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Astrid Tenden Stormorken

Peutz–Jeghers syndrome: a systematic review and recommendations for management
2010 · A D Beggs, A R Latchford, et al. · Gut · 822
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Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
2013 · Hans F A Vasen, Ignacio Blanco, et al. · Gut · 746
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Guidelines for the clinical management of familial adenomatous polyposis (FAP)
2008 · H F A Vasen, G Möslein, et al. · Gut · 700
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Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)
2007 · H F A Vasen, G Möslein, et al. · Journal of Medical Genetics · 552
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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance
2004 · Yvonne M.C. Hendriks, Anja Wagner, et al. · Gastroenterology · 425
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Familial endometrial cancer in female carriers of MSH6 germline mutations
1999 · Juul Wijnen, Wiljo de Leeuw, et al. · Nature Genetics · 415
MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families
2001 · H. F.A. Vasen, A. Stormorken, et al. · Journal of Clinical Oncology · 406
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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients
2000 · Wiljo J. F. de Leeuw, JanWillem Dierssen, et al. · The Journal of Pathology · 188
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
2009 · H. F. A. Vasen, G. Möslein, et al. · Familial Cancer · 119
Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer
2009 · Eli Marie Grindedal, Pål Møller, et al. · Cancer Epidemiology Biomarkers & Prevention · 113
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
2021 · Elizabeth K Bancroft, Elizabeth C Page, et al. · The Lancet Oncology · 99
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Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers
2010 · Wenche Sjursen, Bjørn Ivar Haukanes, et al. · Journal of Medical Genetics · 97
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Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds
2009 · Eli Marie Grindedal, Laura Renkonen-Sinisalo, et al. · Journal of Medical Genetics · 73
Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program
2013 · Pål Møller, Astrid Stormorken, et al. · Breast Cancer Research and Treatment · 57
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations
2005 · Amy Østertun Geirdal, Jon G. Reichelt, et al. · Familial Cancer · 48
Immunohistochemistry Identifies Carriers of Mismatch Repair Gene Defects Causing Hereditary Nonpolyposis Colorectal Cancer
2005 · Astrid T. Stormorken, Inger Marie Bowitz-Lothe, et al. · Journal of Clinical Oncology · 41
Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer
2006 · Astrid T. Stormorken, Neal Clark, et al. · Scandinavian Journal of Gastroenterology · 21
Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers
2013 · Anne Irene Hagen, Lovise Mæhle, et al. · The Breast · 19
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The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry
2014 · Eli Marie Grindedal, Harald Aarset, et al. · Hereditary Cancer in Clinical Practice · 17
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High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers
2008 · Eli Marie Grindedal, Ignacio Blanco, et al. · Familial Cancer · 14
Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry
2001 · Astrid T. Stormorken, Wolfram Müller, et al. · Familial Cancer · 13
AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature
2023 · Laura Roht, Hanne K. Hyldebrandt, et al. · Molecular Genetics & Genomic Medicine · 12
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The clinical utility of genetic testing in breast cancer kindreds: a prospective study in families without a demonstrable BRCA mutation
2014 · Pål Møller, Astrid Stormorken, et al. · Breast Cancer Research and Treatment · 11
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APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis
2018 · Astrid Tenden Stormorken, Thomas Berg, et al. · Familial Cancer · 9
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MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer
2006 · Astrid Stormorken, Karen-Marie Heintz, et al. · Hereditary Cancer in Clinical Practice · 8
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Works count: 44
Citation count: 5,127
H-index: 19
I10-index: 24
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