SISE matters: the sum of information on seventy-yr-old equivalents measures pedigree information content when assessing the risk of HNPCC in a family. (Q50765059)

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scientific article published in January 2005

Language	Label	Description	Also known as
English	SISE matters: the sum of information on seventy-yr-old equivalents measures pedigree information content when assessing the risk of HNPCC in a family.	scientific article published in January 2005

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

SISE matters: the sum of information on seventy-yr-old equivalents measures pedigree information content when assessing the risk of HNPCC in a family. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

1 reference

based on heuristic

inferred from title

information content

1 reference

based on heuristic

inferred from title

author name string

R C Green

1

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

J R McLaughlin

2

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

H B Younghusband

3

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

Familial Cancer

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

4

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

2

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

169-175

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

https://scigraph.springernature.com/pub.10.1007/s10689-004-7251-5

0 references

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

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A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alleles of the APC gene: an attenuated form of familial polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of DNA mismatch repair defects in the pathogenesis of human cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability analysis and/or immunostaining for the diagnosis of hereditary nonpolyposis colorectal cancer?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family history and colorectal cancer: predictors of risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of APC and DNA mismatch repair genes in the development of colorectal cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15951969

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-004-7251-5

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 March 2018

http://europepmc.org/abstract/MED/15951969

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