(Q35209967)

7 August 2017

title

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus (English)

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7 August 2017

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Olli-Pekka Kallioniemi

11

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7 August 2017

35

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7 August 2017

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Olsson H

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7 August 2017

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Grönberg H

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7 August 2017

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Holmberg E

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7 August 2017

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Bailey-Wilson J

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7 August 2017

Kainu T

1

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7 August 2017

Juo SH

2

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7 August 2017

Desper R

3

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7 August 2017

Schaffer AA

4

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7 August 2017

Gillanders E

5

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7 August 2017

Rozenblum E

6

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7 August 2017

Freas-Lutz D

7

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7 August 2017

Weaver D

8

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7 August 2017

Stephan D

9

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7 August 2017

Tirkkonen M

12

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7 August 2017

Syrjäkoski K

13

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7 August 2017

Kuukasjärvi T

14

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7 August 2017

Koivisto P

15

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7 August 2017

Karhu R

16

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7 August 2017

Holli K

17

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7 August 2017

Arason A

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7 August 2017

Johannesdottir G

19

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7 August 2017

Bergthorsson JT

20

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7 August 2017

Johannsdottir H

21

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7 August 2017

Egilsson V

22

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7 August 2017

Barkardottir RB

23

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7 August 2017

Johannsson O

24

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7 August 2017

Haraldsson K

25

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7 August 2017

Sandberg T

26

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7 August 2017

Borg A

30

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7 August 2017

Vehmanen P

31

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7 August 2017

Eerola H

32

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7 August 2017

Heikkila P

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7 August 2017

Pyrhönen S

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7 August 2017

language of work or name

English

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publication date

1 August 2000

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Proceedings of the National Academy of Sciences of the United States of America

7 August 2017

published in

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7 August 2017

volume

97

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7 August 2017

issue

17

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7 August 2017

page(s)

9603-9608

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Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Three distinct regions of allelic loss at 13q14, 13q21-22, and 13q33 in prostate cancer

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Inferring tree models for oncogenesis from comparative genome hybridization data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Optimizing DOP-PCR for universal amplification of small DNA samples in comparative genomic hybridization

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Parametric and nonparametric linkage analysis: a unified multipoint approach

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Faster sequential genetic linkage computations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Strategies for multilocus linkage analysis in humans

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Mutation and cancer: statistical study of retinoblastoma

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Computer-simulation methods in human linkage analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Parameters of the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Avoiding recomputation in linkage analysis.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Statistical analysis of cytogenetic abnormalities in human cancer cells.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16911

Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.97.17.9603

Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations

21 January 2018

1 reference

12 December 2020

Molecular cytogenetics of primary breast cancer by CGH

1 reference

12 December 2020

Mapping loss of heterozygosity at chromosome 13q: loss at 13q12-q13 is associated with breast tumour progression and poor prognosis

1 reference

12 December 2020

Two distinct regions of deletion on chromosome 13q in primary nasopharyngeal carcinoma

1 reference

12 December 2020

Limiting the location of a putative human prostate cancer tumor suppressor gene at chromosome 13q14.3.

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.97.17.9603

1 reference

7 August 2017

0 references

1 reference

7 August 2017

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