Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study (Q30361978)

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English	Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

13 August 2017

Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

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based on heuristic

inferred from title

immunohistochemistry

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based on heuristic

inferred from title

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based on heuristic

inferred from title

gynecologic oncology

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based on heuristic

inferred from title

object named as

Floor Backes

15

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object named as

Feng Gao

13

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Louise A. Brinton

14

object named as

Louise A Brinton

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Europe PubMed Central

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13 August 2017

object named as

David E Cohn

5

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ORCID Public Data File 2021

author name string

Paul J Goodfellow

1

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Europe PubMed Central

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13 August 2017

Caroline C Billingsley

2

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13 August 2017

Heather A Lankes

3

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Europe PubMed Central

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13 August 2017

Shamshad Ali

4

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Europe PubMed Central

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13 August 2017

Russell J Broaddus

6

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Europe PubMed Central

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13 August 2017

Nilsa Ramirez

7

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13 August 2017

Colin C Pritchard

8

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13 August 2017

Heather Hampel

9

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13 August 2017

Alexis S Chassen

10

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Europe PubMed Central

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13 August 2017

Luke V Simmons

11

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13 August 2017

Amy P Schmidt

12

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13 August 2017

Lisa M Landrum

16

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13 August 2017

Melissa A Geller

17

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Europe PubMed Central

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13 August 2017

Paul A DiSilvestro

18

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Europe PubMed Central

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13 August 2017

Michael L Pearl

19

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Europe PubMed Central

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13 August 2017

Shashikant B Lele

20

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Europe PubMed Central

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13 August 2017

Matthew A Powell

21

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Europe PubMed Central

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13 August 2017

Richard J Zaino

22

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13 August 2017

David Mutch

23

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13 August 2017

language of work or name

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publication date

9 November 2015

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13 August 2017

Journal of Clinical Oncology

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Europe PubMed Central

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13 August 2017

33

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Europe PubMed Central

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13 August 2017

36

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Europe PubMed Central

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13 August 2017

4301-4308

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Europe PubMed Central

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13 August 2017

Comparative effectiveness of screening strategies for Lynch syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Society of Gynecologic Oncology statement on risk assessment for inherited gynecologic cancer predispositions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Cost-effectiveness and diagnostic effectiveness analyses of multiple algorithms for the diagnosis of Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Evaluation of clinical criteria for the identification of Lynch syndrome among unselected patients with endometrial cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Endometrial cancer and a family history of cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Relationship between PTEN, DNA mismatch repair, and tumor histotype in endometrial carcinoma: retained positive expression of PTEN preferentially identifies sporadic non-endometrioid carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Etiologic heterogeneity in endometrial cancer: evidence from a Gynecologic Oncology Group trial.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Improving identification of lynch syndrome patients: a comparison of research data with clinical records

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

MLH1 methylation screening is effective in identifying epimutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Aberrant methylation of the X-linked ribosomal S6 kinase RPS6KA6 (RSK4) in endometrial cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

One to 2-year surveillance intervals reduce risk of colorectal cancer in families with Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

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=4678181

3 June 2018

ATR mutation in endometrioid endometrial cancer is associated with poor clinical outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Frequent HOXA11 and THBS2 promoter methylation, and a methylator phenotype in endometrial adenocarcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

3 June 2018

One size may not fit all: the debate of universal tumor testing for Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

26 November 2018

Milestones of Lynch syndrome: 1895-2015.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

26 November 2018

Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

26 November 2018

Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

26 November 2018

Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4678181

26 November 2018

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/26552419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/26552419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Are prediction models for Lynch syndrome valid for probands with endometrial cancer?

1 reference

https://pubmed.ncbi.nlm.nih.gov/26552419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1200/JCO.2015.63.9518

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

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