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Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

Gastroenterology (New York, N.Y. 1943), 2014-03, Vol.146 (3), p.643-646.e8

2014

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Revertant Somatic Mosaicism by Mitotic Recombination in Dyskeratosis Congenita

American journal of human genetics, 2012-03, Vol.90 (3), p.426-433

2012

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Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool

European journal of medical genetics, 2016-03, Vol.59 (3), p.116-125

2016

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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

Nature genetics, 2009-01, Vol.41 (1), p.112-117

2009

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Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1

Gastroenterology (New York, N.Y. 1943), 2015-10, Vol.149 (4), p.897-906.e19

2015

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Effect of Pneumatic Tube System Transport on Cell-Free DNA

Clinical chemistry (Baltimore, Md.), 2021-02, Vol.67 (2), p.434-435

2021

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Mutational analysis of cervical cytology improves diagnosis of endometrial cancer: A prospective multicentre cohort study

International journal of cancer, 2020-05, Vol.146 (9), p.2628-2635

2020

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Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer

Scientific reports, 2015-09, Vol.5 (1), p.14060-14060, Article 14060

2015

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BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Nature genetics, 1997-11, Vol.17 (3), p.341-345

1997

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Nationwide evaluation of mutation-tailored treatment of gastrointestinal stromal tumors in daily clinical practice

Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2021-09, Vol.24 (5), p.990-1002

2021

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Functional characterisation of a novel class of in-frame insertion variants of KRAS and HRAS

Scientific reports, 2019-06, Vol.9 (1), p.8239, Article 8239

2019

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Germline Mutations in the Spindle Assembly Checkpoint Genes BUB1 and BUB3 Are Risk Factors for Colorectal Cancer

Gastroenterology (New York, N.Y. 1943), 2013-09, Vol.145 (3), p.544-547

2013

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A Brief Retrospective Report on the Feasibility of Epidermal Growth Factor Receptor and KRAS Mutation Analysis in Transesophageal Ultrasound- and Endobronchial Ultrasound-Guided Fine Needle Cytological Aspirates

Journal of thoracic oncology, 2010-10, Vol.5 (10), p.1664-1667

2010

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Epigenetic targeting in pancreatic cancer

Cancer treatment reviews, 2014-06, Vol.40 (5), p.656-664

2014

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Identification of candidate predisposing copy number variants in familial and early‐onset colorectal cancer patients

International journal of cancer, 2011-10, Vol.129 (7), p.1635-1642

2011

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Universal genetic assessment for women with ovarian cancer not yet achieved: The promises of universal tumor DNA testing

Gynecologic oncology reports, 2021-11, Vol.38, p.100825-100825, Article 100825

2021

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High sensitivity of both sequencing and real‐time PCR analysis of KRAS mutations in colorectal cancer tissue

Journal of cellular and molecular medicine, 2010-08, Vol.14 (8), p.2122-2131

2010

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High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling

Journal of genetic counseling, 2016-06, Vol.25 (3), p.504-514

2016

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Germline Epigenetic Silencing of the Tumor Suppressor Gene PTPRJ in Early-Onset Familial Colorectal Cancer

Gastroenterology (New York, N.Y. 1943), 2010-12, Vol.139 (6), p.2221-2224

2010

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Higher Quality of Molecular Testing, an Unfulfilled Priority

The Journal of molecular diagnostics : JMD, 2014-05, Vol.16 (3), p.371-377

2014

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A multicenter study to validate the reproducibility of MSI testing with a panel of 5 quasimonomorphic mononucleotide repeats

Diagnostic molecular pathology, 2010-12, Vol.19 (4), p.236-242

2010

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Toward New Strategies to Select Young Endometrial Cancer Patients for Mismatch Repair Gene Mutation Analysis

Journal of clinical oncology, 2003-12, Vol.21 (23), p.4364-4370

2003

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Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers

Journal of Medical Genetics, 2015-06, Vol.52 (6), p.361-374

2015

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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

Cancer cell, 2019-02, Vol.35 (2), p.256-266.e5

2019

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Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

Revertant Somatic Mosaicism by Mitotic Recombination in Dyskeratosis Congenita

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1

Effect of Pneumatic Tube System Transport on Cell-Free DNA

Mutational analysis of cervical cytology improves diagnosis of endometrial cancer: A prospective multicentre cohort study

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Nationwide evaluation of mutation-tailored treatment of gastrointestinal stromal tumors in daily clinical practice

Functional characterisation of a novel class of in-frame insertion variants of KRAS and HRAS

Germline Mutations in the Spindle Assembly Checkpoint Genes BUB1 and BUB3 Are Risk Factors for Colorectal Cancer

A Brief Retrospective Report on the Feasibility of Epidermal Growth Factor Receptor and KRAS Mutation Analysis in Transesophageal Ultrasound- and Endobronchial Ultrasound-Guided Fine Needle Cytological Aspirates

Epigenetic targeting in pancreatic cancer

Identification of candidate predisposing copy number variants in familial and early‐onset colorectal cancer patients

Universal genetic assessment for women with ovarian cancer not yet achieved: The promises of universal tumor DNA testing

High sensitivity of both sequencing and real‐time PCR analysis of KRAS mutations in colorectal cancer tissue

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling

Germline Epigenetic Silencing of the Tumor Suppressor Gene PTPRJ in Early-Onset Familial Colorectal Cancer

Higher Quality of Molecular Testing, an Unfulfilled Priority

A multicenter study to validate the reproducibility of MSI testing with a panel of 5 quasimonomorphic mononucleotide repeats

Toward New Strategies to Select Young Endometrial Cancer Patients for Mismatch Repair Gene Mutation Analysis

Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

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