(Q37194147)

18 August 2017

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer (English)

1 reference

18 August 2017

1 reference

11

1 reference

18 August 2017

5

Clare Turnbull

1 reference

18 August 2017

10

Michael R Stratton

1 reference

18 August 2017

2

Elise Ruark

1 reference

18 August 2017

4

Anthony Renwick

1 reference

18 August 2017

6

Sheila Seal

1 reference

18 August 2017

Katie Snape

1

1 reference

18 August 2017

Patrick Tarpey

3

1 reference

18 August 2017

Anne Murray

7

1 reference

18 August 2017

Sandra Hanks

8

1 reference

18 August 2017

Jenny Douglas

9

1 reference

18 August 2017

language of work or name

English

0 references

publication date

18 April 2012

1 reference

Breast Cancer Research and Treatment

18 August 2017

1 reference

18 August 2017

134

1 reference

18 August 2017

1

1 reference

18 August 2017

429-433

1 reference

https://scigraph.springernature.com/pub.10.1007/s10549-012-2057-x

18 August 2017

0 references

cites work

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Design considerations for massively parallel sequencing studies of complex human disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

The GENCODE exome: sequencing the complete human exome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Revisiting Mendelian disorders through exome sequencing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Loss-of-function variants in the genomes of healthy humans

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

ToppGene Suite for gene list enrichment analysis and candidate gene prioritization

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Genetic predisposition to breast cancer: past, present, and future

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Positional cloning of the Werner's syndrome gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781770

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

6 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10549-012-2057-X

Polygenic inheritance of breast cancer: Implications for design of association studies

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22527104

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10549-012-2057-X

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

22527104

1 reference