increases Neuroblastoma Risk by Affecting HSD17B12 Expression and Lipid Metabolism
inferred← citeshttps://doi.org/10.1002/cai2.103openalex-snapshot
ALKBH5 gene polymorphisms and risk of neuroblastoma in Chinese children from Jiangsu Province
inferred← citeshttps://doi.org/10.1002/cam4.3458openalex-snapshot
Genetic variation associated with childhood and adult stature and risk of MYCN‐amplified neuroblastoma
inferred← citeshttps://doi.org/10.1002/cncr.29706openalex-snapshot
Advances in the translational genomics of neuroblastoma: From improving risk stratification and revealing novel biology to identifying actionable genomic alterations
inferred← citeshttps://doi.org/10.1002/cncr.31353openalex-snapshot
HOTAIR gene polymorphisms contribute to increased neuroblastoma susceptibility in Chinese children
inferred← citeshttps://doi.org/10.1002/cnr2.1875openalex-snapshot
miR ‐100 rs1834306 a > G polymorphism decreases neuroblastoma risk in Chinese children
inferred← citeshttps://doi.org/10.1002/dvdy.24600openalex-snapshot
hace1 Influences zebrafish cardiac development via ROS‐dependent mechanisms
inferred← citeshttps://doi.org/10.1002/em.21799openalex-snapshot
Next generation sequencing and rare genetic variants: From human population studies to medical genetics
inferred← citeshttps://doi.org/10.1002/hep4.1185openalex-snapshot
MicroRNA‐26‐5p functions as a new inhibitor of hepatoblastoma by repressing lin‐28 homolog B and aurora kinase a expression
inferred← citeshttps://doi.org/10.1002/ijc.29077openalex-snapshot
Recent insights into the biology of neuroblastoma
inferred← citeshttps://doi.org/10.1002/ijc.31195openalex-snapshot
Genome‐wide association study identifies the GLDC / IL33 locus associated with survival of osteosarcoma patients
inferred← citeshttps://doi.org/10.1002/ijc.31822openalex-snapshot
Fine mapping of 2q35 high‐risk neuroblastoma locus reveals independent functional risk variants and suggests full‐length BARD1 as tumor‐suppressor
inferred← citeshttps://doi.org/10.1002/iub.2791openalex-snapshot
Functional TET2 gene polymorphisms increase the risk of neuroblastoma in Chinese children
inferred← citeshttps://doi.org/10.1002/jcla.22200openalex-snapshot
The correlation between LIN 28B gene potentially functional variants and Wilms tumor susceptibility in Chinese children
inferred← citeshttps://doi.org/10.1002/jcp.30946openalex-snapshot
LIN28 expression and function in medulloblastoma
inferred← citeshttps://doi.org/10.1002/jgm.3190openalex-snapshot
Association of MYC gene polymorphisms with neuroblastoma risk in Chinese children: A four‐center case–control study
inferred← citeshttps://doi.org/10.1002/med.21750openalex-snapshot
Molecular targeting therapies for neuroblastoma: Progress and challenges
inferred← citeshttps://doi.org/10.1002/pbc.24433openalex-snapshot
Children's Oncology Group's 2013 blueprint for research: Neuroblastoma
inferred← citeshttps://doi.org/10.1002/pbc.24927openalex-snapshot
Lack of association betweenMDM2promoter SNP309 and clinical outcome in patients with neuroblastoma
inferred← citeshttps://doi.org/10.1002/pbc.25051openalex-snapshot
The promises and pitfalls of genetic epidemiologic approaches to pediatric cancers: Lessons from MDM2
inferred← citeshttps://doi.org/10.1002/pbc.25723openalex-snapshot
Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non‐Polyalanine Repeat Expansion Mutations
inferred← citeshttps://doi.org/10.1002/pbc.26244openalex-snapshot
Socioeconomic status and global variations in the incidence of neuroblastoma: call for support of population-based cancer registries in low-middle-income countries
inferred← citeshttps://doi.org/10.1002/pbc.27901openalex-snapshot
Congenital malformation syndromes associated with peripheral neuroblastic tumors: A systematic review
inferred← citeshttps://doi.org/10.1002/pbc.29571openalex-snapshot
Exploration of genetic ancestry and socioeconomic status in the incidence of neuroblastoma: An ecological study
inferred← citeshttps://doi.org/10.1002/ped4.12455openalex-snapshot
The relative contributions of genetic and non‐genetic factors to the risk of neuroblastoma
inferred← citeshttps://doi.org/10.1007/978-3-030-18396-7_3openalex-snapshot
Neuroblastoma Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-46038-3_5openalex-snapshot
Molecular Genetics of Neuroblastoma
inferred← citeshttps://doi.org/10.1007/978-3-319-89626-7_8openalex-snapshot
Neuroblastoma and Neuroblastic Tumors
inferred← citeshttps://doi.org/10.1007/978-94-007-5842-1_17openalex-snapshot
Genome-Wide Analysis and Gene Expression Profiling of Neuroblastoma: What Contribution Did They Give to the Tumor Treatment?
inferred← citeshttps://doi.org/10.1007/s00383-012-3239-7openalex-snapshot
The role of genetic and epigenetic alterations in neuroblastoma disease pathogenesis
inferred← citeshttps://doi.org/10.1007/s00383-025-06025-7openalex-snapshot
RAS gene polymorphisms confer the risk of neuroblastoma in Chinese children from Jiangsu province
inferred← citeshttps://doi.org/10.1007/s00439-024-02700-2openalex-snapshot
Integrative genomic analyses identify neuroblastoma risk genes involved in neuronal differentiation
inferred← citeshttps://doi.org/10.1007/s00441-018-2820-3openalex-snapshot
Genetic susceptibility to neuroblastoma: current knowledge and future directions
inferred← citeshttps://doi.org/10.1007/s10552-016-0799-1openalex-snapshot
A family-based study of gene variants and maternal folate and choline in neuroblastoma: a report from the Children’s Oncology Group
inferred← citeshttps://doi.org/10.1007/s10555-020-09843-4openalex-snapshot
Genetic predisposition and chromosome instability in neuroblastoma
inferred← citeshttps://doi.org/10.1007/s10555-020-09855-0openalex-snapshot
Mouse models of high-risk neuroblastoma
inferred← citeshttps://doi.org/10.1007/s11427-020-1784-7openalex-snapshot
MYC-associated protein X binding with the variant rs72780850 in RNA helicase DEAD box 1 for susceptibility to neuroblastoma
inferred← citeshttps://doi.org/10.1007/s12035-024-04501-0openalex-snapshot
Pharmacologically Targeting Ferroptosis and Cuproptosis in Neuroblastoma
inferred← citeshttps://doi.org/10.1007/s13277-015-3936-7openalex-snapshot
Evaluation of GWAS-identified SNPs at 6p22 with neuroblastoma susceptibility in a Chinese population
inferred← citeshttps://doi.org/10.1007/s13277-015-4192-6openalex-snapshot
Single nucleotide polymorphism rs11669203 in TGFBR3L is associated with the risk of neuroblastoma in a Chinese population
inferred← citeshttps://doi.org/10.1007/s40471-015-0049-1openalex-snapshot
Hard Work Ahead: Fine Mapping and Functional Follow-up of Susceptibility Alleles in Cancer GWAS
inferred← citeshttps://doi.org/10.1016/b978-0-12-812005-7.00014-xopenalex-snapshot
Novel Therapeutic Targets in Neuroblastoma
inferred← citeshttps://doi.org/10.1016/b978-0-12-824550-7.00013-8openalex-snapshot
Clinical implications of noncoding RNAs in neuroblastoma patients
inferred← citeshttps://doi.org/10.1016/b978-1-4557-5414-4.00054-1openalex-snapshot
10.1016/b978-1-4557-5414-4.00054-1
inferred← citeshttps://doi.org/10.1016/j.ajhg.2019.07.020openalex-snapshot
Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.03.024openalex-snapshot
Mammalian HECT ubiquitin-protein ligases: Biological and pathophysiological aspects
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115696openalex-snapshot
The molecular basis of tumor metastasis and current approaches to decode targeted migration-promoting events in pediatric neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.bcp.2026.118192openalex-snapshot
HACE1 suppresses cell migration, invasion, and chemoresistance in neuroblastoma by regulating the PKN1/PA2G4 axis
inferred← citeshttps://doi.org/10.1016/j.canep.2019.06.009openalex-snapshot
Neuroblastoma in relation to joint effects of vitamin A and maternal and offspring variants in vitamin A-related genes: A report of the Children’s Oncology Group
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The Risk-Associated Long Noncoding RNA NBAT-1 Controls Neuroblastoma Progression by Regulating Cell Proliferation and Neuronal Differentiation
inferred← citeshttps://doi.org/10.1016/j.ccell.2015.09.012openalex-snapshot
A LIN28B-RAN-AURKA Signaling Network Promotes Neuroblastoma Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.ccell.2018.01.020openalex-snapshot
Sense-Antisense lncRNA Pair Encoded by Locus 6p22.3 Determines Neuroblastoma Susceptibility via the USP36-CHD7-SOX9 Regulatory Axis
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.05.015openalex-snapshot
Ubiquitylation of Autophagy Receptor Optineurin by HACE1 Activates Selective Autophagy for Tumor Suppression
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.09.046openalex-snapshot
Expression Quantitative Trait Loci and Receptor Pharmacology Implicate Arg1 and the GABA-A Receptor as Therapeutic Targets in Neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.08.086openalex-snapshot
A Single Let-7 MicroRNA Bypasses LIN28-Mediated Repression
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2026.109415openalex-snapshot
In silico identification of robust stage-specific gene signatures in neuroblastoma: Integrating microarray meta-analysis with machine learning and cross-platform validation
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Functional Polymorphisms at ERCC1/XPF Genes Confer Neuroblastoma Risk in Chinese Children
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Biology and treatment of renal tumours in childhood
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Neuroblastoma survivors are at increased risk for second malignancies: A report from the International Neuroblastoma Risk Group Project
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Persistence of racial and ethnic disparities in risk and survival for patients with neuroblastoma over two decades
inferred← citeshttps://doi.org/10.1016/j.gde.2017.03.008openalex-snapshot
Genetic susceptibility to neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.gene.2018.04.015openalex-snapshot
RSRC1 and CPZ gene polymorphisms with neuroblastoma susceptibility in Chinese children
inferred← citeshttps://doi.org/10.1016/j.gene.2019.144262openalex-snapshot
NRAS rs2273267 A>T polymorphism reduces neuroblastoma risk in Chinese children
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e23658openalex-snapshot
Genetic variants of m7G modification genes influence neuroblastoma susceptibility
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e27988openalex-snapshot
TET3 gene rs828867 G>A polymorphism reduces neuroblastoma risk in Chinese children
inferred← citeshttps://doi.org/10.1016/j.jns.2015.07.041openalex-snapshot
Retroperitoneal catecholamine-producing ganglioneuroma with a birth history of monozygotic twins who both suffered from neuroblastoma during their childhoods: A case report with genome analysis
inferred← citeshttps://doi.org/10.1016/j.leukres.2016.04.007openalex-snapshot
HACE1 is a putative tumor suppressor gene in B-cell lymphomagenesis and is down-regulated by both deletion and epigenetic alterations
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.122275openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neo.2020.04.001openalex-snapshot
LIN28B promotes neuroblastoma metastasis and regulates PDZ binding kinase
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Association of Common Genetic Variants in Pre-microRNAs and Neuroblastoma Susceptibility: A Two-Center Study in Chinese Children
inferred← citeshttps://doi.org/10.1016/j.omtn.2020.08.009openalex-snapshot
METTL14 Gene Polymorphisms Confer Neuroblastoma Susceptibility: An Eight-Center Case-Control Study
inferred← citeshttps://doi.org/10.1016/j.omto.2020.12.004openalex-snapshot
Association between NER pathway gene polymorphisms and neuroblastoma risk in an eastern Chinese population
inferred← citeshttps://doi.org/10.1016/j.oncohp.2016.06.003openalex-snapshot
Biology and treatment of Wilms’ tumours in childhood
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inferred← citeshttps://doi.org/10.1016/j.stem.2013.03.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tem.2015.12.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tranon.2019.06.008openalex-snapshot
Association of miR-34b/c rs4938723 and TP53 Arg72Pro Polymorphisms with Neuroblastoma Susceptibility: Evidence from Seven Centers
inferred← citeshttps://doi.org/10.1016/j.trecan.2015.11.002openalex-snapshot
Fingering the Correct Culprit: NonRANdom Target Selection for Therapy of Neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.xcrm.2024.101468openalex-snapshot
Histone lysine demethylase 4 family proteins maintain the transcriptional program and adrenergic cellular state of MYCN-amplified neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.xhgg.2022.100158openalex-snapshot
CFDP1 is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identity
inferred← citeshttps://doi.org/10.1038/clpt.2014.37openalex-snapshot
Integrating Cell-Based and Clinical Genome-Wide Studies to Identify Genetic Variants Contributing to Treatment Failure in Neuroblastoma Patients
inferred← citeshttps://doi.org/10.1038/leu.2016.296openalex-snapshot
The LIN28B/let-7 axis is a novel therapeutic pathway in multiple myeloma
inferred← citeshttps://doi.org/10.1038/nature12119openalex-snapshot
A role for the Perlman syndrome exonuclease Dis3l2 in the Lin28–let-7 pathway
inferred← citeshttps://doi.org/10.1038/nature15540openalex-snapshot
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism
inferred← citeshttps://doi.org/10.1038/nature18632openalex-snapshot
Multiple mechanisms disrupt the let-7 microRNA family in neuroblastoma
inferred← citeshttps://doi.org/10.1038/ncomms3180openalex-snapshot
Hace1 controls ROS generation of vertebrate Rac1-dependent NADPH oxidase complexes
inferred← citeshttps://doi.org/10.1038/ng.2529openalex-snapshot
The genetic landscape of high-risk neuroblastoma
inferred← citeshttps://doi.org/10.1038/nrc3526openalex-snapshot
Neuroblastoma: developmental biology, cancer genomics and immunotherapy
inferred← citeshttps://doi.org/10.1038/nrc3932openalex-snapshot
MicroRNA biogenesis pathways in cancer
inferred← citeshttps://doi.org/10.1038/nrclinonc.2014.168openalex-snapshot
Mechanisms of neuroblastoma regression
inferred← citeshttps://doi.org/10.1038/onc.2014.316openalex-snapshot
Loss of the tumor suppressor Hace1 leads to ROS-dependent glutamine addiction
inferred← citeshttps://doi.org/10.1038/s41392-018-0026-5openalex-snapshot
RNA-binding protein LIN28B inhibits apoptosis through regulation of the AKT2/FOXO3A/BIM axis in ovarian cancer cells
inferred← citeshttps://doi.org/10.1038/s41418-019-0386-6openalex-snapshot
The SRCIN1/p140Cap adaptor protein negatively regulates the aggressiveness of neuroblastoma
inferred← citeshttps://doi.org/10.1038/s41419-017-0060-1openalex-snapshot
Cell death-based treatment of neuroblastoma
inferred← citeshttps://doi.org/10.1038/s41419-021-03790-wopenalex-snapshot
MYCN mediates TFRC-dependent ferroptosis and reveals vulnerabilities in neuroblastoma
inferred← citeshttps://doi.org/10.1038/s41467-017-00408-8openalex-snapshot
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
inferred← citeshttps://doi.org/10.1038/s41467-020-15046-wopenalex-snapshot
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
inferred← citeshttps://doi.org/10.1038/s41467-024-47166-yopenalex-snapshot
Lineage specific transcription factor waves reprogram neuroblastoma from self-renewal to differentiation
inferred← citeshttps://doi.org/10.1038/s41467-024-52128-5openalex-snapshot
Germline functional variants contribute to somatic mutation and outcomes in neuroblastoma
inferred← citeshttps://doi.org/10.1038/s41568-024-00775-7openalex-snapshot
Re-envisioning genetic predisposition to childhood and adolescent cancers
inferred← citeshttps://doi.org/10.1038/s41571-022-00643-zopenalex-snapshot
Advancing therapy for neuroblastoma
inferred← citeshttps://doi.org/10.1038/srep01351openalex-snapshot
Neuroblastoma tumorigenesis is regulated through the Nm23-H1/h-Prune C-terminal interaction
inferred← citeshttps://doi.org/10.1038/srep14364openalex-snapshot
Translational compensation of genomic instability in neuroblastoma
inferred← citeshttps://doi.org/10.1038/srep44779openalex-snapshot
Identification of cancer-associated missense mutations in hace1 that impair cell growth control and Rac1 ubiquitylation
inferred← citeshttps://doi.org/10.1042/bsr20180292openalex-snapshot
Lack of associations between AURKA gene polymorphisms and neuroblastoma susceptibility in Chinese children
inferred← citeshttps://doi.org/10.1042/bsr20181907openalex-snapshot
Association of miR-146a, miR-149 and miR-196a2 polymorphisms with neuroblastoma risk in Eastern Chinese population: a three-center case–control study
inferred← citeshttps://doi.org/10.1042/bsr20200854openalex-snapshot
TP53 Arg72Pro polymorphism and neuroblastoma susceptibility in eastern Chinese children: a three-center case–control study
inferred← citeshttps://doi.org/10.1053/j.semdp.2021.06.007openalex-snapshot
Mediastinal neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: Pathology review and diagnostic approach
inferred← citeshttps://doi.org/10.1073/pnas.1922692117openalex-snapshot
LIN28B regulates transcription and potentiates MYCN-induced neuroblastoma through binding to ZNF143 at target gene promotors
inferred← citeshttps://doi.org/10.1080/07357907.2017.1405016openalex-snapshot
Association Between HACE1 Gene Polymorphisms and Wilms' Tumor Risk in a Chinese Population
inferred← citeshttps://doi.org/10.1080/14737140.2017.1285230openalex-snapshot
Overview and recent advances in the treatment of neuroblastoma
inferred← citeshttps://doi.org/10.1080/15384101.2015.1137712openalex-snapshot
LIN28B: an orchestrator of oncogenic signaling in neuroblastoma
inferred← citeshttps://doi.org/10.1080/15384101.2020.1808382openalex-snapshot
lncRNA-uc003opf.1 rs11752942 A>G polymorphism decreases neuroblastoma risk in Chinese children
inferred← citeshttps://doi.org/10.1089/scd.2015.0322openalex-snapshot
LIN28: A Stem Cell Factor with a Key Role in Pediatric Tumor Formation
inferred← citeshttps://doi.org/10.1093/carcin/bgs380openalex-snapshot
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility
inferred← citeshttps://doi.org/10.1093/carcin/bgv085openalex-snapshot
Lin28B promotes melanoma growth by mediating a microRNA regulatory circuit
inferred← citeshttps://doi.org/10.1093/gigascience/giy050openalex-snapshot
The long noncoding RNA landscape of neuroendocrine prostate cancer and its clinical implications
inferred← citeshttps://doi.org/10.1093/hmg/ddw092openalex-snapshot
GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer
inferred← citeshttps://doi.org/10.1093/jnci/djaa024openalex-snapshot
Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma
inferred← citeshttps://doi.org/10.1093/jnci/djac012openalex-snapshot
Identification of Mitochondrial DNA Variants Associated With Risk of Neuroblastoma
inferred← citeshttps://doi.org/10.1093/jnci/djad183openalex-snapshot
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival
inferred← citeshttps://doi.org/10.1093/jnci/dju047openalex-snapshot
Rare Variants in TP53 and Susceptibility to Neuroblastoma
inferred← citeshttps://doi.org/10.1093/jnci/djx093openalex-snapshot
Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma
inferred← citeshttps://doi.org/10.1093/molbev/msu230openalex-snapshot
Genome-Wide SNP Analysis Reveals Population Structure and Demographic History of the Ryukyu Islanders in the Southern Part of the Japanese Archipelago
inferred← citeshttps://doi.org/10.1093/neuonc/noaa130openalex-snapshot
European genetic ancestry associated with risk of childhood ependymoma
inferred← citeshttps://doi.org/10.1097/md.0000000000051037openalex-snapshot
Two siblings presented with spastic paraplegia and psychomotor retardation with or without seizures with HACE1 variants
inferred← citeshttps://doi.org/10.1097/mop.0000000000000296openalex-snapshot
Genetic discoveries and treatment advances in neuroblastoma
inferred← citeshttps://doi.org/10.1097/mop.0000000000001419openalex-snapshot
Overview of the etiology of childhood cancer and future directions
inferred← citeshttps://doi.org/10.1101/2020.07.23.218503openalex-snapshot
Lineage specific transcription factor waves reprogram neuroblastoma from self-renewal to differentiation
inferred← citeshttps://doi.org/10.1101/2023.01.23.23284864openalex-snapshot
Germline pathogenic variants in 786 neuroblastoma patients
inferred← citeshttps://doi.org/10.1101/gad.224659.113openalex-snapshot
LIN28B promotes growth and tumorigenesis of the intestinal epithelium via Let-7
inferred← citeshttps://doi.org/10.1101/gad.237149.113openalex-snapshot
Lin28 sustains early renal progenitors and induces Wilms tumor
inferred← citeshttps://doi.org/10.1101/gad.256693.114openalex-snapshot
LIN28 cooperates with WNT signaling to drive invasive intestinal and colorectal adenocarcinoma in mice and humans
inferred← citeshttps://doi.org/10.1111/cas.12721openalex-snapshot
A role of uridylation pathway for blockade of let‐7 micro RNA biogenesis by Lin28B
inferred← citeshttps://doi.org/10.1111/jcmm.12836openalex-snapshot
Association of potentially functional variants in the XPG gene with neuroblastoma risk in a Chinese population
inferred← citeshttps://doi.org/10.1111/jcmm.12846openalex-snapshot
Potentially functional polymorphisms in the LIN 28B gene contribute to neuroblastoma susceptibility in Chinese children
inferred← citeshttps://doi.org/10.1111/jcmm.13226openalex-snapshot
The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma
inferred← citeshttps://doi.org/10.1111/jcmm.14827openalex-snapshot
LIN28A gene polymorphisms modify neuroblastoma susceptibility: A four‐centre case‐control study
inferred← citeshttps://doi.org/10.1111/jcmm.14836openalex-snapshot
LMO1 polymorphisms and the risk of neuroblastoma: Assessment of meta‐analysis of case‐control studies
inferred← citeshttps://doi.org/10.1111/jcmm.15576openalex-snapshot
Association between METTL3 gene polymorphisms and neuroblastoma susceptibility: A nine‐centre case‐control study
inferred← citeshttps://doi.org/10.1111/jcmm.17820openalex-snapshot
Functional polymorphisms of the TET1 gene increase the risk of neuroblastoma in Chinese children
inferred← citeshttps://doi.org/10.1155/2016/2932049openalex-snapshot
Lack of Associations betweenXPCGene Polymorphisms and Neuroblastoma Susceptibility in a Chinese Population
inferred← citeshttps://doi.org/10.1155/2018/4868045openalex-snapshot
Precocious Puberty and the Lin28/Let7 Pathway: The Therapeutic Effect of the Nourishing “Yin” and Purging “Fire” Traditional Chinese Medicine Mixture in a Rat Model
inferred← citeshttps://doi.org/10.1155/2019/3518149openalex-snapshot
Association ofNEFLGene Polymorphisms with Wilms’ Tumor Susceptibility in Chinese Children
inferred← citeshttps://doi.org/10.1155/2019/5736175openalex-snapshot
APEX1 Polymorphisms and Neuroblastoma Risk in Chinese Children: A Three-Center Case-Control Study
inferred← citeshttps://doi.org/10.1155/2019/6514608openalex-snapshot
miR-34b/crs4938723 T>C Decreases Neuroblastoma Risk: A Replication Study in the Hunan Children
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6511801.v1openalex-snapshot
Data from Transcription Factors Involved in Tumorigenesis Are Over-Represented in Mutated Active DNA-Binding Sites in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6512115openalex-snapshot
Data from Subcellular Distribution of p53 by the p53-Responsive lncRNA NBAT1 Determines Chemotherapeutic Response in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6513640openalex-snapshot
Data from Somatic Mutations Enriched in Cis-Regulatory Elements Affect Genes Involved in Embryonic Development and Immune System Response in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6513640.v1openalex-snapshot
Data from Somatic Mutations Enriched in Cis-Regulatory Elements Affect Genes Involved in Embryonic Development and Immune System Response in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.can-14-0431openalex-snapshot
Common Genetic Variants in NEFL Influence Gene Expression and Neuroblastoma Risk
inferred← citeshttps://doi.org/10.1158/0008-5472.can-14-3613openalex-snapshot
CASC15-S Is a Tumor Suppressor lncRNA at the 6p22 Neuroblastoma Susceptibility Locus
inferred← citeshttps://doi.org/10.1158/0008-5472.can-19-2270openalex-snapshot
HACE1 Prevents Lung Carcinogenesis via Inhibition of RAC-Family GTPases
inferred← citeshttps://doi.org/10.1158/0008-5472.can-19-2883openalex-snapshot
Transcription Factors Involved in Tumorigenesis Are Over-Represented in Mutated Active DNA-Binding Sites in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.can-19-3499openalex-snapshot
Subcellular Distribution of p53 by the p53-Responsive lncRNA NBAT1 Determines Chemotherapeutic Response in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-3788openalex-snapshot
Somatic Mutations Enriched in Cis -Regulatory Elements Affect Genes Involved in Embryonic Development and Immune System Response in Neuroblastoma
inferred← citeshttps://doi.org/10.1158/1055-9965.epi-19-0941openalex-snapshot
Cancer Progress and Priorities: Childhood Cancer
inferred← citeshttps://doi.org/10.1158/1055-9965.epi-21-0782openalex-snapshot
Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-17-0514openalex-snapshot
Differential Regulation of LET-7 by LIN28B Isoform–Specific Functions
inferred← citeshttps://doi.org/10.1159/000367962openalex-snapshot
Genome-Wide Association Studies in Africans and African Americans: Expanding the Framework of the Genomics of Human Traits and Disease
inferred← citeshttps://doi.org/10.1159/000382066openalex-snapshot
Genomic Alterations and Abnormal Cell Cycle in High-Risk Neuroblastoma
inferred← citeshttps://doi.org/10.1172/jci.insight.165703openalex-snapshot
N6-methyladenosine–mediated overexpression of long noncoding RNA ADAMTS9-AS2 triggers neuroblastoma differentiation via regulating LIN28B/let-7/MYCN signaling
inferred← citeshttps://doi.org/10.1172/jci145142openalex-snapshot
LIN28B alters ribosomal dynamics to promote metastasis in MYCN-driven malignancy
inferred← citeshttps://doi.org/10.1172/jci166919openalex-snapshot
Genetic predisposition to neuroblastoma results from a regulatory polymorphism that promotes the adrenergic cell state
inferred← citeshttps://doi.org/10.1186/1471-2377-13-178openalex-snapshot
Circulating miR-30a, miR-126 and let-7b as biomarker for ischemic stroke in humans
inferred← citeshttps://doi.org/10.1186/s12885-018-4847-yopenalex-snapshot
The rs2147578 C > G polymorphism in the Inc-LAMC2–1:1 gene is associated with increased neuroblastoma risk in the Henan children
inferred← citeshttps://doi.org/10.1186/s12885-025-14310-wopenalex-snapshot
Association between MYCN gene polymorphisms and neuroblastoma susceptibility: a case-control study in Chinese children from Jiangsu Province
inferred← citeshttps://doi.org/10.1186/s12935-019-0788-zopenalex-snapshot
Prognostic value of Lin28A and Lin28B in various human malignancies: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1186/s12943-016-0530-6openalex-snapshot
Long noncoding RNAs in cancer: mechanisms of action and technological advancements
inferred← citeshttps://doi.org/10.1186/s12943-017-0686-8openalex-snapshot
11q deletion in neuroblastoma: a review of biological and clinical implications
inferred← citeshttps://doi.org/10.1186/s13046-024-03113-9openalex-snapshot
RETRACTED ARTICLE: N6-methyladenosine modification of circMARK2 enhances cytoplasmic export and stabilizes LIN28B, contributing to the progression of Wilms tumor
inferred← citeshttps://doi.org/10.1186/s40001-026-04796-wopenalex-snapshot
Association between the lincRNA–TDRG1 rs8506 C > T polymorphism and neuroblastoma risk in children from Jiangsu Province
inferred← citeshttps://doi.org/10.1186/s40246-025-00767-0openalex-snapshot
Genetic variants of m1A modification genes and the risk of neuroblastoma: novel insights from a Chinese case-control study
inferred← citeshttps://doi.org/10.1186/s40478-020-01038-wopenalex-snapshot
Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma
inferred← citeshttps://doi.org/10.1200/edbk_159169openalex-snapshot
Neuroblastoma: A Tough Nut to Crack
inferred← citeshttps://doi.org/10.1200/po-24-00886openalex-snapshot
Anaplastic Lymphoma Kinase Inhibition Therapy for Hereditary Neuroblastoma
inferred← citeshttps://doi.org/10.1212/nxg.0000000000000330openalex-snapshot
HACE1 deficiency leads to structural and functional neurodevelopmental defects
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006787openalex-snapshot
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma
inferred← citeshttps://doi.org/10.1371/journal.pone.0059762openalex-snapshot
Polymorphisms in the Calcium-Sensing Receptor Gene Are Associated with Clinical Outcome of Neuroblastoma
inferred← citeshttps://doi.org/10.1371/journal.pone.0076810openalex-snapshot
Impact of Interleukin-6 –174 G>C Gene Promoter Polymorphism on Neuroblastoma
inferred← citeshttps://doi.org/10.1371/journal.pone.0114696openalex-snapshot
CASP8 SNP D302H (rs1045485) Is Associated with Worse Survival in MYCN-Amplified Neuroblastoma Patients
inferred← citeshttps://doi.org/10.14218/csp.2023.00025sopenalex-snapshot
Association Between miR-492 rs2289030 G>C and Susceptibility to Neuroblastoma in Chinese Children from Jiangsu Province
inferred← citeshttps://doi.org/10.14218/csp.2023.00035openalex-snapshot
miR-618 rs2682818 C>A Polymorphism Decreases Neuroblastoma Risk in Tumors Originating from the Adrenal Gland
inferred← citeshttps://doi.org/10.1517/17460441.2015.974544openalex-snapshot
Neuroblastoma models for insights into tumorigenesis and new therapies
inferred← citeshttps://doi.org/10.1523/jneurosci.2560-15.2015openalex-snapshot
Lin28B and Let-7 in the Control of Sympathetic Neurogenesis and Neuroblastoma Development
inferred← citeshttps://doi.org/10.18632/aging.101429openalex-snapshot
RAN/RANBP2 polymorphisms and neuroblastoma risk in Chinese children: a three-center case-control study
inferred← citeshttps://doi.org/10.18632/aging.101522openalex-snapshot
Relevance of XPD polymorphisms to neuroblastoma risk in Chinese children: a four-center case-control study
inferred← citeshttps://doi.org/10.18632/aging.101601openalex-snapshot
XRCC1 gene polymorphisms and risk of neuroblastoma in Chinese children
inferred← citeshttps://doi.org/10.18632/aging.101920openalex-snapshot
Additional data support the role of LINC00673 rs11655237 C>T in the development of neuroblastoma
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