(Q59159730)

8

object named as

Cathryn Lewis

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author name string

Sara Levene

1

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Gillian Scott

2

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Patricia Price

3

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Jeremy Sanderson

4

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Helen Evans

5

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Claire Taylor

6

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Sylvia Bass

https://scigraph.springernature.com/pub.10.1023/a:1023265919884

7

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language of work or name

English

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publication date

2003

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published in

Familial Cancer

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volume

2

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issue

1

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page(s)

15-25

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exact match

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cites work

The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

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12 December 2020

What is the true incidence of primary fallopian tube carcinoma?

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12 December 2020

Mutations of the BRCA2 gene in ovarian carcinomas

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12 December 2020

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

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Cancer Incidence in BRCA1 mutation carriers

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Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred.

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12 December 2020

BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers

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12 December 2020

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

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12 December 2020

Interpretation of Genetic Test Results for Hereditary Nonpolyposis Colorectal Cancer

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12 December 2020

BRCA2 mutations in primary breast and ovarian cancers

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12 December 2020

Small intestinal neoplasms

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12 December 2020

The protein truncation test: A review

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12 December 2020

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

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12 December 2020

Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas

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12 December 2020

Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England

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12 December 2020

Cancer risks in BRCA2 mutation carriers

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12 December 2020

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

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12 December 2020

Breast cancer as a risk factor for other primary malignant diseases. A nationwide cohort study.

1 reference

12 December 2020

Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome

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12 December 2020

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

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12 December 2020

Validation and simplification of Bethesda guidelines for identifying apparently sporadic forms of colorectal carcinoma with microsatellite instability

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12 December 2020

Germline BRCA1-2 mutations in non-Ashkenazi families with double primary breast and ovarian cancer

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12 December 2020

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families

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12 December 2020

A genetic epidemiological study of carcinoma of the fallopian tube

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12 December 2020

Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations

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12 December 2020

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

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12 December 2020

Bethesda guidelines: relation to microsatellite instability and MLH1 promoter methylation in patients with colorectal cancer.

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High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum

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Recent advances in understanding of genetic susceptibility to breast cancer

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12 December 2020

Identifying and screening patients at high risk of colorectal cancer in general practice

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12 December 2020

Family history of colorectal tumours and implications for the adenoma-carcinoma sequence: a case control study

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12 December 2020

Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls

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12 December 2020

Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families

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12 December 2020

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

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12 December 2020

A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning.

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12 December 2020

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

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12 December 2020

Hereditary nonpolyposis colorectal cancer (HNPCC).

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12 December 2020

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

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12 December 2020

Pancreas cancer as a second primary malignancy. A population-based study.

1 reference

12 December 2020

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria

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12 December 2020

The risk of subsequent primary cancers after colorectal cancer in southeast England.

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12 December 2020

Missense mutations in hMLH1 associated with colorectal cancer

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12 December 2020

Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations

1 reference

12 December 2020

Adenocarcinoma of the proximal small intestine. A marker for familial and multicentric cancer?

1 reference

12 December 2020

Identification of novel germline hMLH1 mutations including a 22 kb Alu-mediated deletion in patients with familial colorectal cancer

1 reference

12 December 2020

Occult cancer of the fallopian tube in BRCA-1 germline mutation carriers at prophylactic oophorectomy: a case for recommending hysterectomy at surgical prophylaxis

1 reference

12 December 2020

Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes

1 reference

12 December 2020

The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes

1 reference

12 December 2020

Increased risk of thyroid and pancreatic carcinoma in familial adenomatous polyposis

1 reference

12 December 2020

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Risk of cancer in BRCA1 and BRCA2 mutation-positive and -negative breast cancer families (Finland)

1 reference

12 December 2020

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

12 December 2020

Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers

1 reference

12 December 2020

Genetic implications of double primary cancers of the colorectum and endometrium

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites

1 reference

12 December 2020

Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations

1 reference

12 December 2020