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Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 175, doi. 10.1002/gcc.20518
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- Publication type:
- Article
Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 5, p. 1017, doi. 10.1002/ijc.22789
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- Publication type:
- Article
Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy.
- Published in:
- International Journal of Cancer, 2002, v. 101, n. 6, p. 555, doi. 10.1002/ijc.10641
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- Publication type:
- Article
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 11, p. 1271
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- Publication type:
- Article
The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 144, n. 3, p. 607, doi. 10.1007/s10549-014-2902-1
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- Publication type:
- Article
Quality of Life and its Relation to Cancer-Related Stress in Women of Families with Hereditary Cancer without Demonstrated Mutation.
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- Quality of Life Research, 2006, v. 15, n. 3, p. 461, doi. 10.1007/s11136-005-3008-3
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- Publication type:
- Article
Inherited Breast Carcinoma: Prospective findings in 1 194 women at risk.
- Published in:
- Acta Oncologica, 1996, v. 35, n. S8, p. 7, doi. 10.3109/02841869609098515
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- Publication type:
- Article
Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome.
- Published in:
- Prostate, 2024, v. 84, n. 10, p. 945, doi. 10.1002/pros.24711
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- Publication type:
- Article
Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway.
- Published in:
- Familial Cancer, 2020, v. 19, n. 2, p. 133, doi. 10.1007/s10689-020-00160-x
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- Publication type:
- Article
Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma ( CDKN2A) in Norway.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 257, doi. 10.1007/s10689-016-9939-8
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- Publication type:
- Article
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 1, doi. 10.1007/s10689-016-9916-2
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- Publication type:
- Article
High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers.
- Published in:
- Familial Cancer, 2009, v. 8, n. 2, p. 145, doi. 10.1007/s10689-008-9219-3
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- Publication type:
- Article
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations.
- Published in:
- Familial Cancer, 2005, v. 4, n. 2, p. 121, doi. 10.1007/s10689-004-7995-y
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- Publication type:
- Article
Amplification of TOP2A and HER-2 genes in breast cancers occurring in patients harbouring BRCA1 germline mutations.
- Published in:
- Acta Oncologica, 2007, v. 46, n. 2, p. 199, doi. 10.1080/02841860600949552
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- Publication type:
- Article
CHEK2 Mutations Affecting Kinase Activity Together With Mutations in TP53 Indicate a Functional Pathway Associated with Resistance to Epirubicin in Primary Breast Cancer.
- Published in:
- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0003062
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- Publication type:
- Article
Fanconi anaemia, BRCA2 and familial considerations - follow up on a previous case report.
- Published in:
- Acta Paediatrica, 2010, v. 99, n. 11, p. 1741, doi. 10.1111/j.1651-2227.2010.01929.x
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- Publication type:
- Article
BRCA1 1675delA and 1135insA Account for One Third of Norwegian Familial Breast-Ovarian Cancer and Are Associated with Later Disease Onset than Less Frequent Mutations.
- Published in:
- Disease Markers, 1999, v. 15, n. 1-3, p. 79, doi. 10.1155/1999/278269
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- Publication type:
- Article
Costs and Benefits of Diagnosing Familial Breast Cancer.
- Published in:
- Disease Markers, 1999, v. 15, n. 1-3, p. 167, doi. 10.1155/1999/751892
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- Publication type:
- Article
Use of Cytology to Diagnose Inherited Breast Cancer.
- Published in:
- 1999
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- Publication type:
- Abstract
Efficacy of Early Diagnosis and Treatment in Women with a Family History of Breast Cancer.
- Published in:
- Disease Markers, 1999, v. 15, n. 1-3, p. 179
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- Publication type:
- Article
Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS).
- Published in:
- Cancers, 2024, v. 16, n. 5, p. 953, doi. 10.3390/cancers16050953
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- Publication type:
- Article
Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program.
- Published in:
- Breast Cancer Research & Treatment, 2013, v. 139, n. 1, p. 155, doi. 10.1007/s10549-013-2540-z
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- Publication type:
- Article
A simplified method for segregation analysis (SISA) to determine penetrance and expression of a genetic variant in a family.
- Published in:
- Human Mutation, 2011, v. 32, n. 5, p. 568, doi. 10.1002/humu.21441
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- Publication type:
- Article
A Nationwide Study of Multiple Endocrine Neoplasia Type 2A in Norway: Predictive and Prognostic Factors for the Clinical Course of Medullary Thyroid Carcinoma.
- Published in:
- Thyroid, 2016, v. 26, n. 9, p. 1225, doi. 10.1089/thy.2015.0673
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- Publication type:
- Article
"It was an important part of my treatment": a qualitative study of Norwegian breast Cancer patients' experiences with mainstreamed genetic testing.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00212-6
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- Publication type:
- Article
Genetic factors influencing prostate cancer risk in Norwegian men.
- Published in:
- Prostate, 2018, v. 78, n. 3, p. 186, doi. 10.1002/pros.23453
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- Publication type:
- Article
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses.
- Published in:
- Prostate, 2010, v. 70, n. 7, p. 735, doi. 10.1002/pros.21106
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- Publication type:
- Article
ANO7 is associated with aggressive prostate cancer.
- Published in:
- International Journal of Cancer, 2018, v. 143, n. 10, p. 2479, doi. 10.1002/ijc.31746
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- Publication type:
- Article
Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations.
- Published in:
- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0113-9
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- Publication type:
- Article
BRCA1 and BRCA2 mutation spectrum -- an update on mutation distribution in a large cancer genetics clinic in Norway.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0085-6
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- Publication type:
- Article
Ten modifiers of penetrance BRCA1 validated in a Norwegian series.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0
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- Publication type:
- Article
Ten modifiers of BRCA1 penetrance validated in a Norwegian series.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0
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- Publication type:
- Article
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-12
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- Publication type:
- Article
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
- Published in:
- 2018
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- Publication type:
- journal article
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Malignt melanom - diagnostikk, behandling og oppfølging i Norge.
- Published in:
- Journal of the Norwegian Medical Association / Tidsskrift for Den Norske Laegeforening, 2013, n. 20, p. 2154, doi. 10.4045/tidsskr.12.1416
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- Publication type:
- Article
Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers.
- Published in:
- 2017
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- Publication type:
- journal article