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AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature

Molecular genetics & genomic medicine, 2023-06, Vol.11 (6), p.e2157-n/a

2023

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Immunohistochemistry Identifies Carriers of Mismatch Repair Gene Defects Causing Hereditary Nonpolyposis Colorectal Cancer

Journal of clinical oncology, 2005-07, Vol.23 (21), p.4705-4712

2005

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Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer

Scandinavian journal of gastroenterology, 2007-01, Vol.42 (5), p.611-617

2007

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Estimated prevalence of hereditary cancers and the need for surveillance in a Norwegian county, Telemark

Scandinavian journal of gastroenterology, 2006, Vol.41 (1), p.71-79

2006

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APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis

Familial cancer, 2018-10, Vol.17 (4), p.539-543

2018

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The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours

Familial cancer, 2003, Vol.2 (1), p.9-13

2003

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Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry

Familial cancer, 2001, Vol.1 (3-4), p.169-173

2001

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Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer

Cancer epidemiology, biomarkers & prevention, 2009-09, Vol.18 (9), p.2460-2467

2009

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The impact of hysterectomy on subsequent colonoscopy in women with Lynch Syndrome

Scandinavian journal of gastroenterology, 2024-08, Vol.59 (8), p.1015-1020

2024

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

Gastroenterology (New York, N.Y. 1943), 2004-07, Vol.127 (1), p.17-25

2004

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Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome

The Prostate, 2024-07, Vol.84 (10), p.945-953

2024

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A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

The lancet oncology, 2021-11, Vol.22 (11), p.1618-1631

2021

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Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

Journal of medical genetics, 2010-02, Vol.47 (2), p.99-102

2010

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Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers

Journal of medical genetics, 2010-09, Vol.47 (9), p.579-585

2010

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Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program

Breast cancer research and treatment, 2013-05, Vol.139 (1), p.155-161

2013

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Familial endometrial cancer in female carriers of MSH6 germline mutations

Nature genetics, 1999-10, Vol.23 (2), p.142-144

1999

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The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation

Breast cancer research and treatment, 2014-04, Vol.144 (3), p.607-614

2014

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A woman in her thirties with breast cancer and bilateral goitre

Tidsskrift for den Norske Lægeforening, 2017-06, Vol.137 (11), p.806

2017

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Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers

Breast (Edinburgh), 2014-02, Vol.23 (1), p.38-43

2014

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Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations

Familial cancer, 2005-06, Vol.4 (2), p.121-126

2005

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

The Journal of pathology, 2000-11, Vol.192 (3), p.328-335

2000

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The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry

Hereditary cancer in clinical practice, 2014-04, Vol.12 (1), p.12-12, Article 12

2014

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Quality of Life and Its Relation to Cancer-Related Stress in Women of Families with Hereditary Cancer without Demonstrated Mutation

Quality of life research, 2006-04, Vol.15 (3), p.461-470

2006

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High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers

Familial cancer, 2009, Vol.8 (2), p.145-151

2009

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AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature

Immunohistochemistry Identifies Carriers of Mismatch Repair Gene Defects Causing Hereditary Nonpolyposis Colorectal Cancer

Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer

Estimated prevalence of hereditary cancers and the need for surveillance in a Norwegian county, Telemark

APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis

The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours

Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry

Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer

The impact of hysterectomy on subsequent colonoscopy in women with Lynch Syndrome

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers

Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program

Familial endometrial cancer in female carriers of MSH6 germline mutations

The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation

A woman in her thirties with breast cancer and bilateral goitre

Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers

Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry

Quality of Life and Its Relation to Cancer-Related Stress in Women of Families with Hereditary Cancer without Demonstrated Mutation

High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers

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