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Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Gastroenterology (New York, N.Y. 1943), 2014-09, Vol.147 (3), p.595-598.e5

2014

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Gene fusions and oncogenic mutations in MLH1 deficient and BRAFV600E wild-type colorectal cancers

Virchows Archiv : an international journal of pathology, 2022-04, Vol.480 (4), p.807-817

2022

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Oncogenic Potential of Bisphenol A and Common Environmental Contaminants in Human Mammary Epithelial Cells

International journal of molecular sciences, 2020-05, Vol.21 (10), p.3735

2020

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Novel insights into tumorigenesis revealed by molecular analysis of Lynch syndrome cases with multiple colorectal tumors

Frontiers in oncology, 2024-04, Vol.14, p.1378392-1378392

2024

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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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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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Converging endometrial and ovarian tumorigenesis in Lynch syndrome: Shared origin of synchronous carcinomas

Gynecologic oncology, 2018-07, Vol.150 (1), p.92-98

2018

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Body Weight, Physical Activity, and Risk of Cancer in Lynch Syndrome

Cancers, 2021-04, Vol.13 (8), p.1849

2021

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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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MicroRNA Methylation in Colorectal Cancer

Advances in experimental medicine and biology, 2016, Vol.937, p.109-122

2016

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Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

Cancers, 2020-07, Vol.12 (7), p.1853

2020

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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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Testing for Lynch Syndrome in Endometrial Carcinoma: From Universal to Age-Selective MLH1 Methylation Analysis

Cancers, 2022-03, Vol.14 (5), p.1348

2022

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Immunoprofiles and DNA Methylation of Inflammatory Marker Genes in Ulcerative Colitis-Associated Colorectal Tumorigenesis

Biomolecules (Basel, Switzerland), 2021-09, Vol.11 (10), p.1440

2021

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

Familial cancer, 2024-06

2024

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Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

Gastroenterology (New York, N.Y. 1943), 2000-05, Vol.118 (5), p.829-834

2000

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Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

Oncotarget, 2017-12, Vol.8 (64), p.108020-108030

2017

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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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Mitotic abnormalities precede microsatellite instability in lynch syndrome-associated colorectal tumourigenesis

EBioMedicine, 2024-05, Vol.103, p.105111-105111, Article 105111

2024

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Cancer-predicting gene expression changes in colonic mucosa of Western diet fed Mlh1+/- mice

PloS one, 2013-10, Vol.8 (10), p.e76865-e76865

2013

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Development of Colorectal Tumors in Colonoscopic Surveillance in Lynch Syndrome

Gastroenterology (New York, N.Y. 1943), 2007-10, Vol.133 (4), p.1093-1098

2007

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Genetic and Epigenetic Modification of MLH1 Accounts for a Major Share of Microsatellite-Unstable Colorectal Cancers

The American journal of pathology, 2000-05, Vol.156 (5), p.1773-1779

2000

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Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Gene fusions and oncogenic mutations in MLH1 deficient and BRAFV600E wild-type colorectal cancers

Oncogenic Potential of Bisphenol A and Common Environmental Contaminants in Human Mammary Epithelial Cells

Novel insights into tumorigenesis revealed by molecular analysis of Lynch syndrome cases with multiple colorectal tumors

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

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

Converging endometrial and ovarian tumorigenesis in Lynch syndrome: Shared origin of synchronous carcinomas

Body Weight, Physical Activity, and Risk of Cancer in Lynch Syndrome

LINE-1 hypomethylation in familial and sporadic cancer

MicroRNA Methylation in Colorectal Cancer

Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

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

Testing for Lynch Syndrome in Endometrial Carcinoma: From Universal to Age-Selective MLH1 Methylation Analysis

Immunoprofiles and DNA Methylation of Inflammatory Marker Genes in Ulcerative Colitis-Associated Colorectal Tumorigenesis

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

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

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

Mitotic abnormalities precede microsatellite instability in lynch syndrome-associated colorectal tumourigenesis

Cancer-predicting gene expression changes in colonic mucosa of Western diet fed Mlh1+/- mice

Development of Colorectal Tumors in Colonoscopic Surveillance in Lynch Syndrome

Genetic and Epigenetic Modification of MLH1 Accounts for a Major Share of Microsatellite-Unstable Colorectal Cancers

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