(Q37344866)

19 August 2017

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer (English)

1 reference

19 August 2017

1 reference

16

Henrik Grönberg

1 reference

19 August 2017

Seong-Tae Kim

6

0 references

Jianfeng Xu

12

object named as

Jianfeng Xu

1 reference

19 August 2017

15

William B Isaacs

1 reference

19 August 2017

11

Pär Stattin

1 reference

19 August 2017

14

John D Carpten

1 reference

19 August 2017

17

S Lilly Zheng

1 reference

19 August 2017

9

Kathleen Wiley

1 reference

19 August 2017

7

Jielin Sun

1 reference

19 August 2017

8

Fredrik Wiklund

1 reference

19 August 2017

13

David Duggan

1 reference

19 August 2017

1

Wennuan Liu

1 reference

19 August 2017

Jishan Sun

2

1 reference

19 August 2017

Ge Li

3

1 reference

19 August 2017

Yi Zhu

4

1 reference

19 August 2017

Scott Zhang

5

1 reference

19 August 2017

Sarah D Isaacs

10

1 reference

19 August 2017

Bao-Li Chang

18

1 reference

19 August 2017

language of work or name

English

0 references

publication date

3 March 2009

1 reference

19 August 2017

1 reference

19 August 2017

69

1 reference

19 August 2017

6

1 reference

19 August 2017

2176-2179

1 reference

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Copy-number variation in control population cohorts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Population stratification of a common APOBEC gene deletion polymorphism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Global variation in copy number in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Fine-scale structural variation of the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Haploview: analysis and visualization of LD and haplotype maps

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Detection of large-scale variation in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Large-scale copy number polymorphism in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

The structure of haplotype blocks in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Characterization of a complex genomic alteration on chromosome 2p that leads to four alternatively spliced fusion transcripts in the neuroblastoma cell lines IMR-5, IMR-5/75 and IMR-32.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

A gene encoding a family with sequence similarity 84, member A (FAM84A) enhanced migration of human colon cancer cells.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Sequence variants of toll-like receptor 4 are associated with prostate cancer risk: results from the CAncer Prostate in Sweden Study

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Common deletion polymorphisms in the human genome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743179

Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19258504

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A high-resolution survey of deletion polymorphism in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19258504

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Germline copy number polymorphisms involving larger than 100 kb are uncommon in normal subjects

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19258504

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1158/0008-5472.CAN-08-3151

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

19258504

1 reference