| P2093 | author name string | Lin Wang | |
| | Kai Wang | |
| | Yao Lu | |
| | Zheng Wang | |
| | Xu Zhang | |
| | Feng Wang | |
| | Chengliang Dong | |
| | Hongbin Zhong | |
| | Haiying Jia | |
| | Jinghui Hou | |
| P2860 | cites work | COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer | Q24608391 |
| | VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing | Q24628978 |
| | Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma | Q24630017 |
| | A census of human cancer genes | Q24647081 |
| | Fast and accurate short read alignment with Burrows-Wheeler transform | Q24653853 |
| | Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH | Q24654938 |
| | The 2007 WHO classification of tumours of the central nervous system | Q24685772 |
| | The biology of VEGF and its receptors | Q27860704 |
| | Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources | Q27860739 |
| | The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 |
| | A method and server for predicting damaging missense mutations | Q27860835 |
| | The Sequence Alignment/Map format and SAMtools | Q27860966 |
| | Loss of DAL-1, a protein 4.1-related tumor suppressor, is an important early event in the pathogenesis of meningiomas | Q28140396 |
| | Common variation at 10p12.31 near MLLT10 influences meningioma risk | Q28943376 |
| | ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data | Q29547161 |
| | Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 |
| | CBTRUS statistical report: Primary brain and central nervous system tumors diagnosed in the United States in 2006-2010. | Q30427255 |
| | Molecular biology of unreresectable meningiomas: implications for new treatments and review of the literature | Q30440977 |
| | Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma. | Q34309433 |
| | Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO | Q34324259 |
| | DNA methylation in the malignant transformation of meningiomas | Q34562612 |
| | Neurofibromatosis 1 and neurofibromatosis 2: a twenty first century perspective. | Q34577777 |
| | Meningiomas | Q35769435 |
| | Loss of SUFU function in familial multiple meningioma. | Q36439334 |
| | Differential mucin phenotypes and their significance in a variation of colorectal carcinoma | Q36987832 |
| | Semaphorin 4D cooperates with VEGF to promote angiogenesis and tumor progression. | Q37069435 |
| | Identification of deleterious mutations within three human genomes | Q37363175 |
| | Roles of Sema4D and Plexin-B1 in tumor progression | Q37790755 |
| | The molecular genetics and tumor pathogenesis of meningiomas and the future directions of meningioma treatments. | Q37870199 |
| | Molecular genetics of meningiomas: a systematic review of the current literature and potential basis for future treatment paradigms | Q37870200 |
| | SWI/SNF nucleosome remodellers and cancer. | Q37886668 |
| | Mapping of the methylation pattern of the MUC2 promoter in pancreatic cancer cell lines, using bisulfite genomic sequencing | Q40383148 |
| | Exome enrichment and SOLiD sequencing of formalin fixed paraffin embedded (FFPE) prostate cancer tissue | Q41872853 |
| | wANNOVAR: annotating genetic variants for personal genomes via the web. | Q42129589 |
| | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma | Q42241120 |
| | Inhibition of endothelial cell migration by gene transfer of tissue inhibitor of metalloproteinases-1. | Q42469568 |
| | Genomic sequencing of meningiomas identifies oncogenic SMO and AKT1 mutations | Q42548316 |
| | A large-scale screen for coding variants predisposing to psoriasis | Q43894399 |
| | Genomic and transcriptome analysis revealing an oncogenic functional module in meningiomas | Q44156113 |
| | Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations | Q44902948 |
| | "Malignancy" in meningiomas: a clinicopathologic study of 116 patients, with grading implications | Q48222606 |
| | Correlation of proto-oncogene expression and proliferation and meningiomas. | Q52514454 |
| | Enhanced expression of the sis and c-myc oncogenes in human meningiomas | Q68502599 |
| | Human KRAS oncogene expression in meningioma | Q69049071 |
| | Apoptotic activity and bcl-2 immunoreactivity in meningiomas. Association with grade and outcome | Q73965124 |
| P433 | issue | 101 | |
| P921 | main subject | neurofibromatosis type II | Q1935832 |
| P304 | page(s) | 301-311 | |
| P577 | publication date | 2014-12-01 | |
| P1433 | published in | Discovery Medicine | Q5281940 |
| P1476 | title | Exome sequencing on malignant meningiomas identified mutations in neurofibromatosis type 2 (NF2) and meningioma 1 (MN1) genes | |
| P478 | volume | 18 | |