A hypothesis-generating search for new genetic breast cancer syndromes--a national study in 803 Swedish families (Q36108214)

12 August 2017

A hypothesis-generating search for new genetic breast cancer syndromes--a national study in 803 Swedish families (English)

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12 August 2017

4

Henrik Grönberg

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12 August 2017

2

Annika Lindblom

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12 August 2017

5

Zakaria Einbeigi

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12 August 2017

Anna von Wachenfeldt

1

1 reference

12 August 2017

South Swedish Oncogenetic Study Group

3

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12 August 2017

Richard Rosenquist

6

1 reference

12 August 2017

Camilla Gardman

7

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12 August 2017

Lennart Iselius

8

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12 August 2017

15 March 2007

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Hereditary Cancer in Clinical Practice

12 August 2017

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12 August 2017

5

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12 August 2017

1

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12 August 2017

17-24

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https://scigraph.springernature.com/pub.10.1186/1897-4287-5-1-17

12 August 2017

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cites work

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

A Ser49Cys variant in the ataxia telangiectasia, mutated, gene that is more common in patients with breast carcinoma compared with population controls

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Dominant Negative ATM Mutations in Breast Cancer Families

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Low frequency of E-cadherin alterations in familial breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Genetic analysis of breast cancer in the cancer and steroid hormone study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Are ATM mutations 7271T-->G and IVS10-6T-->G really high-risk breast cancer-susceptibility alleles?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Is Uterine Papillary Serous Adenocarcinoma a Manifestation of the Hereditary Breast–Ovarian Cancer Syndrome?

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401933

Familial association of histology specific breast cancers with cancers at other sites

21 October 2018

1 reference

12 December 2020

Age at onset as an indicator of familial risk of breast cancer

1 reference

12 December 2020

High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families

1 reference

12 December 2020

BRCA1 screening in patients with a family history of breast or ovarian cancer

1 reference

12 December 2020

The role of ataxia-telangiectasia heterozygotes in familial breast cancer

1 reference

12 December 2020

Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer

1 reference

12 December 2020

The need for oncogenetic counselling. Ten years' experience of a regional oncogenetic clinic

1 reference

12 December 2020

A study of the PTEN/MMAC1 gene in 136 breast cancer families

1 reference

12 December 2020

Identifiers

DOI

10.1186/1897-4287-5-1-17

1 reference

Dimensions Publication ID

12 August 2017

0 references

1 reference

12 August 2017

1 reference