(Q34161196)

31 July 2017

title

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

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31 July 2017

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T Walsh

15

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Marshall Horwitz

M Horwitz

4

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Jinru Shia

J Shia

7

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Jeffrey N Weitzel

23

J N Weitzel

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31 July 2017

William David Foulkes

1

W D Foulkes

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31 July 2017

31

G Rennert

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31 July 2017

30

K Offit

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Brigitte Bressac-de Paillerets

31 July 2017

21

B Bressac-De Paillerets

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31 July 2017

Albert de la Chapelle

28

A De La Chapelle

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31 July 2017

I Thiffault

2

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31 July 2017

S B Gruber

3

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31 July 2017

N Hamel

5

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31 July 2017

C Lee

6

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31 July 2017

A Markowitz

8

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31 July 2017

A Figer

9

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31 July 2017

E Friedman

10

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31 July 2017

D Farber

11

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31 July 2017

C M T Greenwood

12

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31 July 2017

J D Bonner

13

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31 July 2017

K Nafa

14

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31 July 2017

V Marcus

16

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31 July 2017

L Tomsho

17

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31 July 2017

J Gebert

18

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31 July 2017

F A Macrae

19

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31 July 2017

C L Gaff

20

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31 July 2017

P K Gregersen

22

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31 July 2017

P H Gordon

24

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31 July 2017

E MacNamara

25

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31 July 2017

M-C King

26

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31 July 2017

H Hampel

27

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31 July 2017

J Boyd

29

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31 July 2017

G Chong

32

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31 July 2017

N A Ellis

33

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31 July 2017

language of work or name

English

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publication date

26 November 2002

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American Journal of Human Genetics

31 July 2017

published in

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31 July 2017

volume

71

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31 July 2017

issue

6

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31 July 2017

page(s)

1395-1412

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A high-resolution recombination map of the human genome

31 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=420003

Phenotypic analysis of hMSH2 mutations in mouse cells carrying human chromosomes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Deficient DNA mismatch repair: a common etiologic factor for colon cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

A New Statistical Method for Haplotype Reconstruction from Population Data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

The crystal structure of DNA mismatch repair protein MutS binding to a G x T mismatch

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Recurrent germline mutation in MSH2 arises frequently de novo

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Hereditary nonpolyposis colon cancer: analysis of linkage to 2p15-16 places the COCA1 locus telomeric to D2S123 and reveals genetic heterogeneity in seven Canadian families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Founding mutations and Alu-mediated recombination in hereditary colon cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

A genetic profile of contemporary Jewish populations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

Risk of Endometrial Carcinoma Associated with BRCA Mutation

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420003

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

28 October 2018

1 reference

12 December 2020

Inhibition of nonsense-mediated messenger RNA decay in clinical samples facilitates detection of human MSH2 mutations with an in vivo fusion protein assay and conventional techniques

1 reference

12 December 2020

Immunohistochemistry for hMLH1 and hMSH2: a practical test for DNA mismatch repair-deficient tumors

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12 December 2020

Clinicopathologic features of BRCA-linked and sporadic ovarian cancer

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12 December 2020

Mutational analyses ofBRCA1 andBRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

1 reference

12 December 2020

A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population

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12 December 2020

Identifiers

DOI

10.1086/345075

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31 July 2017

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31 July 2017

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