(Q38780723)

6 September 2017

Multigene Panel Testing Provides a New Perspective on Lynch Syndrome (English)

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6 September 2017

Carin R Espenschied

1

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6 September 2017

Holly LaDuca

2

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6 September 2017

Shuwei Li

3

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6 September 2017

Rachel McFarland

4

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6 September 2017

Chia-Ling Gau

5

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6 September 2017

Heather Hampel

6

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6 September 2017

language of work or name

English

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publication date

17 May 2017

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Journal of Clinical Oncology

6 September 2017

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6 September 2017

35

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6 September 2017

22

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6 September 2017

2568-2575

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Beyond DNA: An Integrated and Functional Approach for Classifying Germline Variants in Breast Cancer Genes

6 September 2017

1 reference

12 December 2020

Association of rare MSH6 variants with familial breast cancer

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12 December 2020

Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results

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12 December 2020

Risks of Lynch syndrome cancers for MSH6 mutation carriers

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12 December 2020

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.

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12 December 2020

Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory.

1 reference

12 December 2020

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

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12 December 2020

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

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12 December 2020

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

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12 December 2020

Recurrent and founder mutations in the PMS2 gene.

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12 December 2020

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

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12 December 2020

Identification of Lynch syndrome among patients with colorectal cancer

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12 December 2020

Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer

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12 December 2020

Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation

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12 December 2020

Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

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12 December 2020

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

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12 December 2020

The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history

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12 December 2020

Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.

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12 December 2020

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.

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12 December 2020

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome

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12 December 2020

Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center.

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12 December 2020

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

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12 December 2020

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

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12 December 2020

Neoadjuvant therapy induces loss of MSH6 expression in colorectal carcinoma

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12 December 2020

MSH6 Mutations are Frequent in Hereditary Nonpolyposis Colorectal Cancer Families With Normal pMSH6 Expression as Detected by Immunohistochemistry

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12 December 2020

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer

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12 December 2020

Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology

1 reference

12 December 2020

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

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12 December 2020

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

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12 December 2020

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

1 reference

12 December 2020

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

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12 December 2020

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

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12 December 2020

Recurrent germline mutation in MSH2 arises frequently de novo

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12 December 2020

Inherited Mutations in Women With Ovarian Carcinoma

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12 December 2020

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

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12 December 2020

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

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12 December 2020

Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients

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12 December 2020

A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting

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12 December 2020

Identifiers

DOI

10.1200/JCO.2016.71.9260

1 reference

release_gxfvsmiko5hn7k7eob5v2iuchm

6 September 2017

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Fatcat

https://api.fatcat.wiki/v0/release/gxfvsmiko5hn7k7eob5v2iuchm

24 November 2022

mapped directly with Wikidata item

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