Genetics and Genomics
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Open Access
Featured
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Genetics and Genomics
| Open AccessLINE-1 methylation in leukocyte DNA, interaction with phosphatidylethanolamine N-methyltransferase variants and bladder cancer risk
- S M Tajuddin
- , A F S Amaral
- & J Mosquera
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Genetics and Genomics
| Open AccessFrequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease
- D Leongamornlert
- , E Saunders
- & Z Kote-Jarai
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Genetics and Genomics
| Open AccessFGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
- D Agarwal
- , S Pineda
- & R L Milne
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Molecular Diagnostics
| Open AccessRET-rearranged non-small-cell lung carcinoma: a clinicopathological and molecular analysis
- K Tsuta
- , T Kohno
- & R Kushima
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Letter to the Editor
| Open AccessDistribution of breast cancer risk from SNPs and classical risk factors in women of routine screening age in the UK
- A R Brentnall
- , D G Evans
- & J Cuzick
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Genetics and Genomics
| Open AccessMutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanoma
- M Dono
- , G Angelini
- & U Pfeffer
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Genetics and Genomics
| Open AccessOral contraceptive and reproductive risk factors for ovarian cancer within sisters in the breast cancer family registry
- J S Ferris
- , M B Daly
- & M B Terry
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Short Communication
| Open AccessGermline CDH1 mutations in bilateral lobular carcinoma in situ
- C Petridis
- , I Shinomiya
- & E J Sawyer
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Genetics and Genomics
| Open AccessBOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface
- A J Lee
- , A P Cunningham
- & A C Antoniou
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Genetics and Genomics
| Open AccessIncidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study
- C M Phelan
- , J Iqbal
- & Tomasz Huzarski
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Genetics and Genomics
| Open AccessDICER1 hotspot mutations in non-epithelial gonadal tumours
- L Witkowski
- , J Mattina
- & W D Foulkes
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Genetics and Genomics
| Open AccessMicroRNA-based molecular classification of non-BRCA1/2 hereditary breast tumours
- M Tanic
- , E Andrés
- & B Martinez-Delgado
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Clinical Study
| Open AccessSomatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers
- E Gross
- , C Meul
- & A B P van Kuilenburg
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Genetics and Genomics
| Open AccessThe clinical implication of SS18 -SSX fusion gene in synovial sarcoma
- T Ren
- , Q Lu
- & Y Sun
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Mini Review
| Open AccessReview of processing and analysis methods for DNA methylation array data
- C S Wilhelm-Benartzi
- , D C Koestler
- & R Brown
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Molecular Diagnostics
| Open AccessP2Y2 receptor promotes cell invasion and metastasis in prostate cancer cells
- W-H Li
- , Y Qiu
- & W-G Fang
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Genetics and Genomics
| Open AccessLoss of PTEN expression is an independent predictor of favourable survival in endometrial carcinomas
- A Akiyama-Abe
- , T Minaguchi
- & H Yoshikawa
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Short Communication
| Open AccessMutational analysis of Polycomb genes in solid tumours identifies PHC3 amplification as a possible cancer-driving genetic alteration
- F Crea
- , L Sun
- & C D Helgason
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Short Communication
| Open AccessPigmentation-related phenotypes and risk of prostate cancer
- S J Weinstein
- , J Virtamo
- & D Albanes
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Short Communication
| Open AccessInversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma
- F Gao
- , C Ling
- & K Wang
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Epidemiology
| Open AccessThe NQO1 polymorphism C609T (Pro187Ser) and cancer susceptibility: a comprehensive meta-analysis
- B Lajin
- & A Alachkar
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Short Communication
| Open AccessTERT promoter mutations in ocular melanoma distinguish between conjunctival and uveal tumours
- K G Griewank
- , R Murali
- & M Zeschnigk
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Epidemiology
| Open AccessA comparison of the detection of BRCA mutation carriers through the provision of Jewish population-based genetic testing compared with clinic-based genetic testing
- K A Metcalfe
- , A Poll
- & S A Narod
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Genetics and Genomics
| Open AccessGene expression profiling identifies different sub-types of retinoblastoma
- G Kapatai
- , M-A Brundler
- & C M McConville
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Mini Review
| Open AccessLong noncoding RNAs and the genetics of cancer
- S W Cheetham
- , F Gruhl
- & M E Dinger
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Epidemiology
| Open AccessFluid intake, genetic variants of UDP-glucuronosyltransferases, and bladder cancer risk
- J Wang
- , X Wu
- & J Lin
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Molecular Diagnostics
| Open AccessSox11 expression in astrocytic gliomas: correlation with nestin/c-Met/IDH1-R132H expression phenotypes, p-Stat-3 and survival
- P Korkolopoulou
- , G Levidou
- & C Piperi
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Molecular Diagnostics
| Open AccessFeasibility of proposed single-nucleotide polymorphisms as predictive markers for targeted regimens in metastatic colorectal cancer
- J C Kim
- , Y J Ha
- & Y S Kim
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Genetics and Genomics
| Open AccessLow penetrance susceptibility to glioma is caused by the TP53 variant rs78378222
- V Enciso-Mora
- , F J Hosking
- & R S Houlston
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Genetics and Genomics
| Open AccessMutation analysis of the EGFR gene and downstream signalling pathway in histologic samples of malignant pleural mesothelioma
- R Mezzapelle
- , U Miglio
- & R Boldorini
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Genetics and Genomics
| Open AccessDNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas
- M M Kamieniak
- , I Muñoz-Repeto
- & M J García
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Genetics and Genomics
| Open AccessPutative tumour suppressor gene necdin is hypermethylated and mutated in human cancer
- L E De Faveri
- , C D Hurst
- & E J Chapman
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Short Communication
| Open AccessA retrospective observational study of the relationship between family history and survival from colorectal cancer
- E J A Morris
- , S Penegar
- & R S Houlston
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Molecular Diagnostics
| Open AccessKRAS and BRAF mutations are rare and related to DNA mismatch repair deficiency in gastric cancer from the East and the West: Results from a large international multicentre study
- N C T van Grieken
- , T Aoyma
- & H I Grabsch
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Genetics and Genomics
| Open AccessKRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers
- A I Phipps
- , D D Buchanan
- & P A Newcomb
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Molecular Diagnostics
| Open AccessFrequent GNAS mutations in low-grade appendiceal mucinous neoplasms
- G Nishikawa
- , S Sekine
- & Y Kanai
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Genetics and Genomics
| Open AccessCytosine-based nucleoside analogs are selectively lethal to DNA mismatch repair-deficient tumour cells by enhancing levels of intracellular oxidative stress
- M Hewish
- , S A Martin
- & A Ashworth
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Genetics and Genomics
| Open AccessCommon genetic variants in the 9p21 region and their associations with multiple tumours
- F Gu
- , R M Pfeiffer
- & X R Yang
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Genetics and Genomics
| Open AccessEndogenous BTG2 expression stimulates migration of bladder cancer cells and correlates with poor clinical prognosis for bladder cancer patients
- N Wagener
- , J Bulkescher
- & K Hoppe-Seyler
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Epidemiology
| Open AccessRisk of benign tumours of nervous system, and of malignant neoplasms, in people with neurofibromatosis: population-based record-linkage study
- O O Seminog
- & M J Goldacre
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Epidemiology
| Open AccessHPV16 genetic variation and the development of cervical cancer worldwide
- I Cornet
- , T Gheit
- & G M Clifford
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Genetics and Genomics
| Open AccessAnalysis of gene alterations of mitochondrial DNA D-loop regions to determine breast cancer clonality
- S Masuda
- , T Kadowaki
- & R Y Osamura
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Genetics and Genomics
| Open AccessAn inherited NBN mutation is associated with poor prognosis prostate cancer
- C Cybulski
- , D Wokołorczyk
- & J Lubiński
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Genetics and Genomics
| Open AccessFrequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer
- T Pal
- , M R Akbari
- & S A Narod
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Genetics and Genomics
| Open AccessPatterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancer
- V Abkevich
- , K M Timms
- & J S Lanchbury
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Genetics and Genomics
| Open AccessThe FOXM1-PLK1 axis is commonly upregulated in oesophageal adenocarcinoma
- M Dibb
- , N Han
- & A D Sharrocks
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Letter to the Editor
| Open AccessKRAS mutation in colorectal cancer metastases after adjuvant FOLFOX for the primary
- J-N Vauthey
- , S Kopetz
- & A Andreou
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Letter to the Editor
| Open AccessReply: KRAS mutation in colorectal cancer metastases after adjuvant folfox for the primary
- T Yoshino
- , Y Kawamoto
- & K Tsuchihara
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Letter to the Editor
| Open AccessComment on ‘A comparison of three methods for detecting KRAS mutations in formalin-fixed colorectal cancer specimens’
- N Normanno
- , A Rachiglio
- & C Pinto