(Q54416094)

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

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20697958%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

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

1 reference

Europe PubMed Central

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9 February 2020

colorectal cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

colorectal carcinoma

1 reference

based on heuristic

inferred from title

7

1 reference

Europe PubMed Central

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9 February 2020

1 reference

ORCID Public Data File 2021

author name string

Felipe Carneiro da Silva

1

1 reference

Europe PubMed Central

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9 February 2020

Ligia Petrolini de Oliveira

2

1 reference

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9 February 2020

Erika Monteiro Santos

3

1 reference

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9 February 2020

Wilson Toshihiko Nakagawa

4

1 reference

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9 February 2020

Samuel Aguiar Junior

5

1 reference

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9 February 2020

Mev Dominguez Valentin

6

1 reference

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9 February 2020

Fábio de Oliveira Ferreira

8

1 reference

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9 February 2020

publication date

1 December 2010

1 reference

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9 February 2020

Familial Cancer

1 reference

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9 February 2020

9

1 reference

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9 February 2020

4

1 reference

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9 February 2020

563-570

1 reference

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9 February 2020

https://scigraph.springernature.com/pub.10.1007/s10689-010-9373-2

0 references

Systematic review: surveillance for breast cancer in women treated with chest radiation for childhood, adolescent, or young adult cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-010-9373-2

21 January 2018

Clinical phenotype and prevalence of hereditary nonpolyposis colorectal cancer syndrome in Chinese population

1 reference

https://api.crossref.org/works/10.1007%2FS10689-010-9373-2

21 January 2018

Transmission of Cervical Human Papillomavirus Infection by Sexual Activity: Differences between Low and High Oncogenic Risk Types

1 reference

https://api.crossref.org/works/10.1007%2FS10689-010-9373-2

21 January 2018

Is breast cancer part of the tumor spectrum of hereditary nonpolyposis colorectal cancer?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathology of hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determinants of genital human papillomavirus detection in a US population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of germ-line E-cadherin mutations in gastric cancer families of European origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E-cadherin germline mutations in familial gastric cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Lynch syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An update of HNPCC (Lynch syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tumor spectrum in the Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial colonic cancer without antecedent polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL CANCER OF THE COLON

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of cancer death in first-degree relatives of patients with hereditary non-polyposis cancer syndrome (Lynch type II): a study of 130 kindreds in the United Kingdom

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classics in oncology. Heredity with reference to carcinoma as shown by the study of the cases examined in the pathological laboratory of the University of Michigan, 1895-1913. By Aldred Scott Warthin. 1913

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer in an MSH2 gene mutation carrier

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer family “G” revisited: 1895-1970

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inheritance of Cancer of the Stomach and Large Intestine in Man2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family studies in cancer of the colon and rectum

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosing Lynch syndrome: is the answer in the mouth?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-risk human papillomavirus is sexually transmitted: evidence from a follow-up study of virgins starting sexual activity (intercourse)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic study of carcinoma of the large intestine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in Korea

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to gastric cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family incidence of carcinoma of the colon and rectum in north-east Scotland

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor variation in three extended Lynch syndrome II kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in mismatch repair gene mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colorectal and extracolonic cancer variations in MLH1/MSH2 hereditary nonpolyposis colorectal cancer kindreds and the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chapter 6: Epidemiology and transmission dynamics of genital HPV infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer? A molecular genetic study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gastric cancer: new genetic developments

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family history of uterine and gastro-intestinal cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial clustering of colon, breast, uterine, and ovarian cancers as assessed by family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colorectal cancer: molecules and populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in 348 French MSH2 or MLH1 gene carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of extra-colonic tumors in hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) Brazilian families: An analysis by a Brazilian Hereditary Colorectal Cancer Institutional Registry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

hMLH1 and hMSH2 gene mutation in Brazilian families with suspected hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20697958

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/20697958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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