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The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations

Gastroenterology (New York, N.Y. 1943), 2008-08, Vol.135 (2), p.419-428.e1

2008

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Tumor Microsatellite-Instability Status as a Predictor of Benefit from Fluorouracil-Based Adjuvant Chemotherapy for Colon Cancer

The New England journal of medicine, 2003-07, Vol.349 (3), p.247-257

2003

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Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

JAMA : the journal of the American Medical Association, 2005-04, Vol.293 (16), p.1979

2005

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Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers

Hereditary cancer in clinical practice, 2012-04, Vol.10 (Suppl 2), p.A33-A33, Article A33

2012

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BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

Journal of medical genetics, 2004-09, Vol.41 (9), p.664-668

2004

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A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

Cancer research (Chicago, Ill.), 1998-11, Vol.58 (22), p.5248-5257

1998

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Colorectal cancer screening by detection of altered human DNA in stool: Feasibility of a multitarget assay panel

Gastroenterology (New York, N.Y. 1943), 2000-11, Vol.119 (5), p.1219-1227

2000

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Microsatellite Instability in Cancer of the Proximal Colon

Science (American Association for the Advancement of Science), 1993-05, Vol.260 (5109), p.816-819

1993

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Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability

Cancer research (Chicago, Ill.), 1998-08, Vol.58 (15), p.3455-3460

1998

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BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair

Cancer research (Chicago, Ill.), 2003-09, Vol.63 (17), p.5209-5212

2003

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Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

Science (American Association for the Advancement of Science), 1998-05, Vol.280 (5364), p.750-752

1998

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MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

Gastroenterology (New York, N.Y. 1943), 2004-07, Vol.127 (1), p.9-16

2004

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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 AXIN2 cause colorectal cancer with defective mismatch repair by activating β-catenin/TCF signalling

Nature genetics, 2000-10, Vol.26 (2), p.146-147

2000

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Nonparametric Tests of Association of Multiple Genes with Human Disease

American journal of human genetics, 2005-05, Vol.76 (5), p.780-793

2005

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Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

Cancer research (Chicago, Ill.), 2004-07, Vol.64 (14), p.4721-4727

2004

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The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

American journal of human genetics, 2001-10, Vol.69 (4), p.780-790

2001

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Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci

American journal of human genetics, 2004-12, Vol.75 (6), p.948-965

2004

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Preclinical evidence of Alzheimer's disease in persons homozygous for the epsilon 4 allele for apolipoprotein E

The New England journal of medicine, 1996-03, Vol.334 (12), p.752-758

1996

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Mutations in CHEK2 Associated with Prostate Cancer Risk

American journal of human genetics, 2003-02, Vol.72 (2), p.270-280

2003

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Microsatellite Instability and 8p Allelic Imbalance in Stage B2 and C Colorectal Cancers

JNCI : Journal of the National Cancer Institute, 1999-08, Vol.91 (15), p.1295-1303

1999

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Development of a fluorescent multiplex assay for detection of MSI-High tumors

Disease markers, 2004-01, Vol.20 (4-5), p.237-250

2004

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The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations

Tumor Microsatellite-Instability Status as a Predictor of Benefit from Fluorouracil-Based Adjuvant Chemotherapy for Colon Cancer

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

Colorectal cancer screening by detection of altered human DNA in stool: Feasibility of a multitarget assay panel

Microsatellite Instability in Cancer of the Proximal Colon

Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability

BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating β-catenin/TCF signalling

Nonparametric Tests of Association of Multiple Genes with Human Disease

Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer risk

Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci

AA9int: SNP interaction pattern search using non-hierarchical additive model set

Preclinical evidence of Alzheimer's disease in persons homozygous for the epsilon 4 allele for apolipoprotein E

Mutations in CHEK2 Associated with Prostate Cancer Risk

Microsatellite Instability and 8p Allelic Imbalance in Stage B2 and C Colorectal Cancers

Development of a fluorescent multiplex assay for detection of MSI-High tumors

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