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Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Journal of clinical oncology, 2009-10, Vol.27 (28), p.4793-4797

2009

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Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Journal of surgical oncology, 2016-02, Vol.113 (2), p.209-212

2016

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Epigenetic signatures of familial cancer are characteristic of tumor type and family category

Cancer research (Chicago, Ill.), 2008-06, Vol.68 (12), p.4597-4605

2008

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Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Genes chromosomes & cancer, 2014-10, Vol.53 (10), p.857-864

2014

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BRAF mutation in sporadic colorectal cancer and Lynch syndrome

Virchows Archiv : an international journal of pathology, 2013-11, Vol.463 (5), p.613-621

2013

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Molecular changes preceding endometrial and ovarian cancer: a study of consecutive endometrial specimens from Lynch syndrome surveillance

Modern pathology, 2018-08, Vol.31 (8), p.1291-1301

2018

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Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Genetics in medicine, 2019-08, Vol.21 (8), p.1868-1873

2019

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Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.776-787

2015

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LINE-1 hypomethylation in familial and sporadic cancer

Journal of molecular medicine (Berlin, Germany), 2012-07, Vol.90 (7), p.827-835

2012

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p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome

Clinical cancer research, 2005-10, Vol.11 (19), p.6840-6844

2005

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Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA)-based approach

Molecular medicine (Cambridge, Mass.), 2011-07, Vol.17 (7-8), p.726-735

2011

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Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

Familial cancer, 2024-11, Vol.23 (4), p.647-652

2024

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Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

Clinical cancer research, 2009-09, Vol.15 (18), p.5772-5783

2009

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DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression

EBioMedicine, 2019-01, Vol.39, p.280-291

2019

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Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Oncotarget, 2016-10, Vol.7 (43), p.70685-70698

2016

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Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma

International journal of cancer, 2007-08, Vol.121 (4), p.915-920

2007

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Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin

Cancer epidemiology, biomarkers & prevention, 2012, Vol.21 (1), p.202-211

2012

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Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

Journal of clinical oncology, 2005-07, Vol.23 (21), p.4609-4616

2005

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CYCLIN D1 as a genetic modifier in hereditary nonpolyposis colorectal cancer

Cancer research (Chicago, Ill.), 2001-08, Vol.61 (16), p.6042-6045

2001

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Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

Journal of clinical oncology, 2003-10, Vol.21 (19), p.3629-3637

2003

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Uroepithelial and kidney carcinoma in Lynch syndrome

Familial cancer, 2012-09, Vol.11 (3), p.395-401

2012

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DNA copy number changes in malignant ovarian germ cell tumors

Cancer research (Chicago, Ill.), 2000-06, Vol.60 (11), p.3025-3030

2000

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Cutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer

Genes chromosomes & cancer, 2008-02, Vol.47 (2), p.107-117

2008

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Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

Familial cancer, 2001, Vol.1 (1), p.9-15

2001

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Deletion of 1p loci and microsatellite instability in colorectal polyps

Genes chromosomes & cancer, 1995-11, Vol.14 (3), p.182-188

1995

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Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Epigenetic signatures of familial cancer are characteristic of tumor type and family category

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

BRAF mutation in sporadic colorectal cancer and Lynch syndrome

Molecular changes preceding endometrial and ovarian cancer: a study of consecutive endometrial specimens from Lynch syndrome surveillance

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

LINE-1 hypomethylation in familial and sporadic cancer

p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome

Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA)-based approach

Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression

Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma

Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

CYCLIN D1 as a genetic modifier in hereditary nonpolyposis colorectal cancer

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

Uroepithelial and kidney carcinoma in Lynch syndrome

DNA copy number changes in malignant ovarian germ cell tumors

Cutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer

Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

Deletion of 1p loci and microsatellite instability in colorectal polyps

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