(Q36443837)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Using data mining to characterize DNA mutations by patient clinical features (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

S Evans

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

S J Lemon

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

C Deters

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

R M Fusaro

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

C Durham

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

C Snyder

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

H T Lynch

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 January 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

Proceedings / AMIA Annual Fall Symposium

7 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

253-257

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families

7 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

Heterogeneity and natural history of hereditary breast cancer. Surgical implications

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

Artificial neural networks in mammography: application to decision making in the diagnosis of breast cancer.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2233315

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9357627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical and Pathological Features of Ovarian Cancer in Women with Germ-Line Mutations ofBRCA1

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9357627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9357627%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

9357627

1 reference