A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome (Q37089839)

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scientific article published on 12 July 2016

Language	Label	Description	Also known as
English	A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome	scientific article published on 12 July 2016

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

6

object named as

Jan Lubiński

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Europe PubMed Central

PMC publication ID

18 August 2017

Anna Jakubowska

7

object named as

Anna Jakubowska

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Europe PubMed Central

PMC publication ID

18 August 2017

8

object named as

Ute Hamann

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Europe PubMed Central

PMC publication ID

18 August 2017

2

object named as

Humaira Naeemi

1 reference

Europe PubMed Central

18 August 2017

PMC publication ID

author name string

Muhammad U Rashid

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Noor Muhammad

3

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Europe PubMed Central

PMC publication ID

18 August 2017

Asif Loya

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Muhammed A Yusuf

5

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Europe PubMed Central

PMC publication ID

18 August 2017

publication date

12 July 2016

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Hereditary Cancer in Clinical Practice

1 reference

Europe PubMed Central

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18 August 2017

14

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Europe PubMed Central

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18 August 2017

14

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Hereditary Colorectal Cancer: Genetics and Screening

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29 September 2017

Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

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29 September 2017

Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Hereditary breast cancer: the era of new susceptibility genes

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Clinicopathologic profile of breast cancer patients in Pakistan: ten years data of a local cancer hospital

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series 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=4942885

29 September 2017

Lynch syndrome (HNPCC).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

The risk of extra-colonic, extra-endometrial cancer 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=4942885

29 September 2017

Triple negative tumours: a critical review

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29 September 2017

Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

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=4942885

29 September 2017

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

29 September 2017

Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

3 September 2018

Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

3 September 2018

Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

3 September 2018

Mismatch repair defective breast cancer in the 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=4942885

3 September 2018

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

3 September 2018

Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4942885

3 September 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=4942885

3 September 2018

Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

1 reference

https://api.crossref.org/works/10.1186%2FS13053-016-0056-3

21 January 2018

Society of Gynecologic Oncologists Education Committee Statement on Risk Assessment for Inherited Gynecologic Cancer Predispositions☆

1 reference

https://api.crossref.org/works/10.1186%2FS13053-016-0056-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2FS13053-016-0056-3

21 January 2018

Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suspected hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

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/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA germline mutations in women with uterine serous carcinoma--still a debate

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novelMSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/27413415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S13053-016-0056-3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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