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KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers

British journal of cancer, 2013-04, Vol.108 (8), p.1757-1764

2013

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Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

Scientific reports, 2014-02, Vol.4 (1), p.4026-4026, Article 4026

2014

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Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial colorectal cancer

British journal of cancer, 2014-07, Vol.111 (3), p.598-602

2014

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Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

British journal of cancer, 2011-06, Vol.105 (1), p.162-169

2011

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Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

Clinical genetics, 2015-12, Vol.88 (6), p.523-529

2015

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Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors

Journal of clinical oncology, 2002-02, Vol.20 (4), p.1043-1048

Lindor, N. M.

2002

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Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

Nature genetics, 1999-05, Vol.22 (1), p.82-84

1999

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The concise handbook of family cancer syndromes

JNCI : Journal of the National Cancer Institute, 1998-07, Vol.90 (14), p.1039-1071

1998

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Risks of Primary Extracolonic Cancers Following Colorectal Cancer in Lynch Syndrome

JNCI : Journal of the National Cancer Institute, 2012-09, Vol.104 (18), p.1363-1372

2012

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Familial predisposition for colorectal cancer in chronic ulcerative colitis: A case-control study

Gastroenterology (New York, N.Y. 1943), 1998-11, Vol.115 (5), p.1079-1083

1998

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Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery

Gut, 2011-07, Vol.60 (7), p.950-957

2011

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Increased risk for cancer in patients with the Peutz-Jeghers syndrome

Annals of internal medicine, 1998-06, Vol.128 (11), p.896

1998

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Rothmund–Thomson Syndrome Responsible Gene, RECQL4: Genomic Structure and Products

Genomics (San Diego, Calif.), 1999-11, Vol.61 (3), p.268-276

1999

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Further clinical description of duplication of Williams-Beuren region presenting with congenital glaucoma and brachycephaly

American journal of medical genetics. Part A, 2008-04, Vol.146A (8), p.1055-1058

2008

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Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne Syndrome Maps to Chromosome 15q

American journal of human genetics, 2000-04, Vol.66 (4), p.1443-1448

2000

Volltextzugriff (PDF)

A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne : PAPA syndrome

Mayo Clinic proceedings, 1997-07, Vol.72 (7), p.611-615

1997

Volltextzugriff (PDF)

Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis

Human molecular genetics, 2014-09, Vol.23 (17), p.4729-4737

2014

Volltextzugriff (PDF)

The APC E1317Q Variant in Adenomatous Polyps and Colorectal Cancers

Cancer epidemiology, biomarkers & prevention, 2003-10, Vol.12 (10), p.1023-1028

2003

Volltextzugriff (PDF)

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

JNCI : Journal of the National Cancer Institute, 2004-02, Vol.96 (4), p.261-268

2004

Volltextzugriff (PDF)

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature

Journal of medical genetics, 2006-02, Vol.43 (2), p.e08-e08

2006

Volltextzugriff (PDF)

Microsatellite Instability and Mutation Analysis of hMSH2 and hMLH1 in Patients with Sporadic, Familial and Hereditary Colorectal Cancer

Human molecular genetics, 1996-09, Vol.5 (9), p.1245-1252

1996

Volltextzugriff (PDF)

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Human molecular genetics, 2002-04, Vol.11 (8), p.961-969

2002

Volltextzugriff (PDF)

Care of Patients and Their Families With Familial Adenomatous Polyposis

Mayo Clinic proceedings, 2000, Vol.75 (1), p.57-67

2000

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von Hippel-Lindau disease

Mayo Clinic proceedings, 2000-03, Vol.75 (3), p.265-272

2000

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Motor tics, stereotypies, and self-flagellation in primrose syndrome

Neurology, 2010-07, Vol.75 (3), p.284

2010

Volltextzugriff (PDF)

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KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers

Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial colorectal cancer

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

The concise handbook of family cancer syndromes

Risks of Primary Extracolonic Cancers Following Colorectal Cancer in Lynch Syndrome

Familial predisposition for colorectal cancer in chronic ulcerative colitis: A case-control study

Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery

Increased risk for cancer in patients with the Peutz-Jeghers syndrome

Rothmund–Thomson Syndrome Responsible Gene, RECQL4: Genomic Structure and Products

Further clinical description of duplication of Williams-Beuren region presenting with congenital glaucoma and brachycephaly

Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne Syndrome Maps to Chromosome 15q

A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne : PAPA syndrome

Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis

The APC E1317Q Variant in Adenomatous Polyps and Colorectal Cancers

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature

Microsatellite Instability and Mutation Analysis of hMSH2 and hMLH1 in Patients with Sporadic, Familial and Hereditary Colorectal Cancer

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Care of Patients and Their Families With Familial Adenomatous Polyposis

von Hippel-Lindau disease

Motor tics, stereotypies, and self-flagellation in primrose syndrome

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