The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history (Q30501708)

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scientific article published on 19 August 2010

The PREMM1,2,6 Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History

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English	The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history	scientific article published on 19 August 2010	The PREMM1,2,6 Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history (English)

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Ewout W. Steyerberg

2

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

object named as

Mark A Jenkins

9

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Judith Balmaña

object named as

Judith Balmaña

4

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Steven Gallinger

6

object named as

Steven Gallinger

1 reference

Europe PubMed Central

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12 October 2017

Noralane Lindor

10

object named as

Noralane M Lindor

1 reference

Europe PubMed Central

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12 October 2017

8

object named as

James M Church

1 reference

Europe PubMed Central

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12 October 2017

author name string

Fay Kastrinos

1

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Europe PubMed Central

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12 October 2017

Rowena Mercado

3

1 reference

Europe PubMed Central

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12 October 2017

Spring Holter

5

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Europe PubMed Central

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12 October 2017

Kimberly D Siegmund

7

1 reference

Europe PubMed Central

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12 October 2017

Stephen N Thibodeau

11

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Europe PubMed Central

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12 October 2017

Lynn Anne Burbidge

12

1 reference

Europe PubMed Central

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12 October 2017

Richard J Wenstrup

13

1 reference

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12 October 2017

Sapna Syngal

14

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12 October 2017

language of work or name

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publication date

19 August 2010

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Europe PubMed Central

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12 October 2017

Gastroenterology

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12 October 2017

140

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12 October 2017

1

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12 October 2017

73-81

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Europe PubMed Central

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12 October 2017

Risks of Lynch syndrome cancers for MSH6 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Data reduction for prediction: a case study on robust coding of age and family history for the risk of having a genetic mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Prediction of germline mutations and cancer risk in the Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Genetic testing for high-risk colon cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

20 June 2018

Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Prediction of Lynch syndrome in consecutive patients with colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Comparison of predictive models, clinical criteria and molecular tumour screening for the identification of patients with Lynch syndrome in a population-based cohort of colorectal cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

Decrease in mortality in Lynch syndrome families because of surveillance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125673

26 November 2018

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

https://pubmed.ncbi.nlm.nih.gov/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing New Biomarkers and Predictive Models for Use in Clinical Practice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20727894

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/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20727894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1053/J.GASTRO.2010.08.021

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

ResearchGate publication ID

0 references

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