scholarly article | Q13442814 |
P50 | author | Henne Holstege | Q61281193 |
Jos Jonkers | Q88723772 | ||
Lodewyk F A Wessels | Q89966632 | ||
Christiaan Klijn | Q41050637 | ||
P2093 | author name string | Xiaoling Liu | |
Jeroen de Ridder | |||
Marcel Reinders | |||
P2860 | cites work | The Hallmarks of Cancer | Q221226 |
Cancer as an evolutionary and ecological process | Q22122026 | ||
Characterization of FBX25, encoding a novel brain-expressed F-box protein | Q24294306 | ||
Alterations of anaphase-promoting complex genes in human colon cancer cells | Q24297514 | ||
The zinc finger of the CSN-associated deubiquitinating enzyme USP15 is essential to rescue the E3 ligase Rbx1 | Q24307443 | ||
NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF) | Q24337553 | ||
The BRCA2-interacting protein BCCIP functions in RAD51 and BRCA2 focus formation and homologous recombinational repair | Q24556631 | ||
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization | Q24564349 | ||
Identification and validation of oncogenes in liver cancer using an integrative oncogenomic approach | Q24633776 | ||
A census of human cancer genes | Q24647081 | ||
High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization | Q25257525 | ||
Detecting statistically significant common insertion sites in retroviral insertional mutagenesis screens | Q27339599 | ||
CGHcall: calling aberrations for array CGH tumor profiles. | Q51924133 | ||
Adenovirus E1a prevents the retinoblastoma gene product from complexing with a cellular transcription factor | Q52480364 | ||
Synergistic tumor suppressor activity of BRCA2 and p53 in a conditional mouse model for breast cancer. | Q52544495 | ||
High-resolution analysis of DNA copy number alterations in colorectal cancer by array-based comparative genomic hybridization. | Q53370271 | ||
Amplification of endogenous myc-related DNA sequences in a human myeloid leukaemia cell line | Q53564566 | ||
CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q | Q57903122 | ||
Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays | Q74268267 | ||
Molecular classification of breast carcinomas by comparative genomic hybridization: a specific somatic genetic profile for BRCA1 tumors | Q78598262 | ||
??? | Q59148640 | ||
DAVID: Database for Annotation, Visualization, and Integrated Discovery | Q27499374 | ||
Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene | Q27860693 | ||
Molecular portraits of human breast tumours | Q28032461 | ||
Repeated observation of breast tumor subtypes in independent gene expression data sets | Q28131820 | ||
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation | Q28207115 | ||
TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas | Q28218999 | ||
Cross-species oncogenomics in cancer gene identification | Q28249773 | ||
WD repeat-containing mitotic checkpoint proteins act as transcriptional repressors during interphase | Q28283832 | ||
Cul4A targets p27 for degradation and regulates proliferation, cell cycle exit, and differentiation during erythropoiesis | Q28593723 | ||
On Estimation of a Probability Density Function and Mode | Q29030604 | ||
Circular binary segmentation for the analysis of array-based DNA copy number data | Q29615406 | ||
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays | Q29615979 | ||
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors | Q29618818 | ||
Genome-wide analysis of DNA copy-number changes using cDNA microarrays | Q29618942 | ||
Genomic and transcriptional aberrations linked to breast cancer pathophysiologies | Q29619120 | ||
A comparison study: applying segmentation to array CGH data for downstream analyses | Q30797973 | ||
STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments | Q30821792 | ||
Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data | Q30998407 | ||
Computation of recurrent minimal genomic alterations from array-CGH data | Q31030483 | ||
Robust smooth segmentation approach for array CGH data analysis | Q31120038 | ||
A whole-genome mouse BAC microarray with 1-Mb resolution for analysis of DNA copy number changes by array comparative genomic hybridization | Q33196501 | ||
High resolution array-CGH analysis of single cells | Q33267061 | ||
The emerging role of the COP9 signalosome in cancer | Q34147948 | ||
Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors | Q34190883 | ||
DDEF1 is located in an amplified region of chromosome 8q and is overexpressed in uveal melanoma | Q34419301 | ||
Array-CGH and breast cancer | Q35012854 | ||
Intrinsic molecular signature of breast cancer in a population-based cohort of 412 patients | Q35605761 | ||
Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way. | Q35789595 | ||
Array comparative genomic hybridization and its applications in cancer | Q36141621 | ||
Manifestation, mechanisms and mysteries of gene amplifications | Q36313394 | ||
Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes | Q38444987 | ||
High-resolution global profiling of genomic alterations with long oligonucleotide microarray | Q40534935 | ||
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene | Q41738933 | ||
Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma | Q42466578 | ||
Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer | Q42499457 | ||
Onc gene amplification in promyelocytic leukaemia cell line HL-60 and primary leukaemic cells of the same patient | Q43789288 | ||
PIK3CA is implicated as an oncogene in ovarian cancer. | Q46015944 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | statistics | Q12483 |
P304 | page(s) | e13 | |
P577 | publication date | 2008-01-10 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Identification of cancer genes using a statistical framework for multiexperiment analysis of nondiscretized array CGH data | |
P478 | volume | 36 |
Q44054130 | A Bayesian segmentation approach to ascertain copy number variations at the population level |
Q38471824 | A bayesian integrative model for genetical genomics with spatially informed variable selection. |
Q44762537 | A diagnostic algorithm to identify paired tumors with clonal origin |
Q40366176 | A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control |
Q44943632 | Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors |
Q30497664 | BRCA1-mutated and basal-like breast cancers have similar aCGH profiles and a high incidence of protein truncating TP53 mutations |
Q37137914 | BRCA1185delAG tumors may acquire therapy resistance through expression of RING-less BRCA1 |
Q34962407 | Cancer gene discovery in mouse and man. |
Q34534035 | Comparative analysis of methods for identifying recurrent copy number alterations in cancer |
Q61124716 | Comparative oncogenomics identifies combinations of driver genes and drug targets in BRCA1-mutated breast cancer |
Q36268076 | Comparative oncogenomics implicates the neurofibromin 1 gene (NF1) as a breast cancer driver. |
Q30536665 | Copynumber: Efficient algorithms for single- and multi-track copy number segmentation |
Q33671467 | Cross-species comparison of aCGH data from mouse and human BRCA1- and BRCA2-mutated breast cancers |
Q38068938 | Detection and interpretation of genomic structural variation in health and disease. |
Q37384126 | Detection of recurrent copy number alterations in the genome: taking among-subject heterogeneity seriously |
Q30498218 | DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumors |
Q28483012 | Fenton reaction induced cancer in wild type rats recapitulates genomic alterations observed in human cancer |
Q33481331 | Finding exclusively deleted or amplified genomic areas in lung adenocarcinomas using a novel chromosomal pattern analysis |
Q39543236 | FocalScan: Scanning for altered genes in cancer based on coordinated DNA and RNA change |
Q38484434 | Functional analysis of human cancer-associated genes and their association with the testes and epididymis |
Q34354428 | Genome-wide identification of significant aberrations in cancer genome. |
Q37200784 | Identification of Copy Number Aberrations in Breast Cancer Subtypes Using Persistence Topology |
Q36011694 | Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data |
Q34203669 | Identification of differential aberrations in multiple-sample array CGH studies |
Q33495849 | Identification of significant regional genetic variations using continuous CNV values in aCGH data. |
Q51802432 | Integrative approach for prioritizing cancer genes in sporadic colon cancer. |
Q33744507 | KC-SMARTR: An R package for detection of statistically significant aberrations in multi-experiment aCGH data. |
Q33988970 | Lack of genomic heterogeneity at high-resolution aCGH between primary breast cancers and their paired lymph node metastases |
Q33687060 | Latent factor analysis to discover pathway-associated putative segmental aneuploidies in human cancers |
Q28512158 | Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression |
Q39294303 | Low-grade and high-grade mammary carcinomas in WAP-T transgenic mice are independent entities distinguished by Met expression |
Q43214379 | MSB: a mean-shift-based approach for the analysis of structural variation in the genome |
Q34257684 | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses. |
Q33455313 | Model-based clustering of array CGH data |
Q33692591 | Multiscale representation of genomic signals |
Q34614747 | Pitfalls in experimental designs for characterizing the transcriptional, methylational and copy number changes of oncogenes and tumor suppressor genes |
Q37266084 | RJaCGH: Bayesian analysis of aCGH arrays for detecting copy number changes and recurrent regions |
Q36945532 | RNF138 interacts with RAD51D and is required for DNA interstrand crosslink repair and maintaining chromosome integrity |
Q37248153 | Sequential model selection-based segmentation to detect DNA copy number variation |
Q33761768 | Specific genomic aberrations in primary colorectal cancer are associated with liver metastases |
Q34345632 | TAGCNA: a method to identify significant consensus events of copy number alterations in cancer |
Q41404014 | Whole-exome DNA sequence analysis of Brca2- and Trp53-deficient mouse mammary gland tumours |
Search more.