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- 2016
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Mark
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
2016) In Nature Genetics(
- Contribution to journal › Article
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Mark
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
(
- Contribution to journal › Article
- 2015
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Mark
Ovarialcancer är på många sätt en heterogen sjukdom
(
- Contribution to journal › Article
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Mark
Impact of a paternal origin of germline BRCA1/2 mutations on the age at breast and ovarian cancer diagnosis in a Southern Swedish cohort.
(
- Contribution to journal › Article
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Mark
Passenger strand loading in overexpression experiments using microRNA mimics.
(
- Contribution to journal › Article
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Mutation Screening of 1,237 Cancer Genes across Six Model Cell Lines of Basal-Like Breast Cancer.
(
- Contribution to journal › Article
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Whole genome sequencing of primary breast cancers and matched distant metastases
2015) American Association for Cancer Research (AACR) 106th Annual Meeting 2015 In Cancer Research 75(15).(
- Contribution to journal › Published meeting abstract
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Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing
(
- Contribution to journal › Article
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Mutational and gene fusion analyses of primary large cell and large cell neuroendocrine lung cancer.
(
- Contribution to journal › Article
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Remarkable similarities of chromosomal rearrangements between primary human breast cancers and matched distant metastases as revealed by whole-genome sequencing.
(
- Contribution to journal › Article
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Genome-Wide DNA Methylation Analysis in Melanoma Reveals the Importance of CpG Methylation in MITF Regulation.
(
- Contribution to journal › Article
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The Sweden Cancerome Analysis Network - Breast (SCAN-B) Initiative: a large-scale multicenter infrastructure towards implementation of breast cancer genomic analyses in the clinical routine.
(
- Contribution to journal › Article
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Mark
Serial monitoring of circulating tumor DNA in patients with primary breast cancer for detection of occult metastatic disease.
(
- Contribution to journal › Article
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Molecular characterization of melanoma cases in denmark suspected of genetic predisposition.
(
- Contribution to journal › Article
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Molecular stratification of metastatic melanoma using gene expression profiling: prediction of survival outcome and benefit from molecular targeted therapy.
(
- Contribution to journal › Article
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Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma.
(
- Contribution to journal › Article
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Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.
(
- Contribution to journal › Article
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Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
(
- Contribution to journal › Article
- 2014
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Mark
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
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Mark
CDKN2A-mutation hos en familie med arveligt malignt melanom
(
- Contribution to journal › Article
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Mark
High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
(
- Contribution to journal › Article
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Mark
Cancer-Associated Fibroblasts Expressing CXCL14 Rely upon NOS1-Derived Nitric Oxide Signaling for Their Tumor-Supporting Properties
(
- Contribution to journal › Article
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Mark
High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer.
(
- Contribution to journal › Article
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Mark
Genome-wide DNA methylation analysis of lung carcinoma reveals one neuroendocrine and four adenocarcinoma epitypes associated with patient outcome.
(
- Contribution to journal › Article
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The HER2-Encoded miR-4728-3p Regulates ESR1 through a Non-Canonical Internal Seed Interaction.
(
- Contribution to journal › Article
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Mark
Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer.
(
- Contribution to journal › Article
- 2013
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Mark
Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.
(
- Contribution to journal › Article
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Mutual Exclusivity Analysis of Genetic and Epigenetic Drivers in Melanoma Identifies a Link Between p14(ARF) and RAR beta Signaling
(
- Contribution to journal › Article
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Mark
Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer
(
- Contribution to journal › Article
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Mark
Detecting EGFR alterations in clinical specimens-pitfalls and necessities.
(
- Contribution to journal › Article
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A BAP1 Mutation in a Danish Family Predisposes to Uveal Melanoma and Other Cancers
(
- Contribution to journal › Article
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Histological specificity of alterations and expression of KIT and KITLG in non-small cell lung carcinoma.
(
- Contribution to journal › Article
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High expression of ZNF703 independent of amplification indicates worse prognosis in patients with luminal B breast cancer
(
- Contribution to journal › Article
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Contralateral breast cancer after radiotherapy among BRCA1 and BRCA2 mutation carriers: A WECARE Study Report
(
- Contribution to journal › Article
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Mark
Signatures of mutational processes in human cancer
(
- Contribution to journal › Article
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
(
- Contribution to journal › Article
- 2012
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Mark
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: A population-based survey.
(
- Contribution to journal › Article
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Mark
The gene expression landscape of breast cancer is shaped by tumor protein p53 status and epithelial-mesenchymal transition
(
- Contribution to journal › Article
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Mark
Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer
(
- Contribution to journal › Article
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Mark
Cancer predisposing BARD1 mutations in breast-ovarian cancer families
(
- Contribution to journal › Article
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Mark
Characterisation of amplification patterns and target genes at chromosome 11q13 in CCND1-amplified sporadic and familial breast tumours.
(
- Contribution to journal › Article
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Mark
Global H3K27 trimethylation and EZH2 abundance in breast tumor subtypes.
(
- Contribution to journal › Article
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Mark
Molecular profiling reveals low- and high-grade forms of primary melanoma
(
- Contribution to journal › Article
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Mark
The retinoblastoma gene undergoes rearrangements in BRCA1-deficient basal-like breast cancer.
(
- Contribution to journal › Article
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Mark
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
(
- Contribution to journal › Article
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Mark
The Life History of 21 Breast Cancers
(
- Contribution to journal › Article
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Mark
Mutational Processes Molding the Genomes of 21 Breast Cancers
(
- Contribution to journal › Article
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Mark
Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer
(
- Contribution to journal › Article
- 2011
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Mark
GOBO: Gene Expression-Based Outcome for Breast Cancer Online.
(
- Contribution to journal › Article
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Mark
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
(
- Contribution to journal › Article
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Mark
Breast tumors from CHEK2 1100delC-mutation carriers: genomic landscape and clinical implications
(
- Contribution to journal › Article
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Mark
Identification of new microRNAs in paired normal and tumor breast tissue suggests a dual role for the ERBB2/Her2 gene.
(
- Contribution to journal › Article
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Mark
Endothelial Induced EMT in Breast Epithelial Cells with Stem Cell Properties
(
- Contribution to journal › Article
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High-resolution genomic profiling of male breast cancer reveals differences hidden behind the similarities with female breast cancer
(
- Contribution to journal › Article
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Mark
CD44 isoforms are heterogeneously expressed in breast cancer and correlate with tumor subtypes and cancer stem cell markers.
(
- Contribution to journal › Article
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Mark
A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing
(
- Contribution to journal › Article
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Mark
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
(
- Contribution to journal › Article
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Mark
Exploring the link between MORF4L1 and risk of breast cancer
(
- Contribution to journal › Article
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Mark
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.
(
- Contribution to journal › Article
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Mark
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2010
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Mark
Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.
(
- Contribution to journal › Article
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Mark
Improving Surveillance and Quality of Life of BRCA Mutation Carriers.
(
- Contribution to journal › Article
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Mark
Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
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Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype.
(
- Contribution to journal › Article
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Mark
Genetic profiles distinguish different types of hereditary ovarian cancer.
(
- Contribution to journal › Article
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Mark
Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array-comparative genomic hybridization
(
- Contribution to journal › Article
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Mark
Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns
(
- Contribution to journal › Article
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Multiple metastases from cutaneous malignant melanoma patients may display heterogeneous genomic and epigenomic patterns.
(
- Contribution to journal › Article
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Mark
Gene Expression Profiling-Based Identification of Molecular Subtypes in Stage IV Melanomas with Different Clinical Outcome.
(
- Contribution to journal › Article
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Mark
High-resolution genomic and expression analyses of copy number alterations in HER2-amplified breast cancer
(
- Contribution to journal › Article
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Oral contraceptives and postmenopausal hormones and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers and noncarriers: the WECARE Study
(
- Contribution to journal › Article
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Mark
Reproductive factors and risk of contralateral breast cancer by BRCA1 and BRCA2 mutation status: results from the WECARE study
(
- Contribution to journal › Article
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Identification of Subtypes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Reveals a Gene Signature Prognostic of Outcome.
(
- Contribution to journal › Article
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Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study
(
- Contribution to journal › Article
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Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families
(
- Contribution to journal › Article
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Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
(
- Contribution to journal › Article
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Population-Based Study of the Risk of Second Primary Contralateral Breast Cancer Associated With Carrying a Mutation in BRCA1 or BRCA2.
(
- Contribution to journal › Article
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Mark
Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics
(
- Contribution to journal › Article
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Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
(
- Contribution to journal › Article
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Mark
International network of cancer genome projects
(
- Contribution to journal › Article
- 2009
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Mark
The non-coding RNA of the multidrug resistance-linked vault particle encodes multiple regulatory small RNAs.
(
- Contribution to journal › Article
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Mark
IDENTIFICATION OF NOVEL SECRETED TUMOR STROMA-DERIVED STIMULATORS OF PROSTATE CANCER GROWTH
2009) 7th International Symposium on Targeted Anticancer Therapies In Annals of Oncology 20(Suppl 3). p.34-34(
- Contribution to journal › Published meeting abstract
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Mark
Indistinguishable genomic profiles and shared prognostic markers in undifferentiated pleomorphic sarcoma and leiomyosarcoma: different sides of a single coin?
(
- Contribution to journal › Article
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Mark
CXCL14 is an autocrine growth factor for fibroblasts and acts as a multi-modal stimulator of prostate tumor growth
(
- Contribution to journal › Article
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Comparison of cisplatin sensitivity and the 18F fluoro-2-deoxy 2 glucose uptake with proliferation parameters and gene expression in squamous cell carcinoma cell lines of the head and neck
(
- Contribution to journal › Article
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MiRNA expression in urothelial carcinomas: Important roles of miR-10a, miR-222, miR-125b, miR-7 and miR-452 for tumor stage and metastasis, and frequent homozygous losses of miR-31.
(
- Contribution to journal › Article
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Mark
A Comprehensive Model for DNA Repair Genes and Radiation in Second Breast Cancers: The WECARE Collaborative Study Group
2009) 18th Annual Meeting of the International-Genetic-Epidemiology-Society In Genetic Epidemiology 33(8). p.189-189(
- Contribution to journal › Published meeting abstract
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Mark
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1
(
- Contribution to journal › Article
- 2008
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Mark
Gene products of chromosome 11q and their association with CCND1 gene amplification and tamoxifen resistance in premenopausal breast cancer.
(
- Contribution to journal › Article
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Mark
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.
(
- Contribution to journal › Article
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Genetic profiling differentiates second primary tumors from metastases in adult metachronous soft tissue sarcoma.
(
- Contribution to journal › Article
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Mark
Genomic alterations in coleorectal cencer in relationship to stage and survival assesed by tiling BAC array CGH
(
- Contribution to journal › Published meeting abstract
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Mark
Confirmed cancer trends in families of patients with multiple cancers including cutaneous melanoma.
(
- Contribution to journal › Article
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Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
(
- Contribution to journal › Article
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Mark
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
(
- Contribution to journal › Article
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Mark
Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors.
(
- Contribution to journal › Article
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Mark
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding
(
- Contribution to journal › Article
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Mark
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
(
- Contribution to journal › Article
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Mark
The CD44(+)/CD24(-) phenotype is enriched in basal-like breast tumors
(
- Contribution to journal › Article
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Mark
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms
(
- Contribution to journal › Article