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Surveillance in von Hippel-Lindau disease (vHL)

Clinical genetics, 2010-01, Vol.77 (1), p.49-59

2010

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis

Gastroenterology (New York, N.Y. 1943), 1996-04, Vol.110 (4), p.1020-1027

1996

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Whole-Gene APC Deletions Cause Classical Familial Adenomatous Polyposis, but not Attenuated Polyposis or "Multiple" Colorectal Adenomas

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (5), p.2954-2958

2002

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Young age colorectal cancer and identification of hereditary non-polyposis colorectal cancer cohorts

British journal of surgery, 2007-09, Vol.94 (9), p.1055-1056

Bisgaard, M. L.

2007

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Familial adenomatous polyposis patients without an identified APC germline mutation have a severe phenotype

Gut, 2004-02, Vol.53 (2), p.266-270

2004

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The role of hPMS1 and hPMS2 in predisposing to colorectal cancer

Cancer research (Chicago, Ill.), 2001-11, Vol.61 (21), p.7798-7802

2001

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Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32–31.1

Journal of medical genetics, 2006-02, Vol.43 (2), p.e07-e07

2006

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MUTYH Associated Polyposis (MAP)

Current genomics, 2008-09, Vol.9 (6), p.420-435

2008

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Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

American journal of human genetics, 1996-02, Vol.58 (2), p.300-307

1996

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Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome

The New England journal of medicine, 2008-12, Vol.359 (24), p.2567-2578

2008

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Hereditary Non-Polyposis Colorectal Cancer: Clinical Features and Survival Results from the Danish HNPCC Register

Scandinavian journal of gastroenterology, 1997, Vol.32 (6), p.572-576

1997

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Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression

American journal of human genetics, 1997-07, Vol.61 (1), p.129-138

1997

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Mutations predisposing to hereditary nonpolyposis colorectal cancer : Database and results of a Collaborative study

Gastroenterology (New York, N.Y. 1943), 1997, Vol.113 (4), p.1146-1158

1997

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Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families

Thrombosis and haemostasis, 2001-12, Vol.86 (6), p.1392-1399

2001

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Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis

Gastroenterology (New York, N.Y. 1943), 2000-12, Vol.119 (6), p.1454-1460

2000

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Familial adenomatous polyposis (FAP): Frequency, penetrance, and mutation rate

Human mutation, 1994, Vol.3 (2), p.121-125

1994

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Allelic Loss of Chromosome 2p21-16.3 is Associated with Reduced Survival in Sporadic Colorectal Cancer

Scandinavian journal of gastroenterology, 2001-01, Vol.36 (4), p.405-409

M. L. Bisgaard, A. C. Jäger, P. Dalgaard, J. O. Søndergaard, J. F. Rehfeld, F. C. Nielsen

2001

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Founder effect in protein S-deficient families sharing a hot spot mutation in PROS1

Blood, 1999-01, Vol.93 (2), p.759-759

1999

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Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

Journal of clinical oncology, 2015-11, Vol.33 (31), p.3591-3597

2015

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MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer

Cancer research (Chicago, Ill.), 2001-02, Vol.61 (4), p.1619-1623

2001

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Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis

Diseases of the colon & rectum, 1999-06, Vol.42 (6), p.710-5; discussion 715-6

1999

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The establishment of an HNPCC register

Anticancer research, 1994-07, Vol.14 (4B), p.1647

1994

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Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material

Clinical genetics, 1987-08, Vol.32 (2), p.118-119

1987

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The incidence rate of familial adenomatous polyposis : Results from the Danish polyposis register

International journal of colorectal disease, 1996, Vol.11 (2), p.88-91

1996

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De novo mutations in familial adenomatous polyposis (FAP)

European journal of human genetics : EJHG, 2002-12, Vol.10 (12), p.887

2002

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Surveillance in von Hippel-Lindau disease (vHL)

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis

Whole-Gene APC Deletions Cause Classical Familial Adenomatous Polyposis, but not Attenuated Polyposis or "Multiple" Colorectal Adenomas

Young age colorectal cancer and identification of hereditary non-polyposis colorectal cancer cohorts

Familial adenomatous polyposis patients without an identified APC germline mutation have a severe phenotype

The role of hPMS1 and hPMS2 in predisposing to colorectal cancer

Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32–31.1

MUTYH Associated Polyposis (MAP)

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome

Hereditary Non-Polyposis Colorectal Cancer: Clinical Features and Survival Results from the Danish HNPCC Register

Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression

Mutations predisposing to hereditary nonpolyposis colorectal cancer : Database and results of a Collaborative study

Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families

Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis

Familial adenomatous polyposis (FAP): Frequency, penetrance, and mutation rate

Allelic Loss of Chromosome 2p21-16.3 is Associated with Reduced Survival in Sporadic Colorectal Cancer

Founder effect in protein S-deficient families sharing a hot spot mutation in PROS1

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer

Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis

The establishment of an HNPCC register

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material

The incidence rate of familial adenomatous polyposis : Results from the Danish polyposis register

De novo mutations in familial adenomatous polyposis (FAP)

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