(Q33767027)

29 July 2017

title

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

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29 July 2017

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26

Loic Le Marchand

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Sally-Ann Pearson

Sally-Ann Pearson

4

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Sonja Woodall

Sonja Woodall

20

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Daniel D Buchanan

Daniel D Buchanan

2

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Michael A McGuckin

Michael A McGuckin

30

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Mark Jenkins

Mark A Jenkins

11

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Amanda Spurdle

Amanda B Spurdle

9

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John Potter

John D Potter

25

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Margaret C Cummings

Margaret C Cummings

3

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Elise Pelzer

Elise Pelzer

18

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John Hopper

10

John L Hopper

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29 July 2017

29

Noralane M Lindor

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29 July 2017

22

Finlay A Macrae

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29 July 2017

Michael D Walsh

1

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29 July 2017

Sven T Arnold

5

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29 July 2017

Mark Clendenning

6

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29 July 2017

Rhiannon Walters

7

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29 July 2017

Diane M McKeone

8

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29 July 2017

Kerry D Phillips

12

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29 July 2017

Graeme K Suthers

13

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29 July 2017

Jill George

14

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29 July 2017

Jack Goldblatt

15

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29 July 2017

Amanda Muir

16

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29 July 2017

Kathy Tucker

17

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29 July 2017

Michael R Gattas

19

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29 July 2017

Susan Parry

21

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29 July 2017

Robert W Haile

23

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29 July 2017

John A Baron

24

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29 July 2017

Bharati Bapat

27

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29 July 2017

Stephen N Thibodeau

28

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29 July 2017

Joanne P Young

31

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29 July 2017

language of work or name

English

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publication date

9 March 2010

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29 July 2017

published in

Clinical Cancer Research

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29 July 2017

volume

16

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29 July 2017

issue

7

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29 July 2017

page(s)

2214-2224

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Inherited susceptibility to common cancers

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Hereditary breast cancer: from molecular pathology to tailored therapies

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Molecular, pathologic, and clinical features of early-onset endometrial cancer: identifying presumptive Lynch syndrome patients

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

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

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

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

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Microsatellite instability markers in breast cancer: a review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancer

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Frequency of extra-colonic tumors in hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) Brazilian families: An analysis by a Brazilian Hereditary Colorectal Cancer Institutional Registry.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Loss of hMSH2 expression in primary breast cancer with p53 alterations.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Is breast cancer part of the tumor spectrum of hereditary nonpolyposis colorectal cancer?

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Familial risks in in situ cancers from the Family-Cancer Database.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Determination of the replication error phenotype in human tumors without the requirement for matching normal DNA by analysis of mononucleotide repeat microsatellites

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

The assessment of histological differentiation in breast cancer.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848890

Four novelMSH2 andMLH1 frameshift mutations and occurrence of a breast cancer phenocopy in hereditary nonpolyposis colorectal cancer

30 October 2018

1 reference

12 December 2020

Microsatellite instability is infrequent in medullary breast cancer

1 reference

12 December 2020

Age at onset as an indicator of familial risk of breast cancer

1 reference

12 December 2020

Microsatellite instability and loss of heterozygosity in breast cancer

1 reference

12 December 2020

Familiality of cancer in Utah

1 reference

12 December 2020

Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome

1 reference

12 December 2020

The genetic attributable risk of breast and ovarian cancer

1 reference

12 December 2020

Infrequent occurrence of microsatellite instability in sporadic and familial breast cancer

1 reference

12 December 2020

Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Second primary neoplasms in 633,964 cancer patients in Sweden, 1958-1996

1 reference

12 December 2020

Genotype and phenotype of a new 2-bp deletion of hMSH2 at codon 233

1 reference

12 December 2020

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

12 December 2020

Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Microsatellite instability in early-onset breast cancer

1 reference

12 December 2020

Correspondence re: A. Müller et al., Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer. Cancer Res., 62: 1014-1019, 2002

1 reference

12 December 2020

Genetic alterations and MSI status in primary, synchronous, and metachronous tumors in a family with hereditary nonpolyposis colorectal cancer (HNPCC)

1 reference

12 December 2020

Microsatellite instability in ductal carcinomain situ of the breast

1 reference

12 December 2020

Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

1 reference

12 December 2020

Microsatellite instability in medullary breast carcinomas

1 reference

12 December 2020

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.

1 reference

12 December 2020

Breast cancer in an MSH2 gene mutation carrier

1 reference

12 December 2020

A new variant database for mismatch repair genes associated with Lynch syndrome

1 reference

12 December 2020

Breast cancer immunohistochemistry can be useful in triage of some HNPCC families

1 reference

12 December 2020

10.1158/1078-0432.CCR-09-3058

Identifiers

DOI

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29 July 2017

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29 July 2017

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