(Q37798758)

23 August 2017

Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review (English)

1 reference

23 August 2017

Molly S Daniels

11

0 references

Cecelia A. Bellcross

2

object named as

Cecelia Bellcross

1 reference

23 August 2017

Scott M Weissman

1

1 reference

23 August 2017

Christina Chimera Bittner

3

1 reference

23 August 2017

Mary E Freivogel

4

1 reference

23 August 2017

Joy Larsen Haidle

5

1 reference

23 August 2017

Pardeep Kaurah

6

1 reference

23 August 2017

Anna Leininger

7

1 reference

23 August 2017

Selvi Palaniappan

8

1 reference

23 August 2017

Kelle Steenblock

9

1 reference

23 August 2017

Thuy M Vu

10

1 reference

23 August 2017

8 October 2010

1 reference

Journal of Genetic Counseling

23 August 2017

1 reference

23 August 2017

20

1 reference

23 August 2017

1

1 reference

23 August 2017

5-19

1 reference

Cancer risk in mutation carriers of DNA-mismatch-repair genes

23 August 2017

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Cutaneous sebaceous neoplasms as markers of Muir-Torre syndrome: a diagnostic algorithm

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Risks of Lynch syndrome cancers for MSH6 mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Evolution of the nomenclature for the hereditary colorectal cancer syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Promoter hypermethylation is associated with tumor location, stage, and subsequent progression in transitional cell carcinoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Prediction of germline mutations and cancer risk in the Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Decrease in mortality in Lynch syndrome families because of surveillance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Mismatch repair gene expression defects contribute to microsatellite instability in ovarian carcinoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The molecular basis of Turcot's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Genetic testing for hereditary colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The role of microsatellite instability in gastric carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

DNA microsatellite instability and mismatch repair protein loss in adenomas presenting in hereditary non-polyposis colorectal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Evolution of hereditary non-polyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Comparative lesion sequencing provides insights into tumor evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Risk of pancreatic cancer in families with Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Management of extracolonic tumours in patients with Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Role of heredity in multiple primary cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Decision model of segmental compared with total abdominal colectomy for colon cancer in hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Clinical features of colorectal carcinoma in cancer family syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

PMS2 involvement in patients suspected of Lynch syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Towards identification of hereditary DNA mismatch repair deficiency: sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Systematic review and meta-analysis of ovarian cancers: estimation of microsatellite-high frequency and characterization of mismatch repair deficient tumor histology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Systematic review of microsatellite instability and colorectal cancer prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Proximal adenomas in hereditary non-polyposis colorectal cancer are prone to rapid malignant transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Gynecologic screening in hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Microsatellite instability as indicator of MSH2 gene mutation in patients with upper urinary tract transitional cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Microsatellite instability as a tool for the classification of gastric cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The frequency of Muir-Torre syndrome among Lynch syndrome families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Germline epimutation of MLH1 in individuals with multiple cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Biallelic PMS2 mutations and a distinctive childhood cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Familial endometrial cancer in female carriers of MSH6 germline mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Cancer risk associated with germline DNA mismatch repair gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Distinct patterns of microsatellite instability are seen in tumours of the urinary tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Compound heterozygosity for twoMSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

No Support for Endoscopic Surveillance for Gastric Cancer in Hereditary Non-Polyposis Colorectal Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Better survival rates in patients with MLH1-associated hereditary colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Site and Tumor Type Predicts DNA Mismatch Repair Status in Cutaneous Sebaceous Neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9325-X

MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers

21 January 2018

1 reference

12 December 2020

Microsatellite instability is frequently observed in rectal cancer and influenced by neoadjuvant chemoradiation

1 reference

12 December 2020

MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

12 December 2020

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Frequency and application of the hot spot BRAF gene mutation (p.V600E) in the diagnostic strategy for Hereditary Nonpolyposis Colorectal Cancer

1 reference

12 December 2020

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

1 reference

12 December 2020

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

1 reference

12 December 2020

The accuracy of endometrial sampling in the diagnosis of patients with endometrial carcinoma and hyperplasia: a meta-analysis

1 reference

12 December 2020

Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome

1 reference

12 December 2020

Correlation of mismatch repair genes immunohistochemistry and microsatellite instability status in HNPCC-associated tumours

1 reference

12 December 2020

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

1 reference

12 December 2020

MSH6 mutations in hereditary nonpolyposis colon cancer: another slice of the pie

1 reference

12 December 2020

Different types of microsatellite instability in ovarian carcinoma

1 reference

12 December 2020

Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome

1 reference

12 December 2020

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

1 reference

12 December 2020

The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC

1 reference

12 December 2020

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

1 reference

12 December 2020

A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor

1 reference

12 December 2020

Low rate of microsatellite instability in young patients with adenomas: reassessing the Bethesda guidelines

1 reference

12 December 2020

The reduction in risk of ovarian cancer associated with oral-contraceptive use

1 reference

12 December 2020

Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome

1 reference

12 December 2020

The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma

1 reference

12 December 2020

Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC

1 reference

12 December 2020

Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer

1 reference

12 December 2020

Interval cancers in hereditary non-polyposis colorectal cancer (Lynch syndrome)

1 reference

12 December 2020

Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in Korea

1 reference

12 December 2020

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

12 December 2020

Assessment of markers for the identification of microsatellite instability phenotype in gastric neoplasms

1 reference

12 December 2020

Adenomas in young patients: what is the optimal evaluation?

1 reference

12 December 2020

Prospective Determination of Prevalence of Lynch Syndrome in Young Women With Endometrial Cancer

1 reference

12 December 2020

Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study

1 reference

12 December 2020

Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review

1 reference

12 December 2020

AGA technical review on hereditary colorectal cancer and genetic testing.

1 reference

12 December 2020

BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair

1 reference

12 December 2020

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

12 December 2020

Frequent microsatellite instability in sporadic tumors of the upper urinary tract

1 reference

12 December 2020

Combination oral contraceptive use and the risk of endometrial cancer. The Cancer and Steroid Hormone Study of the Centers for Disease Control and the National Institute of Child Health and Human Development

1 reference

12 December 2020

Analysis of a correlation between the BRAF V600E mutation and abnormal DNA mismatch repair in patients with sporadic endometrial cancer.

1 reference

12 December 2020

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

1 reference

12 December 2020

10.1007/S10897-010-9325-X

Identifiers

DOI

1 reference

23 August 2017

1 reference