An Updated and Comprehensive Meta-Analysis of Association Between Seven Hot Loci Polymorphisms from Eight GWAS and Glioma Risk

[1]  Alexander R. Pico,et al.  Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk , 2014, Nature Genetics.

[2]  Matthew J. Oborski,et al.  Cancer Management and Research Dovepress Malignant Gliomas: Current Perspectives in Diagnosis, Treatment, and Early Response Assessment Using Advanced Quantitative Imaging Methods , 2022 .

[3]  B. Das,et al.  Molecular investigation of isocitrate dehydrogenase gene (IDH) mutations in gliomas: first report of IDH2 mutations in Indian patients. , 2013, Asian Pacific journal of cancer prevention : APJCP.

[4]  E. Gillanders,et al.  Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk , 2013, Cancer Causes & Control.

[5]  Chao Wang,et al.  P53 codon 72 Arg/Pro polymorphism and glioma risk: an updated meta-analysis , 2013, Tumor Biology.

[6]  Shiwen Chen,et al.  Association of the MTHFR C677T polymorphism with primary brain tumor risk , 2013, Tumor Biology.

[7]  L. Kang,et al.  RTEL1 and TERT polymorphisms are associated with astrocytoma risk in the Chinese Han population , 2013, Tumor Biology.

[8]  Hang Liu,et al.  Associations between three XRCC1 polymorphisms and glioma risk: a meta-analysis , 2013, Tumor Biology.

[9]  G. Gao,et al.  RTEL1 tagging SNPs and haplotypes were associated with glioma development , 2013, Diagnostic Pathology.

[10]  Leah E. Mechanic,et al.  Known glioma risk loci are associated with glioma with a family history of brain tumours—A case–control gene association study , 2013, International journal of cancer.

[11]  Weiping Liu,et al.  Association between epidermal growth factor gene rs4444903 polymorphism and risk of glioma , 2013, Tumor Biology.

[12]  Alexander R. Pico,et al.  Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology. , 2013, Neuro-oncology.

[13]  K. Hoang-Xuan,et al.  Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies. , 2013, Neuro-oncology.

[14]  N. Rothman,et al.  Genome-wide association study of glioma and meta-analysis , 2012, Human Genetics.

[15]  Huiling Lou,et al.  Polymorphisms of TREH, IL4R and CCDC26 genes associated with risk of glioma. , 2012, Cancer epidemiology.

[16]  Brooke L. Fridley,et al.  SSBP2 Variants Are Associated with Survival in Glioblastoma Patients , 2012, Clinical Cancer Research.

[17]  S. Chanock,et al.  Joint associations between genetic variants and reproductive factors in glioma risk among women. , 2011, American journal of epidemiology.

[18]  M. Kon,et al.  Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk , 2011, BMC Medical Genomics.

[19]  Melissa Bondy,et al.  Chromosome 7p11.2 (EGFR) variation influences glioma risk. , 2011, Human molecular genetics.

[20]  A. Jemal,et al.  Cancer statistics, 2011 , 2011, CA: a cancer journal for clinicians.

[21]  Ying Mao,et al.  Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population. , 2011, American journal of epidemiology.

[22]  D. Brat,et al.  Cancer susceptibility variants and the risk of adult glioma in a US case–control study , 2011, Journal of Neuro-Oncology.

[23]  Q. Wei,et al.  Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck. , 2010, Carcinogenesis.

[24]  G. Marshall,et al.  Targeting the Dimerization of Epidermal Growth Factor Receptors with Small‐Molecule Inhibitors , 2010, Chemical biology & drug design.

[25]  D. Lambright,et al.  A Novel Pleckstrin Homology Domain-containing Protein Enhances Insulin-stimulated Akt Phosphorylation and GLUT4 Translocation in Adipocytes , 2010, The Journal of Biological Chemistry.

[26]  A. Auvinen,et al.  Interaction between 5 genetic variants and allergy in glioma risk. , 2010, American journal of epidemiology.

[27]  S. Shete,et al.  Genetic advances in glioma: susceptibility genes and networks. , 2010, Current opinion in genetics & development.

[28]  Melissa Bondy,et al.  Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[29]  Melissa Bondy,et al.  Genome-wide association study identifies five susceptibility loci for glioma , 2009, Nature Genetics.

[30]  Alexander R. Pico,et al.  Variants in the CDKN2B and RTEL1 regions are associated with high grade glioma susceptibility , 2009, Nature Genetics.

[31]  A. Jemal,et al.  Cancer Statistics, 2009 , 2009, CA: a cancer journal for clinicians.

[32]  Charles Duyckaerts,et al.  The 2007 WHO classification of tumors of the central nervous system – what has changed? , 2008, Current opinion in neurology.

[33]  Tony Fletcher,et al.  Sequence variant on 8q24 confers susceptibility to urinary bladder cancer , 2008, Nature Genetics.

[34]  Stephen C. West,et al.  RTEL1 Maintains Genomic Stability by Suppressing Homologous Recombination , 2008, Cell.

[35]  Tarik Tihan,et al.  Brain tumor epidemiology: Consensus from the Brain Tumor Epidemiology Consortium , 2008, Cancer.

[36]  J. Lahti,et al.  Retinoic acid induces caspase-8 transcription via phospho-CREB and increases apoptotic responses to death stimuli in neuroblastoma cells. , 2008, Biochimica et biophysica acta.

[37]  B. Bataille,et al.  Prognostic molecular markers with no impact on decision-making: the paradox of gliomas based on a prospective study , 2008, British Journal of Cancer.

[38]  N. Banik,et al.  Differentiation Decreased Telomerase Activity in Rat Glioblastoma C6 Cells and Increased Sensitivity to IFN-γ and Taxol for Apoptosis , 2007, Neurochemical Research.

[39]  Oliver Sieber,et al.  A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 , 2007, Nature Genetics.

[40]  Lester L. Peters,et al.  Genome-wide association study identifies novel breast cancer susceptibility loci , 2007, Nature.

[41]  P. Fearnhead,et al.  Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 , 2007, Nature Genetics.

[42]  E. Blackburn,et al.  Telomeres and telomerase: the path from maize, Tetrahymena and yeast to human cancer and aging , 2006, Nature Medicine.

[43]  R. Pallini,et al.  Telomerase inhibition impairs tumor growth in glioblastoma xenografts , 2006, Neurological research.

[44]  Luo Wang,et al.  Survival prediction in patients with glioblastoma multiforme by human telomerase genetic variation. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[45]  P. Kleihues,et al.  Epidemiology and etiology of gliomas , 2005, Acta Neuropathologica.

[46]  P. Lansdorp,et al.  Regulation of Murine Telomere Length by Rtel An Essential Gene Encoding a Helicase-like Protein , 2004, Cell.

[47]  J. Hackett,et al.  Balancing instability: dual roles for telomerase and telomere dysfunction in tumorigenesis , 2002, Oncogene.

[48]  F. Davis,et al.  Current epidemiological trends and surveillance issues in brain tumors , 2001, Expert review of anticancer therapy.

[49]  V. P. Collins,et al.  Adenovirus-mediated overexpression of p15INK4B inhibits human glioma cell growth, induces replicative senescence, and inhibits telomerase activity similarly to p16INK4A. , 2000, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[50]  R. Jenkins,et al.  Investigation of germline PTEN, p53, p16(INK4A)/p14(ARF), and CDK4 alterations in familial glioma. , 2000, American journal of medical genetics.

[51]  R Miike,et al.  Familial and personal medical history of cancer and nervous system conditions among adults with glioma and controls. , 1997, American journal of epidemiology.

[52]  G. Gao,et al.  CCDC26 gene polymorphism and glioblastoma risk in the Han Chinese population. , 2014, Asian Pacific journal of cancer prevention : APJCP.

[53]  X. Tong,et al.  Associations between the rs6010620 polymorphism in RTEL1 and risk of glioma: a meta-analysis of 20,711 participants. , 2014, Asian Pacific journal of cancer prevention : APJCP.

[54]  Xu Chen,et al.  Association of XRCC3 Thr241Met polymorphisms and gliomas risk: evidence from a meta-analysis. , 2013, Asian Pacific journal of cancer prevention : APJCP.

[55]  Wei-dong Cao,et al.  Glioblastoma multiforme: Molecular characterization and current treatment strategy (Review). , 2012, Experimental and therapeutic medicine.

[56]  A. Jemal,et al.  Global Cancer Statistics , 2011 .

[57]  B. O'neill,et al.  Distinct germ line polymorphisms underlie glioma morphologic heterogeneity. , 2011, Cancer genetics.

[58]  J. Uhm.  Comprehensive genomic characterization defines human glioblastoma genes and core pathways , 2009 .

[59]  Paul Fearnhead,et al.  Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Yeager M, Orr N, Hayes RB, Jacobs KB, Kraft , 2007 .

[60]  H. Grönberg,et al.  Microsatellite instability, PTEN and p53 germline mutations in glioma families. , 2001, Acta oncologica.

[61]  N. Dubrawsky.  Cancer statistics , 1989, CA: a cancer journal for clinicians.