Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer (Q36385676)

13 August 2017

Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer (English)

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13 August 2017

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15

S A Narod

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13 August 2017

T Pal

1

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13 August 2017

M R Akbari

2

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13 August 2017

P Sun

3

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13 August 2017

J-H Lee

4

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13 August 2017

J Fulp

5

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13 August 2017

Z Thompson

6

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13 August 2017

D Coppola

7

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13 August 2017

S Nicosia

8

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13 August 2017

T A Sellers

9

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13 August 2017

J McLaughlin

10

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13 August 2017

H A Risch

11

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13 August 2017

B Rosen

12

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13 August 2017

P Shaw

13

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J Schildkraut

14

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13 August 2017

language of work or name

English

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publication date

9 October 2012

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British Journal of Cancer

13 August 2017

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13 August 2017

107

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10

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13 August 2017

1783-1790

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https://scigraph.springernature.com/pub.10.1038/bjc.2012.452

13 August 2017

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Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical management

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

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A review of the clinical relevance of mismatch-repair deficiency in ovarian cancer

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Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts

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Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

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Cancer risk in mismatch repair gene mutation carriers

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

30 September 2017

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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

30 September 2017

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Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer

30 September 2017

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Association of tumour site and sex with survival benefit from adjuvant chemotherapy in colorectal cancer

30 September 2017

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Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

30 September 2017

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Familial endometrial cancer in female carriers of MSH6 germline mutations

30 September 2017

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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

30 September 2017

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Mutation of a mutL homolog in hereditary colon cancer

30 September 2017

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Clinical impact of unclassified variants of the BRCA1 and BRCA2 genes.

30 September 2017

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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

21 January 2018

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Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations

21 January 2018

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

21 January 2018

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Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer

21 January 2018

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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

21 September 2018

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12 December 2020

P53 alteration and microsatellite instability have predictive value for survival benefit from chemotherapy in stage III colorectal carcinoma

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12 December 2020

Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families

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12 December 2020

Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1

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12 December 2020

Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect

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12 December 2020

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. II. Invasive epithelial ovarian cancers in white women. Collaborative Ovarian Cancer Group

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12 December 2020

Screening for early ovarian cancer

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12 December 2020

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

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12 December 2020

BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing

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12 December 2020

Ovarian cancer linked to Lynch syndrome typically presents as early-onset, non-serous epithelial tumors

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12 December 2020

A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers

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12 December 2020

The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer

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12 December 2020

Identifiers

DOI

10.1038/BJC.2012.452

1 reference

13 August 2017

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13 August 2017

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