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Whole genome DNA copy number changes identified by high density oligonucleotide arrays.
- Published in:
- Human Genomics, 2004, v. 1, n. 4, p. 287, doi. 10.1186/1479-7364-1-4-287
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- Article
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data.
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- Biostatistics, 2010, v. 11, n. 1, p. 164, doi. 10.1093/biostatistics/kxp045
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- Article
Journeys into the genome of cancer cells.
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- EMBO Molecular Medicine, 2013, v. 5, n. 2, p. 169, doi. 10.1002/emmm.201202388
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- Article
Localisation of susceptibility genes for familial testicular germ cell tumour.
- Published in:
- APMIS, 2003, v. 111, n. 1, p. 128, doi. 10.1034/j.1600-0463.2003.11101171.x
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- Publication type:
- Article
Statistical Analysis of Pathogenicity of Somatic Mutations in Cancer.
- Published in:
- Genetics, 2006, v. 173, n. 4, p. 2187, doi. 10.1534/genetics.105.044677
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- Publication type:
- Article
Short inverted repeats contribute to localized mutability in human somatic cells.
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- Nucleic Acids Research, 2017, v. 45, n. 19, p. 11213, doi. 10.1093/nar/gkx731
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- Article
COSMIC: exploring the world's knowledge of somatic mutations in human cancer.
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- Nucleic Acids Research, 2015, v. 43, n. D1, p. D805, doi. 10.1093/nar/gku1075
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- Publication type:
- Article
Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells.
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- Nucleic Acids Research, 2013, v. 41, p. D955, doi. 10.1093/nar/gks1111
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- Publication type:
- Article
COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.
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- Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D945, doi. 10.1093/nar/gkq929
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- Publication type:
- Article
Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance.
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- Nucleic Acids Research, 2010, v. 38, n. 16, p. 5432, doi. 10.1093/nar/gkq306
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- Publication type:
- Article
COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer.
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- Nucleic Acids Research, 2010, v. 38, p. D652, doi. 10.1093/nar/gkp995
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- Publication type:
- Article
Mutational landscape of normal epithelial cells in Lynch Syndrome patients.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29920-2
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- Publication type:
- Article
High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma.
- Published in:
- Nature Medicine, 2015, v. 21, n. 1, p. 81, doi. 10.1038/nm.3773
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- Publication type:
- Article
Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.
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- Journal of Pathology, 2012, v. 227, n. 4, p. 446, doi. 10.1002/path.4042
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- Publication type:
- Article
Genetic alterations in 'normal' luminal and myoepithelial cells of the breast.
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- Journal of Pathology, 1999, v. 189, n. 4, p. 496, doi. 10.1002/(SICI)1096-9896(199912)189:4<496::AID-PATH485>3.0.CO;2-D
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- Publication type:
- Article
Loss of heterozygosity in ductal carcinoma in situ of the breast.
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- Journal of Pathology, 1995, v. 175, n. 2, p. 195, doi. 10.1002/path.1711750207
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- Publication type:
- Article
Recurrent histone mutations in T‐cell acute lymphoblastic leukaemia.
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- British Journal of Haematology, 2019, v. 184, n. 4, p. 676, doi. 10.1111/bjh.15155
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- Publication type:
- Article
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 505, doi. 10.1038/ng.3252
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- Publication type:
- Article
Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer.
- Published in:
- Nature Genetics, 2014, v. 46, n. 5, p. 487, doi. 10.1038/ng.2955
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- Publication type:
- Article
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.
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- Nature Genetics, 2013, v. 45, n. 6, p. 686, doi. 10.1038/ng.2635
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- Publication type:
- Article
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.
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- Nature Genetics, 2010, v. 42, n. 7, p. 604, doi. 10.1038/ng.607
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- Publication type:
- Article
A genome-wide association study of testicular germ cell tumor.
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- Nature Genetics, 2009, v. 41, n. 7, p. 807, doi. 10.1038/ng.394
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- Article
The emerging landscape of breast cancer susceptibility.
- Published in:
- Nature Genetics, 2008, v. 40, n. 1, p. 17, doi. 10.1038/ng.2007.53
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- Publication type:
- Article
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 165, doi. 10.1038/ng1959
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- Publication type:
- Article
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.
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- Nature Genetics, 2006, v. 38, n. 11, p. 1239, doi. 10.1038/ng1902
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- Article
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.
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- Nature Genetics, 2006, v. 38, n. 8, p. 873, doi. 10.1038/ng1837
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- Publication type:
- Article
Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.
- Published in:
- Bioinformatics, 2023, v. 39, n. 12, p. 1, doi. 10.1093/bioinformatics/btad756
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- Publication type:
- Article
Combinations of PARP Inhibitors with Temozolomide Drive PARP1 Trapping and Apoptosis in Ewing’s Sarcoma.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0140988
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- Publication type:
- Article
A Pathogenic Mosaic <i>TP53</i> Mutation in Two Germ Layers Detected by Next Generation Sequencing.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096531
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- Publication type:
- Article
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
- Published in:
- Human Genetics, 2008, v. 123, n. 5, p. 469, doi. 10.1007/s00439-008-0498-4
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- Publication type:
- Article
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
- Published in:
- 1999
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- Publication type:
- journal article
Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays.
- Published in:
- Oncogene, 2003, v. 22, n. 8, p. 1247, doi. 10.1038/sj.onc.1206247
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- Publication type:
- Article
Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08512-7
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- Publication type:
- Article
Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07842-2
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- Publication type:
- Article
Data mining using the Catalogue of Somatic Mutations in Cancer BioMart.
- Published in:
- Database: The Journal of Biological Databases & Curation, 2011, v. 2011, n. 18, p. 1
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- Publication type:
- Article
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation.
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- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1010, doi. 10.1038/ejhg.2012.114
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- Publication type:
- Article
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.
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- European Journal of Human Genetics, 2010, v. 18, n. 5, p. 544, doi. 10.1038/ejhg.2009.220
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- Publication type:
- Article
Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.
- Published in:
- 2010
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- Publication type:
- Correction Notice
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 330, doi. 10.1038/ejhg.2009.175
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- Publication type:
- Article
The cancer genome.
- Published in:
- Nature, 2009, v. 458, n. 7239, p. 719, doi. 10.1038/nature07943
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- Publication type:
- Article
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.
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- Oncogene, 2000, v. 19, n. 36, p. 4170, doi. 10.1038/sj.onc.1203735
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- Publication type:
- Article
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.
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- Oncogene, 1997, v. 14, n. 25, p. 3099, doi. 10.1038/sj.onc.1201107
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- Publication type:
- Article
Evaluation of RAD50 in familial breast cancer predisposition.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 11, p. 2911, doi. 10.1002/ijc.21738
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- Publication type:
- Article
Mutations of BRAF and KRAS in gastric cancer and their association with microsatellite instability(There is no commercial sponsorship or competing financial interests.).
- Published in:
- International Journal of Cancer, 2004, v. 108, n. 1, p. 167, doi. 10.1002/ijc.11553
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- Publication type:
- Article
A mutational signature in gastric cancer suggests therapeutic strategies.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8683, doi. 10.1038/ncomms9683
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- Publication type:
- Article
Cancer: Understanding the target.
- Published in:
- Nature, 2004, v. 430, n. 6995, p. 30, doi. 10.1038/430030a
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- Publication type:
- Article
Cancer and genomics.
- Published in:
- Nature, 2001, v. 409, n. 6822, p. 850, doi. 10.1038/35057046
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- Publication type:
- Article
Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 4, p. 1169, doi. 10.1093/hmg/ddu511
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- Publication type:
- Article
Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 11, p. 1062, doi. 10.1002/gcc.20815
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- Publication type:
- Article
GLO1-A novel amplified gene in human cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 8, p. 711, doi. 10.1002/gcc.20784
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- Publication type:
- Article