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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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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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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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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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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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Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

JNCI : Journal of the National Cancer Institute, 2007-02, Vol.99 (4), p.291-299

2007

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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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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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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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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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Distinct molecular profiles in Lynch syndrome‐associated and sporadic ovarian carcinomas

International journal of cancer, 2013-12, Vol.133 (11), p.2596-2608

2013

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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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Epigenetic analysis of sporadic and Lynch-associated ovarian cancers reveals histology-specific patterns of DNA methylation

Epigenetics, 2014-12, Vol.9 (12), p.1577-1587

2014

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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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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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Loss of Imprinting of the Insulin-Like Growth Factor II Gene Occurs by Biallelic Methylation in a Core Region of H19-Associated CTCF-binding Sites in Colorectal Cancer

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.591-596

2001

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BMPR1A Mutations in Hereditary Nonpolyposis Colorectal Cancer Without Mismatch Repair Deficiency

Gastroenterology (New York, N.Y. 1943), 2011-07, Vol.141 (1), p.e23-e26

2011

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Reducing the risk of type 2 diabetes with nutrition and physical activity – efficacy and implementation of lifestyle interventions in Finland

Public health nutrition, 2010-06, Vol.13 (6A), p.993-999

2010

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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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Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

Breast cancer research : BCR, 2012-06, Vol.14 (3), p.R90-R90, Article R90

2012

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

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

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

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

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

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

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

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

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

Distinct molecular profiles in Lynch syndrome‐associated and sporadic ovarian carcinomas

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

Epigenetic analysis of sporadic and Lynch-associated ovarian cancers reveals histology-specific patterns of DNA methylation

Development of Colorectal Tumors in Colonoscopic Surveillance in Lynch Syndrome

Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma

Loss of Imprinting of the Insulin-Like Growth Factor II Gene Occurs by Biallelic Methylation in a Core Region of H19-Associated CTCF-binding Sites in Colorectal Cancer

BMPR1A Mutations in Hereditary Nonpolyposis Colorectal Cancer Without Mismatch Repair Deficiency

Reducing the risk of type 2 diabetes with nutrition and physical activity – efficacy and implementation of lifestyle interventions in Finland

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

Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

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